2004
DOI: 10.1128/jvi.78.24.13804-13811.2004
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Recombinant Infectious Bronchitis Coronavirus Beaudette with the Spike Protein Gene of the Pathogenic M41 Strain Remains Attenuated but Induces Protective Immunity

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Cited by 123 publications
(187 citation statements)
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References 42 publications
(80 reference statements)
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“…A similar finding has been reported previously, with the titres of several IB strains decreasing in TOCs after 24 h inoculation (Hodgson et al, 2004). Conversely, qRT-PCR results showed an increase in total viral amount by 4 days p.i.…”
supporting
confidence: 73%
“…A similar finding has been reported previously, with the titres of several IB strains decreasing in TOCs after 24 h inoculation (Hodgson et al, 2004). Conversely, qRT-PCR results showed an increase in total viral amount by 4 days p.i.…”
supporting
confidence: 73%
“…Thus when the S gene of the non-pathogenic Beaudette strain was replaced with that of the pathogenic M41 strain, the host range of Beaudette was altered in vitro : the virus no longer replicated in Vero cells (Casais et al ., , 2003. When this spike-swapped recombinant was inoculated (by nose and eye drop) into chickens, it was still nonpathogenic */although it did stimulate protective immunity against challenge by M41 (Hodgson et al ., 2004). In addition to the four structural proteins (S, E, M and N) that are possessed by all coronaviruses, Group 2 coronaviruses contain a fourth membrane-associated protein, the haemagglutinin-esterase protein (reviewed by Enjuanes et al ., 2000;Cavanagh, 2005).…”
Section: Structural Features Of Coronavirusesmentioning
confidence: 99%
“…This leaves us far short of understanding the molecular basis of cross-protection -or lack of itas cellular immune responses play a role in protection, and these are poorly understood. We do know that the S protein alone is sufficient to induce good protective immunity [12,20,46,51,53,93,96]. There is increasing evidence that only a few amino acid differences amongst S proteins are sufficient to have a detrimental impact on cross-protection.…”
Section: Introductionmentioning
confidence: 99%
“…The development of reverse genetic ('infectious clone') systems for IBV has opened up the possibility of precisely modifying the IBV genome for vaccine development as well as for defining the roles of the virus proteins in pathogenicity -two interrelated areas of research [7,10,11,46,47,104].…”
Section: Introductionmentioning
confidence: 99%