4.5 Article

Success rates of inoculation of the various compartments of embryonated chicken eggs at different incubation days

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AVIAN PATHOLOGY
卷 50, 期 1, 页码 61-77

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TAYLOR & FRANCIS LTD
DOI: 10.1080/03079457.2020.1834503

关键词

In ovo; inoculation; success rates; embryo; chicken; methylene blue; magnetic resonance imaging

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The study examined the success rates of inoculating chicken embryos in brown eggs and found that targeting albumen, yolk, amniotic cavity, and embryo yielded low scores. Magnetic resonance imaging was used to understand the reasons behind this, leading to adjustments in the inoculation method. Despite challenges, full scores were obtained for most compartments, making this study a useful guide for future inoculation procedures.
Inoculation of embryonated chicken eggs has been widely used during the past decades; however, inoculation success rates have not been investigated systematically. In this study named success rates were assessed in brown eggs incubated between 5 and 19 days, which were inoculated with 0.2 ml methylene blue per egg. Inoculations were performed in a simple and fully standardized way. Five embryonic compartments were targeted blindly (amniotic cavity, embryo, allantoic cavity, albumen and yolk) with needles of four different lengths; albumen and yolk were targeted with eggs in upside down position. Three compartments were inoculated within sight (air chamber, chorioallantoic membrane and blood vessel). Twenty embryos were used per incubation day, intended deposition site and needle length. Success rates were assessed by visual inspection after breaking the eggs. The inoculations targeting albumen, yolk, amniotic cavity and embryo yielded low scores. Magnetic resonance imaging was performed to elucidate the reason(s) for these low success rates: needles used were of appropriate length, but embryo and amniotic cavity had variable positions in the eggs, while albumen and yolk rapidly changed position after turning the eggs upside down. The latter led to adjustment of the inoculation method for albumen and yolk. Failures to inoculate compartments within sight were immediately visible; therefore, these eggs could be discarded. Except for the amniotic cavity, full scores (20/20) were obtained for all compartments although not always on every day of incubation. In conclusion, the present study may serve as a guide to more accurately inoculate the various chicken embryo compartments.

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