Generalized data on the possible current use of microbiome therapy.
When diagnosing sepsis, it is common to look for pathogens, microbe’s DNA, lipopolysaccharide (LPS), or host biomarkers while missing out on microbiota. The next-generation sequencing of 16S rRNA gene allowed characterizing the gut microbiota taxonomy and clarifying the gut microbial population being more complex than was previously thought. We suppose that significant disruption of the microbiota is an indicator of the major role it plays in sepsis. Serious metabolic disorders of the gut microbiota may contribute to an unfavorable outcome in septic patients. With the changes not only in the composition but also in the metabolic activity of the gut microbiota taken into account, the characteristics of the mechanisms of interactions in the “septic” microbiome will allow the advances in the optimization of the diagnostics and therapy of sepsis to be made.
- gut microbiome
- critical states
- aromatic microbial metabolites
- organ dysfunction
In recent years, the microbiome has been considered as an important player in the pathophysiology of various types of diseases, including trauma and sepsis [1, 2]. Over 70% of species of microorganisms are nonculturable and cannot be isolated as a pure culture for identification. Omics technologies (genomics, transcriptomics, metagenomic sequencing, proteomics, and metabolomics) have fully changed our concepts about the composition and function of the “invisible organ” . Widespread distribution of microbiomic studies became possible about 10 years ago with the emergence of high-performance new-generation sequencing (NGS), allowing transcribing in mass the collective genome of microbiomes—metagenome. The 16S rRNA gene encodes highly specific RNA of bacterial ribosomes and is present in genomes of all known microorganisms. Its structure is quite conservative, but variable-specific regions allow identifying microorganisms of different species and strains. The study pattern is quite simple but rather laborious: at the first stage, DNA is isolated from a sample, and then a so-called genome library containing copies of gene 16S rRNA belonging to different bacteria is obtained. The library is “read” using high-performance sequenators providing reception of several thousand nucleotide sequences of gene 16S rRNA for each sample. The next stage deals with analysis of a huge body of received data using bioinformatic techniques. Results are represented in a way most suitable in each particular case. The introduction of latest technologies, for example, nanopore sequencing, allows fast identification of bacteria in samples and finding markers of resistance to antimicrobial drugs within 5–10 minutes with the portable real-time device for DNA and RNA sequencing “MinION” that weighs less than 100 grams. This method is currently undergoing clinical testing . However, in a typical microbiome experiment, several aspects of microbial communities still remain inaccessible. These include low-abundance but potentially crucial taxa whose genetic material is not sampled by sequencing techniques due to being present below the level of detection . The real value of all this novel knowledge to understand the pathogenesis of sepsis has yet to be established. In this chapter, we are discussing the important role of bacterial metabolites in comparison with taxonomic structure of the septic gut microbiota.
2. The gap between healthy and septic gut microbiomes
Sepsis is a multifaceted host response to an infecting pathogen that may be significantly amplified by endogenous factors . The broader perspective also emphasizes the significant biological and clinical heterogeneity in affected individuals such as their age, underlying comorbidities, concurrent injuries (including surgery) and medications, and source of infection adding to further complexity . The success of antibiotic treatment depends on rapid and accurate identification of relevant pathogens and is complicated by the increasing rate of antimicrobial resistance conditioned by the dynamic changes in the bacterial population in which aerobic and facultative anaerobic bacteria predominant at the onset of sepsis are replaced by anaerobic species as the oxygen levels deplete. Broad-spectrum therapy is administered in the absence of bacterial identification, but this may not accurately reflect causative pathogens .
For a better understanding of how to treat, we probably should change the paradigm from “anthropocentrism” to “microbiocentrism,” as we think.
The presence of over hundreds of species in the gut of a healthy adult host is a way to survive in an ever-changing world and the ability to receive energy from different sources of food. In critical condition, the advantage is obtained by those species that are capable of surviving in more extreme conditions with less oxygen and a lack of nutrients and trace elements. For example,
In our preliminary study, we used gas chromatography-mass spectrometry (GC-MS) analysis of blood serum and feces simultaneously and at the same time analyzed the taxonomic composition of the gut microbiota using 16S rRNA gene-based metagenomic analysis in groups of patients with sepsis, n = 9, and healthy, n = 5. The sepsis was diagnosed according to the Sepsis 3 definition .
