Analyze Diet
Journal of medical virology1986; 20(1); 67-78; doi: 10.1002/jmv.1890200109

Preliminary characterisation of torovirus-like particles of humans: comparison with Berne virus of horses and Breda virus of calves.

Abstract: Pleomorphic virus-like particles have been observed by electron microscopy in the faeces of children and adults with diarrhoea. Some of these particles were approximately 100 nm in diameter and had a "fringe" of closely applied peplomers approximately 10 nm long; they closely resembled Berne virus of horses and Breda virus of calves, the two representatives of a newly proposed family called the Toroviridae. In one sample a toroidal nucleoprotein-like structure was observed within the particles. For two samples a buoyant density of 1.14 g/ml was determined by centrifugation through a sucrose density gradient. One sample possessed a haemagglutinin for rat erythrocytes. The serological relationship between these different viruses was observed by immune electron microscopy, haemagglutination inhibition, and serum neutralisation. The role of these virus-like particles as candidate pathogens of humans is discussed.
Publication Date: 1986-09-01 PubMed ID: 3093635PubMed Central: PMC7166937DOI: 10.1002/jmv.1890200109Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research investigates virus-like particles in human feces, specifically focusing on their potential relationship to the horse’s Berne virus and the cow’s Breda virus, part of the newly identified Toroviridae family. The researchers discuss the physical properties of these particles and their possible role in causing human illnesses.

Observed Virus-like Particles

  • Researchers observed pleomorphic (shapeshifting) virus-like particles in the feces of adults and children suffering from diarrhea using electron microscopy.
  • Some of the observed particles were approximately 100 nanometers (nm) in diameter, with a “fringe” of closely applied peplomers around 10 nm long.
  • The particles resembled the Berne virus found in horses and the Breda virus found in calves. Both of these viruses belong to the new family named Toroviridae.

Physical Properties of the Particles

  • In one sample, a round-ribbon-shaped nucleoprotein-like structure was observed within the particles.
  • Centrifugation through a sucrose density gradient revealed a buoyant density of 1.14 g/ml for two samples, contributing to the detailed physical characterization of these particles.
  • One of the samples had a haemagglutinin, a substance causing red blood cells to agglutinate, for rat erythrocytes, suggesting possible compatibility with animal cells.

Serological Relationship with Other Viruses

  • The study looked into the serological relationship (the relationship based on detection of antibodies in the serum) between these virus-like particles and other viruses.
  • The researchers used methods such as immune electron microscopy, haemagglutination inhibition, and serum neutralisation to observe these serological relationships.
  • The understanding of such relationships helps map the spread and potential hazards of these viruses.

Potential Pathogenic Role in Humans

  • The researchers discuss the role that these virus-like particles might play as pathogenic candidates in humans, suggesting that they could potentially cause disease.
  • This preliminary characterization lays the foundation for further studies to understand the potential risks these particles pose to human health.

Cite This Article

APA
Beards GM, Brown DW, Green J, Flewett TH. (1986). Preliminary characterisation of torovirus-like particles of humans: comparison with Berne virus of horses and Breda virus of calves. J Med Virol, 20(1), 67-78. https://doi.org/10.1002/jmv.1890200109

Publication

ISSN: 0146-6615
NlmUniqueID: 7705876
Country: United States
Language: English
Volume: 20
Issue: 1
Pages: 67-78

Researcher Affiliations

Beards, G M
    Brown, D W
      Green, J
        Flewett, T H

          MeSH Terms

          • Adult
          • Animals
          • Cattle
          • Centrifugation, Density Gradient
          • Child
          • Feces / microbiology
          • Hemagglutination Inhibition Tests
          • Hemagglutination Tests
          • Horses
          • Humans
          • Microscopy, Electron
          • Neutralization Tests
          • Viruses, Unclassified / immunology
          • Viruses, Unclassified / ultrastructure

