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肠炎沙门氏菌都柏林血清型的分子分析:搭建群体遗传学与分子流行病学研究之间的桥梁

Molecular analysis of Salmonella enterica serotype Dublin: building bridges between population genetic and molecular epidemiological studies.

作者信息

Platt D J, Browning L M, Candlish D

机构信息

University Department of Bacteriology, Glasgow Royal Infirmary, Scotland.

出版信息

Electrophoresis. 1996 Apr;17(4):667-71. doi: 10.1002/elps.1150170407.

Abstract

Population genetic studies of Salmonella enterica serotype Dublin using multilocus enzyme electrophoresis have recognised two dominant clones termed Du1 and Du3. The characterisation of plasmids in Dublin suggests greater strain diversity. The application of restriction enzyme fragmentation pattern (REFP) analysis of genomic DNA using Sau3A and HincII together with plasmid subtractive analysis can resolve anomalies in earlier comparisons. Twenty-six isolates were selected for inclusion in the study. All had been previously characterised with respect to their plasmids, and were isolated from the USA, Canada and five European countries. On the basis of plasmid profiles, 17 were predicted to correspond with Du1 and Du3. Sau3A digestion generated two distinct REFPs (A and B) of < 70% similarity, which corresponded with Du1 and Du3. After the contribution of plasmid-derived bands was subtracted, two variants of A (A1 and A2) and four of B (B1, B2, B3 and B4) were recognised. Seventeen were concordant with predictions from population genetic studies. Nine that could not be predicted on the basis of atypical plasmid profiles all showed REFP A1 (Du1) and were consistent with the incursion of additional plasmids or plasmid cointegration. REFPs from HincII digests generally corroborated Sau3A data but showed greater overall similarity between the strains and more influence from plasmid DNA.

摘要

利用多位点酶电泳对肠炎沙门氏菌都柏林血清型进行的群体遗传学研究识别出了两个主要克隆,分别称为Du1和Du3。对都柏林血清型菌株中质粒的表征表明存在更大的菌株多样性。使用Sau3A和HincII对基因组DNA进行限制性酶切片段模式(REFP)分析,并结合质粒消减分析,可以解决早期比较中出现的异常情况。选择了26株分离株纳入该研究。所有分离株之前都已对其质粒进行了表征,并且分离自美国、加拿大和五个欧洲国家。根据质粒图谱,预计有17株与Du1和Du3相对应。Sau3A酶切产生了两个相似度小于70%的不同REFP(A和B),分别对应Du1和Du3。在减去质粒衍生条带的贡献后,识别出了A的两个变体(A1和A2)以及B的四个变体(B1、B2、B3和B4)。17株与群体遗传学研究的预测结果一致。9株基于非典型质粒图谱无法预测的菌株均显示REFP A1(Du1),并且与额外质粒的侵入或质粒共整合一致。HincII酶切产生的REFP通常证实了Sau3A的数据,但显示出菌株之间总体相似度更高,并且受质粒DNA的影响更大。

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