1992
DOI: 10.1099/0022-1317-73-11-2849
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Analysis of a 9.6 kb sequence from the 3' end of canine coronavirus genomic RNA

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Cited by 65 publications
(90 citation statements)
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(46 reference statements)
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“…More than 10 coronavirus N genes have now been sequenced, including those of HCV 229E, TGEV, PRCV, FIPV, CCV, murine hepatitis virus (MHV), HCV OC43, bovine coronavirus (BCV) and infectious bronchitis virus (IBV) (Schreiber et al, 1989;Kapke & Brian, 1986;Britton et al, 1991 ;Vennema et al, 1991 ;Horsburgh et al, 1992;Parker & Masters, 1990;Kamahora et al, 1989;Lapps et al, 1987;Boursnell et al, 1985). Many of these viruses have been sequenced by more than one group; the references quoted here were those used in the sequence analyses shown in Fig.…”
Section: Discussionmentioning
confidence: 99%
“…More than 10 coronavirus N genes have now been sequenced, including those of HCV 229E, TGEV, PRCV, FIPV, CCV, murine hepatitis virus (MHV), HCV OC43, bovine coronavirus (BCV) and infectious bronchitis virus (IBV) (Schreiber et al, 1989;Kapke & Brian, 1986;Britton et al, 1991 ;Vennema et al, 1991 ;Horsburgh et al, 1992;Parker & Masters, 1990;Kamahora et al, 1989;Lapps et al, 1987;Boursnell et al, 1985). Many of these viruses have been sequenced by more than one group; the references quoted here were those used in the sequence analyses shown in Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The S protein of strain CB/05 had the highest identity to FCoV type II strain 79-1683 (Figure 2). Comparison with strain CB/05 was possible only with CCoV type II strains Insavc-1 ( 10 ) and BGF ( 11 ) and CCoV type I strains Elmo/02 and 23/03 ( 3 , 12 ) because of a lack of data on the 3´ end of the CCoV genome in the genes encoding for nonstructural proteins (NSPs) 3a, 3b, 3c, 7a, and 7b. NSPs 3a, 7a, and 7b were not altered.…”
Section: The Studymentioning
confidence: 99%
“…Ten µl RNA, 50 mM KCl, 10 mM Tris-HCl (pH 8), 400 µM dNTP, and 10 units RNAse inhibitor were added to a reaction mixture. CCV RNA was detected by semi-nested RT-PCR using three primers created from the 3' end of spike gene of CCV strain Insavc-1 (Horsburgh et al, 1992). In the first amplification step, 2 µl cDNA sample were amplified in a 50 µl reaction volume containing 50 mM KCl, 1.5 mM MgCl 2 , 10 mM Tris-HCl (pH 8), 200 µM dNTP, 1.5 units Taq DNA polymerase (QIAGEN, Germany) and 15 pM each of outer sense primer; CCV1 (located at position 1691: 5' GGC GTA ACT GAT GGA CCA CG 3') and outer anti-sense primer; CCV2 (located at position 2451: 5' CTT GTA CGG GCG GCA ACA TC 3').…”
Section: Reverse Transcription-polymerase Chain Reaction Detection Ofmentioning
confidence: 99%