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The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi

Soil‐dwelling entomopathogenic nematodes (EPNs) kill arthropod hosts by injecting their symbiotic bacteria into the host hemolymph and feed on the bacteria and the tissue of the dying host for several generations cycles until the arthropod cadaver is completely depleted. The EPN–bacteria–arthropod c...

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Autores principales: Shan, Shaojie, Wang, Wenwu, Song, Chunxu, Wang, Minggang, Sun, Bingjiao, Li, Yang, Fu, Yaqi, Gu, Xinghui, Ruan, Weibin, Rasmann, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465237/
https://www.ncbi.nlm.nih.gov/pubmed/30618110
http://dx.doi.org/10.1111/1751-7915.13365
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author Shan, Shaojie
Wang, Wenwu
Song, Chunxu
Wang, Minggang
Sun, Bingjiao
Li, Yang
Fu, Yaqi
Gu, Xinghui
Ruan, Weibin
Rasmann, Sergio
author_facet Shan, Shaojie
Wang, Wenwu
Song, Chunxu
Wang, Minggang
Sun, Bingjiao
Li, Yang
Fu, Yaqi
Gu, Xinghui
Ruan, Weibin
Rasmann, Sergio
author_sort Shan, Shaojie
collection PubMed
description Soil‐dwelling entomopathogenic nematodes (EPNs) kill arthropod hosts by injecting their symbiotic bacteria into the host hemolymph and feed on the bacteria and the tissue of the dying host for several generations cycles until the arthropod cadaver is completely depleted. The EPN–bacteria–arthropod cadaver complex represents a rich energy source for the surrounding opportunistic soil fungal biota and other competitors. We hypothesized that EPNs need to protect their food source until depletion and that the EPN symbiotic bacteria produce volatile and non‐volatile exudations that deter different soil fungal groups in the soil. We isolated the symbiotic bacteria species (Alcaligenes faecalis) from the EPN Oscheius spp. and ran infectivity bioassays against entomopathogenic fungi (EPF) as well as against plant pathogenic fungi (PPF). We found that both volatile and non‐volatile symbiotic bacterial exudations had negative effects on both EPF and PPF. Such deterrent function on functionally different fungal strains suggests a common mode of action of A. faecalis bacterial exudates, which has the potential to influence the structure of soil microbial communities, and could be integrated into pest management programs for increasing crop protection against fungal pathogens.
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spelling pubmed-64652372019-04-23 The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi Shan, Shaojie Wang, Wenwu Song, Chunxu Wang, Minggang Sun, Bingjiao Li, Yang Fu, Yaqi Gu, Xinghui Ruan, Weibin Rasmann, Sergio Microb Biotechnol Research Articles Soil‐dwelling entomopathogenic nematodes (EPNs) kill arthropod hosts by injecting their symbiotic bacteria into the host hemolymph and feed on the bacteria and the tissue of the dying host for several generations cycles until the arthropod cadaver is completely depleted. The EPN–bacteria–arthropod cadaver complex represents a rich energy source for the surrounding opportunistic soil fungal biota and other competitors. We hypothesized that EPNs need to protect their food source until depletion and that the EPN symbiotic bacteria produce volatile and non‐volatile exudations that deter different soil fungal groups in the soil. We isolated the symbiotic bacteria species (Alcaligenes faecalis) from the EPN Oscheius spp. and ran infectivity bioassays against entomopathogenic fungi (EPF) as well as against plant pathogenic fungi (PPF). We found that both volatile and non‐volatile symbiotic bacterial exudations had negative effects on both EPF and PPF. Such deterrent function on functionally different fungal strains suggests a common mode of action of A. faecalis bacterial exudates, which has the potential to influence the structure of soil microbial communities, and could be integrated into pest management programs for increasing crop protection against fungal pathogens. John Wiley and Sons Inc. 2019-01-07 /pmc/articles/PMC6465237/ /pubmed/30618110 http://dx.doi.org/10.1111/1751-7915.13365 Text en © 2019 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Shan, Shaojie
Wang, Wenwu
Song, Chunxu
Wang, Minggang
Sun, Bingjiao
Li, Yang
Fu, Yaqi
Gu, Xinghui
Ruan, Weibin
Rasmann, Sergio
The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi
title The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi
title_full The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi
title_fullStr The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi
title_full_unstemmed The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi
title_short The symbiotic bacteria Alcaligenes faecalis of the entomopathogenic nematodes Oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi
title_sort symbiotic bacteria alcaligenes faecalis of the entomopathogenic nematodes oscheius spp. exhibit potential biocontrol of plant‐ and entomopathogenic fungi
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465237/
https://www.ncbi.nlm.nih.gov/pubmed/30618110
http://dx.doi.org/10.1111/1751-7915.13365
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