Esposito J J, Knight J C
Virology. 1985 May;143(1):230-51. doi: 10.1016/0042-6822(85)90111-4.
Characteristic DNA endonuclease digest fragment electropherograms and restriction site maps permitted differentiation and genome structure analysis of 38 orthopoxviruses that included isolates of monkeypox virus from humans and animals, monkeypox white variants, variola, vaccinia, ectromelia, Tatera (gerbil) and raccoon poxviruses, and cowpox and camelpox viruses. HindIII cleavage sites mapped on the 38 virus genome DNAs plus SmaI, BglI, SacI, KpnI, XhoI, and SalI maps for variola (Harvey) and monkeypox (Copenhagen) virus DNAs were derived essentially by cross-hybridizations with monkeypox, vaccinia, and variola virus-cloned DNA restriction fragments, thus digest fragments could be assigned homologous regions on previously established genome maps. Salient of our observations, the DNA HindIII maps correlated to a high degree, but variations in middle and especially terminal DNA region cleavage sites provided a basis for discerning species, strains and variants. The extent of the inverted terminal repetitions (ITRs) for 37 DNAs were determined with HindIII, PvuI, SalI, and ClaI, plus nine more restriction enzymes for Bangladesh variola virus DNA by hybridizations with either the terminal tandemly repeated 70-bp segment or an EcoRI-PvuI near hairpin-end 75-bp segment from WR vaccinia virus. The opposite terminal regions of variola DNA were considerably asymmetrical compared to the large symmetrical ITRs of the other species examined. An apparent DNA inversion and concurrent deletion (1 kbp) with subsequent repair of DNA to original structure was suggested from right terminal region maps of four viruses chosen from a variola virus passage series in monkeys. Correlative with virus geographic distribution, two strains of monkeypox virus, each containing two variants, were differentiated by DNA profiles of isolates from smallpox-like disease (SLD) patients of the African rainforest region. The DNAs of five monkeypox viruses isolated from laboratory and zoo animals resembled most DNAs from SLD monkeypox viruses from Sierra Leone. A poxvirus from an American raccoon contained 40% DNA that did not cross-hybridize with orthopoxvirus DNA probes. The DNAs of recent isolates from a gerbil and from a camel each mapped as unique African orthopoxvirus species and differed from variola virus.
特征性DNA内切酶消化片段电泳图和限制性酶切位点图谱有助于对38种正痘病毒进行鉴别和基因组结构分析,这些病毒包括来自人和动物的猴痘病毒分离株、猴痘白色变种、天花病毒、痘苗病毒、鼠痘病毒、沙鼠痘病毒、浣熊痘病毒以及牛痘病毒和骆驼痘病毒。通过与猴痘病毒、痘苗病毒和天花病毒克隆的DNA限制性片段进行交叉杂交,基本确定了38种病毒基因组DNA上的HindIII切割位点,以及天花病毒(哈维株)和猴痘病毒(哥本哈根株)DNA的SmaI、BglI、SacI、KpnI、XhoI和SalI图谱,因此可以在先前建立的基因组图谱上确定消化片段的同源区域。我们观察到的一个显著现象是,DNA HindIII图谱高度相关,但中间尤其是末端DNA区域切割位点的差异为区分病毒种类、毒株和变种提供了依据。通过与WR痘苗病毒末端串联重复的70bp片段或靠近发夹末端的75bp EcoRI - PvuI片段杂交,用HindIII、PvuI、SalI和ClaI以及另外九种限制性酶确定了37种DNA的反向末端重复序列(ITR)的长度,对于孟加拉国天花病毒DNA还使用了更多限制性酶。与其他被检测物种的大的对称ITR相比,天花病毒DNA的相对末端区域明显不对称。从猴天花病毒传代系列中选取的四种病毒的右末端区域图谱显示,存在明显的DNA倒位和同时发生的缺失(1kbp),随后DNA修复为原始结构。与病毒的地理分布相关,通过对非洲雨林地区类天花疾病(SLD)患者分离株的DNA图谱分析,区分出了两株猴痘病毒,每株包含两个变种。从实验室和动物园动物中分离出的五种猴痘病毒的DNA与来自塞拉利昂的SLD猴痘病毒的大多数DNA相似。一种来自美国浣熊的痘病毒含有40%与正痘病毒DNA探针不发生交叉杂交的DNA。从沙鼠和骆驼中最近分离出的病毒的DNA各自被定位为独特的非洲正痘病毒种类,且与天花病毒不同。