Human rotavirus infection. Strategies for the vaccinal prevention
- Authors: Alekseev K.P.1, Kalnov S.L.1, Grebennikova T.V.1, Aliper T.I.1
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Affiliations:
- Virology «Federal Research Centre of Epidemilogy and Microbiology named after the honorary academician N.F. Gamaleya»
- Issue: Vol 61, No 4 (2016)
- Pages: 154-159
- Section: REVIEWS
- Submitted: 20.01.2020
- Published: 28.08.2016
- URL: https://virusjour.crie.ru/jour/article/view/71
- DOI: https://doi.org/10.18821/0507-4088-2016-61-4-154-159
- ID: 71
Cite item
Full Text
Abstract
Rotavirus was first isolated in 1973 in Australia from children with diarrhea. Hundreds of thousands of children die annually in developing countries from this virus with the mortality peaks in the most impoverished among them. According to wHo, rotavirus infection claims about 440 thousands children lives each year, being third in the mortality rate after pneumonia and malaria. Rotavirus is widely spread throughout the world and by the age of five years almost every child encountered this pathogen at least once. Rotavirus has a high genetic and antigenic diversity. The most important for humans is the group A rotavirus, and the most common by far genotypes are G1P [8], G2P [4], G3P [8], G4P [8], G9P [8], and to a lesser extent G12P [8]. There are three gene constellations described in rotavirus designated Wa, Ds-1, and Au-1. It is believed that they originated from rotaviruses of pigs, cattle, dogs, and cats, respectively. Cases of rotavirus interspecies transmission from animal to humans were reported. The first vaccines against rotavirus infection were based on naturally attenuated virus of the animal origin. Their efficiency, especially in developing countries, was inadequate, but today China and India use vaccines based on animal rotaviruses. Using the method of gene reassortation with the cattle rotavirus WC3 as a backbone, pentavalent vaccine against most common human rotavirus serotypes was developed and now successfully used as RotaTeq. The ability of rotavirus to protect against heterologous isolates was taken into account in the development of other vaccine, Rotarix, created on the basis of rotavirus genotype G1P1A [8]. The efficacy of these vaccines in developing countries is significantly reduced (51%), the cost of a dose is high, and so the search for more effective, safe, and inexpensive vaccines against rotavirus continues around the world.
Keywords
About the authors
K. P. Alekseev
Virology «Federal Research Centre of Epidemilogy and Microbiology named after the honorary academician N.F. Gamaleya»
Author for correspondence.
Email: kkendwell@mail.ru
Russian Federation
S. L. Kalnov
Virology «Federal Research Centre of Epidemilogy and Microbiology named after the honorary academician N.F. Gamaleya»
Email: noemail@neicon.ru
Russian Federation
T. V. Grebennikova
Virology «Federal Research Centre of Epidemilogy and Microbiology named after the honorary academician N.F. Gamaleya»
Email: noemail@neicon.ru
Russian Federation
T. I. Aliper
Virology «Federal Research Centre of Epidemilogy and Microbiology named after the honorary academician N.F. Gamaleya»
Email: noemail@neicon.ru
Russian Federation
References
- Matthews R.E. The classification and nomenclature of viruses. Summary of results of meetings of the International Committee on Taxonomy of Viruses in The Hague, September 1978. Intervirology. 1979; 11 (3): 133-5.
- Львов Д.К. Ротавирусные инфекции. В кн.: Львов Д.К. Руководство по вирусологии. Вирусы и вирусные инфекции человека и животных. М.: МИА; 2013: 520-2.
- Estes M.K., Greenberg H.B. Rotaviruses. In: Knipe D.M., Howley P.M., eds. Fields Virology. 6th ed. Phyladelphia: Lippincott Williams & Wilkins; 2013: 1347-401.
- Attoni H., Mertens P.P., Becnel J. et al. Genus Rotavirus. In: King A.M., Adams M.J., Castens E.B., Lefrowitz E.J., eds. Virus Taxonomy. Ninth report of the international committee on taxonomy of viruses. London: Elsevier Academic Press; 2012: 603-13.
- Desselberger U. Rotaviruses. Virus Res. 2014; 190: 75-96.
- Сергеев В.А., Непоклонов Е.А., Алипер Т.И. Ротавирусы. Вирусы и вирусные инфекции. М.: Библионика; 2007: 365-9.
