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Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
Author(s) -
Mo Jongseo,
Spackman Erica,
Stephens Christopher B.
Publication year - 2021
Publication title -
transboundary and emerging diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.392
H-Index - 63
eISSN - 1865-1682
pISSN - 1865-1674
DOI - 10.1111/tbed.13721
Subject(s) - newcastle disease , virus , contamination , outbreak , veterinary medicine , cage , titer , sampling (signal processing) , biology , virology , mathematics , medicine , ecology , computer science , filter (signal processing) , combinatorics , computer vision
Abstract Environmental testing of poultry premises after an outbreak of an infectious disease like avian influenza (AI) or Newcastle disease is essential to promptly verify virus‐free status and subsequently return to normal operations. In an attempt to establish an optimized sampling protocol, a laboratory study simulating an AI virus‐contaminated poultry house with wire layer cages was conducted. Three sample collection devices, pre‐moistened cotton gauze, dry cotton gauze and a foam swab, were evaluated with each of four sample locations within a cage and when sampling all four locations with one device. Virus was detected with quantitative real‐time RT‐PCR utilizing a standard curve of a quantified homologous isolate of AI virus to determine titre equivalents of virus. The pre‐moistened gauze detected the most virus RNA (100% positive, geometric mean titre [GMT): 3.2 log 10 50% embryo infectious doses [EID 50 ] equivalents per 25 cm 2 ) in all four sample locations compared to dry gauze (93% positive, GMT: 2.6 EID 50 equivalents per 25 cm 2 ) and foam swabs (95% positive, GMT: 2.8 log10 EID 50 equivalents per 25 cm 2 ). The highest viral RNA loads were observed from the cage floor, and when the four locations were sampled with the same device. Overall, the pre‐moistened gauze performed the best, and sampling multiple locations within a cage with the same device would likely optimize detection of residual virus.