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dc.contributor.authorM. Yu, Shchelkanoven_US
dc.contributor.authorV. Yu., Ananyeven_US
dc.contributor.authorD. N., Lvoven_US
dc.contributor.authorD. Ye., Kireyeven_US
dc.contributor.authorYe. L., Guryeven_US
dc.contributor.authorD. S., Akaninaen_US
dc.contributor.authorI. V., Galkinaen_US
dc.contributor.authorV. A., Aristovaen_US
dc.contributor.authorT. M., Moskvinaen_US
dc.contributor.authorV. M., Chumakoven_US
dc.contributor.authorN. I., Baranoven_US
dc.contributor.authorV. N., Gorelikoven_US
dc.contributor.authorYe. V, Usacheven_US
dc.contributor.authorS. V., Alkhovskyen_US
dc.contributor.authorO. V., Lyapinaen_US
dc.contributor.authorА. п., Poglazoven_US
dc.contributor.authorO. V., Shlyapnikovaen_US
dc.contributor.authorYe. G., Burukhinaen_US
dc.contributor.authorO. N., Borisovaen_US
dc.contributor.authorI. Т., Fedyakinaen_US
dc.contributor.authorYe. I., Burtsevaen_US
dc.contributor.authorT. N., Morozovaen_US
dc.contributor.authorYe. P., Grenkovaen_US
dc.contributor.authorT. V., Grebennikovaen_US
dc.contributor.authorA. G., Prilipoven_US
dc.contributor.authorYe. I., Samokhvaloven_US
dc.contributor.authorA. D., Zabarezhnyien_US
dc.contributor.authorS. A., Kolomeyetsen_US
dc.contributor.authorV. A., Miroshnikoven_US
dc.contributor.authorP. L., Oropaien_US
dc.contributor.authorV. V., Gaponoven_US
dc.contributor.authorV. L, Semenoven_US
dc.contributor.authorI. O., Susloven_US
dc.contributor.authorV. A., Volkoven_US
dc.contributor.authorS. S., Yamnikovaen_US
dc.contributor.authorT. I., Aliperen_US
dc.contributor.authorV. G., Dunayeven_US
dc.contributor.authorV. L., Gromashevskyen_US
dc.contributor.authorD. V., Masloven_US
dc.contributor.authorF. Т., Novikoven_US
dc.contributor.authorN. A., Vlasoven_US
dc.contributor.authorP. G., Deryabinen_US
dc.contributor.authorYe. A., Nepoklonoven_US
dc.contributor.authorV. L, Zlobinen_US
dc.contributor.authorD. K., Lvoven_US
dc.description.abstractThe paper presents the results of monitoring of viruses of Western Nile (WN), Japanese encephalitis (JE), tick-borne encephalitis (TBE), Geta, influenza A, as well as avian paramicroviruses type 1 (virus of Newcastle disease (ND)) and type 6 (APMV-6) in the Primorye Territory in 2003-2006. Totally throughout the period, specific antibodies to the viruses were detected by neutralization test in wild birds (7.3%, WN; 8.0%, Geta; 0.7% Batai; 2.8%, Alpine hare (Lepus timidus); by hemagglutination-inhibition test in cattle (11.4% WN; 5.9%, JE; j 3.0%, TBE; 11.6%, Geta), horses (6.1, 6.8, 0, and 25.3%, respectively), and pigs (5.4, 1.5, 0, and 5.9%, respectively) by enzyme immunoassay (IgG) in human beings (0.8, 0.5, 6.8, and 3.2%, respectively. Reverse-transcription polymerase chain reaction (RT-PCR) was used to reveal RNA of the NP segment of influenza A virus in 57.9 and 65% of the cloacal swabs from wild and domestic birds, respectively; and the HA-segment of subtype HH was not detected in 2005. HA/H5 RNA was recorded in 5.5 and 6.7% of the swabs from wild and domestic birds, respectively; 6% of the specimens from domestic birds were M-segment positive in 2006. RNA of influenza A virus NA/H7 and RNA was not detected throughout the years. In 2004, the cloacal swabs 8 isolated influenza A strains: two H3N8 and two H4N8 strains from European teals (Anas crecca), two (H3N8 and H6N2) strains from Baikal teals (A. formosa), one (H10N4) strain from shovelers (A. clypeata), and one (H4N8) from garganeys (A. querquedula). In 2004, one ND virus strain was isolated from the cloacal swabs from European teals (A. crecca). RT-PCR revealed RNA of this virus in some 8 more cloacal swabs from black ducks (A. poecilorhyncha) (3 positive specimens), pheasants (Phasianus colchicus) (n = 2), garganeys (A. querquedula) (n = 1), gadwalls (A. strepera) (n = 1), and geese (Anser anser domesticus) (n = 1). Sequencing of the 374-member fragment of the ND virus F gene, which included a proteolytic cleavage site, could assign two samples to the weakly pathogenetic variants of genotype 1, one sample to highly pathogenic variants of genotype 3a, five to highly pathogenic ones of genotype 5b. Isolation of APMV-6 (2003) from common egrets (Egretta alba) and geese (Ans. anser domesticus) is first described.en_US
dc.publisherIzdatel'stvo Meditsinaen_US
dc.publisher.placeRussian Federationen_US
dc.relation.ispartofjournalVoprosy Virusologiien_US
dc.titleКомплексный эколого-вирусологический мониторинг на территории Приморского края в 2003-2006 ггen_US
dc.title.alternativeComplex environmental and virological monitoring in the Primorye Territory in 2003—2006en_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.hasfulltextNo Full Text

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