Pajón R, Chinea G, Marrero E, Gonzalez D, Guillén G
División de Vacunas, Centro de Ingenieria Genética y Biotecnología, Ave 31e/ 158 y 190, Cubanacan, Havana, C.P. 10600, Cuba.
Microb Pathog. 1997 Aug;23(2):71-84. doi: 10.1006/mpat.1997.0136.
The gene coding for the 98-kDa meningococcal outer membrane transferrin binding protein 1 (TbpA) from strain B385 was cloned and sequenced. Sequence comparison among its deduced aminoacid sequence and those from TbpA and the closely related LbpA (lactoferrin binding protein) gene from three different meningococcal strains, and four isolates from two other bacterial pathogens, showed that TbpA variability is confined to five specific segments, designated VR1 (199-287), VR2 (306-381), VR3 (480-546), VR4 (618-651) and VR5 (681-708). The third VR was the most variable among strains both at the nucleotide and amino acid levels. Six additional tbpA genes from different meningococcal strains were cloned and its VR3 sequence determined. On the basis of this data we were able to cluster tbpA genes in two groups: D (bearing a deletion in VR3) and N (nondeleted); all N and D strains belonging to the groups of high or low molecular weight transferrin receptor isotype, respectively. However, by phenogram analysis, the prototypical strain M982 (Group II) was clustered with M990 (B16B6 isotype, Group I). These results point to the existence of important exposed regions as well as to the possibility of horizontal gene exchange involving this locus. A topology model with 14 exposed loops and 28 membrane spanning segments was postulated. According to this tentative analysis, TbpA as well as LbpA proteins should form a gated channel in the neisserial outer membrane. The variable regions were located in the fifth, sixth, eighth, 10th and 11th loops respectively. Among TbpAs VR1, VR2, and VR3 resulted the most relevant regions.
对B385菌株编码98-kDa脑膜炎球菌外膜转铁蛋白结合蛋白1(TbpA)的基因进行了克隆和测序。将其推导的氨基酸序列与来自三种不同脑膜炎球菌菌株的TbpA以及密切相关的乳铁蛋白结合蛋白(LbpA)基因的序列进行比较,并与来自其他两种细菌病原体的四个分离株进行比较,结果表明TbpA的变异性局限于五个特定区段,分别命名为VR1(199 - 287)、VR2(306 - 381)、VR3(480 - 546)、VR4(618 - 651)和VR5(681 - 708)。第三个VR在菌株间的核苷酸和氨基酸水平上是最可变的。克隆了来自不同脑膜炎球菌菌株的另外六个tbpA基因,并测定了其VR3序列。基于这些数据,我们能够将tbpA基因分为两组:D组(VR3中有缺失)和N组(无缺失);所有N组和D组菌株分别属于高分子量或低分子量转铁蛋白受体同种型组。然而,通过系统发育树分析,原型菌株M982(II组)与M990(B16B6同种型,I组)聚类在一起。这些结果表明存在重要的暴露区域,也表明涉及该基因座的水平基因交换的可能性。推测了一个具有14个暴露环和28个跨膜区段的拓扑模型。根据这一初步分析,TbpA以及LbpA蛋白应在奈瑟菌外膜中形成一个门控通道。可变区分别位于第五、第六、第八、第十和第十一环中。在TbpA中,VR1、VR2和VR3是最相关的区域。