Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

Seroepidemiology of group A rotavirus in suburban São Paulo, Brazil

Tools
- Tools
+ Tools

Cox, M. J., Azevedo, R. S., Nokes, D. James, Beards, G. M., McCrae, Malcolm A., Massad, Eduardo and Medley, Graham. (1998) Seroepidemiology of group A rotavirus in suburban São Paulo, Brazil. Epidemiology and Infection, Vol.120 . pp. 327-334. ISSN 0950-2688

[img] PDF
WRAP_Cox_Seroepidemiology.pdf - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader

Download (394Kb)
Official URL: http://dx.doi.org/10.1017/S0950268898008759

Abstract

Age-specifc patterns of rotavirus infection were investigated using a randomly selected and representative sample of sera from a suburban community of São Paulo, Brazil screened for class-specifc antibodies to group A rotavirus. Age-serology of anti-rotavirus IgG showed primary infection predominant in young infants with a median age of around 18 months consistent with IgM serology suggesting highest rates of recent infection between ages 4 and 48 months. Anti-rotavirus serum IgA prevalence increased gradually with age. Paired samples from infants, collected 1 month apart, indicated high exposure rates with seroconversion occurring in several infants during the reported low transmission season. Between 5 and 10% of adults had elevated IgM levels indicative of recent infection and, potentially, of an important contribution adults may play to rotavirus transmission. Further understanding of the dynamics of rotavirus transmission within populations, at group and serotype level, would benefit the design and monitoring of future immunization programmes.

