Mooi F R, van Oirschot H, Heuvelman K, van der Heide H G, Gaastra W, Willems R J
Research Laboratory for Infectious Diseases, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
Infect Immun. 1998 Feb;66(2):670-5. doi: 10.1128/IAI.66.2.670-675.1998.
The Bordetella pertussis proteins P.69 (also designated pertactin) and pertussis toxin are important virulence factors and have been shown to confer protective immunity in animals and humans. Both proteins are used in the new generation of acellular pertussis vaccines (ACVs), and it is therefore important to study the degree of antigenic variation in these proteins. Sequence analysis of the genes for P.69 and the pertussis toxin S1 subunit, using strains collected from Dutch patients in the period 1949 to 1996, revealed three P.69 and three S1 variants which show differences in amino acid sequence. Polymorphism in P.69 was confined to a region comprised of repeats and located proximal to the RGD motif involved in adherence to host tissues. Variation in S1 was observed in two regions previously identified as T-cell epitopes. P.69 and S1 variants, identical to those included in the Dutch whole-cell pertussis vaccine (WCV), were found in 100% of the strains from the 1950s, the period when the WCV was introduced in The Netherlands. However, nonvaccine types of P.69 and S1 gradually replaced the vaccine types in later years and were found in approximately 90% strains from 1990 to 1996. These results suggest that vaccination has selected for strains which are antigenically distinct from vaccine strains. Analysis of strains from vaccinated and nonvaccinated individuals indicated that the WCV protects better against strains with the vaccine type P.69 than against strains with non-vaccine types (P = 0.024). ACVs contain P.69 and S1 types which are found in only 10% of recent Dutch B. pertussis isolates, implying that they do not have an optimal composition. Our findings cast a new light on the reemergence of pertussis in highly vaccinated populations and may have major implications for the long-term efficacy of both WCVs and ACVs.
百日咳博德特氏菌蛋白P.69(也称为百日咳黏附素)和百日咳毒素是重要的毒力因子,已证明可在动物和人类中提供保护性免疫。这两种蛋白都用于新一代无细胞百日咳疫苗(ACV),因此研究这些蛋白的抗原变异程度很重要。使用1949年至1996年期间从荷兰患者收集的菌株对P.69和百日咳毒素S1亚基的基因进行序列分析,发现了三种P.69变体和三种S1变体,它们在氨基酸序列上存在差异。P.69的多态性局限于一个由重复序列组成的区域,该区域位于与宿主组织黏附相关的RGD基序附近。在先前确定为T细胞表位的两个区域中观察到S1的变异。与荷兰全细胞百日咳疫苗(WCV)中包含的变体相同的P.69和S1变体,在20世纪50年代(荷兰引入WCV的时期)的100%菌株中被发现。然而,非疫苗类型的P.69和S1在随后几年逐渐取代了疫苗类型,在1990年至1996年的约90%菌株中被发现。这些结果表明,疫苗接种选择了与疫苗菌株抗原不同的菌株。对接种疫苗和未接种疫苗个体的菌株分析表明,WCV对具有疫苗类型P.69的菌株的保护作用比对具有非疫苗类型的菌株更好(P = 0.024)。ACV包含的P.69和S1类型仅在最近荷兰百日咳博德特氏菌分离株的不到10%中被发现,这意味着它们的组成并非最佳。我们的研究结果为高接种率人群中百日咳的再次出现提供了新的线索,可能对WCV和ACV的长期效力产生重大影响。