de Jong J C, Bijlsma K, Wermenbol A G, Verweij-Uijterwaal M W, van der Avoort H G, Wood D J, Bailey A S, Osterhaus A D
Laboratory of Virology, Rijksinstituut voor Volksgezondheid en Milieuhygiëne, Bilthoven, The Netherlands.
J Clin Microbiol. 1993 Jun;31(6):1562-9. doi: 10.1128/jcm.31.6.1562-1569.1993.
Monoclonal antibody (MAb) preparations specific for the enteric adenoviruses of subgenus F (AdF) were generated and evaluated as typing reagents in virus neutralization tests and enzyme-linked immunosorbent assays (ELISAs). A panel of 11 genome types of adenovirus 40 (Ad40), 24 genome types of Ad41, and 47 adenovirus prototype strains was used to determine the specificities of the MAbs in the two assays. In this way two MAbs, MAb 40-1 (anti-Ad40) and MAb 41-1 (anti-Ad41) were selected. These two MAbs showed strict type specificity in both assays. A third MAb reacted in an ELISA with all 47 human adenovirus types. With two other MAbs, three antigenic subtypes of Ad41 could be distinguished by their reactivities in virus neutralization tests and ELISAs. On the basis of the five selected MAbs, a sensitive ELISA system was developed for the direct detection and simultaneous typing and subtyping of Ad40 and Ad41 present in stool specimens. The five MAbs were also used to study the epidemiology of infections with Ad40 and Ad41 in The Netherlands in the period 1981 through 1989. It was shown that there were no significant fluctuations in the annual incidence of the cluster of enteric adenoviruses as a whole. This cluster should therefore be considered to belong to the "endemic" rather than the "epidemic" adenoviruses. The relative incidence of Ad40 infections compared with that of Ad41 infections changed considerably during the period studied; the proportion of Ad41 infections rose from about 30% in 1981 to about 95% in 1986, after which it stabilized at 90 to 95%. The proportion of one of the subtypes of Ad41 (Ad41 subtype M3) increased from about 40 to 80% in the same period.
制备了针对F亚属肠道腺病毒(AdF)的单克隆抗体(MAb)制剂,并在病毒中和试验和酶联免疫吸附测定(ELISA)中作为分型试剂进行了评估。使用一组包含11种腺病毒40(Ad40)基因组类型、24种Ad41基因组类型和47种腺病毒原型株,来确定这两种测定中MAb的特异性。通过这种方式,选择了两种MAb,即MAb 40-1(抗Ad40)和MAb 41-1(抗Ad41)。这两种MAb在两种测定中均表现出严格的型特异性。第三种MAb在ELISA中与所有47种人腺病毒类型发生反应。利用另外两种MAb,可通过它们在病毒中和试验和ELISA中的反应性区分Ad41的三种抗原亚型。基于所选择的五种MAb,开发了一种灵敏的ELISA系统,用于直接检测粪便标本中存在的Ad40和Ad41,并同时进行分型和亚型分析。这五种MAb还用于研究1981年至1989年期间荷兰Ad40和Ad41感染的流行病学。结果表明,整个肠道腺病毒群的年发病率没有显著波动。因此,该病毒群应被视为属于“地方性”而非“流行性”腺病毒。在所研究的期间内,Ad40感染与Ad41感染的相对发病率发生了相当大的变化;Ad41感染的比例从1981年的约30%上升至1986年的约95%,此后稳定在90%至95%。Ad41的一种亚型(Ad41亚型M3)的比例在同一时期从约40%增加到80%。