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本文引用的文献

1
Role for streptococcal collagen-like protein 1 in M1T1 group A Streptococcus resistance to neutrophil extracellular traps.链球菌胶原样蛋白1在M1T1型A组链球菌抵抗中性粒细胞胞外诱捕网中的作用。
Infect Immun. 2014 Oct;82(10):4011-20. doi: 10.1128/IAI.01921-14. Epub 2014 Jul 14.
2
The classical lancefield antigen of group a Streptococcus is a virulence determinant with implications for vaccine design.A群链球菌的经典兰斯菲尔德抗原是一种毒力决定因素,对疫苗设计具有重要意义。
Cell Host Microbe. 2014 Jun 11;15(6):729-740. doi: 10.1016/j.chom.2014.05.009.
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Disease manifestations and pathogenic mechanisms of Group A Streptococcus.A 组链球菌的疾病表现及致病机制
Clin Microbiol Rev. 2014 Apr;27(2):264-301. doi: 10.1128/CMR.00101-13.
4
DrsG from Streptococcus dysgalactiae subsp. equisimilis inhibits the antimicrobial peptide LL-37.来自无乳链球菌似马亚种的 DrsG 抑制抗菌肽 LL-37。
Infect Immun. 2014 Jun;82(6):2337-44. doi: 10.1128/IAI.01411-13. Epub 2014 Mar 24.
5
The globally disseminated M1T1 clone of group A Streptococcus evades autophagy for intracellular replication.A 群链球菌 M1T1 克隆在全球传播,逃避自噬作用进行细胞内复制。
Cell Host Microbe. 2013 Dec 11;14(6):675-82. doi: 10.1016/j.chom.2013.11.003.
6
Pneumococcal infection in adults: burden of disease.成人肺炎链球菌感染:疾病负担。
Clin Microbiol Infect. 2014 May;20 Suppl 5:45-51. doi: 10.1111/1469-0691.12461. Epub 2014 Jan 24.
7
The spectrum of perinatal group B streptococcal disease.围产期 B 群链球菌病的谱。
Vaccine. 2013 Aug 28;31 Suppl 4:D3-6. doi: 10.1016/j.vaccine.2013.02.030.
8
IgG protease Mac/IdeS is not essential for phagocyte resistance or mouse virulence of M1T1 group A Streptococcus.M1T1 群 A 链球菌的 IgG 蛋白酶 Mac/IdeS 对于吞噬细胞的抵抗力或小鼠毒力并非必需。
mBio. 2013 Jul 30;4(4):e00499-13. doi: 10.1128/mBio.00499-13.
9
The two-component response regulator LiaR regulates cell wall stress responses, pili expression and virulence in group B Streptococcus.双组分应答调节子 LiaR 调控 B 群链球菌细胞壁应激反应、菌毛表达和毒力。
Microbiology (Reading). 2013 Jul;159(Pt 7):1521-1534. doi: 10.1099/mic.0.064444-0. Epub 2013 May 23.
10
A bacterial pathogen co-opts host plasmin to resist killing by cathelicidin antimicrobial peptides.一种细菌病原体劫持宿主纤溶酶来抵抗抗菌肽 cathelicidin 的杀伤。
J Biol Chem. 2012 Nov 30;287(49):40891-7. doi: 10.1074/jbc.M112.404582. Epub 2012 Oct 4.

链球菌病原体的阳离子抗菌肽耐药机制

Cationic antimicrobial peptide resistance mechanisms of streptococcal pathogens.

作者信息

LaRock Christopher N, Nizet Victor

机构信息

Department of Pediatrics, University of California, San Diego, La Jolla, CA, USA.

Department of Pediatrics, University of California, San Diego, La Jolla, CA, USA; Skaggs School of Medicine and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA, USA; Rady Children's Hospital, San Diego, CA, USA.

出版信息

Biochim Biophys Acta. 2015 Nov;1848(11 Pt B):3047-54. doi: 10.1016/j.bbamem.2015.02.010. Epub 2015 Feb 17.

DOI:10.1016/j.bbamem.2015.02.010
PMID:25701232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4539303/
Abstract

Cationic antimicrobial peptides (CAMPs) are critical front line contributors to host defense against invasive bacterial infection. These immune factors have direct killing activity toward microbes, but many pathogens are able to resist their effects. Group A Streptococcus, group B Streptococcus and Streptococcus pneumoniae are among the most common pathogens of humans and display a variety of phenotypic adaptations to resist CAMPs. Common themes of CAMP resistance mechanisms among the pathogenic streptococci are repulsion, sequestration, export, and destruction. Each pathogen has a different array of CAMP-resistant mechanisms, with invasive disease potential reflecting the utilization of several mechanisms that may act in synergy. Here we discuss recent progress in identifying the sources of CAMP resistance in the medically important Streptococcus genus. Further study of these mechanisms can contribute to our understanding of streptococcal pathogenesis, and may provide new therapeutic targets for therapy and disease prevention. This article is part of a Special Issue entitled: Bacterial Resistance to Antimicrobial Peptides.

摘要

阳离子抗菌肽(CAMP)是宿主抵御侵袭性细菌感染的关键一线防御因子。这些免疫因子对微生物具有直接杀伤活性,但许多病原体能够抵抗其作用。A组链球菌、B组链球菌和肺炎链球菌是人类最常见的病原体,它们表现出多种表型适应性以抵抗CAMP。致病性链球菌中CAMP抗性机制的共同主题包括排斥、隔离、输出和破坏。每种病原体都有不同的CAMP抗性机制组合,侵袭性疾病的潜力反映了可能协同作用的几种机制的利用情况。在此,我们讨论了在确定医学上重要的链球菌属中CAMP抗性来源方面的最新进展。对这些机制的进一步研究有助于我们理解链球菌的发病机制,并可能为治疗和疾病预防提供新的治疗靶点。本文是名为“细菌对抗菌肽的抗性”的特刊的一部分。