Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-05T09:10:31.106Z Has data issue: false hasContentIssue false

Parainfluenza virus infections in the Cirencester Survey: Seasonal and other characteristics

Published online by Cambridge University Press:  25 March 2010

R. Edgar Hope-Simpson
Affiliation:
Epidemiological Research Unit, 86 Dyer Street, Cirencester, Gloucestershire, England
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Parainfluenza viruses were isolated 165 times during 14 years surveillance of the illnesses of a general practice population of around 3700. Type 1 isolations numbered 57, type 2 isolations 22 and type 3 isolations 86, representing annual rates of 33, 13 and 50 infections respectively per 10000 of population. Type 4 parainfluenza virus was not isolated. Three major classes of illness gave the following rates: sore throats (Throats) nine, acute febrile respiratory diseases (FRD) 23, acute non-febrile respiratory diseases (non-FRD) 71. The illnesses caused by the three types isolated were similar. Type 1 infections were most abundant in November and type 2 infections in December, and only 11.4 % of these types were isolated in the warm semester April through September. Type 3 infections were seasonally bi-modal, with a winter peak in January and an even greater prevalence (66% of the total) in the warm semester. Type 3 infections in the warmer months and in the later years of the Survey were usually more severe. Type 3 virus may therefore be heterogeneous, one subtype possessing and the other lacking the genetic mechanism of ‘cold-season’ prevalence. Geographical discontinuity between summer and winter isolations strengthens the case for the existence of the two subtypes of type 3 parainfluenza virus.

Type 3 infections caused the majority of the infections in very young infants. Type 2 infections were widely distributed at all ages. Females were attacked more often than males: type 1, 68.4%; type 2,636%; type 3, 53.5%. Type 3 infections in males outnumbered those in females up to 60 years of age, whereas female predominance became apparent in types 1 and 2 before 10 years of age.

All types were widely and sparsely distributed, areas of prevalence changing from year to year. Recurrences occurred only twice, both with type 3 infections. Six persons suffered both a type 1 and a type 3 infection, and one person suffered both a type 2 and a type 3 infection.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1981

References

Gavrilov, V. I., Asher, D. M., Vyalushkina, S. D., Ratushkina, L. S., Zmieva, R. G. & Tumyan, B. G. (1972). Persistent infection of continuous line of pig kidney cells with a variant of the WSN strain of influenza A0 virus (36405). Proceedings of the Society for Experimental Biology and Medicine 140, 109.CrossRefGoogle Scholar
Golubev, Von D. B., Paramonova, M. S., Medvedeva, M. N. & Poljakov, Yu. M. (1975). Influenza A, neuraminidases and their changes during persistence of viruses in tissue cultures. Zeitschrift für gesmte Hygiene 21, 324.Google ScholarPubMed
Hope-Simpson, R. E. (1975). Viruses in acute respiratory diseases. In Viral Diseases (ed. Proudfoot, A. T.), pp. 3653. Edinburgh: Royal College of Physicians of Edinburgh.Google Scholar
Hope-Simpson, R. E. (1979 a). The influence of season upon type A influenza. In The Impact of Weather and Climate on Animals and Man (Period 1973–1978), (ed. Tromp, Solco W.). London:Heyden.Google Scholar
Hope-Simpson, R. E. (1979 b). Epidemic mechanisms of type A influenza. Journal of Hygiene 83, 1126.CrossRefGoogle ScholarPubMed
Hope-Simpson, R. E. (1981 a). The role of season in the epidemiology of influenza. Journal of Hygiene 86, 35.CrossRefGoogle ScholarPubMed
Hope-Simpson, R. E. (1981 b). Streptococcus pyogenes in the throat. Journal of Hygiene 87, 109129.CrossRefGoogle ScholarPubMed
Hope-Simpson, R. E. & Higgins, P. G. (1969). A respiratory virus study in Great Britain – review and evaluation. Progress in Medical Virology 11, 354407. Basel: Karger.Google Scholar
Muchmore, H. G., Parkinson, A. J., Humphries, J. E., Nan Scott, E., McIntosh, D. A., Scott, L. V., Cooney, M. K. & Miles, J. A. R. (1981). Persistent parainfluenza virus shedding during isolation at the South Pole. Nature 289, 187.CrossRefGoogle ScholarPubMed
Parkinson, A. J., Muchmore, H. G., McConnell, T. A., Scott, L. V. & Miles, J. A. R. (1980). Serologic evidence for parainfluenza virus infection during isolation at South Pole Station, Antarctica, American Journal of Epidemiology 112, 334.CrossRefGoogle ScholarPubMed
Woodbury, A. M. (1954). Principles of General Ecology, New York, pp. 120134.Google Scholar