          References

          This article includes 19 references
          1. Beards GM, Hall C, Green J, Flewett TH, Lamouliatte F, Du Pasquier P. An enveloped virus in stools of children and adults with gastroenteritis that resembles the Breda virus of calves.. Lancet 1984 May 12;1(8385):1050-2.
          2. Caul EO, Paver WK, Clarke SK. Letter: Coronavirus particles in faeces from patients with gastroenteritis.. Lancet 1975 May 24;1(7917):1192.
            pmc: PMC7135678pubmed: 48810doi: 10.1016/s0140-6736(75)93176-1google scholar: lookup
          3. Caul EO, Ashley CR, Egglestone SI. Recognition of human enteric coronaviruses by electron microscopy.. Med Lab Sci 1977 Jul;34(3):259-63.
            pubmed: 70735
          4. Dourmashkin RR, Davies HA, Smith H, Bird RG. Are coronavirus-like particles seen in diarrhoea stools really viruses?. Lancet 1980 Nov 1;2(8201):971-2.
          5. Flewett TH, Bryden AS, Davies H, Woode GN, Bridger JC, Derrick JM. Relation between viruses from acute gastroenteritis of children and newborn calves.. Lancet 1974 Jul 13;2(7872):61-3.
            pubmed: 4137164doi: 10.1016/s0140-6736(74)91631-6google scholar: lookup
          6. Horzinek MC, Weiss M, Ederveen J. Berne virus is not 'coronavirus-like'.. J Gen Virol 1984 Mar;65 ( Pt 3):645-9.
            pubmed: 6699624doi: 10.1099/0022-1317-65-3-645google scholar: lookup
          7. Horzinek MC, Weiss M. Toroviridae: a taxonomic proposal.. Zentralbl Veterinarmed B 1984 Oct;31(9):649-59.
            pubmed: 6393658
          8. Horzinek MC, Ederveen J, Weiss M. The nucleocapsid of Berne virus.. J Gen Virol 1985 Jun;66 ( Pt 6):1287-96.
            pubmed: 3925076doi: 10.1099/0022-1317-66-6-1287google scholar: lookup
          9. Macnaughton MR, Davies HA. Human enteric coronaviruses. Brief review.. Arch Virol 1981;70(4):301-13.
            pmc: PMC7087291pubmed: 7034689doi: 10.1007/bf01320245google scholar: lookup
          10. Mathan M, Mathan VI, Swaminathan SP, Yesudoss S. Pleomorphic virus-like particles in human faeces.. Lancet 1975 May 10;1(7915):1068-9.
            pmc: PMC7173216pubmed: 48733doi: 10.1016/s0140-6736(75)91832-2google scholar: lookup
          11. Mortensen ML, Ray CG, Payne CM, Friedman AD, Minnich LL, Rousseau C. Coronaviruslike particles in human gastrointestinal disease. Epidemiologic, clinical, and laboratory observations.. Am J Dis Child 1985 Sep;139(9):928-34.
          12. Moscovici O, Chany C, Lebon P, Rousset S, Laporte J. [Association of coronavirus infection with hemorrhagic entercolitis in newborn infants].. C R Seances Acad Sci D 1980 Mar 31;290(13):869-72.
            pubmed: 6248262
          13. Schnagl RD, Holmes IH, Mackay-Scollay EM. Coronavirus-like particles in Aboriginals and non-Aboriginals in Western Australia.. Med J Aust 1978 Mar 25;1(6):307-9.
            pubmed: 661689
          14. Sitbon M. Human-enteric-coronaviruslike particles (CVLP) with different epidemiological characteristics.. J Med Virol 1985 May;16(1):67-76.
            pmc: PMC7167018pubmed: 2995569doi: 10.1002/jmv.1890160110google scholar: lookup
          15. Weiss M, Steck F, Horzinek MC. Purification and partial characterization of a new enveloped RNA virus (Berne virus).. J Gen Virol 1983 Sep;64 (Pt 9):1849-58.
            pubmed: 6886677doi: 10.1099/0022-1317-64-9-1849google scholar: lookup
          16. Weiss M, Steck F, Kaderli R, Horzinek MC. Antibodies to Berne virus in horses and other animals.. Vet Microbiol 1984 Oct;9(6):523-31.
            pmc: PMC7117441pubmed: 6506447doi: 10.1016/0378-1135(84)90014-2google scholar: lookup
          17. Woode GN, Reed DE, Runnels PL, Herrig MA, Hill HT. Studies with an unclassified virus isolated from diarrheic calves.. Vet Microbiol 1982 Jul;7(3):221-40.
            pmc: PMC7117454pubmed: 7051518doi: 10.1016/0378-1135(82)90036-0google scholar: lookup
          18. Woode GN, Mohammed KA, Saif LJ, Winand NJ, Quesada M, Kelso NE, Pohlenz JF. Diagnostic methods for the newly discovered Breda group of calf enteritis‐inducing viruses. Proceedings of the 3rd International Sympsium of the World Association of Veterinary Lab Diagnosis 1983 2: 533–538.
          19. Woode GN, Saif LJ, Quesada M, Winand NJ, Pohlenz JF, Gourley NK. Comparative studies on three isolates of Breda virus of calves.. Am J Vet Res 1985 May;46(5):1003-10.
            pubmed: 2408519

