BackgroundHuman and animal influenza are inextricably linked. In particular, the pig is uniquely important as a mixing vessel for genetic reassortment of influenza viruses, leading to emergence of novel strains which may cause human pandemics. Significant reduction in transmission of influenza viruses from humans, and other animals, to swine may therefore be crucial for preventing future influenza pandemics. This study investigated the presence of the 2009 pandemic influenza A/H1N1 virus, A(H1N1)pdm09, in Nigerian and Ghanaian pigs, and also determined levels of acceptance of preventive measures which could significantly reduce the transmission of this virus from humans to pigs.MethodsNasal swab specimens from 125 pigs in Ibadan, Nigeria, and Kumasi, Ghana, were tested for the presence of influenza A/California/04/2009 (H1N1) by quantitative antigen-detection ELISA. A semi-structured questionnaire was also administered to pig handlers in the two study areas and responses were analyzed to evaluate their compliance with seven measures for preventing human-to-swine transmission of influenza viruses.ResultsThe virus was detected among pigs in the two cities, with prevalence of 8% in Ibadan and 10% in Kumasi. Levels of compliance of pig handlers with relevant preventive measures were also found to be mostly below 25 and 40% in Ibadan and Kumasi, respectively.ConclusionDetection of influenza A(H1N1)pdm09 among pigs tested suggests the possibility of human-to-swine transmission, which may proceed even more rapidly, considering the very poor acceptance of basic preventive measures observed in this study. This is also the first report on detection of influenza A(H1N1)pdm09 in Ghanaian pigs. We recommend improvement on personal hygiene among pig handlers, enforcement of sick leave particularly during the first few days of influenza-like illnesses, and training of pig handlers on recognition of influenza-like signs in humans and pigs. These could be crucial for prevention of future influenza pandemics.
Since the first detection of human H3N2 influenza virus in Taiwanese pigs in 1970, infection of pigs with wholly human viruses has been known to occur in other parts of the world. These viruses, referred to as human-like H3N2 viruses, have been known to cause clinical and subclinical infections of swine populations. Due to the paucity and complete unavailability of information on transmission of influenza viruses from other species, especially humans, to swine in Nigeria and Ghana, respectively, this study was designed to investigate the presence and prevalence of a human strain of influenza A (H3N2) in swine populations at three locations in two cities within these two West African countries in January and February, 2014. Using stratified random technique, nasal swab specimens were collected from seventy-five (75) pigs at two locations in Ibadan, Nigeria and from fifty (50) pigs in Kumasi, Ghana. These specimens were tested directly by a sensitive Quantitative Solid Phase Antigen-detection Sandwich ELISA using anti-A/Brisbane/10/2007 haemagglutinin monoclonal antibody. Influenza virus A/Brisbane/10/2007 (H3N2) was detected among pigs at the three study locations, with an aggregate prevalence of 4.0% for the two locations in Ibadan, Nigeria and also 4.0% for Kumasi, Ghana. Transmission of influenza viruses from other species to swine portends serious sinister prospects for genetic reassortment and evolvement of novel viruses. We therefore recommend that further studies should be carried out to investigate the presence of other circulating human and avian influenza viruses in swine populations in West Africa and also determine the extent of genetic reassortment of strains circulating among these pigs. This would provide an early warning system for detection of novel influenza viruses, which could have pandemic potentials.
Agricultural and commercial activities have continued to bring people and pigs into regular, close contact in Ibadan, Nigeria. This study was therefore designed to investigate the transmission of human influenza viruses to pigs in Ibadan, using serological surveillance. Serum specimens were collected from ninety-one (91/199) apparently healthy, unvaccinated Landrace pigs at three locations within Ibadan from April to June, 2008. Two strains of human influenza virus A: A/Brisbane/59/2007 (H1N1) and A/Brisbane/10/2007 (H3N2) were used in Haemagglutination-Inhibition Assay for antibody detection. Prevalence of HI antibodies to the two subtypes was 90.1%. Antibodies to influenza A/Brisbane/59/2007 (H1N1) were significantly (P < 0.05) more prevalent (80.2%) than those of influenza A/Brisbane/10/2007 (H3N2) (51.6%). Titres of HI antibodies to influenza A/Brisbane/59/2007 [mean = 3331.5] were significantly higher (P < 0.05) than those of influenza A/Brisbane/10/2007 [mean = 2212.3]. This study shows that these pigs were exposed to human strains of influenza A(H1N1) and A(H3N2) either prior to or during this study. The implications of these high prevalence and antibody titres are discussed in relation to influenza virus infection among pig handlers in Ibadan, Nigeria. We recommend that periodic investigation of circulating strains of influenza viruses in pigs and humans who handle pigs regularly in Nigeria and molecular characterization of such isolates be carried out to ensure early detection of interspecies transmission and potential future pandemic strains.
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