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2,3-丁二醇的合成与霍乱弧菌埃尔托生物型的出现。

2,3-butanediol synthesis and the emergence of the Vibrio cholerae El Tor biotype.

作者信息

Yoon Sang Sun, Mekalanos John J

机构信息

Department of Microbiology and Molecular Genetics, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Infect Immun. 2006 Dec;74(12):6547-56. doi: 10.1128/IAI.00695-06. Epub 2006 Oct 2.

Abstract

Vibrio cholerae is an aquatic bacterium that causes the severe diarrheal disease cholera. V. cholerae strains of the O1 serogroup exist as two biotypes, classical and El Tor. Toxigenic strains of the El Tor biotype emerged to cause the seventh pandemic of cholera in 1961 and subsequently displaced strains of the classical biotype both in the environment and as a cause of cholera within a decade. The factors that drove emergence of the El Tor biotype and the displacement of the classical biotype are unknown. Here, we show a unique difference in carbohydrate metabolism between these two biotypes. When grown with added carbohydrates, classical biotype strains generated a sharp decrease in medium pH, resulting in loss of viability. However, growth of El Tor biotype strain N16961 was enhanced due to its ability to produce 2,3-butanediol, a neutral fermentation end product, and suppress the accumulation of organic acids. An N16961 mutant (SSY01) defective in 2,3-butanediol synthesis showed the same defect in growth that classical biotype strains show in media rich in carbohydrates. Importantly, the SSY01 mutant was attenuated in its ability to colonize the intestines of infant mice, suggesting that host carbohydrates may be available to V. cholerae within the intestinal environment. Similarly, the SSY01 mutant failed to develop biofilms when utilizing N-acetyl-D-glucosamine as a carbon source. Because growth on N-acetyl-D-glucosamine likely reflects the ability of a strain to grow on chitin in certain aquatic environments, we conclude that the strains of classical biotype are likely defective compared to those of El Tor in growth in any environmental niche that is rich in chitin and/or other metabolizable carbohydrates. We propose that the ability to metabolize sugars without production of acid by-products might account for the improved evolutionary fitness of the V. cholerae El Tor biotype compared to that of the classical biotype both as a global cause of cholera and as an environmental organism.

摘要

霍乱弧菌是一种水生细菌,可引发严重的腹泻疾病霍乱。O1血清群的霍乱弧菌菌株存在两种生物型,即古典生物型和埃尔托生物型。埃尔托生物型的产毒菌株于1961年引发了霍乱的第七次大流行,随后在十年内取代了环境中的古典生物型菌株,并成为霍乱的致病源。推动埃尔托生物型出现以及古典生物型被取代的因素尚不清楚。在此,我们展示了这两种生物型在碳水化合物代谢方面的独特差异。当添加碳水化合物进行培养时,古典生物型菌株会使培养基pH值急剧下降,导致活力丧失。然而,埃尔托生物型菌株N16961的生长得到增强,这是因为它能够产生2,3 - 丁二醇(一种中性发酵终产物)并抑制有机酸的积累。一株在2,3 - 丁二醇合成方面存在缺陷的N16961突变体(SSY01)在生长方面表现出与古典生物型菌株在富含碳水化合物的培养基中相同的缺陷。重要的是,SSY01突变体在定殖于幼鼠肠道的能力上有所减弱,这表明肠道环境中的宿主碳水化合物可能可供霍乱弧菌利用。同样,当以N - 乙酰 - D - 葡萄糖胺作为碳源时,SSY01突变体无法形成生物膜。由于在N - 乙酰 - D - 葡萄糖胺上的生长可能反映了菌株在某些水生环境中在几丁质上生长的能力,我们得出结论,与埃尔托生物型菌株相比,古典生物型菌株在任何富含几丁质和/或其他可代谢碳水化合物的环境生态位中的生长可能存在缺陷。我们提出,不产生酸性副产物而代谢糖类的能力可能解释了霍乱弧菌埃尔托生物型在作为霍乱的全球致病源以及作为一种环境生物方面比古典生物型具有更高的进化适应性。

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本文引用的文献

1
Modeling the role of bacteriophage in the control of cholera outbreaks.模拟噬菌体在控制霍乱暴发中的作用。
Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4652-7. doi: 10.1073/pnas.0600166103. Epub 2006 Mar 14.
9
The Vibrio cholerae chitin utilization program.霍乱弧菌几丁质利用程序
Proc Natl Acad Sci U S A. 2004 Feb 24;101(8):2524-9. doi: 10.1073/pnas.0308707101.

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