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本文引用的文献

1
Pneumococcal modification of host sugars: a major contributor to colonization of the human airway?肺炎链球菌对宿主糖的修饰:是人呼吸道定植的主要因素?
Mol Oral Microbiol. 2010 Feb;25(1):15-24. doi: 10.1111/j.2041-1014.2009.00564.x.
2
A novel sialic acid utilization and uptake system in the periodontal pathogen Tannerella forsythia.牙周病原体福赛坦纳菌中一种新型唾液酸利用和摄取系统。
J Bacteriol. 2010 May;192(9):2285-93. doi: 10.1128/JB.00079-10. Epub 2010 Feb 26.
3
Three surface exoglycosidases from Streptococcus pneumoniae, NanA, BgaA, and StrH, promote resistance to opsonophagocytic killing by human neutrophils.肺炎链球菌的三种表面外糖苷酶,NanA、BgaA 和 StrH,促进了对人中性粒细胞吞噬杀伤作用的抵抗。
Infect Immun. 2010 May;78(5):2108-16. doi: 10.1128/IAI.01125-09. Epub 2010 Feb 16.
4
Characterization of a novel sialic acid transporter of the sodium solute symporter (SSS) family and in vivo comparison with known bacterial sialic acid transporters.新型唾液酸转运蛋白(SSS)家族钠离子协同转运体的特性及其与已知细菌唾液酸转运蛋白的体内比较。
FEMS Microbiol Lett. 2010 Mar;304(1):47-54. doi: 10.1111/j.1574-6968.2009.01881.x. Epub 2009 Dec 17.
5
Advances in the biology and chemistry of sialic acids.唾液酸的生物学和化学研究进展。
ACS Chem Biol. 2010 Feb 19;5(2):163-76. doi: 10.1021/cb900266r.
6
The surface-anchored NanA protein promotes pneumococcal brain endothelial cell invasion.表面锚定的NanA蛋白促进肺炎球菌对脑内皮细胞的侵袭。
J Exp Med. 2009 Aug 31;206(9):1845-52. doi: 10.1084/jem.20090386. Epub 2009 Aug 17.
7
Insights into the evolution of sialic acid catabolism among bacteria.对细菌中唾液酸分解代谢进化的见解。
BMC Evol Biol. 2009 May 26;9:118. doi: 10.1186/1471-2148-9-118.
8
Identification of a pneumococcal glycosidase that modifies O-linked glycans.一种修饰O-连接聚糖的肺炎球菌糖苷酶的鉴定。
Infect Immun. 2009 Apr;77(4):1389-96. doi: 10.1128/IAI.01215-08. Epub 2009 Jan 12.
9
The ability to utilize mucin affects the regulation of virulence gene expression in Streptococcus pneumoniae.利用黏蛋白的能力影响肺炎链球菌毒力基因表达的调控。
FEMS Microbiol Lett. 2008 Jan;278(2):231-5. doi: 10.1111/j.1574-6968.2007.01003.x. Epub 2007 Dec 5.
10
Growth of Streptococcus pneumoniae on human glycoconjugates is dependent upon the sequential activity of bacterial exoglycosidases.肺炎链球菌在人糖缀合物上的生长取决于细菌外切糖苷酶的顺序活性。
J Bacteriol. 2008 Jan;190(1):221-30. doi: 10.1128/JB.01251-07. Epub 2007 Nov 2.

唾液酸转运促进肺炎链球菌定植。

Sialic acid transport contributes to pneumococcal colonization.

机构信息

Center for Microbial Pathogenesis, The Research Institute at Nationwide Children’s Hospital, Columbus, OH 43205-2696, USA.

出版信息

Infect Immun. 2011 Mar;79(3):1262-9. doi: 10.1128/IAI.00832-10. Epub 2010 Dec 28.

DOI:10.1128/IAI.00832-10
PMID:21189320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3067482/
Abstract

Streptococcus pneumoniae is a major cause of pneumonia and meningitis. Airway colonization is a necessary precursor to disease, but little is known about how the bacteria establish and maintain colonization. Carbohydrates are required as a carbon source for pneumococcal growth and, therefore, for colonization. Free carbohydrates are not readily available in the naso-oropharynx; however, N- and O-linked glycans are common in the airway. Sialic acid is the most common terminal modification on N- and O-linked glycans and is likely encountered frequently by S. pneumoniae in the airway. Here we demonstrate that sialic acid supports pneumococcal growth when provided as a sole carbon source. Growth on sialic acid requires import into the bacterium. Three genetic regions have been proposed to encode pneumococcal sialic acid transporters: one sodium solute symporter and two ATP binding cassette (ABC) transporters. Data demonstrate that one of these, satABC, is required for transport of sialic acid. A satABC mutant displayed significantly reduced growth on both sialic acid and the human glycoprotein alpha-1. The importance of satABC for growth on human glycoprotein suggests that sialic acid transport may be important in vivo. Indeed, the satABC mutant was significantly reduced in colonization of the murine upper respiratory tract. This work demonstrates that S. pneumoniae is able to use sialic acid as a sole carbon source and that utilization of sialic acid is likely important during pneumococcal colonization.

摘要

肺炎链球菌是肺炎和脑膜炎的主要病因。呼吸道定植是疾病发生的必要前提,但人们对细菌如何建立和维持定植知之甚少。碳水化合物是肺炎链球菌生长和定植所必需的碳源。鼻咽部通常没有游离的碳水化合物,但气道中存在大量的 N-和 O-连接聚糖。唾液酸是 N-和 O-连接聚糖上最常见的末端修饰,肺炎链球菌在气道中可能经常遇到。在这里,我们证明了唾液酸作为唯一碳源支持肺炎链球菌的生长。生长在唾液酸上需要将其导入细菌内。已经提出了三个基因区域来编码肺炎链球菌的唾液酸转运蛋白:一个钠离子协同转运蛋白和两个 ATP 结合盒(ABC)转运蛋白。数据表明,其中一个,satABC,是唾液酸转运所必需的。satABC 突变体在唾液酸和人糖蛋白 alpha-1 上的生长明显减少。satABC 对人糖蛋白生长的重要性表明,唾液酸转运可能在体内很重要。事实上,satABC 突变体在上呼吸道定植中的数量明显减少。这项工作表明,肺炎链球菌能够将唾液酸用作唯一的碳源,并且在肺炎链球菌定植过程中利用唾液酸可能很重要。