Specimens of dipteran included in the study.
Anthropogenic actions, including deforestation, disorganized urbanization, and globalization, contribute to emergence and reemergence of arboviruses worldwide, where Flavivirus is the most prevalent, and its continuous monitoring can help in preventive control strategies. Thus, the aim of this study was to detect flavivirus RNA in single hematophagous insects, which are used as sentinels. Total RNA was extracted from six Aedes aegypti stored since 2003 and from 100 Culicidae and collected through CDC trap in a public park of a Brazilian Northwest city of São Paulo State. Flavivirus was detected through RT/PCR targeting 230–250 bp of the RNA polymerase coding sequence (NS5). PCR amplicons were sequenced by Sanger method, used in comparative analysis over Basic Local Alignment Search Tool (BLAST) in GenBank, and subjected to Neighbor-Joining phylogenetic analyses. Efficiency of Flavivirus diagnosis was confirmed by detection of Dengue virus serotype 2 in Ae. aegypti. From the 100 collected insects, 19 were positive for Culex flavivirus (CxFV). NS5 partial sequence phylogenetic analysis clustered all CxFV in one branch separated from vertebrate flaviviruses, being applicable to the identification of Flavivirus species. The dipteran RNA extraction methodology described in this work supports detection of flaviviruses in single insects maintained in 80% ethanol, which can be used to constant arbovirus surveillance.
- hematophagous insect
- molecular diagnosis
- RNA extraction
- single-insect virus diagnosis
In recent years, due to anthropogenic actions, including deforestation, disorganized urbanization, and globalization, arboviruses have emerged as a major challenge to global health [1, 2]. The arboviruses (arthropod borne viruses) are transmitted to humans through the bite of infected hematophagous insects, causing febrile diseases , with a broad variety of clinical manifestations, ranging from the absence of symptoms to the severe hemorrhagic and encephalitic disorders [4, 5]. The arbovirus vectors include different species of mosquitoes, flies, and ticks. The most worldwide prevalent arboviruses encompass Dengue Virus (DENV), Yellow Fever Virus (YFV), West Nile Virus (WNV), and Zika Virus (ZIKV) from Flaviviridae family and
Arbovirus transmissions occur principally in tropical and subtropical areas, since the presence of vector mosquitoes is associated, mainly, with hot and humid environments, fundamental requirements for their reproduction . Recently, with the global warming and increase in international traveling, the dispersion of arthropod vectors is rising, especially mosquitoes of the genus
Dengue is the most prevalent arbovirus and is responsible for an estimate of 390 million annual cases worldwide , and 3.9 billion people, living in 128 countries, are on risk of infection . Since 2010, dengue cases have been reported in nonendemic countries in Europe, including France, Croatia, and Portugal, where in 2012, an outbreak occurred with more than 2000 reported cases. In this period, 10 other European countries were affected by dengue fever. Further, among European travelers returning from low incoming endemic countries, dengue fever is the most diagnosed disease, after malaria [10, 15]. In 2016, more than 3.34 million cases of dengue were reported in American countries, Southeast Asia, and the Western Pacific. Only in the Americas, approximately 2.38 million people were affected, with 1032 deaths, including Brazil, responsible for almost 1.5 million of the reported cases . In addition to Dengue, in Brazil, a South American country with high international touristic activity, according to the Ministry of Health, occurred 216,207 cases of Zika fever, another important emerging
There are no effective vaccines available for Dengue, Zika, and Chikungunya fevers , and the control of these arboviruses is exclusively implemented by chemical arthropod vector elimination . Therefore, active searching for vectors is necessary to prevent the circulation of known arboviruses. Detection of arboviruses occurs only after detection of human cases, which causes delay in the disease and vector dissemination controls. Thus, to prevent emergency and reemergence of arboviruses, very early detection of vectors and arbovirus and the understanding of their diversity and infection cycle are of great importance. These strategies include also the identification of factors related to the dispersion and entrance of arboviruses in previous indene areas and the identification of wild animal natural reservoirs . Considering the current difficulties in detecting silent circulation of arboviruses and also in obtaining samples from arthropod vectors, human and animal febrile cases, principally in the forests areas, the use of sentinels could be an alternative surveillance approach. Hematophagous insects are present in different wild natural and urban environments, being an excellent group of animal to be used as sentinel. Thus, in this work, the single-insect nucleic acid extraction method  was evaluated in hematophagous dipterans collected in a Brazilian municipal public park using CDC traps, in order to detect RNA from flaviviruses.
