4.4 Article

Vibrio cholerae Infection Induces Strain-Specific Modulation of the Zebrafish Intestinal Microbiome

Journal

INFECTION AND IMMUNITY
Volume 89, Issue 9, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.00157-21

Keywords

Vibrio cholerae; cholera; microbiome; zebrafish

Funding

  1. Public Health Service grant from the National Institute of Allergy and Infectious Diseases [R01AI127390]

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Zebrafish provide an attractive model for studying host-microbe interactions, with the core intestinal microbiome primarily consisting of Proteobacteria. Vibrio cholerae can significantly alter the zebrafish intestinal microbiome, with different strains inducing varying changes. Specific microbes targeted by V. cholerae for colonization in zebrafish hosts depend on the genotype of the V. cholerae strain.
Zebrafish (Danio rerio) is an attractive model organism to use for an array of scientific studies, including host-microbe interactions. Zebrafish contain a core (i.e., consistently detected) intestinal microbiome consisting primarily of Proteobacteria. Furthermore, this core intestinal microbiome is plastic and can be significantly altered due to external factors. Zebrafish are particularly useful for the study of aquatic microbes that can colonize vertebrate hosts, including Vibrio cholerae. As an intestinal pathogen, V. cholerae must colonize the intestine of an exposed host for pathogenicity to occur. Members of the resident intestinal microbial community likely must be reduced or eliminated by V. cholerae for colonization, and subsequent disease, to occur. Many studies have explored a variety of aspects of the pathogenic effects of V. choierae on zebrafish and other model organisms but few have researched how a V. cholerae infection changes the resident intestinal microbiome. In this study, 16S rRNA gene sequencing was used to examine how five genetically diverse V. cholerae strains alter the intestinal microbiome following an infection. We found that V. cholerae colonization induced significant changes in the zebrafish intestinal microbiome. Notably, changes in the microbial profile were significantly different from each other, based on the particular strain of V. cholerae used to infect zebrafish hosts. We conclude that V. cholerae significantly modulates the zebrafish intestinal microbiota to enable colonization and that specific microbes that are targeted depend on the V. choierae genotype.

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