Robinson Charles F, Khayat Reza
bioRxiv. 2024 Sep 2:2024.09.02.610742. doi: 10.1101/2024.09.02.610742.
is a family of double stranded RNA (dsRNA) phage that infects various strains of , a Gram-negative soil bacteria known to infect various crops. Surrounding the icosahedral capsids of these phages is a bacterial derived phospholipid membrane. Embedded within this membrane is a multi-component protein complex, referred to as the spike complex. The spike complex is responsible for host recognition and membrane fusion. We studied the ability of two members of the family to infect cells in the presence of purified outer membrane vesicles (OMVs) and lipopolysaccharide (LPS) derived from distinct sources. In this study we determined that OMVs from the host strain: East River isolate A (ERA) inhibit Phi 8 and Phi 12 host infection. These OMVs range in size from 30 to 60 nm and bind to Phi 8 and Phi 12. However, OMV purified from pv. phaseolicola LM2691 and Δ Δ did not inhibit Phi 8 or Phi 12 host infection. However, LPS derived from ERA and LM2691 inhibited Phi 8 and Phi 12 infection, demonstrating that LPS is the receptor for these two viruses, and that OMV biogenesis is selective of LPS. LPS derived from other non Gram-negative bacteria, did not inhibit infection. We confirmed that host proteins are not required for Phi 8 or Phi 12 host interaction. Our results also suggest that differences in lipid A and the core polysaccharide in LPS may influence Phi 8 and Phi 12 host binding.
Most phage families studied to date use a tailed appendage, composed of a multitude of proteins, for cellular recognition, membrane penetration, and genome injection. This contrasts with members of the family which possess a phospholipid membrane bilayer with embedded proteins responsible for cellular recognition and membrane fusion. Thus, the are akin to enveloped viruses which also use protein complexes embedded into their membrane for cellular recognition and membrane fusion. Examples of such viruses include the , and families. The binding specifics of to the host outer membrane are unknown. Using -OMV interaction we began to uncover the host requirements for binding . The results presented determine that only lipid A and the core polysaccharide of LPS are required for outer membrane binding.
是一类双链RNA(dsRNA)噬菌体,可感染多种菌株,是一种已知会感染多种作物的革兰氏阴性土壤细菌。这些噬菌体的二十面体衣壳周围是一层源自细菌的磷脂膜。嵌入该膜内的是一种多组分蛋白质复合物,称为刺突复合物。刺突复合物负责宿主识别和膜融合。我们研究了该家族的两个成员在存在源自不同来源的纯化外膜囊泡(OMV)和脂多糖(LPS)的情况下感染细胞的能力。在本研究中,我们确定来自宿主菌株:东河分离株A(ERA)的OMV可抑制Phi 8和Phi 12的宿主感染。这些OMV的大小在30至60纳米之间,并与Phi 8和Phi 12结合。然而,从菜豆疫霉pv. phaseolicola LM2691和ΔΔ中纯化的OMV并未抑制Phi 8或Phi 12的宿主感染。然而,源自ERA和LM2691的LPS可抑制Phi 8和Phi 12的感染,表明LPS是这两种病毒的受体,并且OMV生物合成对LPS具有选择性。源自其他非革兰氏阴性细菌的LPS并未抑制感染。我们证实Phi 8或Phi 12与宿主的相互作用不需要宿主蛋白。我们的结果还表明,LPS中脂质A和核心多糖的差异可能会影响Phi 8和Phi 12与宿主的结合。
迄今为止研究的大多数噬菌体家族使用由多种蛋白质组成的尾部附属物进行细胞识别、膜穿透和基因组注入。这与该家族的成员形成对比,该家族拥有磷脂膜双层,其中嵌入的蛋白质负责细胞识别和膜融合。因此,类似于包膜病毒,包膜病毒也使用嵌入其膜中的蛋白质复合物进行细胞识别和膜融合。这类病毒的例子包括、和家族。与宿主外膜的结合细节尚不清楚。利用-OMV相互作用,我们开始揭示结合的宿主需求。所呈现的结果确定,外膜结合仅需要LPS的脂质A和核心多糖。