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Host microbiota can facilitate pathogen infection

['Emily J. Stevens', 'Department Of Zoology', 'University Of Oxford', 'Oxford', 'United Kingdom', 'Kieran A. Bates', 'Kayla C. King']

Date: None

Animals live in symbiosis with numerous microbe species. While some can protect hosts from infection and benefit host health, components of the microbiota or changes to the microbial landscape have the potential to facilitate infections and worsen disease severity. Pathogens and pathobionts can exploit microbiota metabolites, or can take advantage of a depletion in host defences and changing conditions within a host, to cause opportunistic infection. The microbiota might also favour a more virulent evolutionary trajectory for invading pathogens. In this review, we consider the ways in which a host microbiota contributes to infectious disease throughout the host’s life and potentially across evolutionary time. We further discuss the implications of these negative outcomes for microbiota manipulation and engineering in disease management.

Copyright: © 2021 Stevens et al. This is an open access article distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

To understand the multifaceted contributors to infectious disease, the potentially harmful aspects of the microbiota and its components warrant consideration. Microbe-based therapies for disease are being investigated as alternatives to antimicrobials for a wide range of animal hosts, from endangered amphibians to humans [ 36 – 38 ]. A thorough evaluation of the potential for host microbiota to contribute to infectious disease is necessary to establish their utility in disease management as anti-infective prophylactics, probiotics, and prebiotics. In this review, we will discuss the conditions under which microbiota can promote or worsen infection outcomes, with evolutionary consequences. We will then discuss the implications of this potential to facilitate pathogen invasion and infection from within for microbiota manipulation.

It is well established that host microbiota generally play a beneficial role in preventing or fighting infection [ 17 – 20 ]. Microbe-mediated protection can be mediated via resource competition [ 21 , 22 ], interference competition [ 23 ], or the host immune response [ 24 , 25 ]. However, the relative magnitude of these benefits might decrease when microbiota components, in some cases, directly or indirectly facilitate the onset of disease caused by invading pathogens or pathobionts ( Table 1 ). Although some invading pathogens can exploit cues or changes in the resource/immunological environment shaped by the microbiota itself, the context of host health is also an important determinant of infection. Diminished host health can remove the beneficial services the microbiota normally provides. Changes in host health can correlate with dysbiosis of host microbiota [ 26 – 28 ], and opportunistic microbiota components can transition to become harmful among the perturbation [ 26 , 29 – 31 ]. This perturbation and transition of commensals towards pathogenicity can sometimes even be caused by invading pathogens [ 32 , 33 ]. Moreover, protective microbes can become relatively costly to their host in the absence of the invading pathogens they would otherwise suppress [ 31 , 34 , 35 ] (i.e., the same microbial species is protective in one context, but costly in another; see “Costly protective symbionts”).

Microbiota are vital to the functioning of their multicellular host organisms. This realisation has fuelled great interest in the effects of microbes on plant [ 9 ] and animal host health [ 10 ]. Microbe-mediated protection against infection is a widespread phenomenon across host species [ 11 ], with components of the microbiota and their interactions with a host and the wider microbial community mediating susceptibility to invading pathogens and internal pathobionts [ 12 , 13 ]. There are several ways to categorise and define pathogens based on their biology [ 3 ]. Here, we use the term “pathobiont” to mean normally harmless components of the microbiota which have pathogenic potential in some contexts [ 14 – 16 ]. We distinguish these from “invading pathogens,” by which we mean pathogens (including parasites) acquired from a source external to the host (i.e., from a different host or from the environment).

An infection by pathogens (and parasites) can vary from relatively benign to lethal. The degree of harm caused during infection can be driven by aspects of pathogen biology, such as transmissibility [ 1 ], infective dose [ 2 ], or whether they are facultative/obligate [ 3 ], as well as by host biology, and the surrounding biotic or abiotic environment [ 4 ]. While hosts can be genetically predisposed to susceptibility [ 5 ], disease outcomes can be made worse if hosts have a comorbidity [ 6 ] or an impaired or over-reactive immune response [ 7 ]. When invading a host, pathogens will also interact with other microbial species [ 8 ]. The outcome of infection is thus held in the balance by the complex interactions between a host, its microbiota, and both the biotic and abiotic environment [ 4 ].

