Couderc T, Martin A, Wychowski C, Girard M, Horaud F, Crainic R
Unité de Virologie Médicale, Institut Pasteur, Paris, France.
J Gen Virol. 1991 Apr;72 ( Pt 4):973-7. doi: 10.1099/0022-1317-72-4-973.
A chimeric type 1/type 2 poliovirus (v510), in which the antigenic site 1 (Ag1) of poliovirus type 1 (PV-1) Mahoney was replaced by the corresponding site of poliovirus type 2 (PV-2) Lansing, is known to be neurovirulent for mice and neutralized by both type 1 and type 2 monoclonal antibodies. Neutralization-escape mutants to monoclonal antibodies specifically recognizing the PV-2 sequence were obtained from v510. The nucleotide sequence and the mouse neurovirulence of mutants were determined. Amino acid substitutions obtained inside the replaced sequence, at positions 95 and 99, and outside this site, at positions 93 or 104, rendered the virus attenuated for mice. One of the escape mutants harboured a deletion of the entire substituted nonapeptide sequence in v510. This particular virus, which is a PV-1 Mahoney lacking the natural Ag1 loop, does not react with PV-2-specific monoclonal antibodies, has a ts phenotype, is heat-labile and is devoid of neurovirulence for mice.
一种1型/2型嵌合脊髓灰质炎病毒(v510),其中1型脊髓灰质炎病毒(PV-1)Mahoney株的抗原位点1(Ag1)被2型脊髓灰质炎病毒(PV-2)Lansing株的相应位点所取代,已知对小鼠具有神经毒性,并且能被1型和2型单克隆抗体中和。从v510中获得了对特异性识别PV-2序列的单克隆抗体的中和逃逸突变体。测定了突变体的核苷酸序列和小鼠神经毒性。在被取代序列内部的第95和99位以及该位点外部的第93或104位获得的氨基酸取代使病毒对小鼠减毒。其中一个逃逸突变体在v510中缺失了整个被取代的九肽序列。这种特殊的病毒是一种缺乏天然Ag1环的PV-1 Mahoney株,不与PV-2特异性单克隆抗体反应,具有温度敏感型表型,对热不稳定,并且对小鼠没有神经毒性。