Summary Statistic of Water quality characteristics of Samaru stream and standard values for water quality.
\r\n\tThe properties of metamaterials are designed not from the properties of their base materials, but rather from the metamaterial's newly designed structures. The precise shapes, geometries, sizes, orientations, and arrangements of metamaterial composing elements render metamaterials versatile ‘smart’ properties related to manipulating electromagnetic waves, by blocking, absorbing, enhancing, or bending waves of specific wavelengths. This allows achieving benefits extending far beyond what could be achieved by employing conventional materials.
\r\n\tMetamaterials have broad and diverse potential applications including optical filters, medical devices, remote aerospace devices and materials, sensors, infrastructure monitoring, highly effective management of solar power, high-frequency battlefield communication, lenses for high-gain antennas, shielding structures to prevent earthquake damage, acoustic materials, etc. Metamaterial research area is highly interdisciplinary: it involves electrical engineering, electromagnetics, classical optics, studies in the solid-state physics field, antenna engineering, optoelectronics, material science, nanoscience and nanotechnology, semiconductor design, and even can involve computational chemistry.
Water bodies are important economically, aesthetically and intellectually. The livelihood of many communities is hinged to the water bodies around them. Water bodies mirror the environment in which they are found and accumulate substances generated in their catchment (Yongendra and Puttaiah, 2008).
\n\t\t\tAssessment of water quality is very important for knowing its suitability for different uses (Choubey et al., 2008). Urbanization and rapidly growing human population results in an increase in waste water dischargeinto fresh water ecosystems, thus impairing water quality, sometimes to unacceptable levels, thereby, limiting its beneficial use (Tanimu et al., 2011).
\n\t\t\tThe contaminants in domestic sewage have been categorized by Wang et al. (2007) into Suspended Solids (SS) and dissolved solids (DS), organic matter (Chemical Oxygen Demand and Biochemical Oxygen Demand) and nutrients (nitrogen and phosphorus). Raw sewage can carry a number of pathogens including bacteria, viruses, protozoa, helminths (intestinal worms) and fungi (RMCG, Chigoret al., 2011).
\n\t\t\tThe Samaru stream is the major drain of domestic waste of Samaru village, several researchers have lamented the poor state of water quality in the stream Smith (1975), Tiseer et al. (2008 and 2008b), Olubgenga (2009), and Chigor et al. (2011). During a field visit to the Samaru stream in May 2010, the water in the stream was observed to be blackish in colour with an offensive odour due to sewage pollution. Therefore this study was carried out to evaluate water quality characteristics of the stream.
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Samples of water were collected in prewashed sample bottles and transported to the laboratory for analysis of other parameters. Dissolved Oxygen (DO) and Biochemical Oxygen Demand (BOD) were determined using the Azide Modification of the Winkler method, Nitrate-Nitrogen (NO3-N) was determined using the phenoldisulphonic acid method, Phosphate-Phosphorus using the Stannous Chloride method (all as described by APHA, 1998).
\n\t\t\tSample for metal analysis were digested by Nitric acid (HNO3) and the concentration of metals in the samples was determined by Atomic Absorption spectrophotometry (AAS)(APHA 1998).
\n\t\tWater Quality Index (WQI) was determined by methods described by Yogendra and Puttaiah (2008).
\n\t\t\tThe WQI of a water sample in which n number of parameters (characteristics) have been determined is expressed as a summation of the product of quality rating for the nth Water quality parameter (qn) and the unit weight of each parameter (Wn) divided by sum of the unit weights of all the (n) parameters (Wn).
\n\t\t\tMathematically: \n\t\t\t\t\t
qn= quality rating for the nth Water quality parameter, corresponding to the nth parameter is a number reflecting the relative value of this parameter in the polluted water with respect to its standard permissible value and is given by = 100(Vn-Vio)/(Sn-Vio)
\n\t\t\tVn= Estimated value of the nth parameter at a given sampling station.
\n\t\t\tSn= standard permissible value of the nth parameter.
\n\t\t\tVio= ideal value of the nth parameter in pure water (i.e. 0, for all parameters except pH, 7.0 and Dissolved Oxygen, 14.6 mg/L).
\n\t\t\tWn= unit weight of nth parameter = K/Sn\n\t\t\t
\n\t\t\tMetal Index (MI) for the concentration of n number of metals determined in a water sampleis given by the summation of the observed concentration of each metal divided by its Maximum Allowable Concentration (MAC).
\n\t\t\tMathematically \n\t\t\t\t\t
C = the concentration of each element in solution,
\n\t\t\tMAC is maximum allowed concentration for each element
\n\t\t\ti = the ith sample.
\n\t\t\tThe higher the concentration of a metal compared to its respective MAC value, the worse the quality of the water.
\n\t\t\tPearson Correlation Coefficient was used to determine the relationships between observed water quality characteristics.
\n\t\tThe mean pH of the water in the stream was found to be 7.68, with a maximum value of 8, minimum of 7.30 and a standard deviation 0.12 (Table 1). EC and TDS showed a similar trend across the stream cross, increasing from concentrations of 1000 to 1049 and 500 mg/L to 525 mg/L in stations 1 and 2, respectively and then decreasing steadily across stations 3, 4 and 5 (Fig 1). The mean EC was 816.20µS/cm with a standard Error of 134.71µS/cm while a mean of 409.80mg/L was recorded for TDS with a Standard Error of 134.71mg/L (Table 1).
\n\t\t\tDissolved Oxygen decreased from station 1 (0.85mg/L) to station 2 (0.25mg/L) and then increased steadily in stations 3 (0.3mg/L), 4(0.4mg/L) and 5 (0.85mg/L) (Fig 2). Biochemical Oxygen Demand declined from station 1 (0.4mg/L), 2 (0.25mg/L), 3 and 4 (0.05mg/L) and then a slight increase in station 5 (0.1mg/L) Fig 2). Table 1 shows mean and standard errors for DO and BOD of 0.53,013 and 0.17, 0.07 respectively.
\n\t\t\tNO3-N increased from station 1 to 2, decreased in 3 and then increased and decreased in stations 4 and 5 in a zigzag manner giving a similar trend with PO4-P concentration in the five (5) stations. (Fig.2). the maximum NO3-N concentration observed was 3.80mg/L and a lowest of 0.90mg/L. PO4-P mean concentration observed in the stream was 0.44mg/L with a standard error of 0.17.
\n\t\t\tSurface Water Temperature had the highest value of 31°C and lowest of 27°C, Cu and Cr had concentrations below detectable limits (Table 1). Zn, Ni and Cd showed a similar concentrations gradient from station 1 to 5 while Fe showed an opposite trend with the other metals, decreasing in concentration were the others increase and increasing where they decrease (Fig 3). Among the four (4) metals, only Zn concentration was within the acceptable limits (Table 1).