Promotion of pathogen invaders

Microbiota components modify the within-host environment Metabolic environment. Microbiota metabolites are beneficial to hosts in myriad ways. They help to prime the immune system, act as antimicrobials to combat infection, and aid host metabolism [24,80–82]. However, microbiota metabolites can also provide a convenient and easily attainable source of food for invading pathogens to exploit. Metabolic cross-feeding, in which a product of metabolism from one strain is used by another strain, generates novel niches that may benefit pathogens [83]. This assimilation of resources can enhance energy production within the pathogen, enabling increased virulence and rapid growth, and thus more severe disease. For example, the human gut commensal Bacteroides thetaiotaomicron (Bt) can exacerbate infection caused by enterohaemorrhagic Escherichia coli (EHEC) via metabolic cross-feeding [84]. Bt modifies the metabolic environment at the site of EHEC infection, increasing metabolites involved in gluconeogenesis which are then sensed by the virulence-regulating transcription factor Cra. Virulence is up-regulated as a result and, concurrent with invasion of the gut epithelial barrier (also facilitated by Bt), EHEC induces a greater degree of host pathology and higher risk of mortality. Individual species of the microbiota cannot always be pinpointed for their role in facilitating infection. While Bt was specifically identified in the previous example as a contributor to EHEC infection [84], microbial metabolites from multiple components of the microbiota can also collectively enhance EHEC virulence [85]. A comparison between human and mouse microbiota metabolites illustrated that the increased severity of EHEC infection in humans, compared to that in mice, is driven by distinct human gut microbiota metabolites [29]. These metabolites specifically induce increased expression of flagellin in the pathogen, increasing its ability to invade host tissues. Distinct microbial communities can thus shape different infection outcomes via metabolite production. The metabolic environment within a host is a crucial contributor to the pathogenesis of invading organisms. It can be extensively modified by components of the microbiota to both the detriment and the benefit of the host. Changes in host health can likewise alter the within-host metabolic environment, contributing to disease onset from resident commensals [62]. Given the diversity of species housed by the animal gut, there are complex interactions to pick apart. Research is moving towards characterising the functionality of the microbiome by holistically sampling its taxonomic and genomic repertoire in addition to the chemical phenotype. Progress has been made in uncovering pathogen-induced disease phenotypes that are enhanced by the microbiota through application of multi-omics strategies [86,87] (see Table 2). Nonetheless, data integration and interpreting meaningful biological signatures of infection (e.g., biomarkers of infection) remain a challenge [88]. PPT PowerPoint slide

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larger image TIFF original image Download: Table 2. Representative examples of omics approaches used to deduce the role of microbiota components in facilitating infection and worsening infection outcomes. https://doi.org/10.1371/journal.ppat.1009514.t002 Immunological environment. Microbiota can prime the host immune response, altering their susceptibility to invading pathogens. Pathogen infectivity can be indirectly reduced by host microbiota this way [89–93]. Conversely, launching the immune response can inadvertently boost infection by some infectious agents [49]. Reynolds and colleagues [49] found that Lactobacillaceae species abundance in the mouse duodenum positively correlated with susceptibility to the nematode parasite Heligmosomoides polygyrus and heightened immunosuppressive regulatory T-cell and Th17 responses. Subsequent treatment of mice with Lactobacillus taiwanensis—a rodent commensal dominant in infected mice—elevated regulatory T-cell frequencies and promoted the establishment of H. polygyrus. The fact that microbiota composition changed after H. polygyrus exposure towards more “helpful” bacterial species suggests that parasites could actively modify the microbiota to improve their survival. This manipulation could occur directly via antimicrobials [94] or by pathogen-induced host inflammation [95]. Physical disruption of the host site might also cause changes in resource availability, shifting microbiota composition [96].

