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Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara
Bacteria colonize specific niches in the animal gut. However, the genetic basis of these associations is often unclear. The proteobacterium Frischella perrara is a widely distributed gut symbiont of honey bees. It colonizes a specific niche in the hindgut and causes a characteristic melanization res...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104596/ https://www.ncbi.nlm.nih.gov/pubmed/37057993 http://dx.doi.org/10.7554/eLife.76182 |
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author | Schmidt, Konstantin Santos-Matos, Gonçalo Leopold-Messer, Stefan El Chazli, Yassine Emery, Olivier Steiner, Théodora Piel, Joern Engel, Philipp |
author_facet | Schmidt, Konstantin Santos-Matos, Gonçalo Leopold-Messer, Stefan El Chazli, Yassine Emery, Olivier Steiner, Théodora Piel, Joern Engel, Philipp |
author_sort | Schmidt, Konstantin |
collection | PubMed |
description | Bacteria colonize specific niches in the animal gut. However, the genetic basis of these associations is often unclear. The proteobacterium Frischella perrara is a widely distributed gut symbiont of honey bees. It colonizes a specific niche in the hindgut and causes a characteristic melanization response. Genetic determinants required for the establishment of this association, or its relevance for the host, are unknown. Here, we independently isolated three point mutations in genes encoding the DNA-binding protein integration host factor (IHF) in F. perrara. These mutants abolished the production of an aryl polyene metabolite causing the yellow colony morphotype of F. perrara. Inoculation of microbiota-free bees with one of the mutants drastically decreased gut colonization of F. perrara. Using RNAseq, we found that IHF affects the expression of potential colonization factors, including genes for adhesion (type 4 pili), interbacterial competition (type 6 secretion systems), and secondary metabolite production (colibactin and aryl polyene biosynthesis). Gene deletions of these components revealed different colonization defects depending on the presence of other bee gut bacteria. Interestingly, one of the T6SS mutants did not induce the scab phenotype anymore despite colonizing at high levels, suggesting an unexpected role in bacteria-host interaction. IHF is conserved across many bacteria and may also regulate host colonization in other animal symbionts. |
format | Online Article Text |
id | pubmed-10104596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-101045962023-04-15 Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara Schmidt, Konstantin Santos-Matos, Gonçalo Leopold-Messer, Stefan El Chazli, Yassine Emery, Olivier Steiner, Théodora Piel, Joern Engel, Philipp eLife Microbiology and Infectious Disease Bacteria colonize specific niches in the animal gut. However, the genetic basis of these associations is often unclear. The proteobacterium Frischella perrara is a widely distributed gut symbiont of honey bees. It colonizes a specific niche in the hindgut and causes a characteristic melanization response. Genetic determinants required for the establishment of this association, or its relevance for the host, are unknown. Here, we independently isolated three point mutations in genes encoding the DNA-binding protein integration host factor (IHF) in F. perrara. These mutants abolished the production of an aryl polyene metabolite causing the yellow colony morphotype of F. perrara. Inoculation of microbiota-free bees with one of the mutants drastically decreased gut colonization of F. perrara. Using RNAseq, we found that IHF affects the expression of potential colonization factors, including genes for adhesion (type 4 pili), interbacterial competition (type 6 secretion systems), and secondary metabolite production (colibactin and aryl polyene biosynthesis). Gene deletions of these components revealed different colonization defects depending on the presence of other bee gut bacteria. Interestingly, one of the T6SS mutants did not induce the scab phenotype anymore despite colonizing at high levels, suggesting an unexpected role in bacteria-host interaction. IHF is conserved across many bacteria and may also regulate host colonization in other animal symbionts. eLife Sciences Publications, Ltd 2023-04-14 /pmc/articles/PMC10104596/ /pubmed/37057993 http://dx.doi.org/10.7554/eLife.76182 Text en © 2023, Schmidt, Santos-Matos et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Microbiology and Infectious Disease Schmidt, Konstantin Santos-Matos, Gonçalo Leopold-Messer, Stefan El Chazli, Yassine Emery, Olivier Steiner, Théodora Piel, Joern Engel, Philipp Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara |
title | Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara |
title_full | Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara |
title_fullStr | Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara |
title_full_unstemmed | Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara |
title_short | Integration host factor regulates colonization factors in the bee gut symbiont Frischella perrara |
title_sort | integration host factor regulates colonization factors in the bee gut symbiont frischella perrara |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104596/ https://www.ncbi.nlm.nih.gov/pubmed/37057993 http://dx.doi.org/10.7554/eLife.76182 |
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