J Korean Soc Microbiol.
2000 Apr;35(2):191-201.
Detection and differentiation of Herpes Simplex Virus 1 and 2, and
Varicella-Zoster virus in vesicle fluid, joint fluid and serum using PCR
method
- Affiliations
-
- 1Department of Microbiology, Division of Molecular
Biology, Ewha Medical Center and College of Medicine, Ewha Womans
University, Seoul, 158-056, South Korea.
Abstract
-
The viruses of Herpes Simplex Virus 1 (HSV-1), Herpes Simplex
Virus 2 (HSV-2) and Varicella-Zoster virus (VZV) which belong to the
alpha herpes subfamily are important human pathogens. When eruptions were
not fully developed from these viral infections, clinical diagnosis was
not always easy and required virological confirmation test. The above
viruses were reactivated in individuals who were compromised in immune
competence for one reason or another. Polymerase chain reaction (PCR)
enables rapid and sensitive detection of HSV and VZV DNAs. Its
sensitivity was largely influenced by choice of primers. Authors
conducted a study to detect of those three viruses in human specimens
including vesicle fluid and joint fluid and serum using PCR methods.
Primers used for this study were the general primer pair GPHV-RU which
was known to amplify within the genes enjoying the highest degree of
homology between UL15 of HSV and UL42 of VZV. PCR with primers hybridized
pair GPHV-RU amplifies a 396 bp with HSV-1 and HSV-2 standard stain DNA
and 405 bp with VZV standard strain DNA. Restriction enzyme cleavage with
HpaII and DdeI were used to detect and distinguish DNAs of HSV-1 and
HSV-2 and VZV. The purpose of this study was a rapid and easy detection
of VZV and HSV-1 or HSV-2 from various clinical specimens (vesicle fluid,
serum and joint fluid) by PCR method. Used methods were: HSV PCR with
primer 1, 2 and HpaII RE digestion; VZV nested PCR; HSV PCR with primer
A, B and BssHII RE digestion. 1) In 33 cases (33/42, 78.6%) VZV was
detected single or mixed infection from 42 clinical specimens which
included vesicle fluid (5), serum from respiratory infected children
(10), serum from immune suppressed adult cancer patients (7) and joint
fluid from arthritis patients (20). 2) In 20 cases (20/42, 42.6%) HSV was
detected singly or mixed infection and 19 of the cases were HSV-2 and 1
case was HSV-1. 3) In 19 cases (19/42, 45.2%) VZV was singly detected
which included serum from respiratory infected children (6 cases), joint
fluid from arthritis patients (9 cases), vesicle fluid (2 cases) and
serum form immunosuppressed cancer patients (2 cases). 4) HSV was singly
detected in 6 cases (6/42, 14.3%) which included joint fluid from
arthritis patients (5 cases) and serum form respiratory infected children
(1 cases). 5) 14 cases of VZV and HSV mixed infection (14/42, 33.3%) were
detected. They included vesicle fluid (3 cases), serum form
immunosuppressed cancer patients (4 cases), serum from respiratory
infected children (2 cases) and joint fluid from arthritis patients (5
cases). 6) HSV-1 and HSV-2 detection and typing by HSV PCR with primer A,
B and BssHII RE digestion method was more sensitive and the results were
easier to detect than on other method.