Fujiwara Nagatoshi, Nakata Noboru, Naka Takashi, Yano Ikuya, Doe Matsumi, Chatterjee Delphi, McNeil Michael, Brennan Patrick J, Kobayashi Kazuo, Makino Masahiko, Matsumoto Sohkichi, Ogura Hisashi, Maeda Shinji
Department of Host Defense, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan.
J Bacteriol. 2008 May;190(10):3613-21. doi: 10.1128/JB.01850-07. Epub 2008 Mar 7.
Mycobacterium avium-Mycobacterium intracellulare complex (MAC) is the most common isolate of nontuberculous mycobacteria and causes pulmonary and extrapulmonary diseases. MAC species can be grouped into 31 serotypes by the epitopic oligosaccharide structure of the species-specific glycopeptidolipid (GPL) antigen. The GPL consists of a serotype-common fatty acyl peptide core with 3,4-di-O-methyl-rhamnose at the terminal alaninol and a 6-deoxy-talose at the allo-threonine and serotype-specific oligosaccharides extending from the 6-deoxy-talose. Although the complete structures of 15 serotype-specific GPLs have been defined, the serotype 16-specific GPL structure has not yet been elucidated. In this study, the chemical structure of the serotype 16 GPL derived from M. intracellulare was determined by using chromatography, mass spectrometry, and nuclear magnetic resonance analyses. The result indicates that the terminal carbohydrate epitope of the oligosaccharide is a novel N-acyl-dideoxy-hexose. By the combined linkage analysis, the oligosaccharide structure of serotype 16 GPL was determined to be 3-2'-methyl-3'-hydroxy-4'-methoxy-pentanoyl-amido-3,6-dideoxy-beta-hexose-(1-->3)-4-O-methyl-alpha-L-rhamnose-(1-->3)-alpha-L-rhamnose-(1-->3)-alpha-L-rhamnose-(1-->2)-6-deoxy-alpha-L-talose. Next, the 22.9-kb serotype 16-specific gene cluster involved in the glycosylation of oligosaccharide was isolated and sequenced. The cluster contained 17 open reading frames (ORFs). Based on the similarity of the deduced amino acid sequences, it was assumed that the ORF functions include encoding three glycosyltransferases, an acyltransferase, an aminotransferase, and a methyltransferase. An M. avium serotype 1 strain was transformed with cosmid clone no. 253 containing gtfB-drrC of M. intracellulare serotype 16, and the transformant produced serotype 16 GPL. Together, the ORFs of this serotype 16-specific gene cluster are responsible for the biosynthesis of serotype 16 GPL.
鸟分枝杆菌-胞内分枝杆菌复合体(MAC)是最常见的非结核分枝杆菌分离株,可引起肺部和肺外疾病。根据种特异性糖肽脂(GPL)抗原的表位寡糖结构,MAC菌种可分为31个血清型。GPL由一个血清型共同的脂肪酰肽核心组成,在末端丙氨醇处有3,4-二-O-甲基-鼠李糖,在别苏氨酸处有6-脱氧塔罗糖,以及从6-脱氧塔罗糖延伸出的血清型特异性寡糖。尽管已经确定了15种血清型特异性GPL的完整结构,但血清型16特异性GPL的结构尚未阐明。在本研究中,通过色谱法、质谱法和核磁共振分析确定了源自胞内分枝杆菌的血清型16 GPL的化学结构。结果表明,寡糖的末端碳水化合物表位是一种新型的N-酰基-二脱氧己糖。通过联合连锁分析,确定血清型16 GPL的寡糖结构为3-2'-甲基-3'-羟基-4'-甲氧基-戊酰氨基-3,6-二脱氧-β-己糖-(1→3)-4-O-甲基-α-L-鼠李糖-(1→3)-α-L-鼠李糖-(1→3)-α-L-鼠李糖-(1→2)-6-脱氧-α-L-塔罗糖。接下来,分离并测序了参与寡糖糖基化的22.9 kb血清型16特异性基因簇。该基因簇包含17个开放阅读框(ORF)。根据推导的氨基酸序列的相似性,推测ORF的功能包括编码三种糖基转移酶、一种酰基转移酶、一种氨基转移酶和一种甲基转移酶。用含有胞内分枝杆菌血清型16的gtfB-drrC的粘粒克隆253转化鸟分枝杆菌血清型1菌株,转化体产生血清型16 GPL。总之,这个血清型16特异性基因簇的ORF负责血清型16 GPL的生物合成。