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曼氏杆菌属中白细胞毒素操纵子垂直遗传和缺失的证据。

Evidence for vertical inheritance and loss of the leukotoxin operon in genus Mannheimia.

作者信息

Larsen Jesper, Pedersen Anders G, Christensen Henrik, Bisgaard Magne, Angen Øystein, Ahrens Peter, Olsen John E

机构信息

Department of Veterinary Pathobiology, Faculty of Life Sciences, University of Copenhagen, Stigbøjlen, Frederiksberg C, Denmark.

出版信息

J Mol Evol. 2007 Apr;64(4):423-37. doi: 10.1007/s00239-006-0065-3. Epub 2007 Apr 13.

Abstract

The Mannheimia subclades belong to the same bacterial genus but have taken divergent paths toward their distinct lifestyles. M. haemolytica + M. glucosida are potential pathogens of the respiratory tract in the mammalian suborder Ruminantia, whereas M. ruminalis, the supposed sister group, lives as a commensal in the ovine rumen. We have tested the hypothesis that horizontal gene transfer of the leukotoxin operon has catalyzed pathogenic adaptation and speciation of M. haemolytica + M. glucosida, or other major subclades, by using a strategy that combines compositional and phylogenetic methods. We show that it has been vertically inherited from the last common ancestor of the diverging Mannheimia subclades, although several strains belonging to M. ruminalis have lost the operon. Our analyses support that divergence within M. ruminalis following colonization of the ovine rumen was very rapid and that functional decay of most of the leukotoxin operons occurred early when the adaptation to the rumen was fastest, suggesting that antagonistic pleiotropy was the main contributor to losses in the radiating lineages of M. ruminalis. To sum up, the scenario derived from these analyses reflects two aspects. On one hand, it opposes the hypothesis of horizontal gene transfer as a catalyst of pathogenic adaptation and speciation. On the other hand, it indicates that losses of the leukotoxin operons in the radiating lineages of M. ruminalis have catalyzed their adaptation to a commensal environment and reproductive isolation (speciation).

摘要

曼氏杆菌亚分支属于同一细菌属,但在各自独特的生活方式上走上了不同的道路。溶血曼氏杆菌+葡萄糖苷曼氏杆菌是反刍亚目哺乳动物呼吸道的潜在病原体,而推测为姐妹群的瘤胃曼氏杆菌则作为共生菌生活在绵羊瘤胃中。我们通过结合成分分析和系统发育方法的策略,检验了白细胞毒素操纵子的水平基因转移催化了溶血曼氏杆菌+葡萄糖苷曼氏杆菌或其他主要亚分支的致病适应和物种形成这一假设。我们发现它是从分化的曼氏杆菌亚分支的最后一个共同祖先垂直遗传而来的,尽管一些属于瘤胃曼氏杆菌的菌株已经失去了该操纵子。我们的分析支持这样的观点,即瘤胃曼氏杆菌在定殖于绵羊瘤胃后分化非常迅速,并且大多数白细胞毒素操纵子的功能衰退在对瘤胃的适应最快时就早早发生了,这表明拮抗多效性是瘤胃曼氏杆菌辐射谱系中基因丢失的主要原因。总之,这些分析得出的情况反映了两个方面。一方面,它反对水平基因转移作为致病适应和物种形成催化剂的假设。另一方面,它表明瘤胃曼氏杆菌辐射谱系中白细胞毒素操纵子的丢失催化了它们对共生环境的适应和生殖隔离(物种形成)。

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