Item Type: Journal Article
Subjects: Q Science > QR Microbiology > QR355 Virology
Divisions: Faculty of Science > Life Sciences (2010- ) > Biological Sciences ( -2010)
Library of Congress Subject Headings (LCSH): Rotaviruses -- Brazil -- São Paulo (State), Rotavirus infections -- Brazil -- São Paulo (State)
Journal or Publication Title: Epidemiology and Infection
Publisher: Cambridge University Press
ISSN: 0950-2688
Date: 1998
Volume: Vol.120
Page Range: pp. 327-334
Identification Number: 10.1017/S0950268898008759
Status: Peer Reviewed
Access rights to Published version: Open Access
References: 1. Kapikian AZ, Chanock RM. Rotaviruses. In: Fields, BN, DM Knipe, RM Chanock et al. Fields virology. New York: Lippincott-Raven, 1996: chapter 55. 2. Kim HW, Brandt CD, Kapikian AZ, et al. Human reovirus-like agent (HRVLA) infection : occurrence in adult contacts of pediatric patients with gastroenteritis. JAMA 1977; 238: 404-7. 3. Ryan MJ, Ramsey M, Brown D, Gay NJ, Farrington CP, Wall PG. Hospital admissions attributable to rotavirus infection in England and Wales. J Infect Dis 1996; 174 (suppl): S12-18. 4. Glass RI, Gentsch J, Smith JC. Rotavirus vaccines: success by reassortment? Science 1994; 265: 1389-91. 5. World Health Organisation. Wkly Epidemiol Rec 1997; 72: 35-40. 6. Anderson RM, May RM. Infectious diseases of humans: dynamics and control. Oxford: Oxford University Press, 1991. 7. White L, Cox MJ, Medley GF. Cross immunity and vaccination against multiple microparasite strains. IMA J Math Appl Biol Med. (In press). 8. Chrystie I, Totterdell B, Banatvala J. Asymptomatic endemic rotavirus infections in the newborn. Lancet 1978; i : 1176-8. 9. Elias MM. Distribution and titres of rotavirus antibodies in different age-groups. J Hyg 1977: 79: 365-73. 10. Jesudoss E, John TJ, Mathan M, Spence L. Prevalence of rotavirus antibody in infants and children. Indian J Med Res 1978; 68: 383-6. 11. Sack DA, Giman R, Kapikian AZ et al. Seroepidemiology of rotavirus infection in rural Bangladesh. J Clin Microbiol 1980; 11: 530-2. 12. Beards GM, Desselberger U. Determination of rotavirus serotype-specific antibodies in sera by competitive enhanced enzyme immunoassay. J Virol Methods 1989; 24: 103-10. 13. Andrade GP, Lima LR, Hoshino-Shimizu S, et al. Humoral immunity patterns based on antibody reactivity to rotavirus antigens in Brazilian children under 5 years of age. J Med Virol 1996; 49: 212-7. 14. Brussow H, Werchau H, Leidtke W, et al. Prevalence of antibodies to rotavirus in different age-groups of infants in Bochum, West Germany. J Infect Dis 1988; 157: 1014-22. 15. Azevedo Neto RS, Silveira ASB, Nokes DJ, et al. Rubella seroepidemiology in a non-immunized population of Sa4o Paulo State, Brazil. Epidemiol Infect 1994; 113: 161-73. 16. Cochran WG, Sampling techniques, 3rd edn. New York; John Wiley & Son Inc., 1977. 17. Candeias JAN, Racz ML, Trabulsi LR, Murahowsky J. Relative prevalence of rotavirus diarrhoea in children attending outpatient departments of hospitals and general practitioners in S. Paulo, Brazil. J Diarrhoeal Dis Res 1989; 7: 24-7. 18. Stewein K, Mos E, Yanagiota M, et al. Viral, bacterial and parasitic pathogens associated with severe diarrhoea in the city of Sa4o Paulo, Brazil. J Diarrhoeal Dis Res 1993; 11: 148-52. 19. Mehnert DU, Stewein KE. Detection and distribution of rotavirus in raw sewage and creeks in Sa4o Paulo, Brazil. Appl Environ Microbiol 1993; 59: 140-3. 20. Grimwood K, Lund JCS, Coulson BS, Hudson IL, Bishop RF, Barnes GL. Comparison of serum and mucosal antibody responses following severe acute rotavirus gastroenteritis in young children. J Clin Microbiol 1988; 26: 732-8. 21. Coulson BS, Grimwood K, Masendycz PJ, et al. Comparison of rotavirus immunoglobulin A coproconversion with other indices of rotavirus infection in a longitudinal study in childhood. J Clin Microbiol 1990; 28: 1367-74. 22. Murphy BR, Alling DW, Snyder M, et al. Effect of age and preexisting antibody on serum antibody response of infants and children to the F and G glycoproteins during respiratory syncytial virus infection. J Clin Microbiol 1986; 24: 894-8. 23. Cox MJ, Anderson RM, Bundy DAP, et al. Seroepidemiological study of the transmission of the mumps virus in St. Lucia, West Indies. Epidemiol Infect 1989; 102: 147-60. 24. Nokes DJ, Anderson RM, Anderson MJ. Rubella epidemiology in South East England. J Hyg 1986; 96: 291-304. 25. Omoigberle AI, Ojukwu JO, Abiodun PO. Asymptomatic rotavirus infection within Benin City urban community, Nigeria. East African Med J 1996; 73: 688-90. 26. Davidson G, Hogg R, Kirubakaran C. Serum and intestinal immune response to rotavirus enteritis in children. Infect Immun 1983; 40: 447-52. 27. Stiehm ER, Fudenburg HH. Serum levels of immune globulin in health and diseases survey. Pediatrics 1966; 37: 715-27. 28. Offit PA. Rotaviruses: Immunological determinants of protection against infection and disease. Adv Virus Res. 1994; 44: 161-201. 29. Offit PA, Dudzik K. Rotavirus-specific cytotoxic T lymphocytes appear at the intestinal mucosal surface after rotavirus infection. J Virol 1989; 63: 3507-12. 30. Heath RR, Stagg S, Xu F, McCrae MA. Mapping of the target antigens of the rotavirus-specific cytotoxic Tcell response. J Gen Virol 1997; 78: 1065-75. 31. Ramachandran M, Das B, Vij A, et al. Unusual diversity of human rotavirus G and P genotypes in India. J Clin Microbiol 1996; 34: 436-9. 32. Beards GM, Graham C. Temporal distribution of rotavirus G-serotypes in the West Midlands region of the United Kingdom, 1983-1994. J Diarrhoeal Dis Res 1995; 13: 235-7. 33. Gouvea V, de Castro L, Timenetsky M, Greenberg H, Santos N. Rotavirus serotype G5 associated with diarrhea in Brazilian Children. J Clin Microbiol 1994; 32: 1408-9. 34. Bru$ssow H, Sidoti J, Barclay D, Sotek J, Dirren H, Freire WB. Prevalence and serotype specificity of rotavirus antibodies in different age groups of Ecuadorian infants. J Infect Dis 1990; 162: 615-20. 35. Urasawa S, Urasawa T, Taniguchi K, Chiba S. Serotype determination of human rotavirus isolates and antibody prevalence in pediatric population in Hokkaido, Japan. Arch Virol 1984; 81: 1-12. 36. Matson DO, O'Ryan M, Pickering LK, Estes MK. Assessment of epitope-blocking assays for measuring antibody to rotavirus. J Virol Methods 1994; 48: 293-300.
URI: http://wrap.warwick.ac.uk/id/eprint/3019

Request changes to a record

Actions (login required)

View Item View Item

Document Downloads

More statistics for this item...
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us