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Ankita Bhattacharyya

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Open access Aug 2026

Genetic regulation of biosynthesis and resistance to redox-active phenazines in Burkholderia spp.

ABSTRACT Burkholderia includes gram-negative saprophytes, nitrogen-fixers, and species associated with nosocomial infections. Numerous strains in the Burkholderia cepacia, Burkholderia pseudomallei, Burkholderia glumae, and Burkholderia gladioli clades carry genes for phenazine (Phz) biosynthesis. Phenazines are a large class of colored, structurally diverse microbial secondary compounds with a common nitrogen-containing tricyclic core. They act as molecular signals and extracellular electron shuttles, contributing to the competitiveness of producer organisms in their natural habitats. Phenazines also undergo redox cycling, generating reactive oxygen species that suppress the growth of other organisms. The study of phenazines has largely been confined to the model opportunistic pathogen Pseudomonas aeruginosa, and many aspects of their biology in other bacterial groups remain poorly understood. In this study, we identified genes involved in phenazine production, regulation, and resistance in Burkholderia lata 383, a member of the B. cepacia complex, which produces dimethyl 4,9-dihydroxy-1,6-phenazinedicarboxylate. We subjected this strain to a transposon mutagenesis screen and characterized the transcriptomes of phenazine and quorum-sensing (QS) mutants of B. lata 383. Our results indicate that QS regulates phenazine production in Burkholderia and confirm that this cell-cell communication also controls other phenotypic traits, including biofilm formation. Analysis of transcriptome responses to phenazine methosulfate in B. lata 383 and two closely related phenazine-non-producing Burkholderia strains revealed that these organisms cope with phenazine toxicity by upregulating pathways involved in the oxidative stress response, iron-sulfur cluster biogenesis, and multidrug efflux. IMPORTANCE Burkholderia is a diverse genus comprising over 100 agriculturally, medically, and environmentally significant species. Many members of this group produce phenazines, yet the regulatory mechanisms governing phenazine biosynthesis and self-resistance remain poorly characterized. Our study sheds light on key aspects of these pathways, revealing parallels with pseudomonads in how Burkholderia species regulate and respond to these versatile, redox-active metabolites. Burkholderia is a diverse genus comprising over 100 agriculturally, medically, and environmentally significant species. Many members of this group produce phenazines, yet the regulatory mechanisms governing phenazine biosynthesis and self-resistance remain poorly characterized. Our study sheds light on key aspects of these pathways, revealing parallels with pseudomonads in how Burkholderia species regulate and respond to these versatile, redox-active metabolites.

Ankita Bhattacharyya, Ashley E Grantham, J. Hinson et al. · 0 citations
Open access Sep 2026

Identification of novel inhibitors of Mycobacterium smegmatis growth through genome-wide overexpression of Cluster P3 mycobacteriophage Xavia genes.

Bacteriophages encode numerous genes with no known function, many of which can affect essential cellular processes when expressed in the bacterial host. For mycobacteriophages, genome-wide overexpression in Mycobacterium smegmatis can be used to identify proteins that impair growth. To evaluate the cytotoxic potential of the Cluster P3 phage Xavia, we constructed a plasmid library containing 71 predicted Xavia genes under the anhydrotetracycline inducible promoter pTet and screened this library in a plate-based cytotoxicity assay to measure impacts on M. smegmatis growth. Two genes prevented transformants recovery, consistent with toxicity under basal promoter leakiness, and inducible expression of 18 additional genes impaired growth. These inhibitory proteins include structural components; factors involved in DNA metabolism, lysogeny, and lysis; and several proteins with no known function. These results extend functional screening into a lineage of actinobacteriophages that has not previously been characterized, and identify new proteins that warrant further mechanistic analysis.

A. Tennakoon, I. Edirisingha, Cole R. Jirsa et al. · 0 citations

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