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荷兰高流行地区脑膜炎奈瑟菌菌株中I类外膜蛋白的抗原变异

Antigenic variation of the class I outer membrane protein in hyperendemic Neisseria meningitidis strains in the netherlands.

作者信息

Bart A, Dankert J, van der Ende A

机构信息

Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.

出版信息

Infect Immun. 1999 Aug;67(8):3842-6. doi: 10.1128/IAI.67.8.3842-3846.1999.

Abstract

Since 1980, the number of cases of meningococcal disease caused by serogroup B isolates with the P1.4 serosubtype has greatly increased in The Netherlands. Screening for this serosubtype in the strain collection of The Netherlands Reference Laboratory for Bacterial Meningitis revealed that a low number of P1.4 strains had been present in the Dutch meningococcal population since 1965. Genotyping of P1.4 strains showed that one cluster of strains, the hyperendemic lineage III (D. A. Caugant et al., J. Infect. Dis. 162:867-874, 1990), is responsible for the increase since 1980. The diversity of the porA genes, which encode the P1 protein on which serosubtyping is based, was studied for genotypically different P1.4 strains and for lineage III strains expressing antigenically different P1 proteins. Sequence analysis showed that porA genes of genotypically distinct strains that express antigenically indistinguishable P1 proteins are identical only in the epitope-encoding region, suggesting that this region has spread through the meningococcal population via horizontal gene transfer. Analysis of porA genes of lineage III strains showed that both horizontal gene transfer and partial deletion of the epitope-encoding region may contribute to the different antigenic properties for P1 of these strains. Phase variation of expression of the porA gene seems to account for most nonreacting strains. These results show that serosubtyping may underestimate the rise of a hyperendemic clone.

摘要

自1980年以来,荷兰由具有P1.4血清亚型的B群分离株引起的脑膜炎球菌病病例数大幅增加。在荷兰细菌性脑膜炎参考实验室的菌株收集中对该血清亚型进行筛查发现,自1965年以来荷兰脑膜炎球菌群体中就存在少量P1.4菌株。对P1.4菌株进行基因分型表明,其中一组菌株,即高度流行的III型谱系(D. A. Caugant等人,《传染病杂志》162:867 - 874,1990年),是自1980年以来病例数增加的原因。对编码血清分型所依据的P1蛋白的porA基因的多样性进行了研究,对象是基因分型不同的P1.4菌株以及表达抗原性不同的P1蛋白的III型谱系菌株。序列分析表明,表达抗原性无法区分的P1蛋白的基因分型不同的菌株的porA基因仅在表位编码区域相同,这表明该区域是通过水平基因转移在脑膜炎球菌群体中传播的。对III型谱系菌株的porA基因分析表明,水平基因转移和表位编码区域的部分缺失都可能导致这些菌株P1的抗原特性不同。porA基因表达的相变似乎是大多数无反应菌株的原因。这些结果表明,血清分型可能低估了高度流行克隆的增加。

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