\n\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t7.68 | \n\t\t\t\t\t\t0.12 | \n\t\t\t\t\t\t7.30 | \n\t\t\t\t\t\t8.00 | \n\t\t\t\t\t\t< 8 | \n\t\t\t\t\t\tWHO | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t816.20 | \n\t\t\t\t\t\t134.71 | \n\t\t\t\t\t\t298.00 | \n\t\t\t\t\t\t1049.00 | \n\t\t\t\t\t\t1000.00 | \n\t\t\t\t\t\tWHO | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t409.80 | \n\t\t\t\t\t\t67.55 | \n\t\t\t\t\t\t149.00 | \n\t\t\t\t\t\t525.00 | \n\t\t\t\t\t\t500.00 | \n\t\t\t\t\t\tWHO | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t0.53 | \n\t\t\t\t\t\t0.13 | \n\t\t\t\t\t\t0.25 | \n\t\t\t\t\t\t0.85 | \n\t\t\t\t\t\t5.00 | \n\t\t\t\t\t\tWHO | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t0.17 | \n\t\t\t\t\t\t0.07 | \n\t\t\t\t\t\t0.05 | \n\t\t\t\t\t\t0.40 | \n\t\t\t\t\t\t5.00 | \n\t\t\t\t\t\tWHO | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t2.58 | \n\t\t\t\t\t\t0.55 | \n\t\t\t\t\t\t0.90 | \n\t\t\t\t\t\t3.80 | \n\t\t\t\t\t\t10.00 | \n\t\t\t\t\t\tWHO | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t0.44 | \n\t\t\t\t\t\t0.17 | \n\t\t\t\t\t\t0.02 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t5.00 | \n\t\t\t\t\t\tWHO | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t29.20 | \n\t\t\t\t\t\t0.66 | \n\t\t\t\t\t\t27.00 | \n\t\t\t\t\t\t31.00 | \n\t\t\t\t\t\tNA | \n\t\t\t\t\t\tNA | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t0.47 | \n\t\t\t\t\t\t0.12 | \n\t\t\t\t\t\t0.29 | \n\t\t\t\t\t\t0.89 | \n\t\t\t\t\t\t0.30 | \n\t\t\t\t\t\tSON | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\tSON | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\tBDL | \n\t\t\t\t\t\t0.05 | \n\t\t\t\t\t\tSON | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t0.39 | \n\t\t\t\t\t\t0.05 | \n\t\t\t\t\t\t0.25 | \n\t\t\t\t\t\t0.56 | \n\t\t\t\t\t\t3.00 | \n\t\t\t\t\t\tSON | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t0.40 | \n\t\t\t\t\t\t0.04 | \n\t\t\t\t\t\t0.33 | \n\t\t\t\t\t\t0.50 | \n\t\t\t\t\t\t0.02 | \n\t\t\t\t\t\tSON | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t0.09 | \n\t\t\t\t\t\t0.02 | \n\t\t\t\t\t\t0.06 | \n\t\t\t\t\t\t0.16 | \n\t\t\t\t\t\t0.003 | \n\t\t\t\t\t\tSON | \n\t\t\t\t\t
EC= Electrical Conductivity, TDS= Total Dissolved Solids, DO= Dissolved Oxygen, BOD= NO3-N= Nitrate-Nitrogen, PO4-P= Phosphate-Phosphorus, Temp.= Temperature, BDL= Below Detectable Limit, SON= Standard Organisation of Nigeria, NA= not available | \n\t\t\t\t\t
Summary Statistic of Water quality characteristics of Samaru stream and standard values for water quality.
Variation of Electrical Conductivity and Total Dissolved Solids in Samaru stream.
Variation of concentration of Dissolved Oxygen, Biochemical Oxygen Demand, Nitrate-Nitrogen and Phosphate-Phosphorus in Samaru stream.
Variation of concentration of Fe, Zn, Ni and Cd in Samaru stream.
The Water quality index and Metal Index showed a similar pattern of distribution in Stations 1 to 4, increasing from 52.45 and 38.1 (station 1) to 58.95 and 56.11 (station 2) decreasing to 55.25 and 49.51 (station 3) and, 48.31 and 37.65 (station 4). In station 5, the lowest WQI of 45.03 was observed while in contrast station 5 recorded the highest MI value of 79.38 (Table 2).
\n\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t52.45 | \n\t\t\t\t\t\t38.5 | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t58.95 | \n\t\t\t\t\t\t56.11 | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t55.25 | \n\t\t\t\t\t\t49.51 | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t48.31 | \n\t\t\t\t\t\t37.65 | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t45.03 | \n\t\t\t\t\t\t79.38 | \n\t\t\t\t\t
Water Quality and Metal Indices of the five sampling stations in Samaru stream.
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\tExcellent water quality | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\tGood water quality | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\tPoor water quality | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\tVery Poor Water quality | \n\t\t\t\t\t
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\tUnsuitable for drinking | \n\t\t\t\t\t
Water Quality Index and water quality status (Yogendra and Puttaiah 2008).
Significant positive correlation was observed between Fe concentration and pH (r=0.76)(P<0.01); Electrical Conductivity and BOD (r=0.46)(P<0.05), NO3-N (r=0.83)(P<0.01), Surface Water Temperature (0.68)(P<0.05) and Zn (0.57)(P<0.05); TDS with BOD (r=0.45)(P<0.05) and N03-N (r=0.83)(p<0.01), Surface Water Temperature (0.69)(P<0.01) and Zn (r=0.58)(P<0.01); DO with BOD (r=0.40)(p<0.05); N03-N with P04-P (r=0.56), Temperature (r=0.69)(P<0.01) and Zn (r=0.82)(P<0.01); PO4-P with Zn (r=0.62)(P<0.01) and Ni (r=0.50)(P<0.05); Temperature with Zn (r=0.86)(P<0.01); and Ni with Cd (r=0.74)(p<0.01)(Table 4).
\n\t\t\tSignificant negative correlation was observed between EC and DO (r=-0.53)(P<0.05), Ni (r=-0.43)(P<0.05) and Cd (r=0.89)(P<0.01); TDS with DO (r=-0.53)(P<0.05), NI (r=-0.44)(P<0.05) and Cd (r=-0.89)(0.01); DO with NO3-N (r=-0.50)(P<0.05), PO4-P (r=-73)(0.01), Surface Water Temperature (r=-0.64)(P<0.01) and Zn (r=-0.73)(P<0.01); NO3-N with Cd (r=-0.80)(P<0.01); PO4-P and Fe (r=-0.52)(P<0.05); Surface Water Temperature with Ni (r=-0.74)(P<0.01) and Cd (r=-0.83)(P<0.01); Fe with Ni (r=-0.60)(P<0.01); and Zn with Cd (r=-0.64)(P<0.01)(Table 4).
\n\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\t | \n\t\t\t\t\t
pH | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
EC | \n\t\t\t\t\t\t0.37 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
TDS | \n\t\t\t\t\t\t0.36 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
DO | \n\t\t\t\t\t\t-0.23 | \n\t\t\t\t\t\t-0.53* | \n\t\t\t\t\t\t-0.53* | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
BOD | \n\t\t\t\t\t\t0.34 | \n\t\t\t\t\t\t0.46* | \n\t\t\t\t\t\t0.45* | \n\t\t\t\t\t\t0.40* | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t-0.19 | \n\t\t\t\t\t\t0.83** | \n\t\t\t\t\t\t0.83** | \n\t\t\t\t\t\t-0.50* | \n\t\t\t\t\t\t0.26 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
\n\t\t\t\t\t\t\t | \n\t\t\t\t\t\t-0.15 | \n\t\t\t\t\t\t0.30 | \n\t\t\t\t\t\t0.30 | \n\t\t\t\t\t\t-0.73** | \n\t\t\t\t\t\t-0.20 | \n\t\t\t\t\t\t0.56* | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
Temp. | \n\t\t\t\t\t\t-0.05 | \n\t\t\t\t\t\t0.68* | \n\t\t\t\t\t\t0.69** | \n\t\t\t\t\t\t-0.64** | \n\t\t\t\t\t\t-0.24 | \n\t\t\t\t\t\t0.69** | \n\t\t\t\t\t\t0.21 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
Fe | \n\t\t\t\t\t\t0.76** | \n\t\t\t\t\t\t0.21 | \n\t\t\t\t\t\t0.21 | \n\t\t\t\t\t\t-0.15 | \n\t\t\t\t\t\t-0.05 | \n\t\t\t\t\t\t-0.31 | \n\t\t\t\t\t\t-0.52* | \n\t\t\t\t\t\t0.27 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t |
Zn | \n\t\t\t\t\t\t-0.35 | \n\t\t\t\t\t\t0.57* | \n\t\t\t\t\t\t0.58* | \n\t\t\t\t\t\t-0.73** | \n\t\t\t\t\t\t-0.33 | \n\t\t\t\t\t\t0.82** | \n\t\t\t\t\t\t0.62** | \n\t\t\t\t\t\t0.86** | \n\t\t\t\t\t\t-0.21 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | \n\t\t\t\t\t |
NI | \n\t\t\t\t\t\t-0.10 | \n\t\t\t\t\t\t-0.43* | \n\t\t\t\t\t\t-0.44* | \n\t\t\t\t\t\t0.06 | \n\t\t\t\t\t\t0.03 | \n\t\t\t\t\t\t-0.25 | \n\t\t\t\t\t\t0.50* | \n\t\t\t\t\t\t-0.74** | \n\t\t\t\t\t\t-0.60** | \n\t\t\t\t\t\t-0.33 | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t\t\n\t\t\t\t\t |
Cd | \n\t\t\t\t\t\t-0.11 | \n\t\t\t\t\t\t-0.89** | \n\t\t\t\t\t\t-0.90** | \n\t\t\t\t\t\t0.34 | \n\t\t\t\t\t\t-0.33 | \n\t\t\t\t\t\t-0.80** | \n\t\t\t\t\t\t-0.03 | \n\t\t\t\t\t\t-0.83** | \n\t\t\t\t\t\t-0.23 | \n\t\t\t\t\t\t-0.64** | \n\t\t\t\t\t\t0.74** | \n\t\t\t\t\t\t1.00 | \n\t\t\t\t\t
EC= Electrical Conductivity, TDS= Total Dissolved Solids, Temp.= Surface Water Temperature, DO= Dissolved Oxygen, BOD = Biochemical Oxygen Demand, PO4-P= Phosphate-Phosphorus, N03-N = Nitrate-Nitrogen, *Significant P<0.05, **Significant P<0.01 | \n\t\t\t\t\t
Pearson Correlation Coefficient of physicochemical characteristics of water of Samaru stream.
