Hq. Zheng et al., STRAIN-SPECIFIC REVERSE-TRANSCRIPTASE PCR ASSAY - MEANS TO DISTINGUISH CANDIDATE VACCINE FROM WILD-TYPE STRAINS OF RESPIRATORY SYNCYTIAL VIRUS, Journal of clinical microbiology, 34(2), 1996, pp. 334-337
Candidate live-virus vaccines for respiratory syncytial virus are bein
g developed and are beginning to be evaluated in clinical trials. To d
istinguish candidate vaccine strains from wild-type strains isolated d
uring these trials, we developed PCR assays specific to two sets of ca
ndidate vaccine strains, The two sets were a group A strain (3A), its
three attenuated, temperature-sensitive variant strains, a group B str
ain (2B), and its four attenuated, temperature-sensitive variant strai
ns, The PCR assays were evaluated by testing 18 group A wild-type stra
ins, the 3A strains, 9 group B wild-type strains, and the 2B strains,
PCR specific to group A wild-type strains amplified only group wild-ty
pe strains, and 3A-specific PCR amplified only 3A strains, PCR specifi
c to group B wild-type strains amplified all group A and group B strai
ns but gave a 688-bp product for group B wild-type strains, a 279-bp p
roduct for 2B strains, a 547-hp product for all group A strains, and a
n additional 688-bp product for some group A strains, including 3A str
ains. These types of PCR assays can, in conjunction with other methods
, be used to efficiently distinguish candidate vaccine strains from ot
her respiratory syncytial virus strains.