Preview

Journal Infectology

Advanced search

Detection of Nonpolio Enteroviruses among children with acute flaccid paralysis from institutions and from migrants’ families

https://doi.org/10.22625/2072-6732-2014-6-4-43-48

Abstract

Aim: to study of the frequency of isolation and determination of the spectrum of enterovirus serotypes excreted by children living in the North-Western region of Russia and children arriving in this region from unsafe territories.

Materials and methods: we investigated 832 samples of children with acute flaccid paralysis and 1153 samples of healthy children from institutions and migrants’ families. Isolation and identification of enteroviruses were conducted according to WHO recommendations.

Results: enteroviruses of different serotypes were detected in all categories of children. The percentage of detection of enteroviruses in the samples of children from institutions and from migrants’ families was significantly higher than in those of patients with acute flaccid paralysis. In children living in the North-West of Russia we detected enteroviruses ECHO 6, which were not found in children who arrived in the North-Western region of Russia. Enteroviruses ECHO 30 were revealed in resident children more frequently than in children from migrants’ families. Enteroviruses of serotypes which had not circulated earlier in the North-Western region of Russia were revealed in the samples of children from migrants’ families. They were Coxsackieviruses A 13, 17, 24 and enterovirus 99 (species C), enteroviruses 75 and 120 (species B and A).

Conclusion: the difference in the spectrum of enterovirus serotypes excreted by resident children and children who arrived in the North-Western region of Russia from unsafe territories was shown. The obtained data will enlarge the scope of knowledge about enterovirus circulation among various groups of population during different periods of time on different territories.

About the Authors

N. I. Romanenkova
Saint-Petersburg Science Research Institute of Epidemiology and Microbiology named after Pasteur, Saint-Petersburg, Russia
Russian Federation


O. I. Kanaeva
Saint-Petersburg Science Research Institute of Epidemiology and Microbiology named after Pasteur, Saint-Petersburg, Russia
Russian Federation


M. A. Bichurina
Saint-Petersburg Science Research Institute of Epidemiology and Microbiology named after Pasteur, Saint-Petersburg, Russia
Russian Federation


N. R. Rozaeva
Saint-Petersburg Science Research Institute of Epidemiology and Microbiology named after Pasteur, Saint-Petersburg, Russia
Russian Federation


References

1. Domingo E. Basic concepts in RNA virus evolution /E. Domingo et [al.] // Faseb. J. – 1996. – N 10. – P. 859-864.

2. Lukashev A.N., Ivanova O.E., Eremeeva T.P et al. Voprosy virusologii – Problems of Virology. 2004; 5: 12-16 (in Russian).

3. Lukashev A.N., Reznik V.I., Ivanova O.E. et al. Voprosy virusologii – Problems of Virology. 2008; 1: 16-21 (in Russian).

4. Lobzin Yu.V., Skripchenko N.V., Murina E.A. Enterovirus infections: Guidelines for Physicians. Saint-Petersburg; 2012 (in Russian).

5. Romanenkova N.I., Bichurina M.A., Rozaeva N.R. Zhurnal mikrobiologii, epidemiologii i immunobiologii – Journal of Microbiology, Epidemiology and Immunobiology. 2011; 6: 32-36 (in Russian).

6. CDC. Outbreaks of aseptic meningitis associated with echovirus 9 and 30 and preliminary surveillance reports on enterovirus activity – United States, 2003 // Morbid. Mortal. Wkly Rep. – 2003. – Vol. 52. – P. 761-764.

7. Polio laboratory manual. WHO/IVB/04.10.World Health Organization, Geneva, Switzerland. — 2004. — 157 p.

8. Bichurina M.A., Pianykh V.A., Novikova N.A. et al. Infektsiya i immunitet – Infection and Immunity. 2012; 4: 747-752 (in Russian).

9. Golitsyna L.N., Novikova N.A., Fomina S.G. et al. Innovatsionnye tekhnologii v protivoepidemicheskoi zashite naseleniya [Innovation technologies in the antiepidemic protection of the population]. N. Novgorod; 2014. p. 88-92 (in Russian).

10. Lukashev A.N. Analysis of echovirus 30 isolates from Russia and new independent states revealing frequent recombination and reemergence of ancient lineages / A.N. Lukashev et [al.] // J. Clin. Microbiol. – 2008. – Vol. 46. – P. 665-670.

11. Kew O.M. Outbreak of poliomyelitis in Hispaniola associated with circulating type 1 vaccine-derived poliovirus/ O.M. Kew, V. Morris-Glasgow, M. Landaverde et [al.] // Science. — 2002. — Vol. 296. — P.356–359.

12. Kew O.M. Circulating vaccine-derived polioviruses: current state of knowledge/ Kew O.M., Wright P.F., Agol V.I., Delpeyroux F., et [al.] //Bulletin of the WHO.— 2004. — Vol. 82, № 1. — P.16–23.

13. Rousset D. Recombinant vaccine-derived poliovirus in Madagascar/D. Rousset, M. Rakoto-Andrianarivelo, R. Razafindratsimandresy et [al.] // Emerg. Infect. Dis. — 2003. — Vol. 9. — P. 885–887.

14. Shimizu H. Circulation of type 1 vaccine-derived poliovirus in the Philippines in 2001/ H. Shimizu, B. Thorley, F.J. Paladin et [al.] // J. Virology.— 2004.— Vol.78.— P.13512–13521.


Review

For citations:


Romanenkova N.I., Kanaeva O.I., Bichurina M.A., Rozaeva N.R. Detection of Nonpolio Enteroviruses among children with acute flaccid paralysis from institutions and from migrants’ families. Journal Infectology. 2014;6(4):43-48. (In Russ.) https://doi.org/10.22625/2072-6732-2014-6-4-43-48

Views: 587


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2072-6732 (Print)