Agtrevirus phage AV101 recognizes four different O-antigens infecting diverse E. coli

Author:

Sørensen Anders Nørgaard1ORCID,Kalmár Dorottya1,Lutz Veronika Theresa1,Klein-Sousa Victor2,Taylor Nicholas M I2,Sørensen Martine C1,Brøndsted Lone1ORCID

Affiliation:

1. Department of Veterinary and Animal Sciences, University of Copenhagen , Stigbøjlen 4, 1870 Frederiksberg C , Denmark

2. Structural Biology of Molecular Machines Group, Protein Structure & Function Program, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen , Blegdamsvej 3B, 2200 Copenhagen , Denmark

Abstract

Abstract Bacteriophages in the Agtrevirus genus are known for expressing multiple tail spike proteins (TSPs), but little is known about their genetic diversity and host recognition apart from their ability to infect diverse Enterobacteriaceae species. Here, we aim to determine the genetic differences that may account for the diverse host ranges of Agrevirus phages. We performed comparative genomics of 14 Agtrevirus and identified only a few genetic differences including genes involved in nucleotide metabolism. Most notably was the diversity of the tsp gene cluster, specifically in the receptor-binding domains that were unique among most of the phages. We further characterized agtrevirus AV101 infecting nine diverse Extended Spectrum β-lactamase (ESBL) Escherichia coli and demonstrated that this phage encoded four unique TSPs among Agtrevirus. Purified TSPs formed translucent zones and inhibited AV101 infection of specific hosts, demonstrating that TSP1, TSP2, TSP3, and TSP4 recognize O8, O82, O153, and O159 O-antigens of E. coli, respectively. BLASTp analysis showed that the receptor-binding domain of TSP1, TSP2, TSP3, and TSP4 are similar to TSPs encoded by E. coli prophages and distant related virulent phages. Thus, Agtrevirus may have gained their receptor-binding domains by recombining with prophages or virulent phages. Overall, combining bioinformatic and biological data expands the understanding of TSP host recognition of Agtrevirus and give new insight into the origin and acquisition of receptor-binding domains of Ackermannviridae phages.

Funder

Medical Sciences, Danish Council for Independent Research

Faculty of Health and Medical Sciences, University of Copenhagen

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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