2006
DOI: 10.1016/j.vetmic.2006.03.012
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Evaluation of immune effects of fowlpox vaccine strains and field isolates

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Cited by 39 publications
(32 citation statements)
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“…A final extension step was performed for 5 min at 72°C. The primers for the region of FWPV flanking REV 5 0 LTR as described by Wang et al [25] and the env gene [26] were used for the detection of REV integration. The PCR amplification conditions for both the genes were same with annealing temperature at 52°C.…”
Section: Dna Extraction and Pcr Amplificationmentioning
confidence: 99%
“…A final extension step was performed for 5 min at 72°C. The primers for the region of FWPV flanking REV 5 0 LTR as described by Wang et al [25] and the env gene [26] were used for the detection of REV integration. The PCR amplification conditions for both the genes were same with annealing temperature at 52°C.…”
Section: Dna Extraction and Pcr Amplificationmentioning
confidence: 99%
“…While the LTR remnants comprise about 200 or 500 bp, the near-fulllength provirus is about 8000 bp long and missing only a part of the 39 LTR (8,19). In most investigated field isolates the near-fulllength REV provirus or indications of its presence have been found, whereas REV sequences other than remnants of the LTR have been detected only in few vaccine strains (8,12,22).…”
mentioning
confidence: 98%
“…Since REV is an immunosuppressive virus, it is possible that the expression of REV genes influences the pathogenesis of fowlpox by impairing the immune response of the bird (20,22). This could be one possible explanation why antibody formation against FPV is infrequent (2,23,24).…”
mentioning
confidence: 99%
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