Invading pathogens might evolve in response to host microbiota Microbes can evolve quickly [100] because of their large population sizes and rapid generation times. Microbiota components can evolve within their host’s lifetime with consequences for host health [101]. For example, a mildly pathogenic strain of the gut microbiota component Enterococcus faecalis has been shown in nematode hosts to evolve to become more protective due to competitive interactions with a virulent pathogen [23]. Likewise, the pathogen Candida albicans was shown to evolve towards protective mutualism when introduced to a new host in a mouse model [102]. Invading pathogens, in turn, may evolve to overcome or exploit the host microbiota. They can readily overcome barriers to their establishment, including from host resistance [103], antibiotic treatments [104], and vaccines [105]. Theory has shown that pathogens can evolve virulence factors to overcome commensals in the host microbiota, either directly killing their competitors [106] or inducing host inflammation as a form of “proactive invasion” [95]. Experimental evolution approaches in animal model systems have produced mixed evidence on the ability of evolving pathogens to escape suppression by protective microbes. Martinez and colleagues [107] found that niche blocking by Wolbachia in Drosophila melanogaster effectively suppressed the pathogen Drosophila C virus (DCV), which did not evolve to overcome the protective symbiont. In contrast, Rouchet and Vorburger [108] found the parasitoid wasp, Lysiphlebus fabarum, readily counteradapted to the protection given by sympatric Hamiltonella defensa in aphids. A variety of pathogens may have evolved to exploit host microbiota for replication and transmission. Poliovirus and Trichuris muris, for example, have been empirically found to depend on interactions with mouse intestinal microbiota to trigger replication and hatching, respectively, at key host sites [47,48]. Poliovirus was able to better associate with host cells, and its replication was enhanced by up to 500% after binding lipopolysaccharide on enterobacterial surfaces [48]. Similarly, fimbriae on the surface of gut colonisers E. coli and Salmonella typhimurium were found to bind to proteins at the poles of eggs of the parasitic nematode, T. muris. This interaction with enterobacteria provides an essential cue, triggering the emergence of infective larvae [47]. Microbiome-mediated protection can drive the evolution of increased [109] and decreased [110] pathogen virulence. McNally and colleagues [109] found that manipulating the microbiota generated increased competition between commensal competitors and increased the intensity of bacterial warfare. Using theory, they found that stronger competition selected for increased expression of pathogen weapons (virulence factors). Enhanced production of virulence factors by many pathogenic bacteria can inadvertently harm the host. For example, release of Shiga toxin-encoding phage by shigatoxinagenic E. coli [111], and similarly TcdA released by Clostridioides difficile, can clear commensals both directly and via provocation of host inflammation [112,113]. Host microbiota has the potential to influence the evolutionary trajectory of invading pathogens. Manipulating host microbiota offers a promising route to treat or prevent infection, but such approaches should be scrutinised in light of the evolutionary potential of target pathogens.

