For Publishers
DiscoveryMetadataPeer reviewHostingPublishing
For Researchers
JoinPublishReviewCollect
Register
Blog
About
Search
Advanced search
My ScienceOpen
Search
For Publishers
For Researchers
Blog
About
46
views
25
references
 Top references
cited by
14
    
0 reviews
 Review
0
comments
 Comment
0
recommends
+1 Recommend
1 collections
    0
    shares
      316
      similar
       All similar
      • Record: found
      • Abstract: found
      • Article: found

      Sequence Analysis of the Matrix/Nucleocapsid Gene Region of Turkey Coronavirus

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          A reverse transcriptase, polymerase chain reaction (RT-PCR) procedure was used to amplify a segment of the genome of turkey coronavirus (TCV) spanning portions of the matrix and nucleocapsid (MN) protein genes (approximately 1.1 kb). The MN gene region of three epidemiologically distinct TCV strains (Minnesota, NC95, Indiana) was amplified, cloned into pUC19, and sequenced. TCV MN gene sequences were compared with published sequences of other avian and mammalian coronaviruses. A high degree of similarity (>90%) was observed between the nucleotide, matrix protein, and nucleocapsid protein sequences of TCV strains and published sequences of infectious bronchitis virus (IBV). The matrix and nucleocapsid protein sequences of TCV had limited homology (<30%) with MN sequences of mammalian coronaviruses. These results demonstrate a close genetic relationship between the avian coronaviruses, IBV and TCV.

          Related collections

          Most cited references25

          • Record: found
          • Abstract: not found
          • Article: not found

          The biology and pathogenesis of coronaviruses.

          V ter Meulen, S Siddell, H Wege (1981)
          Article 0 comments Cited 119 times – based on 0 reviews     Review now
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Antigenic relationship of the feline infectious peritonitis virus to coronaviruses of other species

            N C Pedersen, J. Ward, W L Mengeling (1978)
            Summary Utilizing the direct and indirect fluorescent antibody procedure, the antigenic relationship of the feline infectious peritonitis virus (FIPV) to 7 other human and animal coronaviruses was studied. FIPV was found to be closely related to transmissible gastroenteritis virus (TGEV) of swine. Transmissible gastroenteritis virus and FIPV were in turn antigenically related to human coronavirus 229E (HCV-229E) and canine coronavirus (CCV). An interesting finding in the study was that the 8 coronaviruses selected for this study fell into one of two antigenically distinct groups. Viruses in each group were antigenically related to each other to varying degrees, but were antigenically unrelated to coronaviruses of the second group. The first antigenically related group was comprised of mouse hepatitis virus, type 3 (MHV-3), hemeagglutinating encephalomyelitis virus 67N (HEV-67N) of swine, calf diarrhea coronavirus (CDCV), and human coronavirus OC43 (HCV-OC43). The second antigenically related group was comprised of FIPV, TGEV, HCV-229E and CCV.
            Article 0 comments Cited 72 times – based on 0 reviews     Review now
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes

              William Lapps, Brenda G. Hogue, David Brian (1987)
              The 3′ end of the 20-kb genome of the Mebus strain of bovine enteric coronavirus (BCV) was copied into cDNA and cloned into the PstI site of the pUC9 vector. Four clones from the 3′ end of the genome were sequenced either completely or in part to determine the sequence of the first 2451 bases. Within this sequence were identified, in order, a 3′-noncoding region of 291 bases, the gene for a 448-amino acid nucleocapsid protein (N) having a molecular weight of 49,379, and the gene for a 230-amino acid matrix protein (M) having a molecular weight of 26,376. A third large open reading frame is contained entirely within the N gene sequence but is positioned in a different reading frame; it potentially encodes a polypeptide of 207 amino acids having a molecular weight of 23,057. A higher degree of amino acid sequence homology was found between the M proteins of BCV and MHV (87%) than between the N proteins (70%). For the M proteins of BCV and MHV, notable differences were found at the amino terminus, the most probable site of O-glycosylation, where the sequence is N-Met-Ser-Ser-Val-Thr-Thr for BCV and N-Met-Ser-Ser-Thr-Thr for MHV. BCV apparently uses two of its six potential O-glycosylation sites.
              Article 0 comments Cited 63 times – based on 0 reviews     Review now
                Bookmark
                All references

                Author and article information

                Journal
                Journal ID (nlm-ta): Intervirology
                Journal ID (iso-abbrev): Intervirology
                Journal ID (publisher-id): INT
                Title: Intervirology
                Publisher: S. Karger AG (Allschwilerstrasse 10, P.O. Box · Postfach · Case postale, CH–4009, Basel, Switzerland · Schweiz · Suisse, Phone: +41 61 306 11 11, Fax: +41 61 306 12 34, karger@karger.com )
                ISSN (Print): 0300-5526
                ISSN (Electronic): 1423-0100
                Publication date (Print): June 1999
                Publication date (Electronic): 16 June 1999
                Volume: 42
                Issue: 1
                Pages: 22-29
                Affiliations
                Department of Microbiology, Pathology, and Parasitology, North Carolina State University, Raleigh, N.C., USA
                Author notes
                *James S. Guy, North Carolina State University, College of Veterinary Medicine, 4700 Hillsborough Street, Raleigh, NC 27606 (USA), Tel. +1 919 829 4287, Fax +1 919 829 4455, E-Mail Jim-Guy@ 123456ncsu.edu
                Article
                Publisher ID: int-0042-0022
                DOI: 10.1159/000024956
                PMC ID: 7179554
                PubMed ID: 10393500
                SO-VID: fbeeca91-8dd0-4180-bf29-017ad14d06e4
                Copyright © Copyright © 1999 by S. Karger AG, Basel
                License:

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                Date received : 31 July 1998
                Date revision received : 8 December 1998
                Date: 1999
                Page count
                Figures: 4, Tables: 2, References: 34, Pages: 8
                Categories
                Subject: Original Paper

                Keywords: coronavirus,infectious bronchitis virus,turkey coronavirus,polymerase chain reaction
                Data availability:
                Keywords: coronavirus, infectious bronchitis virus, turkey coronavirus, polymerase chain reaction

                Comments

                Comment on this article

                scite_

                Similar content316

                See all similar

                Cited by14

                See all cited by

                Most referenced authors283

                See all reference authors