Lapointe L, D'Allaire S, Lebrun A, Lacouture S, Gottschalk M
Groupe de Recherche sur les Maladies Infectieuses du Porc (GREMIP), Faculté de médecine vétérinaire, Université de Montreal, St-Hyacinthe, Québec.
Can J Vet Res. 2002 Jan;66(1):8-14.
An autogenous vaccine was developed, using sonicated bacteria, with a strain of Streptococcus suis capsular type 1/2. The objectives of this study were to evaluate the antibody response following vaccination and to assess the changes in antibody levels in pigs from a herd showing clinical signs of S. suis capsular type 1/2 infection in 6- to 8-week-old pigs. An enzyme-linked immunosorbent assay using the vaccine antigen was standardized. Results from a preliminary study involving 2 control and 4 vaccinated 4-week-old pigs indicated that all vaccinated pigs produced antibodies against 2 proteins of 34 and 43 kDa, respectively, and, in 3 out of 4 vaccinated pigs, against the 117-kDa muramidase-released protein. For the serologic profile, groups of 30 pigs from the infected herd were blood sampled at 2, 4, 6, 8, and 10 weeks of age. The lowest antibody level was observed between weeks 6 and 8, presumably corresponding to a decrease in maternal immunity. A marked increase was seen at 10 weeks of age, shortly after the onset of clinical signs in the herd. For the vaccination field trial, newly weaned, one-week-old piglets were divided into 2 groups of 200 piglets each (control and vaccinated); blood samples were collected from 36 piglets in each group at 2-week intervals for 12 weeks. A significant increase (P < 0.05) in antibody response was observed 4 weeks following vaccination and the level of antibodies stayed high until the end of the experiment. In the control group, the increase was only observed at 13 weeks of age, probably in response to a natural infection. The response to the vaccine varied considerably among pigs and was attributed, in part, to the levels of maternal antibodies at the time of vaccination. No outbreak of S. suis was observed in the control or vaccinated groups, so the protection conferred by the vaccine could not be evaluated.
利用超声处理的细菌,开发出了一种针对1/2型猪链球菌菌株的自体疫苗。本研究的目的是评估接种疫苗后的抗体反应,并评估来自一个在6至8周龄仔猪中出现1/2型猪链球菌感染临床症状的猪群中猪的抗体水平变化。使用疫苗抗原的酶联免疫吸附测定法得到了标准化。一项涉及2头对照猪和4头4周龄接种疫苗猪的初步研究结果表明,所有接种疫苗的猪分别产生了针对34 kDa和43 kDa两种蛋白质的抗体,并且在4头接种疫苗的猪中有3头产生了针对117 kDa溶菌酶释放蛋白的抗体。对于血清学特征,从受感染猪群中选取30头猪组成的组,在2、4、6、8和10周龄时采集血样。在第6至8周期间观察到最低抗体水平,推测这与母源免疫力下降相对应。在10周龄时,即在猪群临床症状出现后不久,观察到抗体水平显著升高。对于疫苗现场试验,将新断奶的1周龄仔猪分为两组,每组200头仔猪(对照组和接种疫苗组);在12周内每隔2周从每组36头仔猪中采集血样。接种疫苗4周后观察到抗体反应显著增加(P<0.05),并且抗体水平在实验结束前一直保持较高。在对照组中,仅在13周龄时观察到抗体增加,可能是对自然感染的反应。猪对疫苗的反应差异很大,部分原因是接种疫苗时母源抗体的水平。在对照组或接种疫苗组中均未观察到猪链球菌爆发,因此无法评估疫苗提供的保护作用。