Maeland Johan A, Radtke Andreas, Lyng Randi V, Mavenyengwa Rooyen T
Department of Laboratory Medicine, Children's and Women's Health, Norwegian University of Science and Technology, Trondheim, Norway.
Clin Vaccine Immunol. 2013 Apr;20(4):607-12. doi: 10.1128/CVI.00581-12. Epub 2013 Feb 13.
Group B streptococci (GBS) are important human and bovine pathogens which can be classified by a variety of phenotype- and gene-based techniques. The capsular polysaccharide and strain-variable, surface-anchored proteins are particularly important phenotypic markers. In an earlier study, a previously unrecognized protein antigen called Z was described. It was expressed by 27.2% of GBS strains from Zimbabwe, usually in combination with R3 protein expression. In this study, a putative Z-specific antiserum actually contained antibodies against two different antigens named Z1 and Z2; Z1 was >250 kDa in molecular mass. Z1, Z2, and R3 generated multiple stained bands on Western blots and showed similar chromatographic characteristics with respect to molecular mass, aggregate formation, and charge. Of 28 reference and prototype GBS strains examined, 8/28 (28.5%) isolates expressed one, two, or all three of the Z1, Z2, and R3 antigens; 4/28 expressed all three antigens; 2/28 expressed Z2 and R3; 1/28 expressed Z1 only; and 1/28 expressed R3 only. Twenty (71.5%) of the 28 isolates expressed none of the three antigens. Expression of one or more of these antigens was shown by isolates of the capsular polysaccharide types Ia, Ib, V, and IX and NT strains and occurred in combination with expression of various other strain-variable and surface-localized protein antigens. When used as serosubtype markers, Z1, Z2, and R3 affected existing GBS serotype designations for some of the isolates. For instance, the R3 reference strain Prague 10/84 (ATCC 49447) changed serotype markers from V/R3 to V/R3, Z1, and Z2. Other isolates may change correspondingly, implying consequences for GBS serotyping and research.
B族链球菌(GBS)是重要的人类和牛病原体,可通过多种基于表型和基因的技术进行分类。荚膜多糖和菌株可变的表面锚定蛋白是特别重要的表型标记。在早期研究中,描述了一种以前未被识别的蛋白质抗原Z。津巴布韦27.2%的GBS菌株表达该抗原,通常与R3蛋白表达同时出现。在本研究中,一种假定的Z特异性抗血清实际上含有针对两种不同抗原Z1和Z2的抗体;Z1的分子量>250 kDa。Z1、Z2和R3在蛋白质印迹上产生多条染色带,并且在分子量、聚集体形成和电荷方面表现出相似的色谱特征。在所检测的28株GBS参考菌株和原型菌株中,8/28(28.5%)的分离株表达Z1、Z2和R3这三种抗原中的一种、两种或全部;4/28表达全部三种抗原;2/28表达Z2和R3;1/28仅表达Z1;1/28仅表达R3。28株分离株中有20株(71.5%)不表达这三种抗原中的任何一种。荚膜多糖Ia、Ib、V和IX型菌株以及非典型菌株的分离株表达这些抗原中的一种或多种,并且与各种其他菌株可变和表面定位的蛋白质抗原的表达同时出现。当用作血清亚型标记时,Z1、Z2和R3影响了一些分离株现有的GBS血清型命名。例如,R3参考菌株布拉格10/84(ATCC 49447)的血清型标记从V/R3变为V/R3、Z1和Z2。其他分离株可能会相应改变,这意味着对GBS血清分型和研究有影响。