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  The intricate triangular interaction between protective microbe, pathogen and host determines fitness of the metaorganism

Griem-Krey, H., Petersen, C., Hamerich, I. K., & Schulenburg, H. (2023). The intricate triangular interaction between protective microbe, pathogen and host determines fitness of the metaorganism. Proceedings of the Royal Society B: Biological Sciences, 290: 20232193. doi:10.1098/rspb.2023.2193.

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griem-krey-et-al-2023-the-intricate-triangular-interaction-between-protective-microbe-pathogen-and-host-determines.pdf (Publisher version), 554KB
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Griem-Krey, Hanne, Author
Petersen, Carola, Author
Hamerich, Inga K., Author
Schulenburg, Hinrich1, Author                 
Affiliations:
1Max Planck Fellow Group Antibiotic Resistance Evolution, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_2600692              

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Free keywords: metaorganism, Caenorhabditis elegans, host–microbiota interactions, protective bacteria, Pseudomonas lurida, Bacillus thuringiensis
 Abstract: The microbiota shapes host biology in numerous ways. One example is protection against pathogens, which is likely critical for host fitness in consideration of the ubiquity of pathogens. The host itself can affect abundance of microbiota or pathogens, which has usually been characterized in separate studies. To date, however, it is unclear how the host influences the interaction with both simultaneously and how this triangular interaction determines fitness of the host–microbe assemblage, the so-called metaorganism. To address this current knowledge gap, we focused on a triangular model interaction, consisting of the nematode Caenorhabditis elegans, its protective symbiont Pseudomonas lurida MYb11 and its pathogen Bacillus thuringiensis Bt679. We combined the two microbes with C. elegans mutants with altered immunity and/or microbial colonization, and found that (i) under pathogen stress, immunocompetence has a larger influence on metaorganism fitness than colonization with the protective microbe; (ii) in almost all cases, MYb11 still improves fitness; and (iii) disruption of p38 MAPK signalling, which contributes centrally to immunity against Bt679, completely reverses the protective effect of MYb11, which further reduces nematode survival and fitness upon infection with Bt679. Our study highlights the complex interplay between host, protective microbe and pathogen in shaping metaorganism biology.

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Language(s): eng - English
 Dates: 2023-09-262023-11-072023-12-062023
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1098/rspb.2023.2193
 Degree: -

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Title: Proceedings of the Royal Society B: Biological Sciences
  Abbreviation : Proc. R. Soc. B
Source Genre: Journal
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Publ. Info: London : Royal Society
Pages: - Volume / Issue: 290 Sequence Number: 20232193 Start / End Page: - Identifier: ISSN: 0962-8452
CoNE: https://pure.mpg.de/cone/journals/resource/110975500577295_2