Three operational taxonomic units of Eimeria are common in Nigerian chickens and may undermine effective molecular diagnosis of coccidiosis.

Autor: Jatau ID; Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria, Nigeria. mail4idjatau@gmail.com., Lawal IA; Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria, Nigeria., Kwaga JK; Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria, Nigeria., Tomley FM; Pathology and Pathogen Biology, Royal Veterinary College, Hawkshead Lane, North Mymms, AL9 7TA, UK., Blake DP; Pathology and Pathogen Biology, Royal Veterinary College, Hawkshead Lane, North Mymms, AL9 7TA, UK. dblake@rvc.ac.uk., Nok AJ; Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria, Nigeria.
Jazyk: angličtina
Zdroj: BMC veterinary research [BMC Vet Res] 2016 Jun 04; Vol. 12, pp. 86. Date of Electronic Publication: 2016 Jun 04.
DOI: 10.1186/s12917-016-0713-9
Abstrakt: Background: Chicken is fast becoming the world's most consumed meat. As a consequence poultry health is more important now than ever before, with pathogens of chickens recognised as serious threats to food security. One such threat are Eimeria species parasites, protozoa which can cause the disease coccidiosis. Eimeria can compromise economic poultry production and chicken welfare, and have serious consequences for poor livestock keepers. Seven Eimeria species that infect chickens are recognised with a global enzootic distribution. More recently three cryptic Operational Taxonomic Units (OTUx, y and z) have been described in populations of Eimeria recovered from chickens in Australia. Two of the three OTUs have also been detected in sub-Saharan Africa, but their occurrence, pathology and the risk they pose is largely unknown.
Results: Nigeria has witnessed a dramatic expansion in poultry production and is now the largest poultry producer in Africa. Here, faecal samples collected from nine of 12 commercial chicken farms sampled in Kaduna state, Nigeria, were found to contain eimerian oocysts. After amplification by in vivo propagation all three cryptic OTU genotypes were detected using polymerase chain reaction (PCR), including OTUy for the first time outside of Australia. Comparison with a widely used, established Eimeria species-specific PCR assay revealed failure to detect the OTU genotypes.
Conclusions: All three of the Eimeria OTU genotypes appear to be common in north-western Nigeria. The failure of a leading species-specific molecular assay to detect these genotypes indicates a risk of false negative Eimeria diagnosis when using molecular tools and suggests that the spatial occurrence of each OTU may be far wider than has been recognised. The risk posed by these novel genotypes is unknown, but it is clear that a better understanding of Eimeria occurrence is required together with the validation of effective diagnostics.
Databáze: MEDLINE