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沙眼衣原体主要外膜蛋白的系统发育分析及潜在致病决定因素的研究。

Phylogenetic analysis of the Chlamydia trachomatis major outer membrane protein and examination of potential pathogenic determinants.

作者信息

Stothard D R, Boguslawski G, Jones R B

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.

出版信息

Infect Immun. 1998 Aug;66(8):3618-25. doi: 10.1128/IAI.66.8.3618-3625.1998.

Abstract

Phylogenetic analysis was utilized to investigate biological relationships (tissue tropism, disease presentation, and epidemiologic success), as evidenced by coevolution, among human strains of Chlamydia trachomatis. Nucleotide sequences of omp1, the gene encoding the major outer membrane protein (MOMP) of C. trachomatis, were determined for 40 strains representing 11 serovars. These data were combined with available omp1 sequences from GenBank for an analysis encompassing a total of 69 strains representing 17 serovars infecting humans. Phylogenetic analysis of the nucleotide and inferred amino acid sequences showed no evolutionary relationships among serovars that corresponded to biological or pathological phenotypes (tissue tropism, disease presentation, and epidemiologic success). In addition, no specific residues that may have evolved to play a role in determining biologically relevant characteristics of chlamydia, such as tissue specificity, disease presentation, and epidemiologic success, were apparent in the MOMP. These results suggest that variation in MOMP may have arisen from a need to be diverse in the presence of immune pressure rather than as a function of pathogenicity. Therefore, the role of MOMP in disease pathogenesis and infection may be passive, and it may not be the major ligand responsible for directing infection of various human cell types.

摘要

利用系统发育分析来研究沙眼衣原体人类菌株之间的生物学关系(组织嗜性、疾病表现和流行病学成功情况),这种关系通过共同进化得以体现。测定了代表11个血清型的40株沙眼衣原体的omp1核苷酸序列,该基因编码沙眼衣原体的主要外膜蛋白(MOMP)。这些数据与来自GenBank的可用omp1序列相结合,进行了一项分析,涵盖了总共69株代表17个感染人类血清型的菌株。对核苷酸和推断的氨基酸序列进行的系统发育分析表明,血清型之间不存在与生物学或病理表型(组织嗜性、疾病表现和流行病学成功情况)相对应的进化关系。此外,在MOMP中没有明显的特定残基可能是为了在确定衣原体的生物学相关特征(如组织特异性、疾病表现和流行病学成功情况)中发挥作用而进化产生的。这些结果表明,MOMP的变异可能是由于在免疫压力下需要多样化,而不是作为致病性的一种功能。因此,MOMP在疾病发病机制和感染中的作用可能是被动的,它可能不是负责指导感染各种人类细胞类型的主要配体。

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