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Infectious diseases are a major obstacle to profitable poultry production in Nigeria due to the mortality and severe economic losses they cause. In particular, they are a potent threat to attainment of the food security goals of government and national self-sufficiency in food production. Thus, there is a need for continuous monitoring of the nation's poultry population for these diseases. As part of an ongoing investigation of enteric viruses associated with poor performance or hatchery diseases in commercial poultry in southwestern Nigeria, intestinal contents from 97 condemned or runted day-old commercial turkey poults were examined for turkey astroviruses, infectious bronchitis virus, chicken astrovirus (CAstV), avian nephritis virus, avian rotavirus, avian reovirus, fowl adenovirus, and chicken parvovirus by virus isolation, electron microscopy (EM), polymerase chain reaction (PCR), and reverse transcription PCR. The samples were collected from five commercial hatcheries and five farms located in southwestern Nigeria. While all samples tested negative for other viruses, CAstV was detected in the majority (83.5%) of the birds, although some pleomorphic virus-like particles with surface projections that appeared fringed or fimbriated were observed in five of the cell culture samples by EM. Phylogenetic analysis revealed these CAstV strains belonged to the Bi clade. These findings not only implicate CAstV as the major cause of hatchery condemnations in commercial turkeys in southwestern Nigeria but also highlight the need for experimental studies to further establish its role in this disease condition.

Infections with divergent strains of astroviruses appear to be endemic in commercial poultry. In order to investigate enteric viruses associated with hatchery condemnations in Nigerian poultry, an indirect immunofluorescence test with CAstV-612- (Group A), CAstV-11672- (Group B) and ANV-1-infected cells was used to screen sera obtained from commercial broilers (n = 164) and turkeys (n = 97) in farms and hatcheries in southwest Nigeria. Of the 261 sera tested, 16 (6.1%) were positive for CAstV antibodies after immunofluorescent staining with CAstV-11672-infected cells. Thirteen (81.3%) of the positive sera were from broilers with three (18.7%) being from turkeys. Conversely, all tested sera were negative for CAstV-612 and ANV-1 antibodies. Since CAstV-11672, a group B CAstV is known to be antigenically and genetically distinct from CAstV-612 that belongs to group A, these findings reveal that the circulating serotype of CAstV in commercial broilers and turkeys in southwest Nigeria belongs to group B of CAstV. Education of veterinary personnel and poultry farmers about this emerging virus and its impact on commercial poultry in Nigeria, as well as continuous monitoring of chicken and turkey flocks for infections caused by it are therefore imperative in order to facilitate the implementation of effective prevention and control measures.