Harmful infection from within Transitions of commensal microbes to pathogens. Commensals in the microbiota can transition along the parasite–mutualist continuum [66,76,114]. Transitions towards pathogenicity can be influenced by changes to the within-host environment—onset of illness or compromised immunity [7], diet [26], antibiotic treatment [115], or stress [28,116]—as well as changes in the external environment [28]. Infection by invading pathogens can also induce otherwise commensal bacteria to become pathogenic [33,117]. A well-studied example of a transition to pathogenicity is that of C. difficile, the causative agent of colitis. C. difficile can be at very low abundance in the human gastrointestinal tract. A healthy gut microbiota usually provides colonisation resistance against C. difficile expansion [52]. However, following a period of antibiotic treatment which diminishes the protective power of the microbiota, this bacterium can proliferate extensively to dominate the intestinal niche [71]. In this context, it is a highly problematic pathogen which can cause recurrent disease. Faecal microbiota transplants have proven useful in such cases, whereby the dysbiotic gut microbiota of a C. difficile patient is replaced with that of a healthy donor to eliminate the infection [118]. How can these transitions to pathogenicity occur among pathobionts? Metabolic changes in components of the microbiota can underpin the transition. Recent work on the Drosophila gut microbiome demonstrates that catabolism of host gut luminal uridine by pathobionts drives the generation of uracil and ribose. These metabolites respectively trigger an inflammatory host immune response and increased expression of virulence genes in pathobionts. Quorum sensing regulates both processes and is therefore necessary for a transition to virulence. Deletion of genes involved in nucleotide metabolism in strains of enteric Drosophila pathobionts blocked quorum sensing and thus the commensal-to-pathogen transition. Metabolites such as uracil and ribose may therefore act as pathogen-specific indicators, used by metazoan hosts to distinguish good from bad within the gut. Recognition of these indicators equips hosts to modulate immunity and gut-microbe homeostasis in response to changes within the microbiota [58]. In polymicrobial infections, metabolic cross-feeding can be an essential source of nutrients, enhancing the ability of commensal microbes to establish infection. The pathobiont Aggregatibacter actinomycetemcomitans, for example, requires L-lactate produced by the commensal bacterium Streptococcus gordonii to establish polymicrobial periodontal infection in a murine abscess model [119]. A. actinomycetemcomitans also exhibits enhanced respiratory metabolism in the presence of S. gordonii [120], as the latter increases the bioavailability of oxygen to the opportunist by providing electron acceptors. A. actinomycetemcomitans uses these electron acceptors to increase energy yield in the form of ATP production, which promotes increased virulence. With more energy available, the pathobiont can invest in the production of toxins, adhesins, and immunomodulatory proteins, among many other virulence factors [120]. Pathobionts have an array of tools available to adapt to environmental change within their niche [69,121–123]. Factors which contribute to the commensal bacterial lifestyle can be repurposed upon immune compromisation in the host or upon nutrient limitation or community disruption of the microbiota. Such changes within the host environment can lead to pathobionts proliferating beyond their niche to invade host tissues [69,123]. Adhesive proteins, for example, are required for asymptomatic colonisation of a new host, yet are also important in attaching to host cells to initiate invasion [123,124]. They can additionally contribute to the development of bacterial biofilms [69,70] to facilitate persistence of an infection under adverse conditions (e.g., antibiotic treatment). Likewise, toxins play a significant destructive role in the onset of disease. Toxins induce host cell lysis and stimulate inflammation, and they are recognised as major drivers of the symptoms of bacterial infection [125]. Recent research has also highlighted the contribution of toxins to pathobiont colonisation or persistence in different niches within the host during asymptomatic carriage, thus they aid both the commensal and pathogenic lifestyles of pathobionts [126]. Gene expression changes underpin transitions to pathogenicity and are driven by the need to adapt to changing conditions [121,122]. Infection can therefore be instigated by pathobionts within the host microbiota, following a transition from commensalism to a pathogenic state. Costly protective symbionts. In wild animal systems, beneficial microbiota components otherwise known as defensive/protective symbionts have been shown to prevent pathogen establishment and reproduction [127]. They are so effective at defending that the evolution of host resistance is slowed in the face of pathogen infection [128]. Many of these symbionts can, however, impose a physiological burden upon their host that is measured in the absence of an invading threat. [127]. For example, while the endosymbiont Wolbachia in numerous arthropod hosts defends against parasitic viruses [129], bacteria [130], and nematodes [131], Wolbachia in Drosophila fruit flies can cause a reduction in colonised host fertility, fecundity, and egg hatch rates, mediated by high symbiont densities [31]. A trade-off emerges in many host-microbe systems whereby increased conferred protection means the symbiont can become more pathogenic [34,35] (albeit, see Cayetano and colleagues [132]). Mathé-Hubert and colleagues [133] further showed that the cost of carrying a protective symbiont (Spiroplasma) in pea aphids can be alleviated by concurrent colonisation with a second symbiont (Regiella insecticola), as co-colonisation improves host lifetime reproduction and population growth. Changes in the abiotic environment can also reveal the costs of these resident protectors in the microbiota. One extreme example is a species of the nematode-infecting bacterium Leucobacter, which under dry laboratory conditions is a protective bacterium against another highly virulent Leucobacter species, but in aqueous conditions causes hosts to become irreversibly fused by their tails leading to death [134]. The abiotic environment can therefore mediate host-associated microbe function to both favour and oppose pathogenicity.