On the basis of water Quality Index, stations 1, 2 and 3 (upstream stations) may be classified to be of poor water quality, whereas stations 4 and 5 may be classified to be of good water quality. The trend where downstream stations are of a better water quality when the source of pollution is upstream may be explained by the role bacteria, algae and aquatic macrophytes play in ultra filtration of polluted water as it flows from upstream-down stream. Similar results have been reported Tiseer et al., (2008a) and Taurai (2012).
\n\t\t\tThe mean metal concentration of Fe, Ni and Cd observed were above the permissible limit in drinking water (SON, 2007), while the high metal index observed in the stream may be a great indication that the sewage entering the stream contains a high concentration of heavy metals. The higher MI observed in station 5 may be as a result of pollution from the University Press and/or the dumpsite behind Icsa/Ramat Halls.
\n\t\t\tAbolude et al., (2009) reported that concentrations of seven (7) out of the nine (9) studied trace elements (including Fe, Ni and Cd) in the Kubanni reservoir were above the recommended levels for drinking water, the present study implicates the Samaru stream to be an important contributor to the problem.
\n\t\t\tThe significant relationships observed between pH and Surface Water Temperature and parameters such as DO, PO4-P, NO3-N, EC, TDS, Fe, Zn, Ni, Cd may be attributed to the reason that the solubility of this chemical substances in water is affected by pH and Temperature.
\n\t\t\tMeasures are required to be taken to halt the continuous inflow of sewage into the Samaru stream from the Samaru village and the some student hostels (Danfodio, Sasakawa and Icsa/Ramat) of the Ahmadu Bello University, Zaria to reduce or totally eliminate the continuous pollution of water in the Samaru stream and the University reservoir by extension.
Pain is an unpleasant sensation that can range from slight discomfort to excruciating agony and can be linked to actual or potential tissue damage [1]. It is a multimodal and biopsychosocial event with an individual objective and subjective occurrences, resulting in significantly diverse perceptions of pain between the individuals. One of the most common reasons for a patient to visit an endodontist is dental pain. Managing dental pain and anxiety during and after treatment is still a difficult task, which depends on the clinician’s skill and knowledge [2].
In symptomatic pulp tissue diagnosed with irreversible pulpitis, extracellular levels of Substance P are elevated. When comparing pulp tissue diagnosed with irreversible pulpitis to clinically normal pulp tissue, an 8-fold rise in Substance P was found [3]. As a result, irreversible pulpitis is linked to high peptidergic system activation. It is generally known that root canal preparation causes inflammation in the periapical tissues, explaining why root canal therapy causes post-treatment pain (such as symptomatic apical periodontitis). SP is released in the periodontal ligaments as a result of varied canal preparation approaches, which was found to be quite interesting. However, the amount of released SP differs among procedures. Inflammation in the periapical tissues could be triggered by an elevation in SP [4]. This might thus be considered a key mediator of neurogenic inflammation and related hyperalgesia, and hence a prospective target for therapeutics targeted at regulating pain and minimizing the harmful effects of tissue injury [5].
When a carious lesion gets close to the pulp, the pulp’s inflammatory alterations get worse. An acute exacerbation of chronic inflammation occurs at this stage, with an influx of neutrophils and the release of inflammatory mediators (prostaglandins and interleukins), proinflammatory neuropeptides and mediators (substance P, Bradykinin, and calcitonin gene related peptide) [6]. These mediators can increase pain perception and neuronal excitability by stimulating peripheral nociceptors within the pulp of the affected tooth. This causes moderate-to-severe discomfort. Conventional procedures may not provide sufficient anesthesia. As a result, endodontists must achieve profound anesthesia in order to alleviate the pain [7].
The use of local anesthetic agents in pain management plays a vital role. It is the safest and most effective medications to prevent and manage pain during dental treatment [8]. Today’s availability of a variety of local anesthetic agents allows dentists to choose an anesthetic with specific properties such as time of onset and duration, hemostatic control, and degree of cardiac side effects that are suited for each individual patient and dental operation [9]. 2 percent lignocaine (Xylotox, Adcock Ingram; Xylesthesin, 3 M) with 1:80000 adrenaline content, 3 percent mepivacaine (Carbocaine) without a vasoconstrictor and 4 percent articaine (Ubistesin 3 M) with either 1:100000 or 1:200000 adrenaline concentration is currently the most commonly used local anesthetic agents in general dentistry [10]. Each local anesthetic has its own maximum recommended dose (MDR) measured in mg/kg body weight. Unfortunately, the literature7 shows that the mg/kg MDR for each drug ranges from 4.4 mg/kg 8 to 6.6 mg/kg [11, 12].
When dealing with a tooth that has been diagnosed with irreversible pulpitis or “Hot” tooth, it’s critical to determine whether enough local anesthetic has been attained. Subjective and objective testing has historically been used to validate successive inferior alveolar nerve block (IANB). Signs such as lip numbness, probing the gingiva surrounding the tooth to be treated, and so forth are examples of subjective tests [13]. Patients should not suffer discomfort throughout therapy if they respond favorably to the subjective results. These approaches, however, are not confirmatory test for detecting pulpal anesthesia.
While it’s possible that the operator’s inability to deposit anesthetic solution close to the targeted nerve would result in an insufficient blockade in both normal and non-inflamed states, it’s also possible that a partial blockade would suffice in neurons that inflammatory mediators did not sensitize. It’s crucial to understand the nerve supply to the anesthetized tissue and the anatomy of the injection site and any changes [14].
