Meier Patricia Stutzmann, Troller Rolf, Heiniger Nadja, Grivea Ioanna N, Syrogiannopoulos George A, Aebi Christoph
Institute for Infectious Diseases, University of Bern, Switzerland.
Vaccine. 2005 Mar 14;23(16):2000-8. doi: 10.1016/j.vaccine.2004.09.036.
The outer membrane proteins UspA1 and UspA2 are candidate antigens for a Moraxella catarrhalis vaccine. We previously reported that 103 of 108 isolates (95%) from young children expressed UspA1 detected by reactivity with the monoclonal antibody mAb24B5. The aim of the present study was to investigate mechanisms controlling UspA1 expression by analysis of five mAb24B5 non-reactive isolates. Four of these strains were characterized by (i) decreased or absent transcription of uspA1 and uspA2 and (ii) clustered mutations and deletions in the promoter region of both uspA1 and uspA2. Antigenic or phase variation were not responsible for reduced levels of UspA1 expression. While mAb24B5-positive isolates expressing normal levels of uspA1 and uspA2 mRNA belonged to the previously described 16S rRNA type 1 phylogenetic group, these four mAb24B5-negative isolates were found to belong to the 16S rRNA gene types 2 or 3. The remaining mAb24B5-negative isolate (#610) belonged to 16S rRNA type 1 and exhibited a posttranscriptional defect of UspA1 expression defined by normal levels of uspA1 mRNA and both recombinant and in vitro expression of mAb24B5-reactive UspA1. In conclusion, M. catarrhalis clinical isolates exhibiting reduced expression of UspA1 and UspA2 belonged to a distinct phylogenetic subpopulation. A UspA-based vaccine is unlikely to be effective against such isolates.
外膜蛋白UspA1和UspA2是卡他莫拉菌疫苗的候选抗原。我们之前报道过,从幼儿中分离出的108株菌株中有103株(95%)通过与单克隆抗体mAb24B5反应检测到表达UspA1。本研究的目的是通过分析5株mAb24B5无反应性的分离株来研究控制UspA1表达的机制。其中4株菌株的特征为:(i)uspA1和uspA2的转录减少或缺失;(ii)uspA1和uspA2启动子区域的聚集性突变和缺失。抗原变异或相变异并非UspA1表达水平降低所致。表达正常水平uspA1和uspA2 mRNA的mAb24B5阳性分离株属于先前描述的16S rRNA 1型系统发育组,而这4株mAb24B5阴性分离株被发现属于16S rRNA基因2型或3型。其余mAb24B5阴性分离株(#610)属于16S rRNA 1型,表现出UspA1表达的转录后缺陷,其定义为uspA1 mRNA水平正常以及mAb24B5反应性UspA1的重组表达和体外表达均正常。总之,UspA1和UspA2表达降低的卡他莫拉菌临床分离株属于一个独特的系统发育亚群。基于UspA的疫苗不太可能对这类分离株有效。