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首页> 外文期刊>Journal of Clinical Microbiology >Typing Neisseria meningitidis by analysis of restriction fragment length polymorphisms in the gene encoding the class 1 outer membrane protein: application to assessment of epidemics throughout the last 4 decades in China.
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Typing Neisseria meningitidis by analysis of restriction fragment length polymorphisms in the gene encoding the class 1 outer membrane protein: application to assessment of epidemics throughout the last 4 decades in China.

机译:通过分析编码1类外膜蛋白的基因中的限制性片段长度多态性来分型脑膜炎奈瑟氏球菌:在中国近40年的流行病评估中的应用。

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A typing method was developed for Neisseria meningitidis serogroup A by analysis of restriction fragment length polymorphisms (RFLP) of the class 1 outer membrane protein gene (porA). By using appropriate primers, an approximately 1,116-bp fragment of the porA gene was amplified by PCR and then was digested with the restriction endonuclease MspI. The digestion products were separated on 10% polyacrylamide gels and were stained with silver. One hundred three clinical isolates of group A N. meningitidis from 17 provinces of China collected over a 26-year period were analyzed. Results of MspI-generated RFLP profiles of PCR-amplified porA genes were compared with those obtained by conventional serosubtyping. There was a band of about 400 bp common to all strains examined, and the 103 strains of serogroup A resulted in 22 unique RFLP patterns. The differences in bands could be observed mainly in the range of 120 to 280 bp. The smaller fragments were useful in distinguishing meningococci with the same serosubtype. Three epidemic periods were characterized by the presence of three distinct genotypes (a1, a2, and a3), accounting for 74.5% of the strains examined (3.88, 26.21, and 44.66%, respectively). Three predominant RFLP patterns were correlated epidemiologically with cycles of epidemic meningococcal meningitis and were well-matched to the predominant serosubtypes (P1.9, P1.7, 10, and P1.9) that presented at the same prevalence cycles. The genotyping yielded information that allowed strains from one epidemic to be distinguished from those from another that would have been indistinguishable if only serotyping and serosubtyping were available. Therefore, the PCR-RFLP typing method was very useful in the epidemiologic investigation of group A meningococcal meningitis.
机译:通过分析1类外膜蛋白基因(porA)的限制性片段长度多态性(RFLP),开发了一种针对脑膜炎奈瑟菌血清群A的分型方法。通过使用适当的引物,通过PCR扩增porA基因的约1,116-bp的片段,然后用限制性核酸内切酶MspI消化。消化产物在10%聚丙烯酰胺凝胶上分离,并用银染色。分析了来自中国17个省的26年内的A组脑膜炎奈瑟氏球菌的临床分离物103个。将MspI生成的PCR扩增的porA基因的RFLP图谱结果与通过常规血清分型获得的结果进行比较。所有检查的菌株共有一条约400 bp的条带,血清群A的103株产生22种独特的RFLP模式。可以主要在120至280bp的范围内观察到带的差异。较小的片段可用于区分具有相同血清亚型的脑膜炎球菌。三个流行时期的特征是存在三种不同的基因型(a1,a2和a3),分别占所检测菌株的74.5%(分别为3.88、26.21和44.66%)。三种主要的RFLP模式在流行病学上与流行性脑膜炎球菌性脑膜炎的发病周期相关,并且与以相同患病率出现的主要血清亚型(P1.9,P1.7、10和P1.9)良好匹配。基因分型产生的信息可以使一种流行病的菌株与另一种流行的菌株区分开,如果仅提供血清分型和血清亚型则无法区分。因此,PCR-RFLP分型方法在A组脑膜炎球菌性脑膜炎的流行病学调查中非常有用。

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