          Citations

          This article has been cited 24 times.
          1. Ujike M, Taguchi F. Recent Progress in Torovirus Molecular Biology. Viruses 2021 Mar 8;13(3).
            doi: 10.3390/v13030435pubmed: 33800523google scholar: lookup
          2. Anbalagan S, Peterson J, Wassman B, Elston J, Schwartz K. Genome sequence of torovirus identified from a pig with porcine epidemic diarrhea virus from the United States. Genome Announc 2014 Dec 18;2(6).
            doi: 10.1128/genomeA.01291-14pubmed: 25523767google scholar: lookup
          3. Zhou L, Wei H, Zhou Y, Xu Z, Zhu L, Horne J. Molecular epidemiology of Porcine torovirus (PToV) in Sichuan Province, China: 2011-2013. Virol J 2014 Jun 5;11:106.
            doi: 10.1186/1743-422X-11-106pubmed: 24903213google scholar: lookup
          4. Gubbay J, Al-Rezqi A, Hawkes M, Williams L, Richardson S, Matlow A. The role of torovirus in nosocomial viral gastroenteritis at a large tertiary pediatric centre. Can J Infect Dis Med Microbiol 2012 Summer;23(2):78-81.
            doi: 10.1155/2012/134961pubmed: 23730313google scholar: lookup
          5. Alonso-Padilla J, Pignatelli J, Simon-Grifé M, Plazuelo S, Casal J, Rodríguez D. Seroprevalence of porcine torovirus (PToV) in Spanish farms. BMC Res Notes 2012 Dec 5;5:675.
            doi: 10.1186/1756-0500-5-675pubmed: 23217216google scholar: lookup
          6. Stanley M, Mayr J, Huber W, Vlasak R, Streicher H. Synthesis and inhibitory activity of sialic acid derivatives targeted at viral sialate-O-acetylesterases. Eur J Med Chem 2011 Jul;46(7):2852-60.
            doi: 10.1016/j.ejmech.2011.04.008pubmed: 21524502google scholar: lookup
          7. Pignatelli J, Grau-Roma L, Jiménez M, Segalés J, Rodríguez D. Longitudinal serological and virological study on porcine torovirus (PToV) in piglets from Spanish farms. Vet Microbiol 2010 Dec 15;146(3-4):260-8.
            doi: 10.1016/j.vetmic.2010.05.023pubmed: 20542392google scholar: lookup
          8. Shin DJ, Park SI, Jeong YJ, Hosmillo M, Kim HH, Kim HJ, Kwon HJ, Kang MI, Park SJ, Cho KO. Detection and molecular characterization of porcine toroviruses in Korea. Arch Virol 2010 Mar;155(3):417-22.
            doi: 10.1007/s00705-010-0595-2pubmed: 20127374google scholar: lookup
          9. Pignatelli J, Jimenez M, Luque J, Rejas MT, Lavazza A, Rodriguez D. Molecular characterization of a new PToV strain. Evolutionary implications. Virus Res 2009 Jul;143(1):33-43.
          10. Park SJ, Oh EH, Park SI, Kim HH, Jeong YJ, Lim GK, Hyun BH, Cho KO. Molecular epidemiology of bovine toroviruses circulating in South Korea. Vet Microbiol 2008 Jan 25;126(4):364-71.
            doi: 10.1016/j.vetmic.2007.07.012pubmed: 17719729google scholar: lookup
          11. Kuwabara M, Wada K, Maeda Y, Miyazaki A, Tsunemitsu H. First isolation of cytopathogenic bovine torovirus in cell culture from a calf with diarrhea. Clin Vaccine Immunol 2007 Aug;14(8):998-1004.
            doi: 10.1128/CVI.00475-06pubmed: 17567770google scholar: lookup
