Specific detection of monkeypox virus by polymerase chain reaction

被引:39
作者
Neubauer, H
Reischl, U
Ropp, S
Esposito, JJ
Wolf, H
Meyer, H
机构
[1] Fed Armed Forces Med Acad, Inst Microbiol, D-80937 Munich, Germany
[2] Univ Regensburg, Inst Med Microbiol & Hyg, D-93053 Regensburg, Germany
[3] Ctr Dis Control & Prevent, Div Viral & Rickettsial Dis, Natl Ctr Infect Dis, Publ Hlth Serv,US Dept Hlth & Human Serv, Atlanta, GA 30333 USA
关键词
orthopoxvirus; DNA sequences; acidophilic inclusion body protein;
D O I
10.1016/S0166-0934(98)00099-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The open reading frame coding for the A-type inclusion body protein (ATI) of monkeypox virus (MPV) was identified and sequenced for two strains. Nucleotide sequence comparison revealed 72-95.3% homology with the reported open reading frame sequences of the ATIs of other orthopoxvirus species, such as variola, vaccinia, cowpox, ectromelia, and camelpox viruses. Each MPV strain contained an 8-bp deletion, which caused a frameshift that introduced a premature stop in the open reading frame at base 2091 relative to the ATI open reading frame of cowpox virus strain Brighten. The sequences enabled a primer pair to be designed that flanked the deletion and specifically amplified a 601-bp fragment that identified and differentiated 19 MPV strains examined from five other Old World orthopoxvirus species examined. The specificity was confirmed by cleavage of the 19 MPV strain amplicons with Bg/II, which produced three subfragments of expected sized, based on the determined MPV sequences. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:201 / 207
页数:7
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