- Saif L.J. Nongroup A rotaviruses of humans and animals. In: Jiang B., Ramig R.F., eds. Current Topics in Microbiology and Immunology. Vol. 185. Berlin: Springer-Verlag; 1994: 339-71.
- Santos N., Hoshino Y. Global distribution of rotavirus serotypes/genotypes and its implication for the development and implementationof an effective rotavirus vaccine. Rev. Med. Virol. 2005; 15 (1): 29-56.
- Koopmans M., Brown D. Seasonality and diversity of Group A rotaviruses in Europe. Acta Paediatr. Suppl. 1999; 88 (426): 14-9.
- Matthijnssens J., Bilcke J., Ciarlet M., Martella V., Bányai K., Rahman M. et al. Rotavirus disease and vaccination: impact on genotype diversity. Future Microbiol. 2009; 4 (10): 1303-16.
- Matthijnssens J., Ciarlet M., McDonald S.M., Attoui H., Bányai K., Brister J.R. et al. Uniformity of rotavirus strain nomenclature proposed by the Rotavirus Classification Working Group (RCWG). Arch. Virol. 2011; 156: 1397-413.
- Bishop R.F., Davidson G.P., Holmes I.H., Ruck B.J. Virus particles in epithelial cells of duodenal mucosa from children with acute nonbacterial gastroenteritis. Lancet. 1973; 2 (7841): 1281-3.
- Tate J.E., Burton A.H., Boschi-Pinto C., Steele A.D., Duque J., Parashar U.D. et al. 2008 estimate of worldwide rotavirus-associated mortality in children younger than 5 years before the introduction of universal rotavirus vaccination programmes: a systematic review and metaanalysis. Lancet Infect. Dis. 2011; 12 (2): 136-41.
- WHO. Rotavirus vaccines: an update. Wkly. Epidemiol. Rec. 2012; 84: 533-40.
- Parashar U.D., Hummelman E.G., Bresee J.S., Miller M.A., Glass R.I. Global illness and deaths caused by rotavirus disease in children. Emerg. Infect. Dis. 2003; 9 (5): 565-72.
- Таточенко В.К. Ротавирусные вакцины. Вакцины и вакцинация. М.: ГЭОТАР-Медиа; 2014: 432-9.
- Liu L., Johnson H.L., Cousens S., Perin J., Scott S., Lawn J.E. et al. Child Health Epidemiology Reference Group of WHO and UNICEF. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet. 2012; 379 (9832): 2151-61.
- Zaman K., Dang D.A., Victor J.C., Shin S., Yunus M., Dallas M.J. et al. Efficacy of pentavalent rotavirus vaccine against severe rotavirus gastroenteritis in infants in developing countries in Asia: a randomised, doubleblind, placebo-controlled trial. Lancet. 2010; 376 (9741): 615-23.
- Matthijnssens J., Rahman M., Ciarlet M., Van Ranst M. Emerging human rotavirus genotypes. In: Palombo E.A., Kirkwood C.D., eds. Viruses in the Environment. Kerala, India: Research Signpost; 2008: 171-219.
- Rahman M., Matthijnssens J., Yang X., Delbeke T., Arijs I., Taniguchi K. et al. Evolutionary history and global spread of the emerging G12 human rotaviruses. J. Virol. 2007; 81 (5): 2382-90.
- Heiman E.M., McDonald S.M., Barro M., Taraporewala Z.F., Bar-Magen T., Patton J.T. Group A human rotavirus genomics:evidence that gene constellations are influenced by viralprotein interactions. J. Virol. 2008; 82: 11 106-16.
- McDonald S.M., Matthijnssens J., McAllen J.K., Hine E., Overton L., Wang S. et al. Evolutionary dynamics of human rotaviruses: balancingreassortment with preferred genome constellations. PloS Pathog. 2009; 5 (10): e1000634.
- Matthijnssens J., Van Ranst M. Genotype constellation and evolution of group A rotavirusesinfecting humans. Curr. Opin. Virol. 2012; 2 (4): 426-33.
- Matthijnssens J., Rahman M., Van Ranst M. Two out of the 11 genes of an unusual human G6P[6] rotavirus isolate are of bovine origin. J. Gen. Virol. 2008; 89 (Pt. 10): 2630-5.
