Bacterial Associates of a Desert Specialist Fungus-Growing Ant Antagonize Competitors with a Nocamycin Analog

02 March 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Fungus-growing ants are defended by antibiotic-producing bacterial symbionts in the genus Pseudonocardia. Nutrients provisioned by the ants support these symbionts but also invite colonization and competition from other bacteria. As an arena for chemically-mediated bacterial competition, this niche offers a window into ecological antibiotic function with well-defined competing organisms. From multiple colonies of the desert specialist ant Trachymyrmex smithi, we isolated Amycolatopsis bacteria that inhibit the growth of Pseudonocardia symbionts. Using bioassay-guided fractionation, we discovered a novel analog of the antibiotic nocamycin that is responsible for this antagonism. We identified the biosynthetic gene cluster for this antibiotic, which has a suite of oxidative enzymes consistent with this molecule's more extensive oxidative tailoring relative to similar tetramic acid antibiotics. High genetic similarity to globally distributed soil Amycolatopsis isolates suggest that this ant-derived Amycolatopsis strain may be an opportunistic soil strain whose antibiotic production allows for competition in this specialized niche. This nocamycin analog adds to the catalog of novel bioactive molecules isolated from bacterial associates of fungus-growing ants and its activity against ant symbionts represents, to our knowledge, the first documented ecological function for the widely distributed enoyl tetramic acid family of antibiotics.

Keywords

Chemical ecology
Natural products
Biosynthetic gene cluster
Tetramic acid
Nocamycin

Supplementary materials

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Supporting information
Description
Summary of bacterial strains used; mass spectra, NMR spectra, and NMR spectral data for nocamycin V; summary of nocamycin V BGC genes; phylogeny of cytochromes P450 from tirandamycin and nocamycin BGCs; summary of all putative nocamycin V BGCs.
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