2. Materials and methods
2.1 Specimens and ethical aspects
A total of 106 insects of the order Diptera were analyzed, of which 100 were collected in the Municipal Park of the city of Marília—São Paulo, and six were specimens of
|Taxon||Storage method||Collection local, data||Number of specimens|
|Anopheles (Culicidae)||Ethanol 80%||Marília-SP, December 2017||3|
|Phlebotomus (Psychodidae)||Ethanol 80%||Marília-SP, December 2017||2|
|Ceratopogonidae||Ethanol 80%||Marília-SP, November 2017||3|
|Cecidomyiidae||Ethanol 80%||Marília-SP, December 2017||1|
|Culicinae (Culicidae)||Ethanol 80%||Marília-SP, June 2017||91|
|Frozen at −20 °C||USP-SP, March 2003||6|
This work did not involve collection of human samples, total or partial, and specimens or tissue samples from vertebrate animals and/or embryos. In addition, no threatened or protected species were collected.
2.2 Single-insect nondestructive RNA extraction
For RNA extraction, each dipteran was digested for 16 h at 56°C, inserted in 200 μL of a lysis buffer composed of 200 mM Tris-HCl (pH 7.5), 250 mM NaCl, 25 mM EDTA (pH 8.0), 0.5% of SDS, and 400 μg/mL of proteinase K as described for DNA extraction . Before digestion, ethanol from insects stored in 80% ethanol was removed after washing twice with 1 mL of 1× PBS (137 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4, and 1.8 mM KH2PO4). Following the incubation period, the digestion buffer was transferred to 1.5 mL RNase free tube and submitted to RNA purification. One milliliter of 80% ethanol was added to the insect specimen, which was stored in freezer at −20°C. Total RNA purification for each insect from the obtained digestion solution was performed through Qiagen® RNA Mini Kit and PureLink® RNA Mini Kit according to the manufacturer’s instructions.
2.3 RNA quality and
Flavivirusnucleic acid detection
The quality and quantity of extracted RNA from each insect were done through agarose gel electrophoresis and by reverse transcription and polymerase chain reaction (RT/PCR), with oligonucleotides that amplify a 464 bp fragment encoding the 28S ribosomal RNA fraction (28S rRNA) of dipteran (Table 2). RNA from each insect was diluted into a final volume of 60 μL of RNase free water, and 4 μL was subjected to 1.5% agarose gel electrophoresis in 0.5× TBE buffer and stained with SafeBlue® according to manufacturer’s instructions. Ten insect samples were used to verify quality by RT/PCR, and before RT reaction, 40 μL of the total RNA was treated with DNase I by means of the Biometra Kit from Analytik Jena, following manufacturer’s instructions, being diluted in 40 μL of RNase free water. Subsequently, three complementary DNA (cDNA) syntheses were performed, each with a different oligonucleotide, detailed in Table 2, being 0.5 μM of oligonucleotide 28SD7r, six bases random primers from Promega, or Oligo dT18. For each cDNA synthesis, 5.5 μL of one insect total extracted RNA, treated with DNase I, was submitted to RT reaction with 200 units of MMLV Reverse Transcriptase (Invitrogen) following fabricator’s instructions, in a total volume of 20 μL. Two microliter of the obtained cDNAs was used in PCR to amplify a 464 bp fragment corresponding to 28S rRNA of Dipteran (Table 2) through Brazil Platinum Taq DNA polymerase (Invitrogen) according to producer’s instructions. PCR condition was one cycle of 94°C for 3 min; 40 cycles of 94°C for 30 s, 50°C for 30 s, and 72°C for 30 s; and 72°C for 7 min. To control DNase I treatment, 5.5 μL of untreated RNA was used directly on PCR. Reaction products were subjected to 1.5% agarose gel electrophoresis in 0.5× TBE buffer, after staining with SafeBlue®.
|Primers||Sequence 5′-3′||Amplicon size||Genomic region||Reference|
|28SD7forw||AGAGAGAGTTCAAGAGTACGTG||464 bp||28S rRNA (Diptera)|||
|D1 forw||TCAATATGCTGAAACGCGCGAGAAACC||511 bp||C/prM (DENV)|||
|cFD2 rev||GTGTCCCAGCCGGCGGTGTCATCAGC||220–250 bp||NS5 (Flavivirus)|||
|Oligo dT18||TTTTTTTTTTTTTTTTTT||Poly A tail|
2.4 Sequencing and phylogenetic analysis
PCR positive fragments were purified by using the Thermo Scientific GeneJET PCR Purification Kit and sequenced with BigDye 3.1 (Applied Biosystems®) and PCR fragment-specific oligonucleotides, according to manufacturer’s instructions. Sequence cycle conditions were 96°C for 1 min; 39 cycles at 96°C for 15 s, 50°C for 15 s, and 60°C for 4 min. After DNA precipitation with 10% of NaOAc (3 M, pH 5.2), 10% of 1.5 μL of glycogen (1 mg/mL), and two volumes of ethanol, the reactions were pelleted by centrifugation and were washed with 70% of ethanol. The reactions were loaded in an ABI PRISM® 3130XL Genetic Analyzer /HITACHI (16 capillaries). The source and specificity of the obtained sequences were evaluated by BLAST in GenBank .