- Nakagomi O., Ohshima A., Aboudy Y., Shif I., Mochizuki M., Nakagomi T. et al. Molecular identification byRNA-RNA hybridization of a human rotavirus that is closely related to rotaviruses of feline and canine origin. J. Clin. Microbiol. 1990; 28: 1198-203.
- Iturriza-Gómara M., Dallman T., Banyai K., Bottiger B., Buesa J., Diedrich S. et al. Rotavirus genotypes co-circulating in Europe between 2006 and 2009 as determined by EuroRotaNet, a pan-Europeancollaborative strain surveillance network. Epidemiol. Infect. 2011; 139 (6): 895-909.
- Matthijnssens J., Potgieter C.A., Ciarlet M., Parrenõ V., Martella V., Bányai K. et al. Are human P[14] rotavirus strains the result of interspeciestransmissions from sheep or other ungulates that belongto the mammalian order Artiodactyla? J. Virol. 2009; 83 (7): 2917-29.
- Ghosh S., Alam M.M., Ahmed M.U., Talukdar R.I., Paul S.K., Kobayashi N. Complete genome constellation of a caprinegroup A rotavirus strain reveals common evolution withruminant and human rotavirus strains. J. Gen. Virol. 2010; 91 (Pt. 9): 2367-73.
- WHO. Rotavirus vaccines. WHO position paper - January 2013. Wkly. Epidemiol. Rec. 2013; 88 (5): 49-64.
- Бахтояров Г.Н., Файзулоев Е.Б., Филатов Н.Н., Линок А.В., Курносова В.В., Зверев В.В. Генетическая структура штаммов ротавирусов Московского региона в период с 2009 по 2014 г. В кн.: Материалы VII Ежегодного Всероссийского Конгресса по инфекционным болезням с международным участием. М.; 2015: 37.
- Подколзин А.Т., Петухов Д.Н., Веселова О.А. Отчет РЦКИ: Данные о циркуляции ротавирусов группы А в РФ в зимний сезон 2011-2012 гг. Публикация Референс-центра по мониторингу возбудителей кишечных инфекций. ФБУН ЦНИИ эпидемиологии Роспотребнадзора, РЦКИ. М.; 2012.
- Fu C., Wang M., Liang J., He T., Wang D., Xu J. Effectiveness of Lanzhou lamb rotavirus vaccine against rotavirus gastroenteritis requiring hospitalization: a matched case-control study. Vaccine. 2007; 25 (52): 8756-61.
- CDC. Withdrawal of rotavirus vaccine recommendation. MMWR Morb. Mortal. Wkly. Rep. 1999; 48 (43): 1007.
- Vesikari T.I., Matson D.O., Dennehy P., Van Damme P., Santosham M., Rodriguez Z. et al. Safety and efficacy of a pentavalent human-bovine (WC3) reassortant rotavirus vaccine. N. Engl. J. Med. 2006; 354 (1): 23-33.
- Ruiz-Palacios G.M., Perez-Schael I., Velazquez F.R., Abate H., Breuer T. Clemens S.C. et al. Safety and efficacy of an attenuated vaccine against severe rotavirus gastroenteritis. N. Engl. J. Med. 2006; 354 (1): 11-22.
- Kandasamy S., Chattha K.S., Vlasova A.N., Saif L.J. Prenatal vitamin A deficiency impairs adaptive immune responses to pentavalent rotavirus vaccine (RotaTeq®) in a neonatal gnotobiotic pig model. Vaccine. 2014; 32 (7): 816-24.
- Bhandari N., Rongsen-Chandola T., Bavdekar A., John J., Antony K., Taneja S. et al. Efficacy of amonovalent human-bovine (116E) rotavirus vaccine in Indian infants: a randomised, double-blind,placebocontrolled trial. Lancet. 2014; 383 (9935): 2136-43.
- Zade J.K., Kulkarni P.S., Desai S.A., Sabale R.N., Naik S.P., Dhere R.M. Bovine rotavirus pentavalent vaccine development in India. Vaccine. 2014; 32 (Suppl. 1): A124-8.
- Fix A., Harrow C., McNeal M., Dally L., Flores J., Robertson G. et al. Safety and immunogenicity of a parenterally administered rotavirus VP8 subunit vaccine in healthyadults. In: Seventh International conference on Vaccinesfor Enteric Diseases. Thailand, Nov 6-8. Bangkok; 2013.