During a local infiltration at the root apex, however, the cortical bone of the body of the mandible can effectively block the anesthetic. The maxillary cortical bone is often thinner. Anesthetic diffusion is more easily achieved through this bone. Therefore, infiltration anesthesia, which is routinely used in the maxilla, would be less affected by anatomic variance. Block anesthesia is advised in the mandible because it is more predictable. Still, it demands a deeper awareness of the deep anatomy of the jaw and is more technique sensitive, which is why anesthetic failures in the mandible are more common. Inadequate local anesthetic has also been linked to accessory innervation of the mandibular teeth from various sources. The nerve to the mylohyoid muscle, in particular, has been linked to the transport of afferent fibers from the mandibular teeth [14]. The clinician has many alternatives for overcoming accessory innervations from the mylohyoid nerve, including using a blocking technique that deposits anesthetic solution higher in the pterygomandibular space.
The pH of the anesthetic solution determines the ratio of RN to RNH+. According to the Henderson–Hasselbalch equation, there are equal amounts of half-charged and half-uncharged molecules when the acid dissociation constant Pka equals the pH of the solution. In a cartridge of local anesthetic solution, both charged (RNH+) and uncharged (RN) molecules exist in equilibrium. The deionized lipid-soluble (RH) form penetrates the neuronal membrane and takes up H+. RNH+ within the nerve, resulting in RNH+, which enters the sodium channel and blocks conduction. To produce anesthesia, the body buffers the pH-injected anesthetic solution to the physiological pH [15].
This becomes potentially critical since inflammation-induced tissue acidosis can cause local anesthetics to get “ion trapped.” According to this theory, the low tissue pH causes a higher proportion of the local anesthetic to be held in the charged acid form of the molecule, preventing it from passing through cell membranes. This theory has been proposed as a primary cause of local anesthetic failures in situations like endodontic pain [16].
Local anesthetic failures may be exacerbated by central sensitization. Increased sensitivity may enhance incoming sensory nerve impulses. There is a significant response to peripheral stimuli in central sensitization, and as a result, the IANB may allow adequate signaling to occur, leading to the experience of pain [16].
According to this hypothesis, the nerves on the exterior of the nerve bundle supply the molar teeth, while the nerves on the inside supply the anterior teeth. Even if the anesthetic solution is placed in the right location, it may not disperse enough into the nerve trunk to reach all nerves and cause a sufficient block. This concept may only apply to the increased failure rates associated with IANB in the anterior teeth, not the posterior teeth [17].
The Tetrodoxin resistant channels (TTXr) family of sodium channels have been demonstrated to be resistant to the effects of local anesthesia. Anesthetic failures in a hot tooth are caused by increased expression of sodium channels in the pulp. The TTXr channels are resistant to lidocaine, resulting in insufficient anesthetic [18]. TTXr channels are expressed on nociceptors, and their activation with Prostaglandin E2 is relatively resistant to lidocaine. Because they are less susceptible to lidocaine, sodium channels that are resistant to TTX. As the concentration of lidocaine rises, the sodium channels get blocked [19].
Inflamed tissue nerves have a lower excitability threshold and an altered resting potential. Lower excitability thresholds are responsible for impulse transmission [20].
Anxiety in the patient may also play a role in the local anesthetic failure. Clinicians who have worked with anxious patients know that they have a lower pain threshold and are more likely to complain about an unpleasant dental experience. The sight of a needle and the sound of the dental handpiece are frequently reported as causes of anxiety in patients. Furthermore, patients may be particularly apprehensive about root canal therapy.
Inflammation has several additional consequences on the physiology of local tissues. Inflammatory mediators cause peripheral vasodilation, which increases the rate of systemic absorption, lowering the concentration of local anesthetics. Local anesthetics, in most circumstances, need formulation with vasoconstrictor drugs. Thus, this is a potentially relevant mechanism. Although regional variations in blood flow occur in inflamed dental pulp, little is known regarding inflammation-induced vascular alterations in periradicular tissue [21]. Furthermore, this vasodilation is likely to be confined and not seen at distant injection sites. As a result, compared to nerve block anesthesia, this concept may be more useful in understanding issues with infiltration anesthesia.
Inflammation alters the production of many proteins in nociceptors, resulting in a rise in neuropeptides such substance P and calcitonin gene-related peptide. These neuropeptides have an essential role to perform have a role in regulating pulpal inflammation. Furthermore, tissue damage can change the composition, distribution, and activity of sodium channels expressed on the nociceptors. Inflammation’s effect on these sodium channels might substantially impact local anesthetic failures [22].
Tachyphylaxis is a condition in which a receptor agonist medication causes a reduction in responsiveness to a subsequent dose of the drug. Because local anesthetics are frequently used in conjunction with vasoconstrictors, the medication may remain in the tissue long enough to trigger tachyphylaxis at the sodium channel. This has been suggested as a factor in decreased anesthetic efficacy, particularly after many administrations [21].
Contrary to popular belief, most moderate-duration anesthetics are equally efficient in inducing deep pulpal anesthetic for root canal treatment. Understanding the anatomical, local, and psychological aspects of each patient against the type of anesthetic utilized is critical to success. Most dentists prefer to employ a combination of anesthetics and a vasoconstrictor. When some types of anesthetic drugs are used, it is possible that the patients would experience more pain. Because of the acidic nature of local anesthetics, lower pH values are considered to produce a burning sensation during injection [23].
The injection location might influence injection discomfort. According to one study, maxillary buccal injections with plain 2% lidocaine Was found to be considerably less discomfort than 2% lidocaine with 1:80000 epinephrine. However, using the same anesthetic drugs, no difference in injection discomfort was recorded at the palatal location [12]. The type of anesthetic solution has little effect on injection discomfort when a location with less connective tissue (such as the palatal site in the maxilla) is injected. Faster injection speed leads to increased drug distribution. It has been proposed that a speed of injection exposes a larger portion of a nerve to the anesthetic solution, resulting in a higher rate of local anesthesia success. The rapid injections, on the other hand, produced more pain and discomfort during the procedure [23, 24, 25].
In individuals with symptomatic irreversible pulpitis, the degree of preoperative pain might impact anesthetic success. The activation of nociceptors during inflammation might be one reason for the lower success rate of inflamed pulp. The peripheral and central pain pathways are altered and modulated by the barrage of painful stimuli, as well as tissue destruction. Another reason for failure is that nerves from inflamed tissue have reduced excitability thresholds and altered resting potentials [26].
Inflamed pulps may have more tetrodotoxin-resistant sodium channels, which are resistant to local anesthetics. Prostaglandins, which can influence tetrodotoxin-resistant receptors and reduce nerve responses to anesthetic drugs, have also risen considerably in inflamed pulps [27]. As a result, premedication with nonsteroidal anti-inflammatory medicines (NSAIDs) and corticosteroids to increase anesthetic success appear to be a viable option. However, the findings of such research do not agree on the effectiveness of premedication on anesthetic success [28, 29]. However, if the patient does not have spontaneous pain, pre-treatment with particular types of NSAIDs may improve the effectiveness of anesthesia when treating irreversible pulpitis [30]. Premedication with corticosteroids before anesthesia with an inferior alveolar nerve block (IANB) injection resulted in a considerably better success rate.
Genetics may play a role in predisposing specific individuals to problems such as discomfort, delayed healing, and abscess development. A range of genetic variations influences pain perception and behavior. Pain becomes significantly more common in women, and various explanations have been proposed, including hormonal and genetically driven sex variations in brain neurochemistry [27].
Intraligamentary anesthesia is a technique wherein local anesthetic solution administered via the periodontal ligament to reach the pulpal nerve supply. The use of conventional or customized syringes can be used for this technique. At the mesiobuccal aspect, the needle is placed as deeply between the root surface and alveolar bone at a 30° angle to the long axis of the tooth. The needle can be placed with the bevel pointing in either direction, and 0.2 ml of the solution should be injected per root using back pressure. For 5 to 10 seconds, the needle is held in place [31]. The anesthetic action begins almost immediately and lasts for around 15–20 minutes [32].
