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


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          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.

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          Coronaviridae 1

          An informal proposal has been made to group together a number of recently recognized viruses under the head of coronaviruses [1]. They affect a variety of hosts causing a diversity of diseases, but they are grouped together mainly because they have similar electron microscopic appearances, are ether-labile, and probably contain RNA. However, remembering that influenza and parainfluenza viruses were once thought to be quite closely related on similar grounds, much of the grouping should be regarded as tentative. Nevertheless, murine strains (MHV) are antigenically related to some human strains and, morphologically, human, avian, and murine viruses replicate in a similar way; it is therefore likely that at least some of the groupings will be confirmed by further investigation. There is now some more detailed information on the structure of the prototype virus IBV (avian infectious bronchitis virus), the striking features being the large number of peptides and the large single RNA strand. Some strains possess hemagglutinin and there seems to be a hemagglutinin receptor-destroying enzyme which is not a neuraminidase; also there is evidence of a viral RNA polymerase. These features confirm that IBV is quite distinct from other viruses. We still have no detailed information about the biochemical characteristics of its nucleic acid, the process of replication or the lipid composition of the envelope. All in all, the time is now ripe for completing these basic studies of IBV and checking whether the same characteristics are found in the other viruses at present included in the group. It may take years to reach certainty on these points, but we believe this early attempt at taxonomy can be valuable in indicating which facts should be sought first, in order to clarify as soon as possible our understanding of this interesting and superficially diverse group. The Study Group believes that the coronaviruses are sufficiently distinct from other viruses to constitute a family, Coronaviridae; at present, it will have to be considered a monogeneric family. To save space, references included in the review by McIntosh [2] will not be repeated. 1 Taxonomy [2] 1.1 Coronaviridae 1.3 Family with only one genus, Coronavirus 2 The virion 2.1 Chemical composition 2.1.1 Nucleic acid RNA IBV2: single-stranded [5, 6]. HCV: single-stranded [7] Number of pieces: IBV, one [5] Sedimentation coefficients: IBV, 50S [5] Molecular weight: IBV, 9 × 10G [5] Infectivity: Not demonstrated for any member. 2.1.2 Proteins Number of polypeptides: HCV: 6-8 polypeptides [8]: IBV: 16 polypeptides [9] Molecular weight of polypeptides: HCV, 13,000-210,000 [8]. IBV, 14,000-180,000 [9] Enzymes: IBV: possible receptor-destroying enzyme activity [10], possible RNA polymerase [10, 11]. HCV: RNA-dependent RNA polymerase [12]. Other functional proteins: hemagglutinin (HCV: some strains; HEV; IBV: some strains [13]). 2.1.3 Lipids: Present 2.1.4 Carbohydrates: IBV. HCV, TGEV: glycopeptides present. 2.2 Physicochemical properties 2.2.1 Density: 1.16-1.23 g/cm3 in sucrose: 1.23-1.24 g/cm3 in CsCl. 2.2.2 Sedimentation coefficient: HCV: 374-416S, strain OC43: 378-400S, strain 229E [8]. IBV: 330S. 2.2.4 Stability of infectivity pH: TGEV: optimum stability at pH 6.5 [14]. IBV: optimum stability between pH 6.0 and 6.5 [11]. Conflicting or no evidence for other viruses. Heat: Rapidly inactivated at 56°; slow inactivation at 37°; moderately stable at 4°, assuming optimal suspending medium. Other agents: Unstable with common disinfectants and detergents. 2.3 Structure 2.3.1 Nucleocapsid: See 2.3.3. 2 See 10.3 for abbreviations of species. 2.3.2 Envelope: Lipid envelope present, containing peptides and glycopeptides. 2.3.3 Cores: Electron-dense inner shell visible in thin section. HCV: ribonucleoprotein (RNP) core, density 1.31 g/cm3 (CsCl), sedimentation 180S [15]; linear appearance by negative staining [12]. Dimensions: 55-nm diameter in thin section. 2.4 Morphology 2.4.1 Overall shape: Round, non-rigid, some elongated forms. 2.4.2 Dimensions: 60-220 nm 2.4.3 Surface projections: Characteristic bulbous projections, 12-24 nm long, widely spaced. 2.4.4 Special features in thin sections: Inner and outer shells, sometimes separated by electron-lucent space. Some reports of internal threadlike structure. 2.4.5 Other features: Fragile attachment of projections to surface of virion. Inner tongue-shaped membrane sometimes visible by negative staining. 3 Replication 3.1 Site of accumulation of viral proteins: Cytoplasm. 3.2 Nonstructural proteins: Probably present. 3.3 Mode of nucleic acid replication 3.3.2 Effect of inhibitors: Sensitive to 6-azauracil, virazole [10]. Insensitive to 5′-iododeoxyuridine, 5′-bromodeoxyuridine, 5′-fluorodeoxyuridine, cytosine arabinoside, aminopterin and actinomycin D. 3.4 Site and mechanism of maturation: Matures in cytoplasm by budding through endoplasmic reticulum. 3.5 Other features: No budding at plasma membrane. 4 Cooperative interactions: No information available. 5 Host range 5.1 Natural: Generally restricted to normal host species. 5.2 Experimental 5.2.1 In vivo: Generally specific for species of origin: chicken embryos (IBV), suckling mice (MHV, some strains of IBV3 and HCV), newborn rabbits (IBV3). suckling white rats (IBV3), suckling hamsters (HCV), hamsters (MHV). 5.2.2 In vitro: HCV: 1°4 and 2° human embryonic cells, 1° monkey kidney cells, human embryonic tracheal organ cultures. IBV3: 1° 3 Isolation in chicken embryos is essential before adaptation to hosts or cells indicated. 4 1° = First passage. chicken and chicken embryonic cells, 1° monkey kidney, chicken tracheal organ cultures, VERO cells. MHV: L cells, WI-38 cells, 1° mouse and mouse embryonic cells, mouse macrophages, NCTC-1469 cells. TGEV and HEV: 1° porcine cells. TGEV: 1° canine kidney cells. RCV and SDAV: 1° rat kidney cells. 6 Pathogenicity 6.1 Association with diseases: IBV: acute respiratory disease and nephritis in chickens. HCV: common colds in humans. MHV: hepatitis and encephalitis in mice (most strains cause primarily one or the other). TGEV: gastroenteritis in pigs. HEV: encephalitis in pigs. RCV: pulmonary infections of rats. SDAV: sialodacryoadenitis in rats. 6.2 Tissue tropisms: IBV: respiratory and reproductive tract. HCV: upper respiratory tract. TGEV: small intestine, lung. HEV: intestine, brain. MHV: brain, liver, spleen. RCV: lung. SDV: salivary gland. 6.3 Cytopathology: Cellular vacuolation and syncytium formation. 7 Geographic distribution: Probably worldwide. 8 Transmission 8.1 Vertical: HCV: no. IBV: yes. No data available for other strains. 8.2 Horizontal: Yes. 8.3 Vectors 8.3.1 Biological: Not known. 8.3.2 Mechanical: IBV: contaminated equipment, personnel, etc. TGEV: fecal-oral route. HCV: presumed airborne. No data for other strains. 9 Antigenic properties 9.1 Number of distinct antigenic molecules in virion: IBV: up to 3. HCV: 3, possibly 4. MHV: 2. 9.2 Antigens involved in virus neutralization: No adequate information. 9.3 Number of distinct nonstructural antigens: No adequate information. 9.4 Specificity of different antigens: No information. 10 Classification 10.1 Definition of family Coronaviridae: Pleomorphic enveloped particles, averaging 100 nm diameter, containing RNA and essential lipid. Bear unique definitive projections. Multiply in cytoplasm, mature by budding through endoplasmic reticulum. No defined subgroups, but a tentative grouping may be made on basis of serology. IBV, many recognized serotypes, however, all seem to be interrelated, possibly by a common antigen. No interrelationship demonstrated with any of the other coronaviruses. HCV, several serotypes, two main groups-those isolated in tissue culture and those isolated in organ culture. Serologically related to MHV. The three rodent coronaviruses, MHV, RCV and SDAV, are interrelated serologically, and also related to HCV. No adequate information on relationship or diversity between individual strains of MHV. TGEV, no antigenic diversity between strains, possible relationship to HEV. HEV, no antigenic diversity between strains, possible relationship to TGEV. TBDV, only one report available, no relationship shown to other coronaviruses. 10.2 Only one Genus, Coronavirus. Type species: IBV. 10.3 Species: Avian infectious bronchitis virus (IBV) Human Coronavirus (HCV) Murine hepatitis virus (MHV) Porcine transmissible gastroenteritis virus (TGEV) Porcine hemagglutinating encephalitis virus (HEV) Rat Coronavirus (RCV) Sialodacryoadenitis virus of rats (SDAV) Turkey bluecomb disease virus (TBDV) [3] Neonatal calf diarrhea Coronavirus (NCDCV) [4]
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            A Hemagglutinating Virus Producing Encephalomyelitis in Baby Pigs.

