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The Gut Microbiota Protects Bees from Invasion by a Bacterial Pathogen
Margaret I Steele1, Erick V S Motta1, Tejashwini Gattu1
1Department of Integrative Biology, University of Texas at Austin, Austin, Texas, USA.
Abstract:
Commensal microbes in animal guts often help to exclude bacterial pathogens. In honey bees, perturbing or depleting the gut microbiota increases host mortality rates upon challenge with the opportunistic pathogen Serratia marcescens, suggesting antagonism between S. marcescens and one or more members of the bee gut microbiota. In laboratory culture, S. marcescens uses a type VI secretion system (T6SS) to kill bacterial competitors, but the role of this T6SS within hosts is unknown. Using infection assays, we determined how the microbiota impacts the abundance and persistence of S. marcescens in the gut and visualized colocalization of S. marcescens with specific community members in situ. Using T6SS-deficient S. marcescens strains, we measured T6SS-dependent killing of gut isolates in vitro and compared the persistence of mutant and wild-type strains in the gut. We found that S. marcescens is rapidly eliminated in the presence of the microbiota but persists in microbiota-free guts. Protection is reduced in monocolonized and antibiotic-treated bees, possibly because different symbionts occupy distinct niches. Serratia marcescens uses a T6SS to antagonize Escherichia coli and other S. marcescens strains but shows limited ability to kill bee symbionts. Furthermore, wild-type and T6SS-deficient S. marcescens strains achieved similar abundance and persistence in bee guts. Thus, an intact gut microbiota offers robust protection against this common pathogen, whose T6SSs do not confer the ability to compete with commensal species. IMPORTANCE Bacteria living within guts of animals can provide protection against infection by pathogens. Some pathogens have been shown to use a molecular weapon known as a T6SS to kill beneficial bacteria during invasion of the mouse gut. In this study, we examined how bacteria native to the honey bee gut work together to exclude the opportunistic pathogen Serratia marcescens. Although S. marcescens has a T6SS that can kill bacteria, bee gut bacteria seem resistant to its effects. This limitation may partially explain why ingestion of S. marcescens is rarely lethal to insects with healthy gut communities.
Insights
A healthy honey bee gut microbiota effectively prevents the pathogen Serratia marcescens from establishing. The pathogen
Area of Science:
- Microbiology
- Insect Pathology
- Microbiome Research
Background:
- Commensal gut microbes protect animal hosts from bacterial pathogens.
- Perturbing the honey bee gut microbiota increases mortality upon challenge with Serratia marcescens.
- Serratia marcescens employs a type VI secretion system (T6SS) to kill competitors in vitro.
Purpose of the Study:
- To investigate the impact of the honey bee gut microbiota on Serratia marcescens abundance and persistence.
- To determine the role of Serratia marcescens T6SS in host-microbe interactions.
- To assess the susceptibility of bee gut symbionts to Serratia marcescens T6SS.
Main Methods:
- Infection assays to track S. marcescens in vivo.
- In vitro killing assays using T6SS-deficient S. marcescens strains.
- In situ visualization of S. marcescens colocalization with gut symbionts.
- Comparison of wild-type and T6SS-mutant S. marcescens persistence in bee guts.
Main Results:
- Serratia marcescens is rapidly cleared in the presence of a normal gut microbiota but persists in microbiota-free guts.
- S. marcescens T6SS antagonizes E. coli and other S. marcescens strains but shows limited killing of bee symbionts.
- Wild-type and T6SS-deficient S. marcescens strains exhibited similar abundance and persistence in honey bee guts.
Conclusions:
- An intact honey bee gut microbiota provides robust protection against Serratia marcescens.
- The T6SS of S. marcescens is not effective against key honey bee gut symbionts.
- Microbiota-mediated exclusion, rather than T6SS-based competition, is the primary mechanism limiting S. marcescens.
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