In comparison to other anesthetic techniques, Intraligamentary anesthesia allows for a substantial reduction in the overall volume of anesthetic solution and vasoconstrictor supplement. At the same time, the unintentional intravascular application is avoided [33]. Furthermore, the effectiveness of Intraligamentary anesthesia is limited in cases of severe marginal periodontitis or teeth with a sclerotic periodontal gap, and alternate anesthetic methods such as inferior alveolar nerve block can be advised [32].
Intraosseous Anesthesia is more invasive and necessitates the use of specialist equipment, such as a perforator (e.g., Stabident, X-Tip). The gingiva must first be sedated for the perforator to penetrate without discomfort. A slow-speed handpiece is used to move the perforator into the anesthetic gingiva and bone until the cancellous bone is felt like a sharp dip. The perforator is then withdrawn, and a small 27-gauge needle is introduced through the perforation, injecting approximately 1 mL of solution over 2 minutes. It’s one of the most effective supplemental methods available [34]. The intraosseous injection permits the local anesthetic solution to be injected directly into the cancellous bone adjacent to the tooth that has to be sedated [35]. The intraosseous anesthetic onset of anesthesia is immediate and lasts for around 15 to 30 minutes, and was found to be more efficient than intraligamentary anesthesia [36].
After a failed IANB, buccal infiltration has been utilized as a supplemental anesthetic for anesthetizing mandibular molar teeth, especially in symptomatic irreversible pulpitis. A mandibular buccal infiltration injection of 4% articaine with 1:100,000 epinephrine as an additional injection to improve the effectiveness of the IANB injection has recently been investigated. The usage of the articaine solution was shown to be better than the lidocaine solution in asymptomatic individuals (88 percent vs. 71 percent, respectively) [37]. Only 58% anesthesia was achievable with buccal infiltration injection when used as a supplement to the IANB in case of symptomatic irreversible pulpitis [38].
Intrapulpal anesthesia is one of the supplementary anesthesia that is beneficial, especially in a hot tooth. The most crucial aspect of this technique is to pump the fluid into the pulp forcefully. If the physician does not feel pressure or resistance to injection, the solution is not reaching the pulp and is most likely running out of the pulp chamber and back into the access cavity [39]. However, this type of anesthesia is excruciating and should only be used as the last option during endodontic therapy. Intrapulpal anesthesia has the drawback of having a limited duration of effect. As a result, it’s critical to remove the pulp from all of the root canals as soon as possible after injection to avoid repeated injection [40]. It is necessary that the patient should be informed that the type of anesthesia will cause moderate to severe discomfort in the beginning.
Buffered local anesthesia technique to one of the techniques to improve the efficiency of the local anesthetics. Alkalinization accelerates the dissociation of the LA molecule, increasing in the uncharged base form that penetrates the nerve membrane and acts in the intraneuronal location. The addition of sodium bicarbonate is the most frequent technique for buffering LAs. The addition of sodium bicarbonate to local anesthetics reacts to form sodium chloride water and carbon dioxide. Alkalinization with sodium bicarbonate raise the pH of the solution. Carbon dioxide produces an independent anesthetic effect by changing the local anesthetic inside the nerve direct depressant effect of carbon dioxide on the nerve axon [41]. 50 mEq is the maximum dose of sodium bicarbonate. 20 ml of 1 or 2% lignocaine is recommended to be added with 2 ml of 8.4 percent sodium bicarbonate. The ratio of lignocaine to bicarbonate should be between 5:1 and 10:1 for best effects. If the bicarbonate level exceeds this ratio, precipitation may occur. In individuals with metabolic acidosis and hypocalcemia, this method is contraindicated [15].
Pain being the most common symptom, every effort should be made to manage it during and after root canal treatment and should be informed priorly the type of anesthesia administered to the patient. Although various anesthetic agents and techniques are available, the choice of them is specific and customized to each patient and their preoperative status and clinical condition. So, ultimately, the clinician should critically decide on a specific agent or a technique for the clinical condition of the patient. It is necessary to provide appropriate pulpal anesthesia when treating teeth with irreversible pulpitis.
The authors declare no conflict of interest.
IntechOpen implements a robust policy to minimize and deal with instances of fraud or misconduct. As part of our general commitment to transparency and openness, and in order to maintain high scientific standards, we have a well-defined editorial policy regarding Retractions and Corrections.
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\\n\\n1. RETRACTIONS
\\n\\nA Retraction of a Chapter will be issued by the Academic Editor, either following an Author’s request to do so or when there is a 3rd party report of scientific misconduct. Upon receipt of a report by a 3rd party, the Academic Editor will investigate any allegations of scientific misconduct, working in cooperation with the Author(s) and their institution(s).
\\n\\nA formal Retraction will be issued when there is clear and conclusive evidence of any of the following:
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\\n\\n1.2. REMOVALS AND CANCELLATIONS
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\\n\\nA Statement of Concern detailing alleged misconduct will be issued by the Academic Editor or publisher following a 3rd party report of scientific misconduct when:
\\n\\nIntechOpen believes that the number of occasions on which a Statement of Concern is issued will be very few in number. In all cases when such a decision has been taken by the Academic Editor the decision will be reviewed by another editor to whom the author can make representations.
\\n\\n3. CORRECTIONS
\\n\\nA Correction will be issued by the Academic Editor when:
\\n\\n3.1. ERRATUM
\\n\\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
\\n\\nA published Erratum will adhere to the Retraction Notice publishing guidelines outlined above.
\\n\\n3.2. CORRIGENDUM
\\n\\nA Corrigendum will be issued by the Academic Editor when it is determined that a mistake in a Chapter is a result of an Author’s miscalculation or oversight. A published Corrigendum will adhere to the Retraction Notice publishing guidelines outlined above.
\\n\\n4. FINAL REMARKS
\\n\\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\\n\\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\\n\\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
\\n\\nAny suggestions or comments on this Policy are welcome and may be sent to permissions@intechopen.com.
\\n\\nPolicy last updated: 2017-09-11
\\n"}]'},components:[{type:"htmlEditorComponent",content:'IntechOpen’s Retraction and Correction Policy has been developed in accordance with the Committee on Publication Ethics (COPE) publication guidelines relating to scientific misconduct and research ethics:
\n\n1. RETRACTIONS
\n\nA Retraction of a Chapter will be issued by the Academic Editor, either following an Author’s request to do so or when there is a 3rd party report of scientific misconduct. Upon receipt of a report by a 3rd party, the Academic Editor will investigate any allegations of scientific misconduct, working in cooperation with the Author(s) and their institution(s).
\n\nA formal Retraction will be issued when there is clear and conclusive evidence of any of the following:
\n\nPublishing of a Retraction Notice will adhere to the following guidelines:
\n\n1.2. REMOVALS AND CANCELLATIONS
\n\n2. STATEMENTS OF CONCERN
\n\nA Statement of Concern detailing alleged misconduct will be issued by the Academic Editor or publisher following a 3rd party report of scientific misconduct when:
\n\nIntechOpen believes that the number of occasions on which a Statement of Concern is issued will be very few in number. In all cases when such a decision has been taken by the Academic Editor the decision will be reviewed by another editor to whom the author can make representations.
\n\n3. CORRECTIONS
\n\nA Correction will be issued by the Academic Editor when:
\n\n3.1. ERRATUM
\n\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
\n\nA published Erratum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n3.2. CORRIGENDUM
\n\nA Corrigendum will be issued by the Academic Editor when it is determined that a mistake in a Chapter is a result of an Author’s miscalculation or oversight. A published Corrigendum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n4. FINAL REMARKS
\n\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\n\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\n\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
\n\nAny suggestions or comments on this Policy are welcome and may be sent to permissions@intechopen.com.