The taxonomic composition of the gut microbiota in a group at the phylum level as determined by the metagenomic analysis of feces is shown in Figure 1. The major four phyla of the human gut microbiota,
As we have shown earlier, high levels of some aromatic microbial metabolites (AMMs) in serum are related to the severity and mortality of critically ill patients . The sum of the level of eight most relevant metabolites, benzoic (BA), phenylpropionic (PhPA), phenyllactic (PhLA), p-hydroxyphenylbenzoic (p-HBA), p-hydroxyphenylacetic (p-HPhAA), p-hydroxyphenylpropionic (p-HPhPA), homovanillic (HVA), and p-hydroxyphenyllactic acids (p-HPhLA), in serum samples from septic patients was higher than in healthy people 3.7 (1.2–8.0) μM and 1.3 (1.0–1.6) μM, respectively (p < 0.05). In the septic group, the maximum values of the sum of these metabolites were more than 10 μM which is higher than in patients with lethal outcome. The differences in the AMM quality profiles of simultaneously serum and fecal samples (SFS) of patients with sepsis and healthy are presented in Figure 2. The results showed that the feces of healthy people abound with such metabolites, p-PhAA, p-HPhPA, and p-HPhLA, supporting data obtained by Jenner et al. . At the same time, we observed prevalence of BA, PhLA, and p-PhAA in sepsis with a higher level of BA in the gut of non-survivors. Differences in the proportion of AMM in the blood compared to the intestine can be explained by the fact that most hydrophilic (p-HPhAA, p-HPhLA, and PhLA) metabolites are excreted by the kidneys, while lipophilic metabolites (BA, PhAA, and PhPA) are absorbed by cells of tissue barriers (intestinal wall, lymphoid tissue, liver, vascular endothelium, etc.).
In particular, serum samples of healthy people are characterized by a predominance of BA and PhPA, while hydrophilic AMMs are detected in sepsis with the appearance of high levels of HVA in the serum of non-survivors. BA is a product of the synthesis of bacteria, plants, and fungi, but a significant content is formed as a result of biodegradation of phenylalanine. Experimental study of the proximal part of the gastrointestinal tract showed that BA had a bacteriostatic and bactericidal dose-dependent effect on coliform and lactic acid bacteria .
On the one hand, it is important to emphasize that the dysfunction of the microbiota is manifested by excessive production of certain microbial metabolites as a reflection of the high microbial load with pathological colonization by bacteria involved in the development of sepsis. On the other hand, microbiota function, which is very important for host homeostasis, such as microbial biodegradation of an excess of endogenous biologically active compounds, due to a decrease in biodiversity in the intestine, primarily a deficiency of indigenous anaerobes, is disturbed . The altered profile of aromatic metabolites in the blood may be an integral indicator reflecting these dramatic disturbances and possibly other functions of the “invisible organ.”
3. The gut microbial metabolites in the pathogenesis of sepsis
It was shown that in vitro some sepsis-associated AMM in clinically significant concentrations can inhibit the phagocytic activity of neutrophils ; cause mitochondrial dysfunction ; influence on platelet aggregation ; reduce tyrosine hydroxylase activity, thus limiting the synthesis of catecholamines; and participate in the pathogenesis of septic shock . Numerous data obtained in vitro allow us to hypothesize that AMM acts as signaling molecules (Figure 3).
It is impossible to exclude the presence of common signaling pathways, cell receptors, transmembrane transporters, and other mechanisms of humans and bacteria, as well as the direct participation of microbial metabolites in the pathogenesis of sepsis. Thus, today, we should not confine ourselves to studying eukaryotic cells while searching for new molecular mechanisms of sepsis-associated organ failure and septic shock . We should consider and simulate experimental changes in the internal environment of a person that occur with a radical “restructuring” of the microbiome in seriously ill patients. This approach opens new prospects for an objective monitoring of diseases, carrying out an assessment of the integral metabolic profile on common metabolites (particularly aromatic) within a given time, and will provide new targets for therapeutic effects in the future.
4. Microbiome-oriented therapy: how to keep balance?
In sepsis, disturbances of physiological parameters caused directly by patient’s conditions and multiple treatment-induced factors might have powerful impact on the gut microbiome. Finding a therapy aimed at restoring the balance between “beneficial” and “harmful” microorganisms is highly relevant. At present, there are several possible approaches (Table 1):
Increase the “beneficial” microorganisms using pro-, pre-, and/or metabiotics.
Use a combination of probiotics and prebiotics known as symbiotics.
Improve the composition by transplantation of fecal microbiota transplantation (FMT).
