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布鲁里溃疡和产(myco)lactone 的分枝杆菌。

Buruli ulcer and mycolactone-producing mycobacteria.

机构信息

Leprosy Research Center, National Institute of Infectious Diseases, Tokyo 189-0002, Japan. nakanaga@nih.go.jp

出版信息

Jpn J Infect Dis. 2013;66(2):83-8. doi: 10.7883/yoken.66.83.

DOI:10.7883/yoken.66.83
PMID:23514902
Abstract

Buruli ulcer (BU) is an emerging human disease caused by Mycobacterium ulcerans, which mainly affects the extremities. It is most endemic in sub-Saharan Africa; however, it has been reported worldwide, including in some non-tropical areas. "M. ulcerans subsp. shinshuense" is proposed as a subspecies of M. ulcerans, which have been reported from Japan and China. A total of 35 BU cases have been reported as of November 2012. Although M. ulcerans is categorized as nontuberculous mycobacteria, it has some unique characteristics that could only be observed in this bacterium. It possesses a giant virulent plasmid, composed of 174-kbp nucleotides, coding polyketide synthase to produce macrolide toxin called mycolactone. The discovery of such a linkage of plasmid and its pathogenesis has not been reported in other human disease-causing mycobacteria.

摘要

布鲁里溃疡(BU)是一种由溃疡分枝杆菌引起的新兴人类疾病,主要影响四肢。它主要流行于撒哈拉以南非洲地区;然而,它已在全球范围内报告,包括一些非热带地区。“溃疡分枝杆菌亚种申津野分枝杆菌”被提议为溃疡分枝杆菌的一个亚种,该亚种已在日本和中国报告。截至 2012 年 11 月,共报告了 35 例布鲁里溃疡病例。虽然溃疡分枝杆菌被归类为非结核分枝杆菌,但它具有一些独特的特征,只能在这种细菌中观察到。它拥有一个巨大的毒性质粒,由 174-kbp 核苷酸组成,编码聚酮合酶以产生大环内酯毒素称为 mycolactone。这种质粒及其发病机制的发现尚未在其他引起人类疾病的分枝杆菌中报道。

相似文献

1
Buruli ulcer and mycolactone-producing mycobacteria.布鲁里溃疡和产(myco)lactone 的分枝杆菌。
Jpn J Infect Dis. 2013;66(2):83-8. doi: 10.7883/yoken.66.83.
2
Mycolactone gene expression is controlled by strong SigA-like promoters with utility in studies of Mycobacterium ulcerans and buruli ulcer.分枝杆菌酸内酯基因的表达受强 SigA 样启动子控制,可用于分枝杆菌溃疡和溃疡分枝杆菌的研究。
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Naturally occurring a loss of a giant plasmid from Mycobacterium ulcerans subsp. shinshuense makes it non-pathogenic.自然发生的巨大质粒丢失使溃疡分枝杆菌亚种信州株丧失致病性。
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Buruli ulcer: reductive evolution enhances pathogenicity of Mycobacterium ulcerans.布鲁里溃疡:还原性进化增强溃疡分枝杆菌的致病性。
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Detection of Mycobacterium ulcerans subsp. shinshuense DNA from a water channel in familial Buruli ulcer cases in Japan.从日本家族性布鲁里溃疡病例的一条水道中检测溃疡分枝杆菌信州亚种DNA。
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Infiltrating leukocytes surround early Buruli ulcer lesions, but are unable to reach the mycolactone producing mycobacteria.浸润的白细胞围绕着早期的布鲁里溃疡病灶,但无法接触到产生分枝杆菌内酯的分枝杆菌。
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引用本文的文献

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Exploring Mycolactone-The Unique Causative Toxin of Buruli Ulcer: Biosynthetic, Synthetic Pathways, Biomarker for Diagnosis, and Therapeutic Potential.探索分枝杆菌内酯——布鲁里溃疡的独特致病毒素:生物合成、合成途径、诊断生物标志物及治疗潜力
Toxins (Basel). 2024 Dec 6;16(12):528. doi: 10.3390/toxins16120528.
2
Membrane Active Immunomodulator As a Novel Therapy for an Infectious Bacterial Disease, Buruli Ulcer.膜活性免疫调节剂作为一种治疗感染性细菌病——布鲁里溃疡的新疗法。
In Vivo. 2022 Nov-Dec;36(6):2615-2629. doi: 10.21873/invivo.12996.
3
Naturally occurring a loss of a giant plasmid from Mycobacterium ulcerans subsp. shinshuense makes it non-pathogenic.
自然发生的巨大质粒丢失使溃疡分枝杆菌亚种信州株丧失致病性。
Sci Rep. 2018 May 29;8(1):8218. doi: 10.1038/s41598-018-26425-1.
4
Membrane perturbing properties of toxin mycolactone from Mycobacterium ulcerans.分枝杆菌溃疡分枝杆菌毒素 mycolactone 的膜扰动特性。
PLoS Comput Biol. 2018 Feb 5;14(2):e1005972. doi: 10.1371/journal.pcbi.1005972. eCollection 2018 Feb.
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Buruli Ulcer, a Prototype for Ecosystem-Related Infection, Caused by Mycobacterium ulcerans.布鲁里溃疡,一种由溃疡分枝杆菌引起的与生态系统相关感染的原型。
Clin Microbiol Rev. 2017 Dec 13;31(1). doi: 10.1128/CMR.00045-17. Print 2018 Jan.
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Overexpression of a Mycobacterium ulcerans Ag85B-EsxH Fusion Protein in Recombinant BCG Improves Experimental Buruli Ulcer Vaccine Efficacy.溃疡分枝杆菌Ag85B-EsxH融合蛋白在重组卡介苗中的过表达提高了实验性布氏杆菌溃疡疫苗的效力。
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