Myxobacteria restrain Phytophthora invasion by scavenging thiamine in soybean rhizosphere via outer membrane vesicle-secreted thiaminase I
Public metabolites such as vitamins play critical roles in maintaining the ecological functions of microbial community. However, the biochemical and physiological bases for fine-tuning of public metabolites in the microbiome remain poorly understood. Here, we examine the interactions between myxobac...
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Veröffentlicht in: | Nature communications 2023-09, Vol.14 (1), p.5646-16, Article 5646 |
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Sprache: | eng |
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Zusammenfassung: | Public metabolites such as vitamins play critical roles in maintaining the ecological functions of microbial community. However, the biochemical and physiological bases for fine-tuning of public metabolites in the microbiome remain poorly understood. Here, we examine the interactions between myxobacteria and
Phytophthora sojae
, an oomycete pathogen of soybean. We find that host plant and soil microbes complement
P. sojae’
s auxotrophy for thiamine. Whereas, myxobacteria inhibits
Phytophthora
growth by a thiaminase I CcThi1 secreted into extracellular environment via outer membrane vesicles (OMVs). CcThi1 scavenges the required thiamine and thus arrests the thiamine sharing behavior of
P. sojae
from the supplier, which interferes with amino acid metabolism and expression of pathogenic effectors, probably leading to impairment of
P. sojae
growth and pathogenicity. Moreover, myxobacteria and CcThi1 are highly effective in regulating the thiamine levels in soil, which is correlated with the incidence of soybean
Phytophthora
root rot. Our findings unravel a novel ecological tactic employed by myxobacteria to maintain the interspecific equilibrium in soil microbial community.
The plant pathogen
Phytophthora sojae
requires exogenous thiamine for growth. Here, Li et al. show that soil myxobacteria inhibit
Phytophthora
’s growth by scavenging thiamine through the secretion a thiaminase via outer membrane vesicles. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-023-41247-0 |