          12. Neuman BW, Adair BD, Yoshioka C, Quispe JD, Orca G, Kuhn P, Milligan RA, Yeager M, Buchmeier MJ. Supramolecular architecture of severe acute respiratory syndrome coronavirus revealed by electron cryomicroscopy. J Virol 2006 Aug;80(16):7918-28.
            doi: 10.1128/JVI.00645-06pubmed: 16873249google scholar: lookup
          13. Smits SL, Lavazza A, Matiz K, Horzinek MC, Koopmans MP, de Groot RJ. Phylogenetic and evolutionary relationships among torovirus field variants: evidence for multiple intertypic recombination events. J Virol 2003 Sep;77(17):9567-77.
          14. Atmar RL, Estes MK. Diagnosis of noncultivatable gastroenteritis viruses, the human caliciviruses. Clin Microbiol Rev 2001 Jan;14(1):15-37.
            doi: 10.1128/CMR.14.1.15-37.2001pubmed: 11148001google scholar: lookup
          15. Duckmanton LM, Tellier R, Liu P, Petric M. Bovine torovirus: sequencing of the structural genes and expression of the nucleocapsid protein of Breda virus. Virus Res 1998 Nov;58(1-2):83-96.
            doi: 10.1016/s0168-1702(98)00104-xpubmed: 9879765google scholar: lookup
          16. Kroneman A, Cornelissen LA, Horzinek MC, de Groot RJ, Egberink HF. Identification and characterization of a porcine torovirus. J Virol 1998 May;72(5):3507-11.
          17. Koopmans M, Petric M, Glass RI, Monroe SS. Enzyme-linked immunosorbent assay reactivity of torovirus-like particles in fecal specimens from humans with diarrhea. J Clin Microbiol 1993 Oct;31(10):2738-44.
          18. Koopmans M, Horzinek MC. Toroviruses of animals and humans: a review. Adv Virus Res 1994;43:233-73.
            doi: 10.1016/s0065-3527(08)60050-0pubmed: 8191955google scholar: lookup
          19. Brown DW, Beards GM, Flewett TH. Detection of Breda virus antigen and antibody in humans and animals by enzyme immunoassay. J Clin Microbiol 1987 Apr;25(4):637-40.
            doi: 10.1128/jcm.25.4.637-640.1987pubmed: 3571473google scholar: lookup
          20. Schnagl RD, Brookes S, Medvedec S, Morey F. Characteristics of Australian human enteric coronavirus-like particles: comparison with human respiratory coronavirus 229E and duodenal brush border vesicles. Arch Virol 1987;97(3-4):309-23.
            doi: 10.1007/BF01314429pubmed: 3426398google scholar: lookup
          21. Brown DW, Selvakumar R, Daniel DJ, Mathan VI. Prevalence of neutralising antibodies to Berne virus in animals and humans in Vellore, South India. Brief report. Arch Virol 1988;98(3-4):267-9.
            doi: 10.1007/BF01322174pubmed: 3348749google scholar: lookup
          22. Beards GM. Laboratory diagnosis of viral gastroenteritis. Eur J Clin Microbiol Infect Dis 1988 Feb;7(1):11-3.
            doi: 10.1007/BF01962164pubmed: 3132369google scholar: lookup
          23. Koopmans M, Herrewegh A, Horzinek MC. Diagnosis of torovirus infection. Lancet 1991 Apr 6;337(8745):859.
            doi: 10.1016/0140-6736(91)92573-kpubmed: 1672953google scholar: lookup
          24. Wang X, Chen Y, Qi C, Li F, Zhang Y, Zhou J, Wu H, Zhang T, Qi A, Ouyang H, Xie Z, Pang D. Mechanism, structural and functional insights into nidovirus-induced double-membrane vesicles. Front Immunol 2024;15:1340332.
            doi: 10.3389/fimmu.2024.1340332pubmed: 38919631google scholar: lookup