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Hia 表达的选择和反选择揭示了不可分型流感嗜血杆菌感染中 Hia 相变异表达的关键作用。

Selection and Counterselection of Hia Expression Reveals a Key Role for Phase-Variable Expression of Hia in Infection Caused by Nontypeable Haemophilus influenzae.

机构信息

Institute for Glycomics, Griffith University, Gold Coast, Australia.

Department of Pediatrics, Saint Louis University School of Medicine Pediatric Research Institute, Cardinal Glennon Children's Medical Center, Saint Louis, Missouri.

出版信息

J Infect Dis. 2015 Aug 15;212(4):645-53. doi: 10.1093/infdis/jiv103. Epub 2015 Feb 23.

Abstract

Hia is a major adhesin of nontypeable Haemophilus influenzae (NTHi) and has long been investigated as a vaccine candidate. Here we show that Hia phase variation is controlled by changes in the length of a polythymidine tract located in the hia promoter. Studies of an invasive clinical isolate (strain R2866) show that strains expressing high Hia levels are more efficiently killed by opsonophagocytosis. An opsonophagocytic assay was used to select for a subpopulation of variants that expressed a low level of Hia, which facilitated their escape from killing by anti-Hia antisera. Conversely, a subpopulation of variants expressing a high level of Hia was selected for during passaging through Chang cells. In both cases, phase variation of Hia expression corresponded directly with discrete modal changes in polythymidine tract length. In the chinchilla model of NTHi infection, we observed consistent selection for high Hia expression upon nasopharyngeal colonization, confirming the key role of phase-variable expression of Hia within a specific niche in vivo.

摘要

Hia 是无定型流感嗜血杆菌(NTHi)的主要黏附素,长期以来一直被作为疫苗候选物进行研究。在这里,我们发现 Hia 相变异由位于 hia 启动子中的聚胸腺嘧啶序列长度变化所控制。对侵袭性临床分离株(菌株 R2866)的研究表明,表达高水平 Hia 的菌株更容易被调理吞噬作用所杀伤。调理吞噬作用测定用于选择表达低水平 Hia 的变体亚群,这有助于它们逃避抗 Hia 抗血清的杀伤。相反,在通过 Chang 细胞传代时,选择了表达高水平 Hia 的变体亚群。在这两种情况下,Hia 表达的相变异都与聚胸腺嘧啶序列长度的离散模式变化直接对应。在 NTHi 感染的豚鼠模型中,我们观察到在鼻咽定植时持续选择高 Hia 表达,这证实了 Hia 相变异在特定生态位中的关键作用。

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