Polymerase chain reaction and restriction fragment length polymorphism analysis of varicella-zoster virus isolates from the United States and other parts of the world

被引:45
作者
LaRussa, P
Steinberg, S
Arvin, A
Dwyer, D
Burgess, M
Menegus, M
Rekrut, K
Yamanishi, K
Gershon, A
机构
[1] Columbia Univ, New York, NY USA
[2] Univ Rochester, Rochester, NY USA
[3] Stanford Univ, Stanford, CA 94305 USA
[4] Kaiser Permanente, Reg Lab, N Hollywood, CA USA
[5] Univ Sydney, Sydney, NSW 2006, Australia
[6] Osaka Univ, Osaka, Japan
关键词
D O I
10.1086/514267
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A polymerase chain reaction (PCR) assay that identifies and differentiates wild-type (,vt) and vaccine strains of varicella-zoster virus (VZV) was used to determine if VZV strains with restriction fragment length polymorphisms resembling those of the Japanese Oka vaccine strain were present in the wt pool outside of Japan. Virus samples (n = 114) from patients with chickenpox and tester from various parts of the United States and Australia were analyzed. The assay correctly identified 113 samples as wt strain. The 1 sample identified as Oka vaccine strain came from a child with leukemia who developed a vaccine-associated rash after receiving the live attenuated varicella vaccine. At this point, there is no evidence that wt strains resembling the vaccine are circulating outside of Japan. This indicates that this PCR assay can be utilized to distinguish rashes due to vaccine and wt VZV.
引用
收藏
页码:S64 / S66
页数:3
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