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Effects of the In Ovo Vaccination of the ts-11 Strain of Mycoplasma gallisepticum in Layer Embryos and Posthatch Chicks.
Alqhtani, Abdulmohsen H; Fatemi, Seyed A; Elliott, Katie E C; Branton, Scott L; Evans, Jeff D; Leigh, Spencer A; Gerard, Patrick D; Peebles, Edgar D.
Afiliación
  • Alqhtani AH; Department of Poultry Science, Mississippi State University, Starkville, MS 39762, USA.
  • Fatemi SA; Department of Animal Production, College of Agriculture and Food Sciences, King Saud University, P.O. Box 2460, Riyadh 11451, Saudi Arabia.
  • Elliott KEC; Department of Poultry Science, Mississippi State University, Starkville, MS 39762, USA.
  • Branton SL; Department of Poultry Science, Mississippi State University, Starkville, MS 39762, USA.
  • Evans JD; Poultry Research Unit, USDA-ARS, Starkville, MS 39762, USA.
  • Leigh SA; Poultry Research Unit, USDA-ARS, Starkville, MS 39762, USA.
  • Gerard PD; Poultry Research Unit, USDA-ARS, Starkville, MS 39762, USA.
  • Peebles ED; Poultry Research Unit, USDA-ARS, Starkville, MS 39762, USA.
Animals (Basel) ; 12(9)2022 Apr 27.
Article en En | MEDLINE | ID: mdl-35565547
ABSTRACT
The transmission of the ts-11 strain of Mycoplasma gallisepticum (MG) vaccine (ts-11MGV) between incubated eggs and between hatchlings that was administrated via in ovo injection, and its subsequent effects on their posthatch performance were evaluated. Marek's disease diluent alone (sham-injected) or containing either 3.63 × 101, 102, 103, or 104 cfu of ts-11MGV was manually in ovo-injected into the amnion on 18 days of incubation. Egg residue analysis, percentage incubational egg weight loss, hatchability of viable injected eggs, and hatchling body weight (BW) were assessed. Selected hatchlings from each treatment replicate group were swabbed in the choanal cleft for MG DNA detection. Female chick live performance was also assessed through 21 days of posthatch age. Unexposed control sentinel chicks were allocated to each treatment replicate group to assess horizontal transmission. Birds were later swabbed and bled respectively, for detection of MG DNA and IgM production at 21 days posthatch. In all birds, no MG DNA was detected and SPA tests for IgM were negative. Among all variables, only 0 to 21 day BW gain was significantly affected by treatment and was lower in the 3.63 × 104 ts-11 MGV treatment in comparison to all the other treatments. Because ts-11MGV does not exhibit vertical or horizontal transmission capabilities under commercial conditions, it may not be a good candidate for in ovo injection.
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