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              Rat coronavirus (RCV): A prevalent, naturally occurring pneumotropic virus of rats

              Summary A new virus isolated from the lungs of rats is prevalent in colony reared and wild rats and induces a fatal pneumonitis in newborn rats. The virus, designated as rat coronavirus (RCV), exhibits properties representative of the coronavirus group: characteristic surface structure, particles somewhat variable in size averaging approximately 90 mμ, apparent RNA content, essential lipid, heat sensitivity, and a close serologie relationship with the mouse hepatitis virus complex. RCV grows well in primary rat kidney cell cultures, exhibits a pathognomonic type CPE, and produces a complement fixing antigen which is sensitive for detection of antibody and useful in sero-epidemiologic studies.

                Author and article information

                Arch Virol
                Arch. Virol
                Archives of Virology
                Springer-Verlag (Vienna )
                : 58
                : 1
                : 45-53
                [1 ]GRID grid.27860.3b, ISNI 0000000419369684, Department of Medicine, School of Veterinary Medicine, , University of California, ; Davis, California USA
                [2 ]GRID grid.94365.3d, ISNI 0000000122975165, National Institute of Health, ; Bethesda, Maryland USA
                [3 ]GRID grid.417548.b, ISNI 0000000404786311, National Animal Disease Center, ; Ames, Iowa USA
                © Springer-Verlag 1978

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                : 23 October 1977
                : 23 February 1978
                Original Papers
                Custom metadata
                © Springer-Verlag 1978

                Microbiology & Virology
                hepatitis,diarrhea,peritonitis,hepatitis virus,gastroenteritis
                Microbiology & Virology
                hepatitis, diarrhea, peritonitis, hepatitis virus, gastroenteritis


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