High genetic diversity of measles virus, World Health Organization European region, 2005-2006

2008
Authors
Kremer, Jacques R.Brown, Kevin E.
Jin, Li
Santibanez, Sabine
Shulga, Sergey V.

Aboudy, Yair
Demchyshyna, Irina V.
Đemileva, Sultana
Echevarria, Juan E.

Featherstone, David F.
Hukić, Mirsada
Johansen, Kari
Litwinska, Bogumila
Lopareva, Elena
Lupulescu, Emilia
Mentis, Andreas F.
Mihneva, Zefira
Mosquera, Maria M.
Muscat, Mark
Naumova, M.A.

Nedeljković, Jasminka
Nekrasova, Ljubov S.
Magurano, Fabio

Fortuna, Claudia

De Andrade, Helena Rebelo

Richard, Jean-Luc
Robo, Alma
Rota, Paul A.
Samoilovich, Elena O.
Sarv, Inna
Semeiko, Galina V.
Shugayev, Nazim
Utegenova, Elmira S.
van Binnendijk, Rob
Vinner, Lasse

Waku-Kouomou, Diane
Wild, Fabian T.
Brown, David W.G.
Mankertz, Annette

Muller, Claude P.
MuldersJJ, Mick N.
article (publishedVersion)
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Show full item recordAbstract
During 2005-2006, nine measles virus (MV) genotypes were identified throughout the World Health Organization European Region. All major epidemics were associated with genotypes D4, D6, and B3. Other genotypes (B2, D5, D8, D9, G2, and H1) were only found in limited numbers of cases after importation from other continents. The genetic diversity of endemic D6 strains was low; genotypes C2 and D7, circulating in Europe until recent years, were no longer identified. The transmission chains of several indigenous MV strains may thus have been interrupted by enhanced vaccination. However, multiple importations from Africa and Asia and virus introduction into highly mobile and unvaccinated communities caused a massive spread of D4 and B3 strains throughout much of the region. Thus, despite the reduction of endemic MV circulation, importation of MV from other continents caused prolonged circulation and large outbreaks after their introduction into unvaccinated and highly mobile communities.
Source:
Emerging Infectious Diseases, 2008, 14, 1, 107-114Publisher:
- Centers Disease Control & Prevention, Atlanta
DOI: 10.3201/eid1401.070778
ISSN: 1080-6040
PubMed: 18258089