Abstract
BackgroundThe threat of poultry-origin H6 avian influenza viruses to human health emphasizes the importance of monitoring their evolution. South Africa’s H6N2 epidemic in chickens began in 2001 and two co-circulating antigenic sub-lineages of H6N2 could be distinguished from the outset. The true incidence and prevalence of H6N2 in the country has been difficult to determine, partly due to the continued use of an inactivated whole virus H6N2 vaccine and the inability to distinguish vaccinated from non-vaccinated birds on serology tests. In the present study, the complete genomes of 12 H6N2 viruses isolated from various farming systems between September 2015 and February 2019 in three major chicken-producing regions were analysed and a serological experiment was used to demonstrate the effects of antigenic mismatch in diagnostic tests.ResultsGenetic drift in H6N2 continued and antigenic diversity in sub-lineage I is increasing; no sub-lineage II viruses were detected. Reassortment patterns indicated epidemiological connections between provinces as well as different farming systems, but there was no reassortment with wild bird or ostrich influenza viruses. The sequence mismatch between the official antigens used for routine hemagglutination inhibition (HI) testing and circulating field strains has increased steadily, and we demonstrated that H6N2 field infections are likely to be missed. More concerning, sub-lineage I H6N2 viruses acquired three of the nine HA mutations associated with human receptor-binding preference (A13S, V187D and A193N) since 2002. Most sub-lineage I viruses isolated since 2015 acquired the K702R mutation in PB2 associated with the ability to infect humans, whereas prior to 2015 most viruses in sub-lineages I and II contained the avian lysine marker. All strains had an unusual HA0 motif of PQVETRGIF or PQVGTRGIF.ConclusionsThe H6N2 viruses in South African chickens are mutating and reassorting amongst themselves but have remained a genetically pure lineage since they emerged more than 18 years ago. Greater efforts must be made by government and industry in the continuous isolation and characterization of field strains for use as HI antigens, new vaccine seed strains and to monitor the zoonotic threat of H6N2 viruses.
Highlights
The threat of poultry-origin H6 avian influenza viruses to human health emphasizes the importance of monitoring their evolution
No viruses were isolated from the Western Cape or other provinces during this period, serological test results suggest that infection is widespread
Viruses isolated in 2015 showed normal patterns of agglutination of chicken red blood cells (RBCs) on the hemagglutination inhibition (HI) tests
Summary
The threat of poultry-origin H6 avian influenza viruses to human health emphasizes the importance of monitoring their evolution. Avian influenza A virus (IAV) serotypes are formed by the combination of two major antigens on the viral surface, namely hemagglutinin protein (H) of which 16 subtypes have been identified, and neuraminidase (N) protein of which nine subtypes are known. The disease “avian influenza” is defined in the World Organization for Animal Health (OIE) Terrestrial Animal Health Code as an infection of poultry caused by any influenza A virus with high pathogenicity (HPAI) (i.e. an intra-venous pathogenicity index of > 1.2 in chickens), and by H5 and H7 subtypes with low pathogenicity (LPAI) [2]. Abolnik et al BMC Veterinary Research (2019) 15:455 opt to use vaccination as a means of control or reducing infections, the OIE recommends that vaccine strains be re-evaluated at least every 2 to 3 years for efficacy against circulating field viruses and updated as required. Evaluating and updating diagnostic tests to keep abreast of genetic and antigenic drift in IAV is important
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