van der Avoort H G, Wermenbol A G, Zomerdijk T P, Kleijne J A, van Asten J A, Jensma P, Osterhaus A D, Kidd A H, de Jong J C
Laboratorium voor Virologie, Rijksinstituut voor Volksgezondheid en Milieuhygiene, Bilthoven, The Netherlands.
Virus Res. 1989 Feb;12(2):139-57. doi: 10.1016/0168-1702(89)90060-9.
The DNA of 48 strains of adenovirus type 40 (Ad40) and of 128 strains of adenovirus type 41 (Ad41), isolated between 1971 and 1986 from various countries, was characterized by restriction enzyme analysis using nine and ten restriction endonucleases respectively. Five new DNA variants of Ad40 and 18 new DNA variants of Ad41 were detected. Most of the restriction sites which differed among the various DNA variants appeared to be distributed at random over the entire length of the viral genomes of the two serotypes. The number of restriction sites by which two DNA variants differed from each other was used as a measure of their relatedness. Several clusters of closely related DNA variants were observed for each of the two serotypes. The 35 DNA variants of Ad40 and Ad41 were used to test monoclonal antibody preparations for their range of reactivity in a neutralization assay. One monoclonal antibody (5-8), raised against Ad40 strain Dugan, showed type-specific neutralization of all 11 Ad40 DNA variants tested. Six monoclonal antibodies, raised against Ad41 strain Tak, neutralized different proportions of the variants of Ad41. Two of these preparations (1-21 and 3-19) neutralized all 24 Ad41 DNA variants, while a third (1-23) reacted with only 12 Ad41 variants. Three other monoclonal antibody preparations (3-10, 3-18, 7-14) reacted specifically with only 6 of these 12 variants. The patterns of reactivity with the monoclonal antibody preparations correlated with the presence or absence of a HindIII restriction site at 56 map units and of an EcoRI restriction site at 52 map units on the Ad41 DNA. This region of the adenovirus DNA codes for the hexon protein, which is known to contain the type-specific neutralizing antigenic determinants.
1971年至1986年间从不同国家分离出的48株40型腺病毒(Ad40)和128株41型腺病毒(Ad41)的DNA,分别用9种和10种限制性内切酶通过限制性酶切分析进行了特征鉴定。检测到5种新的Ad40 DNA变异体和18种新的Ad41 DNA变异体。不同DNA变异体之间不同的大多数限制性位点似乎随机分布在两种血清型病毒基因组的全长上。两个DNA变异体彼此不同的限制性位点数量用作它们亲缘关系的衡量标准。对于两种血清型中的每一种,都观察到了几个密切相关的DNA变异体簇。35种Ad40和Ad41的DNA变异体用于在中和试验中测试单克隆抗体制剂的反应范围。一种针对Ad40 Dugan株产生的单克隆抗体(5-8)对所有测试的11种Ad40 DNA变异体表现出型特异性中和作用。针对Ad41 Tak株产生的6种单克隆抗体中和了不同比例的Ad41变异体。其中两种制剂(1-21和3-19)中和了所有24种Ad41 DNA变异体,而第三种(1-23)仅与12种Ad41变异体反应。另外三种单克隆抗体制剂(3-10、3-18、7-14)仅与这12种变异体中的6种特异性反应。与单克隆抗体制剂的反应模式与Ad41 DNA上56个图谱单位处的HindIII限制性位点和52个图谱单位处的EcoRI限制性位点的有无相关。腺病毒DNA的这个区域编码六邻体蛋白,已知该蛋白含有型特异性中和抗原决定簇。