Literature DB >> 25512533

Revealing bacterial targets of growth inhibitors encoded by bacteriophage T7.

Shahar Molshanski-Mor1, Ido Yosef1, Ruth Kiro1, Rotem Edgar1, Miriam Manor1, Michael Gershovits2, Mia Laserson2, Tal Pupko2, Udi Qimron3.   

Abstract

Today's arsenal of antibiotics is ineffective against some emerging strains of antibiotic-resistant pathogens. Novel inhibitors of bacterial growth therefore need to be found. The target of such bacterial-growth inhibitors must be identified, and one way to achieve this is by locating mutations that suppress their inhibitory effect. Here, we identified five growth inhibitors encoded by T7 bacteriophage. High-throughput sequencing of genomic DNA of resistant bacterial mutants evolving against three of these inhibitors revealed unique mutations in three specific genes. We found that a nonessential host gene, ppiB, is required for growth inhibition by one bacteriophage inhibitor and another nonessential gene, pcnB, is required for growth inhibition by a different inhibitor. Notably, we found a previously unidentified growth inhibitor, gene product (Gp) 0.6, that interacts with the essential cytoskeleton protein MreB and inhibits its function. We further identified mutations in two distinct regions in the mreB gene that overcome this inhibition. Bacterial two-hybrid assay and accumulation of Gp0.6 only in MreB-expressing bacteria confirmed interaction of MreB and Gp0.6. Expression of Gp0.6 resulted in lemon-shaped bacteria followed by cell lysis, as previously reported for MreB inhibitors. The described approach may be extended for the identification of new growth inhibitors and their targets across bacterial species and in higher organisms.

Entities:  

Keywords:  bacterial cytoskeleton; bacteriophage biology; high-throughput DNA sequencing; host takeover; target identification

Mesh:

Substances:

Year:  2014        PMID: 25512533      PMCID: PMC4284602          DOI: 10.1073/pnas.1413271112

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


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