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侵袭性b型和不可分型流感嗜血杆菌中转铁蛋白结合蛋白1和2的特性分析

Characterization of transferrin binding proteins 1 and 2 in invasive type b and nontypeable strains of Haemophilus influenzae.

作者信息

Gray-Owen S D, Schryvers A B

机构信息

Department of Microbiology and Infectious Diseases, Faculty of Medicine, University of Calgary, Alberta, Canada.

出版信息

Infect Immun. 1995 Oct;63(10):3809-15. doi: 10.1128/iai.63.10.3809-3815.1995.

DOI:10.1128/iai.63.10.3809-3815.1995
PMID:7558284
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC173535/
Abstract

Haemophilus influenzae has the ability to obtain iron from human transferrin via two bacterial cell surface transferrin binding proteins, Tbp1 and Tbp2. Although a wide array of strains have been shown to express these receptor proteins, two studies have recently identified a series of isolates which appeared to lack the ability to bind transferrin. Included in this group were the members of a cryptic genospecies of nontypeable biotype IV strains which appear to possess a tropism for female urogenital tissues and are major etiologic agents of neonatal and postpartum bacteremia due to H. influenzae. The present study employed oligonucleotide primers specific for genes encoding the Tbp proteins of a type b biotype I strain of H. influenzae to probe the genomic DNAs of isolates from the previous studies. The tbpA and tbpB genes which encode Tbp1 and Tbp2, respectively, were detected in all of the strains tested either by PCR amplification directly or by Southern hybridization analysis. All of the strains displayed a transferrin binding phenotype, and affinity isolation of receptor proteins with transferrin-conjugated Sepharose recovered Tbp1 and/or Tbp2 from 11 of 14 strains, including 2 of the nontypeable biotype IV strains. In addition, all of the strains were capable of growing on human transferrin specifically, indicating that the mechanism of iron assimilation from transferrin is functional and is not siderophore mediated. These results confirm the presence of tbp genes in all of the invasive H. influenzae isolates characterized to date, suggesting that Tbp-mediated iron acquisition is important in disease which initiates from either the respiratory or urogenital mucosa.

摘要

流感嗜血杆菌能够通过两种细菌细胞表面转铁蛋白结合蛋白Tbp1和Tbp2从人转铁蛋白中获取铁。尽管已显示多种菌株表达这些受体蛋白,但最近有两项研究鉴定出一系列似乎缺乏结合转铁蛋白能力的分离株。这一组包括不可分型生物IV型菌株的一个隐匿基因种的成员,这些菌株似乎对女性泌尿生殖组织具有嗜性,并且是流感嗜血杆菌引起的新生儿和产后菌血症的主要病原体。本研究使用针对流感嗜血杆菌b型生物I型菌株的Tbp蛋白编码基因的寡核苷酸引物来探测先前研究中分离株的基因组DNA。通过直接PCR扩增或Southern杂交分析在所有测试菌株中检测到分别编码Tbp1和Tbp2的tbpA和tbpB基因。所有菌株均表现出转铁蛋白结合表型,用转铁蛋白偶联的琼脂糖凝胶亲和分离受体蛋白从14株中的11株中回收了Tbp1和/或Tbp2,包括2株不可分型生物IV型菌株。此外,所有菌株都能够在人转铁蛋白上特异性生长,表明从转铁蛋白吸收铁的机制是有功能的,且不是由铁载体介导的。这些结果证实了在迄今为止所鉴定的所有侵袭性流感嗜血杆菌分离株中都存在tbp基因,这表明Tbp介导的铁获取在源于呼吸道或泌尿生殖粘膜的疾病中很重要。

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