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

microLife Pub Date : 2023-12-20 DOI:10.1093/femsml/uqad047
Anders Nørgaard Sørensen, Dorottya Kalmar, V. T. Lutz, Victor Klein-Sousa, Nicholas M I Taylor, M. C. H. Sørensen, L. Brøndsted
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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) E. 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.
姬状病毒噬菌体 AV101 可识别感染不同大肠杆菌的四种不同 O 抗原
已知噬菌体阿格雷病毒属表达多种尾尖蛋白(TSP),但除了能感染多种肠杆菌科细菌外,人们对它们的遗传多样性和宿主识别能力知之甚少。在此,我们旨在确定 Agrevirus 噬菌体不同宿主范围的基因差异。我们对 14 种 Agtrevirus 进行了比较基因组学研究,只发现了一些遗传差异,包括涉及核苷酸代谢的基因。最值得注意的是tsp基因簇的多样性,特别是在大多数噬菌体中独一无二的受体结合域。我们进一步鉴定了感染九种不同广谱β-内酰胺酶(ESBL)大肠杆菌的噬菌体 AV101 的特征,并证明这种噬菌体在噬菌体中编码四种独特的 TSP。纯化的 TSP 形成半透明区并抑制特定宿主的 AV101 感染,证明 TSP1、TSP2、TSP3 和 TSP4 可分别识别大肠杆菌的 O8、O82、O153 和 O159 O 抗原。BLASTp 分析表明,TSP1、TSP2、TSP3 和 TSP4 的受体结合结构域与大肠杆菌原噬菌体和远缘毒性噬菌体编码的 TSP 相似。因此,Agtrevirus 可能是通过与噬菌体或毒性噬菌体重组而获得其受体结合域的。总之,结合生物信息学和生物学数据,拓展了对Agtrevirus的TSP宿主识别的理解,并对阿克曼病毒科噬菌体受体结合域的起源和获得有了新的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
5.50
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