A molecular survey on Avian Metapneumovirus (aMPV) diffusion was performed from 2011 to 2013 in 122 turkey and 48 broiler farms, located in a densely populated poultry area of Northern Italy. Turkeys were all vaccinated at 1 day of age in the hatchery. aMPV was detected using RTnested PCR or qRT-PCR; both tests are able to detect and differentiate aMPV subtypes A and B. All samples but one resulted positive for aMPV subtype B confirming the high prevalence of this subtype in Italy. The majority of aMPV detections were of field origin, circulating mainly in 9 to 12- week-old turkeys and 5 to 7 week-old broilers, showing respiratory signs. The reasons for vaccine failure could be due to field virus changes occurred in key antigenic regions, which allow virus replication and disease in well-vaccinated birds. Strains of vaccine origin were detected in turkeys with a high prevalence during the first few weeks after vaccination with aMPV live vaccines. This confirmed the pattern previously seen where vaccine viruses were shown to persist on farm for 4-5 weeks. Uniquely in this study, vaccine derived strains were detected in older turkeys of up to 84 days of age. Moreover, sequence analysis of F and G protein genes of selected strains was performed.
M. Cecchinato, M. Drigo, C. Lupini, M. Martini, V. Listorti, G. Franzo, et al. (2014). AN UPDATE ON THE EPIDEMIOLOGY OF AVIAN METAPNEUMOVIRUS IN ITALY. Giessen : VVB LAUFERSWEILER VERLAG.
AN UPDATE ON THE EPIDEMIOLOGY OF AVIAN METAPNEUMOVIRUS IN ITALY
LUPINI, CATERINA;LISTORTI, VALERIA;LACONI, ANDREA;CATELLI, ELENA
2014
Abstract
A molecular survey on Avian Metapneumovirus (aMPV) diffusion was performed from 2011 to 2013 in 122 turkey and 48 broiler farms, located in a densely populated poultry area of Northern Italy. Turkeys were all vaccinated at 1 day of age in the hatchery. aMPV was detected using RTnested PCR or qRT-PCR; both tests are able to detect and differentiate aMPV subtypes A and B. All samples but one resulted positive for aMPV subtype B confirming the high prevalence of this subtype in Italy. The majority of aMPV detections were of field origin, circulating mainly in 9 to 12- week-old turkeys and 5 to 7 week-old broilers, showing respiratory signs. The reasons for vaccine failure could be due to field virus changes occurred in key antigenic regions, which allow virus replication and disease in well-vaccinated birds. Strains of vaccine origin were detected in turkeys with a high prevalence during the first few weeks after vaccination with aMPV live vaccines. This confirmed the pattern previously seen where vaccine viruses were shown to persist on farm for 4-5 weeks. Uniquely in this study, vaccine derived strains were detected in older turkeys of up to 84 days of age. Moreover, sequence analysis of F and G protein genes of selected strains was performed.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.