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分子技术对脑膜炎球菌病研究的影响。

The Impact o Molecular Techniques on the Study of Meningococcal Disease.

作者信息

Maiden M C

机构信息

Division of Bacteriology, National Institute for Biological Standards and Control, Hertfordshire, Hatfield, UK.

出版信息

Methods Mol Med. 1998;15:265-91. doi: 10.1385/0-89603-498-4:265.

DOI:10.1385/0-89603-498-4:265
PMID:21390752
Abstract

Neisseria meningitidis, the meningococcus, is normally a harmless commensal bacterium that colonises the naso/oropharynx of humans. This antigenically variable gram-negative diplococcus has the potential, however, to cause rapidly progressing meningitis and fulminant septicemia, either separately or together (1,2). Once present in the bloodstream, meningococci grow rapidly and their highly toxic lipo-oligosaccharides frequently cause extensive tissue damage and severe toxic shock. The progress of the disease is swift, and death often occurs within hours of the onset of symptoms (3). Even in countries where meningococcal infection is relatively rare, it remains a high priority for public health services because of the high mortality rates of fulminant septicemic disease (which can be up to 40% even when intensive supportive therapy is available), the high proportion of sequelae in patients who have recovered (including brain damage and digit or limb loss), and the age groups most susceptible (young children and, to a lesser extent, teenagers) (4,5).

摘要

脑膜炎奈瑟菌,即脑膜炎球菌,通常是一种无害的共生细菌,定植于人类的鼻咽/口咽部。然而,这种抗原性多变的革兰氏阴性双球菌有可能单独或同时引发快速进展的脑膜炎和暴发性败血症(1,2)。一旦进入血流,脑膜炎球菌迅速生长,其剧毒的脂寡糖常常导致广泛的组织损伤和严重的中毒性休克。疾病进展迅速,死亡通常在症状出现数小时内发生(3)。即使在脑膜炎球菌感染相对罕见的国家,由于暴发性败血症疾病的高死亡率(即使有强化支持治疗,死亡率也可高达40%)、康复患者中后遗症的高比例(包括脑损伤和手指或肢体丧失)以及最易感的年龄组(幼儿以及程度较轻的青少年)(4,5),它仍然是公共卫生服务的高度优先事项。

相似文献

1
The Impact o Molecular Techniques on the Study of Meningococcal Disease.分子技术对脑膜炎球菌病研究的影响。
Methods Mol Med. 1998;15:265-91. doi: 10.1385/0-89603-498-4:265.
2
Meningococcal disease: recognition, treatment, and prevention.
Nurse Pract. 1998 Aug;23(8):30, 33-6, 39-40 passim.
3
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J Exp Med. 2006 Aug 7;203(8):1939-50. doi: 10.1084/jem.20060482. Epub 2006 Jul 24.
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Meningococcal disease: a review on available vaccines and vaccines in development.脑膜炎球菌病:现有疫苗及正在研发的疫苗综述
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Clin Infect Dis. 2009 Mar 1;48(5):587-94. doi: 10.1086/596707.
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Fulminant septicaemia with purpura fulminans requiring limb amputation.暴发性败血症伴暴发性紫癜,需截肢。
IDCases. 2019 Nov 28;19:e00673. doi: 10.1016/j.idcr.2019.e00673. eCollection 2020.
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Neisseria meningitidis B vaccines.脑膜炎奈瑟菌 B 疫苗。
Expert Rev Vaccines. 2011 Sep;10(9):1337-51. doi: 10.1586/erv.11.103.
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Meningococcal disease: public health burden and control.脑膜炎球菌病:公共卫生负担与防控
World Health Stat Q. 1997;50(3-4):170-7.
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Development of new vaccines against meningococcal disease.新型抗脑膜炎球菌病疫苗的研发
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10
Genetics and evolution of Neisseria meningitidis: importance for the epidemiology of meningococcal disease.脑膜炎奈瑟菌的遗传学与进化:对脑膜炎球菌病流行病学的重要性
Infect Genet Evol. 2008 Sep;8(5):558-65. doi: 10.1016/j.meegid.2008.04.002. Epub 2008 Apr 10.

引用本文的文献

1
Evolutionary changes in antimicrobial resistance of invasive Neisseria meningitidis isolates in Belgium from 2000 to 2010: increasing prevalence of penicillin nonsusceptibility.2000 至 2010 年期间比利时侵袭性脑膜炎奈瑟菌分离株对抗菌药物耐药性的演变变化:青霉素不敏感性的流行率增加。
Antimicrob Agents Chemother. 2012 May;56(5):2268-72. doi: 10.1128/AAC.06310-11. Epub 2012 Jan 30.
2
Ultrasound enhanced detection of individual meningococcal serogroups by latex immunoassay.超声增强乳胶免疫测定法对各型脑膜炎球菌血清群的检测
J Clin Pathol. 2002 Jan;55(1):37-40. doi: 10.1136/jcp.55.1.37.
3
Multilocus sequence typing and antigen gene sequencing in the investigation of a meningococcal disease outbreak.
多位点序列分型和抗原基因测序在脑膜炎球菌病暴发调查中的应用
J Clin Microbiol. 1999 Dec;37(12):3883-7. doi: 10.1128/JCM.37.12.3883-3887.1999.
4
Population genetic and evolutionary approaches to analysis of Neisseria meningitidis isolates belonging to the ET-5 complex.用于分析属于ET-5复合体的脑膜炎奈瑟菌分离株的群体遗传学和进化方法。
J Bacteriol. 1999 Sep;181(18):5551-6. doi: 10.1128/JB.181.18.5551-5556.1999.
5
Heterogeneity of the PorB protein in serotype 22 Neisseria meningitidis.22型脑膜炎奈瑟菌中PorB蛋白的异质性
J Clin Microbiol. 1998 Dec;36(12):3680-2. doi: 10.1128/JCM.36.12.3680-3682.1998.