Takata Tohru, El-Omar Emad, Camorlinga Margarita, Thompson Stuart A, Minohara Yutaka, Ernst Peter B, Blaser Martin J
Division of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Infect Immun. 2002 Jun;70(6):3073-9. doi: 10.1128/IAI.70.6.3073-3079.2002.
Helicobacter pylori strains frequently express Lewis X (Le(x)) and/or Le(y) on their cell surfaces as constituents of the O antigens of their lipopolysaccharide molecules. To assess the effect of Le(x) and Le(y) expression on the ability of H. pylori to colonize the mouse stomach and to adhere to epithelial cells, isogenic mutants were created in which fucT1 alone or fucT1 and fucT2, which encode the fucosyl transferases necessary for Le(x) and Le(y) expression, were deleted. C3H/HeJ mice were experimentally challenged with either wild-type 26695 H. pylori or its isogenic mutants. All strains, whether passaged in the laboratory or recovered after mouse passage, colonized the mice well and without consistent differences. During colonization by the mutants, there was no reversion to wild type. Similarly, adherence to AGS and KatoIII cells was unaffected by the mutations. Together, these findings indicate that Le expression is not necessary for mouse gastric colonization or for H. pylori adherence to epithelial cells.
幽门螺杆菌菌株通常在其细胞表面表达Lewis X(Le(x))和/或Le(y),作为其脂多糖分子O抗原的组成部分。为了评估Le(x)和Le(y)表达对幽门螺杆菌定殖于小鼠胃部及黏附于上皮细胞能力的影响,构建了同基因突变体,其中单独缺失了编码Le(x)和Le(y)表达所需岩藻糖基转移酶的fucT1,或同时缺失了fucT1和fucT2。用野生型26695幽门螺杆菌或其同基因突变体对C3H/HeJ小鼠进行实验性感染。所有菌株,无论是在实验室传代的还是在小鼠传代后回收的,均能很好地定殖于小鼠体内,且无一致差异。在突变体定殖过程中,未出现回复为野生型的情况。同样,突变对幽门螺杆菌黏附AGS和KatoIII细胞也没有影响。这些发现共同表明,Le表达对于幽门螺杆菌在小鼠胃部定殖或黏附于上皮细胞并非必需。