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杜克雷嗜血杆菌产脓性菌素抗性脂寡糖(LOS)突变体的遗传分析:全长LOS的恢复可恢复对脓性菌素的敏感性。

Genetic analysis of a pyocin-resistant lipooligosaccharide (LOS) mutant of Haemophilus ducreyi: restoration of full-length LOS restores pyocin sensitivity.

作者信息

Filiatrault M J, Munson R S, Campagnari A A

机构信息

Department of Microbiology, State University of New York at Buffalo, Buffalo, New York 14214, USA.

出版信息

J Bacteriol. 2001 Oct;183(19):5756-61. doi: 10.1128/JB.183.19.5756-5761.2001.

Abstract

DNA sequence and Southern blot analyses were used to determine the genetic defect of a Haemophilus ducreyi pyocin-resistant lipooligosaccharide (LOS) mutant, HD35000R. The region of the HD35000R chromosome containing the suspected mutation was amplified, and sequence analysis detected a 3,189-bp deletion. This deletion resulted in the loss of the entire waaQ gene, another open reading frame that encodes a putative homolog to a hypothetical protein (HI0461) of H. influenzae, the gene encoding an argininosuccinate synthase homolog, and a change in the 3' sequence of the lgtF gene. Southern blot analysis confirmed that no genomic rearrangements had occurred. Isogenic LOS mutants and the respective complemented mutants were evaluated for susceptibility to pyocin C. The mutants expressing truncated LOS were resistant to lysis by pyocin C, and complementation restored sensitivity to the pyocin. We conclude that HD35000R is defective in both glycosyltransferase genes and that pyocin resistance is due to truncation of the full-length LOS molecule.

摘要

采用DNA序列分析和Southern印迹分析来确定一株杜克雷嗜血杆菌(Haemophilus ducreyi)对绿脓菌素耐药的脂寡糖(LOS)突变体HD35000R的遗传缺陷。扩增了HD35000R染色体上包含疑似突变的区域,序列分析检测到一个3189 bp的缺失。该缺失导致整个waaQ基因、另一个编码与流感嗜血杆菌(H. influenzae)一种假定蛋白(HI0461)的推定同源物的开放阅读框、一个编码精氨琥珀酸合酶同源物的基因缺失,以及lgtF基因3'序列的改变。Southern印迹分析证实未发生基因组重排。评价了同基因LOS突变体和各自的互补突变体对绿脓菌素C的敏感性。表达截短LOS的突变体对绿脓菌素C的裂解具有抗性,互补作用恢复了对绿脓菌素的敏感性。我们得出结论,HD35000R在两个糖基转移酶基因上存在缺陷,并且对绿脓菌素的抗性是由于全长LOS分子的截短所致。

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