4.7 Article

Ecological and evolutionary drivers of haemoplasma infection and bacterial genotype sharing in a Neotropical bat community

Journal

MOLECULAR ECOLOGY
Volume 29, Issue 8, Pages 1534-1549

Publisher

WILEY
DOI: 10.1111/mec.15422

Keywords

16S rRNA; bacterial zoonosis; cophylogeny; host shifts; host specificity; Mycoplasma; parasite sharing

Funding

  1. ARCS Foundation
  2. American Society of Mammalogists
  3. Odum School of Ecology
  4. NSF [DEB-1716698, DEB-1601052]
  5. Defense Advanced Research Projects Agency [DARPA D16AP00113]
  6. Defense Advanced Research Projects Agency (DARPA PREEMPT program) [D18AC00031]
  7. U.S. National Institutes of General Medical Sciences IDeA Program [P20GM103474, P30GM110732]
  8. USDA National Institute of Food and Agriculture (Hatch project) [1015891]
  9. American Museum of Natural History Theodore Roosevelt Memorial Fund
  10. American Museum of Natural History Taxonomic Mammalogy Fund
  11. Sir Henry Dale Fellowship - Wellcome Trust [102507/Z/13/Z]
  12. Sir Henry Dale Fellowship - Royal Society [102507/Z/13/Z]
  13. Explorer's Club
  14. MRC [MC_UU_12014/8] Funding Source: UKRI

Ask authors/readers for more resources

Most emerging pathogens can infect multiple species, underlining the importance of understanding the ecological and evolutionary factors that allow some hosts to harbour greater infection prevalence and share pathogens with other species. However, our understanding of pathogen jumps is based primarily around viruses, despite bacteria accounting for the greatest proportion of zoonoses. Because bacterial pathogens in bats (order Chiroptera) can have conservation and human health consequences, studies that examine the ecological and evolutionary drivers of bacterial prevalence and barriers to pathogen sharing are crucially needed. Here were studied haemotropic Mycoplasma spp. (i.e., haemoplasmas) across a species-rich bat community in Belize over two years. Across 469 bats spanning 33 species, half of individuals and two-thirds of species were haemoplasma positive. Infection prevalence was higher for males and for species with larger body mass and colony sizes. Haemoplasmas displayed high genetic diversity (21 novel genotypes) and strong host specificity. Evolutionary patterns supported codivergence of bats and bacterial genotypes alongside phylogenetically constrained host shifts. Bat species centrality to the network of shared haemoplasma genotypes was phylogenetically clustered and unrelated to prevalence, further suggesting rare-but detectable-bacterial sharing between species. Our study highlights the importance of using fine phylogenetic scales when assessing host specificity and suggests phylogenetic similarity may play a key role in host shifts not only for viruses but also for bacteria. Such work more broadly contributes to increasing efforts to understand cross-species transmission and the epidemiological consequences of bacterial pathogens.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available