Phylogenomic analyses and host range prediction of cluster P mycobacteriophages

Author:

Howell Abigail A12,Versoza Cyril J13,Cerna Gabriella124,Johnston Tyler4,Kakde Shriya1,Karuku Keith1,Kowal Maria1,Monahan Jasmine1,Murray Jillian14,Nguyen Teresa1,Sanchez Carreon Aurely124,Streiff Abigail4,Su Blake15,Youkhana Faith4,Munig Saige1,Patel Zeel1,So Minerva1,Sy Makena1,Weiss Sarah1,Pfeifer Susanne P13ORCID

Affiliation:

1. School of Life Sciences, Arizona State University , Tempe, AZ 85281, USA

2. Biodesign Institute, Arizona State University , Tempe, AZ 85281, USA

3. Center for Evolution and Medicine, Arizona State University , Tempe, AZ 85281, USA

4. School of Molecular Sciences, Arizona State University , Tempe, AZ 85281, USA

5. School of Politics and Global Studies, Arizona State University , Tempe, AZ 85281, USA

Abstract

Abstract Bacteriophages, infecting bacterial hosts in every environment on our planet, are a driver of adaptive evolution in bacterial communities. At the same time, the host range of many bacteriophages—and thus one of the selective pressures acting on complex microbial systems in nature—remains poorly characterized. Here, we computationally inferred the putative host ranges of 40 cluster P mycobacteriophages, including members from 6 subclusters (P1–P6). A series of comparative genomic analyses revealed that mycobacteriophages of subcluster P1 are restricted to the Mycobacterium genus, whereas mycobacteriophages of subclusters P2–P6 are likely also able to infect other genera, several of which are commonly associated with human disease. Further genomic analysis highlighted that the majority of cluster P mycobacteriophages harbor a conserved integration-dependent immunity system, hypothesized to be the ancestral state of a genetic switch that controls the shift between lytic and lysogenic life cycles—a temperate characteristic that impedes their usage in antibacterial applications.

Funder

National Science Foundation CAREER

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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