Suppress “harmful” microorganisms, and create favorable conditions for recovery of one’s own “beneficial” microorganisms using selective antibacterial drugs (similar selective digestive decontamination).
|Study||Population||Type of intervention||Results|
|☺||Panigrahi et al. ||4556 healthy newborns||Reduction in the incidence of sepsis during the first 60 days of life|
|☺||Stadlbauer et al. ||15 patients with early sepsis||The multispecies probiotic in a dose of 109 daily||Probiotic intervention successfully modulates the microbiome|
|☺||Manzanares et al. ||Meta-analysis of 30 trials that enrolled 2972 critically ill patients||Different types of probiotic therapy||Probiotics were associated with a significant reduction in infections (risk ratio 0.80, 95% confidence interval (CI) 0.68, 0.95, P = 0.009; heterogeneity I2 = 36%, P = 0.09)|
|☺||Kasatpibal et al. ||Meta-analysis of 31 articles that enrolled 2952 surgical patients||Different types of probiotic, prebiotic and symbiotic therapy||Symbiotic therapy was the best regimen in reducing surgical site infection (SSI) (RR = 0.28; 95% CI, 0.12–0.64)|
|☺||Besselink et al. ||298 patients with predicted severe acute pancreatitis||4 species of lactic bacterial (||Probiotic prophylaxis is associated with an increased risk of mortality and higher rate of infectious complications|
|☺||Han et al. ||Review of management of ||FMT||The potential effective therapy but not enough data in the ICU patients|
|☺||Moayyedi et al. ||Meta-analysis of 5 trials that enrolled 284 patients with CDI||FMT (including autologous FMT)||FMT was statistically significantly more effective (RR, 0.41; 95% CI, 0.22–0.74; NNT, 3; 95% CI, 2–7) than vancomycin or placebo|
|☺||McClave et al. ||Review of clinical use of fecal microbial transplantation in critical illness||FMT||An attractive option to mitigate multiple organ dysfunction in the ICU|
|☺||FDA ||Two immunocompromised patients||FMT||The development of a severe infection and one death from fecal transplants containing drug-resistant bacteria|
|☺||Price et al. ||Meta-analysis of 29 articles that enrolled patients in general intensive care units||SDD||Favorable effect on mortality, with a direct evidence odds ratio of 0.73 (95% confidence interval 0.64 to 0.84)|
|☺||Buelow et al. ||10 ICU patients||SDD||The limited risks for antibiotic resistance|
|☺||Webster et al. ||Meta-analysis of 37 trials (involving more than 7000 patients)||SDD||SDD reduces ventilator-associated pneumonia (odds ratio (OR) = 0.28; 95% confidence interval (CI) = 0.20–0.38) and mortality (OR = 0.73; CI = 0.64–0.84)|
|Antimicrobial therapy under the control of the metabolic activity of the gut microbiota|
|☺||Beloborodova and Sarshor ||56 patients with pneumonia or abdominal infection||Enteral correction of the metabolic activity of the gut microbiota||The downward trend of mortality by 11%|
The undoubtful effectiveness of probiotics for correction of functional disorders of the gastrointestinal tract has been widely accepted. A randomized placebo-controlled study on 4556 healthy newborns in India proved that oral probiotics
In another study, the use of symbiotics as an adjuvant therapy in surgical patients reduced incidence of such postoperative complications as wound infection . One of the reasons for doubts concerning expediency of applying probiotics in ICU is intestinal barrier failure in critically ill patients. The translocation of bacteria to systemic blood flow and lymph is known to promote a complex chain of events leading to multiple organ failure . On this basis, the use of live bioculture drugs (probiotics) in critically ill patients looks far from harmless and even dangerous. Possible, a NGS-based approach for the detection of bacteremia in patients with sepsis, which has shown promising results, will be a key step in the clinical use of NGS in this indication . In randomized double-blind placebo-controlled independent study on severe acute pancreatitis patients (n = 298)—Probiotics in Pancreatitis Trial (PROPATRIA)—1 group (n = 153), for prophylaxis of suppurative complications received a biomedicine containing 4 species of lactic bacterial (
In our opinion, the use of live microbial cultures of lactic acid bacteria might have aggravated metabolic disturbances and led to adverse consequences in initially severe patients, in particular, because of excessive production of PhLA and p-HPhLA which are typical metabolites of bifido- and lactic bacteria [36, 37]. A group of authors who used probiotics with positive effect in short bowel syndrome patients have reached similar conclusions, namely, the importance of metabolic status evaluation. The colleagues associated high mortality in PROPATRIA study with lethal combination of proteolytic enzymes of pancreas and high level of lactic acid caused by bacterial fermentation of carbohydrates as a key factor related to intake of probiotics. Nevertheless, authors suggest that a probiotic therapy may not be counterindicated for the prevention of secondary infections associated with acute pancreatitis, provided that future clinical studies start probiotic therapy early as possible and prevent bacterial overgrowth not only of patient’s own intestinal flora but also the dose of probiotic bacteria .
