Bacterial-fungal crosstalk is defined by a fungal lactone mycotoxin and its degradation by a bacterial lactonase

Author:

Dor Shlomit1ORCID,Nudel Keren12,Eagan Justin L.3ORCID,Cohen Rami1,Hull Christina M.34,Keller Nancy P.35ORCID,Prusky Dov6,Afriat-Jurnou Livnat12ORCID

Affiliation:

1. Department of Molecular and Computational Biosciences and Biotechnology, Migal-Galilee Research Institute, Kiryat Shmona, Israel

2. Faculty of Sciences and Technology, Tel-Hai College, Upper Galilee, Israel

3. Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, Wisconsin, USA

4. Department of Biomolecular Chemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA

5. Department of Plant Pathology, University of Wisconsin-Madison, Madison, Wisconsin, USA

6. Department of Postharvest Science, Agricultural Research Organization, Rishon LeZion, Israel

Abstract

ABSTRACT Bacteria, fungi, and mammals contain lactonases that can degrade the Gram-negative bacterial quorum sensing (QS) molecules N-acyl homoserine lactones (AHLs). AHLs are critical for bacteria to coordinate gene expression and pathogenicity with population density. However, AHL-degrading lactonases present variable substrate ranges, including degradation of the Pencillium expansum lactone mycotoxin patulin. We selected Erwinia spp. as our model bacteria to further investigate this interaction. We find both native apple microbiome Erwinia spp. and the fruit tree pathogen Erwinia amylovora to be inhibited by patulin. At patulin concentrations that inhibited E. amylovora growth, expression of E. amylovora lactonase encoded by EaaiiA was increased. EaAiiA demonstrated the ability to degrade patulin in vitro, as well, as in vivo where it reduced apple disease and patulin production by P. expansum . Fungal-bacterial co-cultures revealed that the E. amylovora Δ eaaiia strain failed to protect apples from P. expansum infections, which contained significant amounts of patulin. Our results suggest that bacterial lactonase production can modulate the pathogenicity of P. expansum in response to the secretion of toxic patulin. IMPORTANCE Chemical signaling in the microbial world facilitates the regulation of gene expression as a function of cell population density. This is especially true for the Gram-negative bacterial signal N-acyl homoserine lactone (AHL). Lactonases that deactivate AHLs have attracted a lot of attention because of their antibacterial potential. However, the involvement of these enzymes in inhibiting fungal pathogens and the potential role of these enzymes in bacterial-fungal interactions are unknown. Here, we find that a bacterial enzyme involved in the degradation of AHLs is also induced by and degrades the fungal lactone mycotoxin, patulin. This work supports the potential use of bacterial enzymes and/or the producing bacteria in controlling the post-harvest fruit disease caused by the patulin-producing fungus Penicillium expansum .

Funder

Jewish Charitable Association

United States-Israel Binational Agricultural Research and Development Fund

United States-Iarael Binational Agricultural Fund

Publisher

American Society for Microbiology

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