bioRxivBioengineeringPreprint
Allantoic fluid-based qPCR for early-onset in ovo sexing
S. M. B. d. Santos, M. Corion, B. De Ketelaere, J. Lammertyn, D. Spasic
Abstract
The culling of day-old male chickens remains an important welfare issue in the poultry industry. Several governments (e.g., Germany, France or Italy) have prohibited this practice, pushing the hatcheries to look for alternatives. Although different solutions exist for solving this problem, sex determination during embryos incubation (so called in ovo sexing) is considered the most suitable both for consumers and the industry since it aligns with the increasing demand for ethical and sustainable agriculture. However, to be applied in the market, in ovo sexing technologies have to meet a number of requirements, such as being compatible with all egg colors and early developmental stages, while maintaining high hatchability rate and accuracy at low cost and high throughput. To meet these requirements, we studied the use of the sexual genes HINTW (female-specific) and DMRT-1 (present in both males and females) between incubation days 6 and 9. By utilizing quantitative polymerase chain reaction (qPCR) as analysis method and allantoic fluid (AF) as sample, our study confirmed specific detection of these genes in AF, remarkably already at day 6 of development. In a blind study performed with 80 eggs, we achieved a 95% accuracy rate in sorting embryos when using the HINTW gene alone and an outstanding 100% accuracy rate when using {Delta}{lambda} values (difference between the HINTW and DMRT-1 qPCR cycle threshold (Ct)). Importantly, the AF sampling procedure did not reveal any significant detrimental effects on hatchability or embryo development, revealing high potential for this understudied type of sample to be used. In conclusion, the developed assay can provide more in-depth information about AF as a sample for genomic in ovo sexing and open new industrial possibilities for developing faster and cheaper assays. Research highlightsO_LIA highly reliable and accurate method for in ovo sexing in early incubation stages is established. C_LIO_LIAllantoic fluid can be easily extracted with minimal invasiveness while providing the necessary genomic material for sexual sorting. C_LIO_LIHINTW was found to be present in both female and male samples due to possible maternal contamination. C_LIO_LIHINTW alone or combined with DMRT-1 gene enables early-onset sexing with 100% accuracy. C_LI
- organism: chicken / avian
- assay: bulk RNA-seq
- research focus: cell type annotation
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- In Ovo Sexing and Genotyping using PCR techniques: A Contribution to the 3R Principles in Chicken Breeding
Claudia Dierks, A. Förster, … Stefanie Altgilbers·Scientific ReportsPeer-reviewed·Feb 21, 2026
- How to prevent chick culling in the poultry industry? Discovery of a new biomarker for in ovo gender screening
Nicolas Drouin, Hyung Lim Elfrink, … Thomas Hankemeier·bioRxiv·Aug 20, 2023
- A novel qPCR-based technique for identifying avian sex: an illustration within embryonic craniofacial bone
Claire J. Houchen, Maria Bergman‐Gonzalez, Erin Ealba Bumann·genesisPeer-reviewed·Jun 24, 2023
- Gender identification in Chicken (Gallus gallus) by PCR using whole blood and dried blood spot on filter paper as template: without prior DNA isolation
S. Dhanasekaran, G. Dhinakar Raj, … Thambidurai Ganesh Babu·bioRxiv·Apr 3, 2016
- A Quantitative Polymerase Chain Reaction Protocol for Sex Identification of Zebra Finch and Chicken Using Blood Samples
Prakrit Subba, Saidat Omowunmi Adeniran-Obey, … Julia M. George·bioRxiv·Aug 27, 2025
- On-farm hatching and contact with adult hen post hatch induce sex-dependent effects on performance and welfare in broiler chickens
L. A. Guilloteau, A. Bertin, … A. Collin·bioRxiv·May 17, 2023