\n\nPolicy last updated: 2017-09-11
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The Gram-positive pathogen is armed with battery of virulence factors that facilitate to establish infections in the hosts. The organism is well known for its ability to acquire resistance to various antibiotic classes. The emergence and spread of methicillin-resistant S. aureus (MRSA) strains which are often multi-drug resistant in hospitals and subsequently in community resulted in significant mortality and morbidity. The epidemiology of MRSA has been evolving since its initial outbreak which necessitates a comprehensive medical approach to tackle this pathogen. Vancomycin has been the drug of choice for years but its utility was challenged by the emergence of resistance. In the last 10 years or so, newer anti-MRSA antibiotics were approved for clinical use. However, being notorious for developing antibiotic resistance, there is a continuous need for exploring novel anti-MRSA agents from various sources including plants and evaluation of non-antibiotic approaches.",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Arumugam Gnanamani, Periasamy Hariharan and Maneesh Paul-\nSatyaseela",authors:[{id:"192829",title:"Dr.",name:"Arumugam",middleName:null,surname:"Gnanamani",slug:"arumugam-gnanamani",fullName:"Arumugam Gnanamani"},{id:"204388",title:"Dr.",name:"Periasamy",middleName:null,surname:"Hariharan",slug:"periasamy-hariharan",fullName:"Periasamy Hariharan"},{id:"204389",title:"Dr.",name:"Maneesh",middleName:null,surname:"Paul-Satyaseela",slug:"maneesh-paul-satyaseela",fullName:"Maneesh Paul-Satyaseela"}]},{id:"53782",doi:"10.5772/66645",title:"Methicillin-Resistant Staphylococcus aureus (MRSA) in Food- Producing and Companion Animals and Food Products",slug:"methicillin-resistant-staphylococcus-aureus-mrsa-in-food-producing-and-companion-animals-and-food-pr",totalDownloads:2743,totalCrossrefCites:8,totalDimensionsCites:16,abstract:"Methicillin-resistant Staphylococcus aureus (MRSA) has become a growing concern in companion and food-producing animals. The presence of multidrug-resistance with a wide range of extracellular enterotoxin genes, virulence factors, and Panton-Valentine leukocidin (pvl) cytotoxin genes confer life-threatening traits on MRSA and makes them highly pathogenic and difficult to treat. Clonal complex 398 (CC398), a predominant clonal lineage of livestock-associated-MRSA in domestic animals and retail meat, is capable of infecting humans. In order to monitor and prevent MRSA contamination, it is critical to understand its source and transmission dynamics. In this review, we describe MRSA in food-producing animals (pig, cattle, chicken), horses, pet animals (dogs, cats), and food products (pork, beef, chicken, milk, and fish).",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Jungwhan Chon, Kidon Sung and Saeed Khan",authors:[{id:"189634",title:"Dr.",name:"Kidon",middleName:null,surname:"Sung",slug:"kidon-sung",fullName:"Kidon Sung"},{id:"190400",title:"Dr.",name:"Jungwhan",middleName:null,surname:"Chon",slug:"jungwhan-chon",fullName:"Jungwhan Chon"},{id:"190401",title:"Dr.",name:"Saeed",middleName:null,surname:"Khan",slug:"saeed-khan",fullName:"Saeed Khan"}]},{id:"52755",doi:"10.5772/65978",title:"Bee Products and Essential Oils as Alternative Agents for Treatment of Infections Caused by S. aureus",slug:"bee-products-and-essential-oils-as-alternative-agents-for-treatment-of-infections-caused-by-s-aureus",totalDownloads:1916,totalCrossrefCites:4,totalDimensionsCites:8,abstract:"Bacteria of the genus Staphylococcus are important human and veterinary pathogens. A crucial characteristic for this group of bacteria is that they can easily acquire mechanisms of antibiotic resistance for a plethora of antibiotics currently in use for human and animal therapies. Therefore, there is a great need to find novel, non-antibiotic chemotherapeutics with marked antistaphylococcal activity. Promising but still underestimated group of potential antistaphylococcal chemotherapeutics constitute bee products: honey, pollen, royal jelly, fermented pollen and especially propolis. Another group of natural products that exhibit promising antibacterial activity is essential oils. Usefulness of bee products and essential oils in the treatment of infections caused by S. aureus has been confirmed by results of many investigations carried out by researches in different regions of the world. In this chapter, we have presented the review of publication in this area as well as perspectives and limitations of future applications of these two groups of natural products.",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Piotr Szweda and Barbara Kot",authors:[{id:"117528",title:"Dr.",name:"Szweda",middleName:null,surname:"Piotr",slug:"szweda-piotr",fullName:"Szweda Piotr"},{id:"189685",title:"Associate Prof.",name:"Barbara",middleName:null,surname:"Kot",slug:"barbara-kot",fullName:"Barbara Kot"},{id:"195004",title:"Dr.",name:"Barbara",middleName:null,surname:"Kot",slug:"barbara-kot",fullName:"Barbara Kot"}]},{id:"52875",doi:"10.5772/65761",title:"Bacteriophage Therapy: An Alternative for the Treatment of Staphylococcus aureus Infections in Animals and Animal Models",slug:"bacteriophage-therapy-an-alternative-for-the-treatment-of-staphylococcus-aureus-infections-in-animal",totalDownloads:1987,totalCrossrefCites:4,totalDimensionsCites:7,abstract:"Staphylococcus aureus causes hospital-acquired (HA), community-acquired (CA) and companion animal and livestock-associated (LA) infections. Molecular epidemiology studies suggest that although host specificity may be associated with specific genetic lineages, recent human-to-animal and animal-to-human transmissions related to mobile genetic elements have been described. Gene transfers include virulence and antibiotic resistance genes, thus making it difficult to control multidrug resistance S. aureus infections. Bacteriophages (phages) and endolysins, the enzymes responsible for bacterial lysis by phages, are alternatives to the use of antibiotics for the control of S. aureus infections. In this work, we review current advances in the development of phage therapy and the study and design of recombinant endolysins to treat S. aureus infections. Preliminary results of bacteriophage isolation based on molecular epidemiology knowledge show that bacteriophages are specific of genetic lineages and that this strategy may be used as an approach to isolate and evaluate new bacteriophages for therapy.",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Claudia I. Barrera-Rivas, Norma A. Valle-Hurtado, Graciela M.\nGonzález-Lugo, Víctor M. Baizabal-Aguirre, Alejandro Bravo-Patiño,\nMarcos Cajero-Juárez and Juan J. Valdez-Alarcón",authors:[{id:"191123",title:"Dr.",name:"Juan José",middleName:null,surname:"Valdez-Alarcón",slug:"juan-jose-valdez-alarcon",fullName:"Juan José Valdez-Alarcón"},{id:"195005",title:"Mrs.",name:"Claudia Ibeth",middleName:null,surname:"Barrera-Rivas",slug:"claudia-ibeth-barrera-rivas",fullName:"Claudia Ibeth Barrera-Rivas"},{id:"195006",title:"MSc.",name:"Norma Anahí",middleName:null,surname:"Valle-Hurtado",slug:"norma-anahi-valle-hurtado",fullName:"Norma Anahí Valle-Hurtado"},{id:"195007",title:"MSc.",name:"Graciela M.",middleName:null,surname:"González-Lugo",slug:"graciela-m.