Quessy S, Dubreuil J D, Caya M, Higgins R
Groupe de Recherche sur les Maladies Infectieuses du Porc, Faculté de Médecine Vétérinaire, Université de Montréal, Québec, Canada.
Infect Immun. 1995 May;63(5):1975-9. doi: 10.1128/iai.63.5.1975-1979.1995.
In an effort to relate the protein profile to virulence, proteins from the cellular fractions and from culture supernatants of Streptococcus suis capsular type 2 strains from different geographical origins were compared by using Western blots (immunoblots). The protein profiles of the cellular fractions were similar for the majority of virulent and avirulent isolates studied, with the exception of three virulent Canadian strains for which a 135-kDa protein was not detected. Examination of the culture supernatants revealed the presence of a 135-kDa protein in all strains except the same three virulent Canadian isolates. In addition, a 110-kDa protein was present in 14 of 16 virulent strains and not in avirulent isolates. When injected into mice, the 110-kDa protein induced an immunoglobulin G response and protected against infection with homologous and heterologous virulent strains. Four strains (1330, 0891, TD10, and R75/S2) that were avirulent in the mouse model of infection and four other strains (1591, 999, JL590, and AAH4) that were virulent in the mouse model were injected into pigs. All virulent strains reproduced the disease, and all avirulent strains failed to reproduce the disease (with the exception of transient lameness in one case and fever in another case). The 110-kDa protein therefore appears to be a reliable virulence marker and a good candidate for a subunit vaccine.
为了将蛋白质谱与毒力联系起来,通过蛋白质免疫印迹法(免疫印迹)比较了来自不同地理来源的2型猪链球菌菌株细胞组分和培养上清液中的蛋白质。在所研究的大多数有毒和无毒分离株中,细胞组分的蛋白质谱相似,但有三株加拿大有毒菌株未检测到135 kDa的蛋白质。对培养上清液的检测发现,除了同样三株加拿大有毒分离株外,所有菌株中都存在一种135 kDa的蛋白质。此外,16株有毒菌株中有14株存在一种110 kDa的蛋白质,而无毒分离株中不存在。当注射到小鼠体内时,110 kDa的蛋白质诱导了免疫球蛋白G反应,并对同源和异源有毒菌株的感染起到了保护作用。将在小鼠感染模型中无毒的四株菌株(1330、0891、TD10和R75/S2)和在小鼠模型中有毒的另外四株菌株(1591、999、JL590和AAH4)注射到猪体内。所有有毒菌株都引发了疾病,所有无毒菌株都未能引发疾病(有一个案例出现短暂跛行,另一个案例出现发热除外)。因此,110 kDa的蛋白质似乎是一个可靠的毒力标志物,也是亚单位疫苗的良好候选物。