2006
DOI: 10.1007/s00705-005-0695-6
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Genetic diversity of avian infectious bronchitis coronavirus strains isolated in China between 1995 and 2004

Abstract: Twenty-six avian infectious bronchitis (IB) viruses (IBV) were isolated from outbreaks in chickens in China between 1995 and 2004. They were characterized by comparison with twenty-six Chinese reference strains and five other IBV strains. Chinese IBVs, which were mainly nephropathogenic, were placed into seven genotypes. Fourteen Chinese IBV isolates were placed in genotype I, having small evolutionary distances from each other. Genotype II included 6 strains that were isolated in the 1990s in China. Genotype … Show more

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Cited by 113 publications
(170 citation statements)
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(68 reference statements)
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“…The RNA was air-dried for 2 to 10 min, redissolved in 30 ml RNase-free water and stored at (/708C until use. Reverse transcription was carried out in a 40 ml reaction mixture containing 20 ml RNA using IBV genomic antisense IBV-212 oligonucleotide (Table 2), as described elsewhere (Liu et al, 2006).…”
Section: Methodsmentioning
confidence: 99%
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“…The RNA was air-dried for 2 to 10 min, redissolved in 30 ml RNase-free water and stored at (/708C until use. Reverse transcription was carried out in a 40 ml reaction mixture containing 20 ml RNA using IBV genomic antisense IBV-212 oligonucleotide (Table 2), as described elsewhere (Liu et al, 2006).…”
Section: Methodsmentioning
confidence: 99%
“…Therefore, two genome-sense oligonucleotides *S1Uni2 (Adzhar et al, 1997) and IBV-87 (Liu et al, 2006), as summarized in Table 2 *were used with IBV-212 as the antisense primer for PCR amplification of the entire S1 protein genes of vaccine virus strains. The PCR profiles involved an initial denaturation for 5 min at 958C followed by 30 cycles of denaturation at 948C for 1 min, annealing at 508C for 1 min, and polymerization at 728C for 2 min.…”
Section: Methodsmentioning
confidence: 99%
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