-gonzalez-lugo",fullName:"Graciela M. González-Lugo"},{id:"195008",title:"Dr.",name:"Víctor Manuel",middleName:null,surname:"Baizabal-Aguirre",slug:"victor-manuel-baizabal-aguirre",fullName:"Víctor Manuel Baizabal-Aguirre"},{id:"195009",title:"Dr.",name:"Alejandro",middleName:null,surname:"Bravo-Patiño",slug:"alejandro-bravo-patino",fullName:"Alejandro Bravo-Patiño"},{id:"195010",title:"Dr.",name:"Marcos",middleName:null,surname:"Cajero-Juárez",slug:"marcos-cajero-juarez",fullName:"Marcos Cajero-Juárez"}]},{id:"53377",doi:"10.5772/66225",title:"Staphylococcus aureus Bacteremia in Adults",slug:"staphylococcus-aureus-bacteremia-in-adults",totalDownloads:2097,totalCrossrefCites:3,totalDimensionsCites:5,abstract:"Staphylococcus aureus is an important cause of bacteremia, and S. aureus bacteremia constitutes a serious condition with high morbidity and mortality, secondary to multiple complications including infective endocarditis and embolization. The incidence of bacteremia with S. aureus is increasing with more frequent use of medications that lower immune system response, and with the utilization of more invasive medical procedures. In addition, the emergence of resistant S. aureus isolates is becoming more common and can negatively affect the outcome of an individual if not diagnosed and managed properly. Health care workers encounter S. aureus bloodstream infections on a routine basis, and in certain situations, it becomes a very challenging infection to control. Because of the impact this entity has on health care costs and the increased use of resources, it is necessary to highlight the causes, clinical presentation, associated complications, and treatment measures. In this chapter, we will cover each of these points, with somewhat more emphasis on methicillin‐resistant S. aureus that is prevalent in both community and hospital settings and is more commonly associated with worsening prognosis and higher mortality.",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Dima Youssef and Kate Molony",authors:[{id:"190397",title:"Dr.",name:"Dima",middleName:null,surname:"Youssef",slug:"dima-youssef",fullName:"Dima Youssef"},{id:"195814",title:"Dr.",name:"Kate",middleName:null,surname:"Molony",slug:"kate-molony",fullName:"Kate Molony"}]}],mostDownloadedChaptersLast30Days:[{id:"54154",title:"Staphylococcus aureus: Overview of Bacteriology, Clinical Diseases, Epidemiology, Antibiotic Resistance and Therapeutic Approach",slug:"staphylococcus-aureus-overview-of-bacteriology-clinical-diseases-epidemiology-antibiotic-resistance-",totalDownloads:7155,totalCrossrefCites:14,totalDimensionsCites:25,abstract:"Staphylococcus aureus is an important human pathogen that causes wide range of infectious conditions both in nosocomial and community settings. The Gram-positive pathogen is armed with battery of virulence factors that facilitate to establish infections in the hosts. The organism is well known for its ability to acquire resistance to various antibiotic classes. The emergence and spread of methicillin-resistant S. aureus (MRSA) strains which are often multi-drug resistant in hospitals and subsequently in community resulted in significant mortality and morbidity. The epidemiology of MRSA has been evolving since its initial outbreak which necessitates a comprehensive medical approach to tackle this pathogen. Vancomycin has been the drug of choice for years but its utility was challenged by the emergence of resistance. In the last 10 years or so, newer anti-MRSA antibiotics were approved for clinical use. However, being notorious for developing antibiotic resistance, there is a continuous need for exploring novel anti-MRSA agents from various sources including plants and evaluation of non-antibiotic approaches.",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Arumugam Gnanamani, Periasamy Hariharan and Maneesh Paul-\nSatyaseela",authors:[{id:"192829",title:"Dr.",name:"Arumugam",middleName:null,surname:"Gnanamani",slug:"arumugam-gnanamani",fullName:"Arumugam Gnanamani"},{id:"204388",title:"Dr.",name:"Periasamy",middleName:null,surname:"Hariharan",slug:"periasamy-hariharan",fullName:"Periasamy Hariharan"},{id:"204389",title:"Dr.",name:"Maneesh",middleName:null,surname:"Paul-Satyaseela",slug:"maneesh-paul-satyaseela",fullName:"Maneesh Paul-Satyaseela"}]},{id:"53377",title:"Staphylococcus aureus Bacteremia in Adults",slug:"staphylococcus-aureus-bacteremia-in-adults",totalDownloads:2097,totalCrossrefCites:3,totalDimensionsCites:5,abstract:"Staphylococcus aureus is an important cause of bacteremia, and S. aureus bacteremia constitutes a serious condition with high morbidity and mortality, secondary to multiple complications including infective endocarditis and embolization. The incidence of bacteremia with S. aureus is increasing with more frequent use of medications that lower immune system response, and with the utilization of more invasive medical procedures. In addition, the emergence of resistant S. aureus isolates is becoming more common and can negatively affect the outcome of an individual if not diagnosed and managed properly. Health care workers encounter S. aureus bloodstream infections on a routine basis, and in certain situations, it becomes a very challenging infection to control. Because of the impact this entity has on health care costs and the increased use of resources, it is necessary to highlight the causes, clinical presentation, associated complications, and treatment measures. In this chapter, we will cover each of these points, with somewhat more emphasis on methicillin‐resistant S. aureus that is prevalent in both community and hospital settings and is more commonly associated with worsening prognosis and higher mortality.",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Dima Youssef and Kate Molony",authors:[{id:"190397",title:"Dr.",name:"Dima",middleName:null,surname:"Youssef",slug:"dima-youssef",fullName:"Dima Youssef"},{id:"195814",title:"Dr.",name:"Kate",middleName:null,surname:"Molony",slug:"kate-molony",fullName:"Kate Molony"}]},{id:"55253",title:"Clostridium difficile Infection Diagnosis by Biological Molecular Methods",slug:"clostridium-difficile-infection-diagnosis-by-biological-molecular-methods",totalDownloads:1978,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"In the past 15 years, the incidence of Clostridium difficile infection has emerged especially because of the new highly virulent strains. The classical diagnosis methods used to diagnose C. difficile infection take time and the enzyme immunoassay (EIA) test has demonstrated the lack of sensitivity. Even though new modern molecular methods have become available, the diagnosis of C. difficile in patients or healthy carriers remains a big challenge for both clinicians and laboratory staff. In the present chapter, we will list the main genotyping methods, stressing their advantages and disadvantages, as well. A brief presentation of the most useful kit (principle, sensitivity, specificity, benefits and disadvantages) to assess the impact of molecular methods in comparison with classical methods will offer support for future research in the present context of an increasing prevalence of C. difficile infection that represents worldwide, a real public health problem. To improve the patients’ quality of life, to limit hospital transmission, and to save money, we have tried to identify the best diagnosis algorithm as tool in C. difficile diagnosis and surveillance. This algorithm may differ depending on the capacities of the laboratories and on the socioeconomic level of the countries in question.",book:{id:"5831",slug:"clostridium-difficile-a-comprehensive-overview",title:"Clostridium Difficile",fullTitle:"Clostridium Difficile - A Comprehensive Overview"},signatures:"Luminiţa Smaranda Iancu, Andrei Florin Cârlan and Ramona\nGabriela Ursu",authors:[{id:"197809",title:"Prof.",name:"Luminiţa Smaranda",middleName:null,surname:"Iancu",slug:"luminita-smaranda-iancu",fullName:"Luminiţa Smaranda Iancu"},{id:"205531",title:"Dr.",name:"Andrei",middleName:null,surname:"Cârlan",slug:"andrei-carlan",fullName:"Andrei Cârlan"},{id:"205532",title:"Dr.",name:"Ramona Gabriela",middleName:null,surname:"Ursu",slug:"ramona-gabriela-ursu",fullName:"Ramona Gabriela Ursu"}]},{id:"53782",title:"Methicillin-Resistant Staphylococcus aureus (MRSA) in Food- Producing and Companion Animals and Food Products",slug:"methicillin-resistant-staphylococcus-aureus-mrsa-in-food-producing-and-companion-animals-and-food-pr",totalDownloads:2743,totalCrossrefCites:8,totalDimensionsCites:16,abstract:"Methicillin-resistant Staphylococcus aureus (MRSA) has become a growing concern in companion and food-producing animals. The presence of multidrug-resistance with a wide range of extracellular enterotoxin genes, virulence factors, and Panton-Valentine leukocidin (pvl) cytotoxin genes confer life-threatening traits on MRSA and makes them highly pathogenic and difficult to treat. Clonal complex 398 (CC398), a predominant clonal lineage of livestock-associated-MRSA in domestic animals and retail meat, is capable of infecting humans. In order to monitor and prevent MRSA contamination, it is critical to understand its source and transmission dynamics. In this