Crain M J, Turner J S, Robinson D A, Coffey T J, Brooks-Walter A, McDaniel L S, Briles D E
Department of Pediatrics, University of Alabama at Birmingham 35294-0011, USA.
Microb Pathog. 1996 Oct;21(4):265-75. doi: 10.1006/mpat.1996.0060.
Pneumococcal surface protein A (PspA) has been shown to be a serologically variable virulence factor of Streptococcus pneumoniae. In mice, PspA can elicit antibodies capable of protecting them against otherwise fatal infections with encapsulated pneumococci. In previous studies it has been reported that almost all isolates have two apparently unlinked genomic sequences that are highly homologous to the 5' and 3' halves of Rx1 pspA, although out MAbs to PspA have not detected more than one PspA in any given isolate of S. Pneumoniae. Recently, we have identified four isolates from a clone of capsular serotype 6B pneumococci (MC25-28) that simultaneously express two distinct PspAs. Each of the isolates (MC25-28) exhibited the same two Kpn I fragments (each containing a Hind III site) that hybridized with Rx1 pspA. MAbs specific for PspA detected two PspAs characterized by different molecular weights and different serologic patterns of reactivity (PspA type 6 detected by MAbs XiR278 and 2A4, and PspA type 34 detected only by MAb 7D2) in each of the four isolates. In previous studies XiR278 and 2A4 frequently have been observed to react with PspA epitopes of the same strain. Based on molecular weight data both epitopes were always present on the same molecule. Our present findings raise the possibility that pneumococci make a second serologically variable PspA which is generally not detected by currently available MAbs to PspA.
肺炎球菌表面蛋白A(PspA)已被证明是肺炎链球菌的一种血清学可变毒力因子。在小鼠中,PspA可引发能够保护它们免受包膜肺炎球菌致命感染的抗体。在先前的研究中,据报道几乎所有分离株都有两个明显不连锁的基因组序列,它们与Rx1 pspA的5'和3'半部分高度同源,尽管我们针对PspA的单克隆抗体在任何给定的肺炎链球菌分离株中都未检测到超过一种PspA。最近,我们从荚膜血清型6B肺炎球菌克隆(MC25 - 28)中鉴定出四个分离株,它们同时表达两种不同的PspA。每个分离株(MC25 - 28)都展示出相同的两个Kpn I片段(每个片段都含有一个Hind III位点),这些片段与Rx1 pspA杂交。针对PspA的单克隆抗体在这四个分离株中的每一个中都检测到了两种具有不同分子量和不同血清学反应模式的PspA(由单克隆抗体XiR278和2A4检测到的PspA 6型,以及仅由单克隆抗体7D2检测到的PspA 34型)。在先前的研究中,经常观察到XiR278和2A4与同一菌株的PspA表位发生反应。基于分子量数据,这两个表位总是存在于同一分子上。我们目前的发现增加了一种可能性,即肺炎球菌产生了第二种血清学可变的PspA,而目前可用的针对PspA的单克隆抗体通常无法检测到这种PspA。