An alternative to probiotics, “smart” direction, is infusion of liquid filtrate of feces from healthy fecal microbiota transplantation. The potential advantage of this method is enlargement of microbial biodiversity and the presence of biologically active substances and metabolites, which might assist a longer effect of microbiota recovery . This procedure has been successfully used for treating the severe infection caused by
We assume that the main efforts in fighting infection should be directed to decrease microbial metabolic activity. Considering that the intestine is the main reservoir of bacteria and therefore the main source of bacterial metabolites, it seems appropriate to correct the activity of intestinal microbiota in patient with infection. Enteral correction of the metabolic activity of intestinal microbiota contributes to the improvement of the patients’ state .
Selective digestive decontamination (SDD) is often considered a prophylactic mode of antibiotic therapy allowing targeted prevention of bowel colonization by “pathogenic” microorganisms. The effect is achieved thanks to the selective impact on potentially pathogenic aerobic and facultative aerobic bacteria by means of enteral administration of antibacterial drugs that do not suppress anaerobic microorganisms, thus creating conditions for recovery of microbiota balance and assisting its functioning even in the unfavorable environment in ICU. Currently, numerous clinical studies and meta-analyses have shown that SDD helps prevent hospital infection in ICU and reduce mortality . Wide implementation of SDD was restricted, inter alia, because of fears of increasing resistance of nosocomial microorganisms to antibiotics ; however, convincing data have been obtained confirming the absence of resistant bacterial growth at the background of selective decolonization. A number of major investigations are currently underway, and their authors are expected to give shortly new clinical recommendations concerning the use of this method in ICU . The pronounced clinical effect may be associated with a change in the profile of microbial metabolites, which requires additional research.
As shown above, the “harmful/beneficial” gut bacteria disbalance is frequently associated with nosocomial pathogens and adverse outcome. The influence of negative factors related to changed internal environment of the macroorganism, and rather aggressive therapy leads to a drastic change in the species diversity of microbiota  and, as a consequence, a disturbance of functional activity of microbial community and a development of the maximal disorders that may cause irreversible breakdowns of homeostasis and host body death. A “vicious circle” is created: disturbance of gut microbiome function in critically ill patients leads to overproduction of certain microbial metabolites, which, in turn, have pathological impact on macroorganism’s organs and systems (Figure 4).
Two potential points of effect in sepsis treatment can be identified as:
Host state: prognosing negative dynamics of homeostasis indices as critical condition progresses and maximally sparing regimens of antimicrobial therapy taking into account the important role of microbiome
Treatment strategies: suppression of overgrowth and targeted correction of bacterial metabolism 
So, are the microbiota-oriented diagnostics and therapy in sepsis a utopia or necessity? In real clinical practice, it is not yet possible to provide real-time monitoring of the microbiome, due to such diagnostics being time-consuming, expensive, complex, and insufficiently studied. Previous works have noted that the gut is a “motor of multiple organ failure and sepsis” , and its underestimation earned it a name of “forgotten organ.” In the past decades, the number of studies of microbiota in various diseases, including sepsis, has increased drastically and is likely to keep rising. Now it is clear that the “forgotten organ” is a reservoir of pathogens and possibly of genes associated with antibiotic resistance, as well as a marker of disease severity and outcome. Therapy aimed at restoring microbiota equilibrium rather than blindly prescribing broad-spectrum antibiotics may be the best choice. Understanding the metabolic language of microorganisms will serve as a catalyst for the development of new strategies, which will be especially important in the era of antibiotic resistance. New, culturally independent technologies allowing a fast accurate and comprehensive assessment of microbiome will be adapted in the coming years for practical use and wide application. Characterization of changes in ICU patient’s microbiome will enable advancement in the development of diagnostic and therapeutic interventions based on changes not only in the microbiota’s composition but also in its metabolic profile as well.
We used gas chromatography-mass spectrometry (GC-MS) method to quantify metabolites in human serum from septic patients and healthy volunteers. For taxonomic identification of samples, Ion 16S Metagenomics Kits, Ion Reporter metagenomic workflow solution, and Ion Torrent sequencing systems were used. Clinical and laboratory data and APACHE II and SOFA scores in patients were matched. Data were compared by Mann-Whitney U test; p-values less than 0.05 were considered significant.