The nucleotide and amino acid partial 226 bp sequence corresponding to the NS5 protein of
In analysis, partial 16 NS5 sequences of CxFV generated in this study from
Agarose gel electrophoresis analysis of the total RNA extracted from 10 specimens of dipteran maintained in 80% ethanol by the nondestructive nucleic acid extraction method described before  showed integrity, and an approximately amount of 1 μg/mL, per specimen (Figure 1). The presence of RNA was also confirmed by RT/PCR to amplify a 464 bp corresponding to the 28S rRNA from dipteran, after treatment of RNA with DNase I (Figure 2). The presence of DNA was observed in all samples (Figure 2; DNA). After DNase I treatment, DNA was present in samples 1, 2, 6, and 8, corresponding to PCR products obtained from cDNA synthesized with oligo (dT), which should amplify mRNA and not the 28S rRNA. Specific RNA amplification was observed in samples, 3, 4, 5, 7, 9, and 10, after 28S rRNA PCR performed on cDNA synthesized with random six nucleotides and 28S rRNA-specific oligonucleotides (Figure 2).
To verify the feasibility to use the dipteran extracted RNA for
Sixteen CxFV nucleotide (226 bp in length) and translated partial NS5 amino acid (75 residues) sequences, with good quality, were used for phylogenetic reconstruction by the Neighbor-Joining method (Figures 5 and 6). NS5 nucleotide and amino acidic partial sequence of CxFV obtained from culicids of Marilia city varied from 0 to 3% among the same virus species of other Brazilian regions, Africa, Argentina, and China.
The morphological characteristics of 19 CxFV infected dipterans were observed by optical microscopy in order to confirm the taxonomic position and to identify their gender. Nineteen specimens confirmed to belong to the genus
The technique of RNA extraction from a single mosquito preserving their chitinous cytoskeleton is described for the first time, and its use can contribute not only to the detection of infectious agents with RNA genome but also to the evolutionary and morphological studies of Diptera since the RNA molecule is an important tool to understand the physiology and evolutionary relationships among organisms , and the physical structure of the insect is maintained . Also, vectorial capability of arthropods to several infectious agents can be investigated using specific molecules, with conditional expression profiles, as biomarkers. Molecular identification of the arthropod specimen can be performed by RT/PCR on RNA using oligonucleotides complementary to barcode genes. Also, if DNA is necessary, after proteinase K solution treatment, an aliquot of the arthropod nucleic acid solution can be used for DNA extraction.
Genome of the most important medical arboviruses is composed of RNA, and research works on the detection of these viruses in hematophagous mosquitoes are accomplished on pools of 20–50 specimens, which are macerated and destroyed [33, 34, 35, 36]. In this work, a good quality of RNA was obtained from a single dipteran specimen, which was confirmed by electrophoresis in agarose gels (Figure 1) and by a specific amplification of a 464 bp fragment of the 28S fraction of diptera rRNA, after DNase I treatment (Figure 2). The RNA obtained from a single insect was appropriately to detect DENV-2 in frozen
Different geographical regions present divergences in arthropod infectious diseases vectors diversity and distribution. In Brazil, the main urban vector for YFV is
It is believed that
The single dipteran RNA extraction technique described in this work permits the use of hematophagous insects as sentinels to detect arboviruses, preserving the chitinous skeleton of the insect and guaranteeing the subsequent morphological studies. The possibility to obtain RNA from a single dipteran also makes possible the investigation of infectious agent’s vector capability and the identification of the ingurgitated blood meal source, enabling the description of arthropod alimentary habit and an indication of which vertebrates may be implicated in a virus life cycle. The method also opens the possibility for constant arbovirus surveillance, which can be used to prevent and control epidemics that affect millions of people each year. The presence of CxFV in
This work was supported by the Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP) [grant number 2016/14514-4 and scholarships to Leticia Abrantes Andrade, fellow number 2018/05133-2 and Luana Prado Rolim de Oliveira, fellow number 2019/11384-0]; the Pró-reitoria de Extensão da Universidade Federal do ABC (PROEC-UFABC) [grant number PJ010-2017]; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES); and Universidade Federal do ABC (UFABC).
Conflict of interest
The authors declare no conflict of interest.