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2.
J Clin Microbiol ; 51(3): 771-81, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23254128

ABSTRACT

Newcastle disease (ND) is a deadly avian disease worldwide. In Africa, ND is enzootic and causes large economic losses, but little is known about the Newcastle disease virus (NDV) strains circulating in African countries. In this study, 27 NDV isolates collected from apparently healthy chickens in live-bird markets of the West African countries Benin and Togo in 2009 were characterized. All isolates had polybasic fusion (F)-protein cleavage sites and were shown to be highly virulent in standard pathogenicity assays. Infection of 2-week-old chickens with two of the isolates resulted in 100% mortality within 4 days. Phylogenetic analysis of the 27 isolates based on a partial F-protein gene sequence identified three clusters: one containing all the isolates from Togo and one from Benin (cluster 2), one containing most isolates from Benin (cluster 3), and an outlier isolate from Benin (cluster 1). All the three clusters are related to genotype VII strains of NDV. In addition, the cluster of viruses from Togo contained a recently identified 6-nucleotide insert between the hemagglutinin-neuraminidase (HN) and large polymerase (L) genes in a complete genome of an NDV isolate from this geographical region. Multiple strains that include this novel element suggest local emergence of a new genome length class. These results reveal genetic diversity within and among local NDV populations in Africa. Sequence analysis showed that the F and HN proteins of six West African isolates share 83.2 to 86.6% and 86.5 to 87.9% identities, respectively, with vaccine strain LaSota, indicative of considerable diversity. A vaccine efficacy study showed that the LaSota vaccine protected birds from morbidity and mortality but did not prevent shedding of West African challenge viruses.


Subject(s)
Genetic Variation , Newcastle Disease/prevention & control , Newcastle Disease/virology , Newcastle disease virus/classification , Newcastle disease virus/pathogenicity , Viral Vaccines/immunology , Animals , Benin/epidemiology , Chickens , Cluster Analysis , Genotype , Molecular Sequence Data , Newcastle Disease/epidemiology , Newcastle disease virus/genetics , Newcastle disease virus/isolation & purification , Phylogeny , Sequence Analysis, DNA , Survival Analysis , Togo/epidemiology , Viral Vaccines/administration & dosage , Virulence , Virus Shedding
3.
J Virol ; 86(20): 11394-5, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22997417

ABSTRACT

The complete genome sequence of an African Newcastle disease virus (NDV) strain isolated from a chicken in Togo in 2009 was determined. The genome is 15,198 nucleotides (nt) in length and is classified in genotype VII in the class II cluster. Compared to common vaccine strains, the African strain contains a previously described 6-nt insert in the downstream untranslated region of the N gene and a novel 6-nt insert in the HN-L intergenic region. Genome length differences are a marker of the natural history of NDV. This is the first description of a class II NDV strain with a genome of 15,198 nt and a 6-nt insert in the HN-L intergenic region. Sequence divergence relative to vaccine strains was substantial, likely contributes to outbreaks, and illustrates the continued evolution of new NDV strains in West Africa.


Subject(s)
Chickens/virology , Genome, Viral , Newcastle Disease/virology , Newcastle disease virus/genetics , Animals , Base Sequence , Genetic Variation , Molecular Sequence Data , Newcastle disease virus/classification , Newcastle disease virus/isolation & purification , Sequence Analysis, DNA , Togo
4.
Emerg Infect Dis ; 18(9): 1446-52, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22932129

ABSTRACT

To determine the extent of animal influenza virus circulation in Côte d'Ivoire, Benin, and Togo, we initiated systematic year-round active influenza surveillance in backyard birds (predominantly chickens, guinea fowl, and ducks) and pigs. A total of 26,746 swab specimens were screened by using reverse transcription PCR. Animal influenza prevalence was estimated at 0 (95% CIs for each of the 2 study years 0-0.04% to 0-1.48% [birds] and 0-0.28% to 0-5% [pigs]). In addition, 2,276 serum samples from the same populations were negative for influenza-specific antibodies. These data indicate that the environments and host populations previously identified as harboring high levels of influenza virus in Southeast Asia do not do so in these 3 countries. The combination of climate and animal density factors might be responsible for what appears to be the absence of influenza virus in the backyard sector of the 3 countries.


Subject(s)
Influenza A virus/isolation & purification , Influenza in Birds/epidemiology , Orthomyxoviridae Infections/epidemiology , Swine Diseases/epidemiology , Swine Diseases/virology , Animals , Benin/epidemiology , Cote d'Ivoire/epidemiology , Environment , Influenza A virus/classification , Influenza A virus/genetics , Influenza in Birds/virology , Orthomyxoviridae Infections/virology , Population Surveillance , Poultry , Prevalence , Swine , Togo/epidemiology
5.
PLoS One ; 4(3): e4842, 2009.
Article in English | MEDLINE | ID: mdl-19290041

ABSTRACT

Highly pathogenic avian influenza virus A/H5N1 was first officially reported in Africa in early 2006. Since the first outbreak in Nigeria, this virus spread rapidly to other African countries. From its emergence to early 2008, 11 African countries experienced A/H5N1 outbreaks in poultry and human cases were also reported in three of these countries. At present, little is known of the epidemiology and molecular evolution of A/H5N1 viruses in Africa. We have generated 494 full gene sequences from 67 African isolates and applied molecular analysis tools to a total of 1,152 A/H5N1 sequences obtained from viruses isolated in Africa, Europe and the Middle East between 2006 and early 2008. Detailed phylogenetic analyses of the 8 gene viral segments confirmed that 3 distinct sublineages were introduced, which have persisted and spread across the continent over this 2-year period. Additionally, our molecular epidemiological studies highlighted the association between genetic clustering and area of origin in a majority of cases. Molecular signatures unique to strains isolated in selected areas also gave us a clearer picture of the spread of A/H5N1 viruses across the continent. Mutations described as typical of human influenza viruses in the genes coding for internal proteins or associated with host adaptation and increased resistance to antiviral drugs have also been detected in the genes coding for transmembrane proteins. These findings raise concern for the possible human health risk presented by viruses with these genetic properties and highlight the need for increased efforts to monitor the evolution of A/H5N1 viruses across the African continent. They further stress how imperative it is to implement sustainable control strategies to improve animal and public health at a global level.


Subject(s)
Influenza A Virus, H5N1 Subtype/classification , Phylogeny , Africa , Bayes Theorem , Evolution, Molecular , Influenza A Virus, H5N1 Subtype/genetics , Influenza A Virus, H5N1 Subtype/pathogenicity , Mutation
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