review, we describe MRSA in food-producing animals (pig, cattle, chicken), horses, pet animals (dogs, cats), and food products (pork, beef, chicken, milk, and fish).",book:{id:"5471",slug:"frontiers-in-i-staphylococcus-aureus-i-",title:"Frontiers in Staphylococcus aureus",fullTitle:"Frontiers in Staphylococcus aureus"},signatures:"Jungwhan Chon, Kidon Sung and Saeed Khan",authors:[{id:"189634",title:"Dr.",name:"Kidon",middleName:null,surname:"Sung",slug:"kidon-sung",fullName:"Kidon Sung"},{id:"190400",title:"Dr.",name:"Jungwhan",middleName:null,surname:"Chon",slug:"jungwhan-chon",fullName:"Jungwhan Chon"},{id:"190401",title:"Dr.",name:"Saeed",middleName:null,surname:"Khan",slug:"saeed-khan",fullName:"Saeed Khan"}]},{id:"55751",title:"Overview of Clostridium difficile Infection: Life Cycle, Epidemiology, Antimicrobial Resistance and Treatment",slug:"overview-of-clostridium-difficile-infection-life-cycle-epidemiology-antimicrobial-resistance-and-tre",totalDownloads:2735,totalCrossrefCites:3,totalDimensionsCites:4,abstract:"The use of antimicrobial agents and acquired resistances explains in part the emergence and spreading of epidemic strains of Clostridium difficile. Continued use of antimicrobial therapy still represents an acute danger in triggering the emergence and spreading of new resistant and multiresistant strains including against first-line antibiotics. We examine the pathway of peptidoglycan synthesis in this organism and associated resistances, as well as resistance to other classes of antibiotics. The life cycle of C. difficile involves growth, spore formation and germination. Spores endow the organism with a formidable capacity of persistence in the environment and in the host, resistance, dissemination and infectious potential. Highly resistant spores produced by antibiotic-resistant/multiresistant strains may be one of the most serious challenges we face in what concerns the containment of C. difficile. Finally, we review recent developments in the treatment and prevention of C. difficile infection.",book:{id:"5831",slug:"clostridium-difficile-a-comprehensive-overview",title:"Clostridium Difficile",fullTitle:"Clostridium Difficile - A Comprehensive Overview"},signatures:"Joana Isidro, Aristides L. 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The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}}]},series:{item:{id:"13",title:"Veterinary Medicine and Science",doi:"10.5772/intechopen.73681",issn:"2632-0517",scope:"Paralleling similar advances in the medical field, astounding advances occurred in Veterinary Medicine and Science in recent decades. These advances have helped foster better support for animal health, more humane animal production, and a better understanding of the physiology of endangered species to improve the assisted reproductive technologies or the pathogenesis of certain diseases, where animals can be used as models for human diseases (like cancer, degenerative diseases or fertility), and even as a guarantee of public health. Bridging Human, Animal, and Environmental health, the holistic and integrative “One Health” concept intimately associates the developments within those fields, projecting its advancements into practice. This book series aims to tackle various animal-related medicine and sciences fields, providing thematic volumes consisting of high-quality significant research directed to researchers and postgraduates. It aims to give us a glimpse into the new accomplishments in the Veterinary Medicine and Science field. 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A dynamic career research platform which is based on the thematic areas of comparative vertebrate physiology, stress endocrinology, reproductive endocrinology, animal health and welfare, and conservation biology. \nEdward has supervised 40 research students and published over 60 peer reviewed research.",institutionString:null,institution:{name:"University of Queensland",institutionURL:null,country:{name:"Australia"}}},editorTwo:null,editorThree:null},{id:"20",title:"Animal Nutrition",coverUrl:"https://cdn.intechopen.com/series_topics/covers/20.jpg",isOpenForSubmission:!0,editor:{id:"175967",title:"Dr.",name:"Manuel",middleName:null,surname:"Gonzalez Ronquillo",slug:"manuel-gonzalez-ronquillo",fullName:"Manuel Gonzalez Ronquillo",profilePictureURL:"https://mts.intechopen.com/storage/users/175967/images/system/175967.png",biography:"Dr. Manuel González Ronquillo obtained his doctorate degree from the University of Zaragoza, Spain, in 2001. He is a research professor at the Faculty of Veterinary Medicine and Animal Husbandry, Autonomous University of the State of Mexico. He is also a level-2 researcher. He received a Fulbright-Garcia Robles fellowship for a postdoctoral stay at the US Dairy Forage Research Center, Madison, Wisconsin, USA in 2008–2009. He received grants from Alianza del Pacifico for a stay at the University of Magallanes, Chile, in 2014, and from Consejo Nacional de Ciencia y Tecnología (CONACyT) to work in the Food and Agriculture Organization’s Animal Production and Health Division (AGA), Rome, Italy, in 2014–2015. He has collaborated with researchers from different countries and published ninety-eight journal articles. He teaches various degree courses in zootechnics, sheep production, and agricultural sciences and natural resources.\n\nDr. Ronquillo’s research focuses on the evaluation of sustainable animal diets (StAnD), using native resources of the region, decreasing carbon footprint, and applying meta-analysis and mathematical models for a better understanding of animal production.",institutionString:null,institution:{name:"Universidad Autónoma del Estado de México",institutionURL:null,country:{name:"Mexico"}}},editorTwo:null,editorThree:null},{id:"28",title:"Animal Reproductive Biology and Technology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/28.jpg",isOpenForSubmission:!0,editor:{id:"177225",title:"Prof.",name:"Rosa Maria Lino Neto",middleName:null,surname:"Pereira",slug:"rosa-maria-lino-neto-pereira",fullName:"Rosa Maria Lino Neto Pereira",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bS9wkQAC/Profile_Picture_1624519982291",biography:"Rosa Maria Lino Neto Pereira (DVM, MsC, PhD and) is currently a researcher at the Genetic Resources and Biotechnology Unit of the National Institute of Agrarian and Veterinarian Research (INIAV, Portugal). She is the head of the Reproduction and Embryology Laboratories and was lecturer of Reproduction and Reproductive Biotechnologies at Veterinary Medicine Faculty. She has over 25 years of experience working in reproductive biology and biotechnology areas with a special emphasis on embryo and gamete cryopreservation, for research and animal genetic resources conservation, leading research projects with several peer-reviewed papers. Rosa Pereira is member of the ERFP-FAO Ex situ Working Group and of the Management Commission of the Portuguese Animal Germplasm Bank.",institutionString:"The National Institute for Agricultural and Veterinary Research. Portugal",institution:null},editorTwo:null,editorThree:null}]},overviewPageOFChapters:{paginationCount:14,paginationItems:[{id:"82457",title:"Canine Hearing Management",doi:"10.5772/intechopen.105515",signatures:"Peter M. 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She obtained her Ph.D. in Veterinary Sciences from the University of Trás-os-Montes e Alto Douro, Portugal. After almost 32 years of teaching at the University of Trás-os-Montes and Alto Douro, she recently moved to the University of Évora, Department of Veterinary Medicine, where she teaches in the field of Animal Reproduction and Clinics. Her primary research areas include the molecular markers of the endometrial cycle and the embryo–maternal interaction, including oxidative stress and the reproductive physiology and disorders of sexual development, besides the molecular determinants of male and female fertility. She often supervises students preparing their master's or doctoral theses. 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She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. 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Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. 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