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High prevalence and diversity of species D adenoviruses (HAdV-D) in human populations of four Sub-Saharan countries

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    0428335 - ÚBO 2015 RIV GB eng J - Článek v odborném periodiku
    Pauly, M. - Hoppe, E. - Mugisha, L. - Petrželková, Klára Judita - Akoua-Koffi, C. - Couacy-Hymann, E. - Anoh, A. E. - Mossoun, A. - Schubert, G. - Wiersma, L. - Pascale, S. - Muyembe, J.-J. - Karhemere, S. - Weiss, S. - Leendertz, S. A. - Calvignac-Spencer, S. - Leendertz, F. H. - Ehlers, B.
    High prevalence and diversity of species D adenoviruses (HAdV-D) in human populations of four Sub-Saharan countries.
    Virology Journal. Roč. 11, č. 25 (2014), s. 25. E-ISSN 1743-422X
    Grant CEP: GA ČR GA206/09/0927
    Institucionální podpora: RVO:68081766
    Klíčová slova: Adenoviridae * Human adenovirus D * Genotype * Sub-Saharan Africa * PCR
    Kód oboru RIV: GJ - Choroby a škůdci zvířat, veterinární medicína
    Impakt faktor: 2.181, rok: 2014

    Background: Human adenoviruses of species D (HAdV-D) can be associated with acute respiratory illness, epidemic keratoconjunctivitis, and gastroenteritis, but subclinical HAdV-D infections with prolonged shedding have also been observed, particularly in immunocompromised hosts. To expand knowledge on HAdV-D in Sub-Saharan Africa, we investigated the prevalence, epidemiology and pathogenic potential of HAdV-D in humans from rural areas of 4 Sub-Saharan countries, Côte d'Ivoire (CI), Democratic Republic of the Congo (DRC), Central African Republic (CAR) and Uganda (UG). Methods. Stool samples were collected from 287 people living in rural regions in CI, DRC, CAR and UG. HAdV-D prevalence and diversity were determined by PCR and sequencing. A gene block, spanning the genes pV to hexon, was used for analysis of genetic distance. Correlation between adenovirus infection and disease symptoms, prevalence differences, and the effect of age and gender on infection status were analyzed with cross tables and logistic regression models. Results: The prevalence of HAdV-D in the investigated sites was estimated to be 66% in CI, 48% in DRC, 28% in CAR (adults only) and 65% in UG (adults only). Younger individuals were more frequently infected than adults; there was no difference in HAdV-D occurrence between genders. No correlation could be found between HAdV-D infection and clinical symptoms. Highly diverse HAdV-D sequences were identified, among which a number are likely to stand for novel types. Conclusions: HAdV-D was detected with a high prevalence in study populations of 4 Sub-Saharan countries. The genetic diversity of the virus was high and further investigations are needed to pinpoint pathological potential of each of the viruses. High diversity may also favor the emergence of recombinants with altered tropism and pathogenic properties.
    Trvalý link: http://hdl.handle.net/11104/0233685

     
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