Microbiota community structure as an early warning signal Healthy microbiota community compositions can differ between individuals and population groups and also within individuals over time [135]. It is consequently not always feasible to establish what a “typical” dysbiotic microbiota looks like during infectious disease. However, a recent study in apiculture has demonstrated how early microbiota perturbations can have sustained negative consequences on host development and increase pathogen susceptibility within a population [116]. Schwarz and colleagues administered the commensal species Snodgrassella alvi to newly emerged worker bees as a potential probiotic therapy to protect against the parasite Lotmaria passim. Yet, despite S. alvi being part of the usual core microbiota of bees, inoculation of this species alone in young hosts led to microbiota perturbation, possibly reducing the protective benefits normally conferred and ultimately increasing parasite susceptibility [116]. While microbiota dysbiosis in general may correlate with infectious disease onset, microbial taxonomic signatures for specific infections may not always be a reliable indicator of disease [136]. The Anna Karenina principle [137] (“all happy families look alike, but each unhappy family is unhappy in its own way”) has been applied to explain observations in which microbiota community composition varies more between diseased individuals than healthy individuals. Nonetheless, in some instances, pathologies may be predicted by a specific reduction in certain key taxa. Bacterial vaginosis (BV) in humans is one such example, a condition caused by dysbiosis within the vaginal microbiota that affects approximately one-third of reproductive age women [138]. Vaginal microbiota composition varies across demographics [139], but onset of BV is typically associated with a reduction in Lactobacillus species, accompanied by the dominance of anaerobes and increased alpha diversity [140]. In these lactobacilli-depleted communities, the presence of biogenic amines can increase [141]. These amines, and the microbial community composition with which they are associated, could be useful biomarkers of disease in the early stages of BV development. Indeed, multi-omic approaches have been used to characterise the metabolic profiles corresponding to different symptomatic BV types [142]. Yeoman and colleagues [142] took this approach and identified distinct microbial taxa and metabolites which correlated to 2 different symptomatic BV types (and also to host behaviour). The characteristic odour of BV infection was linked to Dialister spp., the presence of discharge was linked with Mobiluncus spp., and Gardnerella spp. were linked with the symptom of pain. These findings provide both potential diagnostic markers for the onset of disease and insights into the determinants of BV. Moving beyond correlative relationships between microbes and infections to establishing causation remains a major challenge [143–146]. Due to the complexities of microbial communities within a host, including the high species richness within a niche and the multitude of microbe–microbe and host–microbe interactions, it is often difficult to attribute specific microbes to a causative role in disease. Furthermore, in some cases, infection may not be attributable to one species, but to polymicrobial interactions which are difficult to pick apart [30]. Host heterogeneity in genotype, lifestyle, and diet further compounds the ability to infer causality. Not all components of the microbiota are culturable in the laboratory setting and are only identifiable as members of the community through sequencing. They are thus often excluded from culture-dependent laboratory experiments aiming to determine causality [86,147–150]. To bridge this gap between correlation and causation in elucidating the relationship between microbiota and infection, current research is benefitting from combining laboratory experiments with multidisciplinary and multi-omic approaches (see Table 2). Tractable, controlled experimental models of defined microbial communities will be important in this transition [151]. Synthetic microbial communities composed of native microbiota components are now being developed for use in model organisms [147,152–154]. Such resources will allow in-depth dissection of host–microbiota interactions in model organisms, using tools which are easily controlled while remaining representative of natural systems. The combination of experimental models with corresponding omics data will further allow functional verification of bacterial phenotypes within the microbiota [155]; this mechanistic insight will be essential in determining causality in microbial infections.

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