The Xenorhabdus nematophila LrhA transcriptional regulator modulates production of γ-keto- N -acyl amides with inhibitory activity against mutualistic host nematode egg hatching

Author:

Lam Yick Chong12,Hamchand Randy12ORCID,Mucci Nicholas C.3,Kauffman Sarah J.3,Dudkina Natavan12,Reagle Emily V.24,Casanova-Torres Ángel M.5,DeCuyper Jessica3,Chen Haiwei6,Song Deguang6,Thomas Michael G.5,Palm Noah W.6ORCID,Goodrich-Blair Heidi35ORCID,Crawford Jason M.124ORCID

Affiliation:

1. Department of Chemistry, Yale University, New Haven, Connecticut, USA

2. Institute of Biomolecular Design & Discovery, Yale University, West Haven, Connecticut, USA

3. Department of Microbiology, University of Tennessee, Knoxville, Tennessee, USA

4. Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut, USA

5. Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA

6. Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut, USA

Abstract

ABSTRACT Xenorhabdus nematophila is a symbiotic Gammaproteobacterium that produces diverse natural products that facilitate mutualistic and pathogenic interactions in their nematode and insect hosts, respectively. The interplay between X. nematophila secondary metabolism and symbiosis stage is tuned by various global regulators. An example of such a regulator is the LysR-type protein transcription factor LrhA, which regulates amino acid metabolism and is necessary for virulence in insects and normal nematode progeny production. Here, we utilized comparative metabolomics and molecular networking to identify small molecule factors regulated by LrhA and characterized a rare γ-ketoacid (GKA) and two new N -acyl amides, GKA-Arg ( 1 ) and GKA-Pro ( 2 ) which harbor a γ-keto acyl appendage. A lrhA null mutant produced elevated levels of compound 1 and reduced levels of compound 2 relative to wild type. N -acyl amides 1 and 2 were shown to be selective agonists for the human G-protein-coupled receptors (GPCRs) C3AR1 and CHRM2, respectively. The CHRM2 agonist 2 deleteriously affected the hatch rate and length of Steinernema nematodes. This work further highlights the utility of exploiting regulators of host-bacteria interactions for the identification of the bioactive small molecule signals that they control. IMPORTANCE Xenorhabdus bacteria are of interest due to their symbiotic relationship with Steinernema nematodes and their ability to produce a variety of natural bioactive compounds. Despite their importance, the regulatory hierarchy connecting specific natural products and their regulators is poorly understood. In this study, comparative metabolomic profiling was utilized to identify the secondary metabolites modulated by the X. nematophila global regulator LrhA. This analysis led to the discovery of three metabolites, including an N -acyl amide that inhibited the egg hatching rate and length of Steinernema carpocapsae nematodes. These findings support the notion that X. nematophila LrhA influences the symbiosis between X. nematophila and S. carpocapsae through N -acyl amide signaling. A deeper understanding of the regulatory hierarchy of these natural products could contribute to a better comprehension of the symbiotic relationship between X. nematophila and S. carpocapsae .

Funder

HHS | NIH | National Institute of General Medical Sciences

NASEM | Ford Foundation Fellowship Programs

HHS | National Institutes of Health

UW-Madison USDA Hatch Multi-state Research Formula Fund

University of Tennessee, Knoxville

Publisher

American Society for Microbiology

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