Müller Ilse, Medina-Selby Angelica, Palacios Jose Luis, Martinez Patricio, Opazo Patricio, Bruce Elsa, Mancilla Marta, Valenzuela Pablo, Yudelevich Arturo, Venegas Alejandro
BIOS Chile IGSA y MIFAB, Avda Marathon 1942, Santiago, Chile.
Biol Res. 2002;35(1):67-84. doi: 10.4067/s0716-97602002000100010.
We have cloned and sequenced ten Helicobacter pylori genes from a Chilean strain (CH-CTX1) including: a cytotoxin VacA fragment, a CagA fragment (A17), a species-specific protein (TsaA), urease subunits (UreA, UreB), a flagellin subunit (FlaB), heat shock proteins (HspA and HspB), adhesin (HpaA) and a lipoprotein (Lpp20). We compared their deduced amino acid sequences with the corresponding sequences from three unrelated H. pylori strains, including fully sequenced strains 26695(UK) and J99(USA), and found that eight of them (UreA, UreB, FlaB, HspA, HspB, Lpp20, TsaA and HpaA) presented more than 97.3% identity. In contrast, VacA partial sequence showed lower identity values (93.2-94.9%). Moreover, we found major differences in the A17 region respect to the number and arrangement of the internal repeated elements when sequences from different strains were aligned. The A17 regions from strains CH-CTX1 and 26695 are very similar (91.8% identity) but lacked 6 repeated elements when compared to the Australian strains ATCC 43526 and NCTC 11637. The CCUG 17874 A17 region showed the largest deletion involving 9 repeats. A17 size differences between strains CCUG 17874 and CH-CTX1 were verified by PCR and polypeptide size. Such differences may explain variations in virulence among H. pylori strains as well as diversity in serum immunoreactivity.
我们从一株智利幽门螺杆菌(CH-CTX1)中克隆并测序了10个基因,包括:细胞毒素VacA片段、CagA片段(A17)、种特异性蛋白(TsaA)、脲酶亚基(UreA、UreB)、鞭毛蛋白亚基(FlaB)、热休克蛋白(HspA和HspB)、黏附素(HpaA)和一种脂蛋白(Lpp20)。我们将它们推导的氨基酸序列与来自三株不相关幽门螺杆菌菌株的相应序列进行了比较,这三株菌株包括已完成全序列测定的菌株26695(英国)和J99(美国),发现其中8个基因(UreA、UreB、FlaB、HspA、HspB、Lpp20、TsaA和HpaA)的序列一致性超过97.3%。相比之下,VacA部分序列的一致性值较低(93.2 - 94.9%)。此外,当比对不同菌株的序列时,我们发现A17区域在内部重复元件的数量和排列方面存在重大差异。CH-CTX1和26695菌株的A17区域非常相似(一致性为91.8%),但与澳大利亚菌株ATCC 43526和NCTC 11637相比,缺少6个重复元件。CCUG 17874菌株的A17区域显示出最大的缺失,涉及9个重复元件。通过PCR和多肽大小验证了CCUG 17874和CH-CTX1菌株之间A17大小的差异。这些差异可能解释了幽门螺杆菌菌株之间毒力的差异以及血清免疫反应性的多样性。