TY - JOUR
T1 - The use of the serum progesterone strip test as a clinical tool for assessing reproductive status in replacement gilts
AU - Taechamaeteekul, Preechaphon
AU - Pimpitak, Umaporn
AU - Suwimonteerabutr, Junpen
AU - Poonlapdecha, Wanwisa
AU - Khun-arwut, Nutthiwut
AU - Komolpis, Kittinan
AU - Rengpipat, Sirirat
AU - Sang-Gassanee, Kridtasak
AU - Lin, Hongyao
AU - Collell, Miquel
AU - Knox, Robert V.
AU - Tummaruk, Padet
N1 - This research project is supported by the National Research Council of Thailand (NRCT) (N42A660892) and Merck Animal Health, USA. P. Taechamaeteekul received PhD Scholarships from the Second Century Fund (C2F), Chulalongkorn University.
PY - 2025/12
Y1 - 2025/12
N2 - Identifying the reproductive status of replacement gilts at the appropriate age can improve mating efficiency and reduce non-productive days. This study aimed to evaluate the reproductive status of gilts and assess the accuracy of a serum progesterone strip test. A total of 112 Landrace × Yorkshire gilts, aged 196–238 days, were enrolled. Estrus detection was performed daily from 189 days of age using the back-pressure test with fence-line boar exposure. Blood samples were collected from all gilts, and serum progesterone levels were determined using both ELISA and a progesterone lateral flow assays (LFAs) strip test. Puberty was defined by an ELISA-based serum progesterone concentration ≥5.0 ng/ml. The LFAs employed a competitive assay using a monoclonal antibody against progesterone. A single test line indicated a ‘positive’ result (pubertal), while two lines indicated ‘negative’ (prepubertal). To perform the test, 2–3 drops of serum were applied to the strip, with results read after 15 min. Based on ELISA, 51.8 % of gilts were pubertal and 48.2 % were prepubertal. Pubertal gilts had significantly higher serum progesterone levels than prepubertal gilts (30.8 ± 11.4 vs. 0.8 ± 0.8 ng/ml; P < 0.001). The LFAs correctly identified 98.2 % of pubertal gilts and 94.4 % of prepubertal gilts, yielding a sensitivity of 98.2 % and specificity of 94.4 %. In conclusion, the progesterone strip test demonstrated high accuracy and shows strong potential for on-farm use in identifying pubertal gilts based on serum progesterone concentration.
AB - Identifying the reproductive status of replacement gilts at the appropriate age can improve mating efficiency and reduce non-productive days. This study aimed to evaluate the reproductive status of gilts and assess the accuracy of a serum progesterone strip test. A total of 112 Landrace × Yorkshire gilts, aged 196–238 days, were enrolled. Estrus detection was performed daily from 189 days of age using the back-pressure test with fence-line boar exposure. Blood samples were collected from all gilts, and serum progesterone levels were determined using both ELISA and a progesterone lateral flow assays (LFAs) strip test. Puberty was defined by an ELISA-based serum progesterone concentration ≥5.0 ng/ml. The LFAs employed a competitive assay using a monoclonal antibody against progesterone. A single test line indicated a ‘positive’ result (pubertal), while two lines indicated ‘negative’ (prepubertal). To perform the test, 2–3 drops of serum were applied to the strip, with results read after 15 min. Based on ELISA, 51.8 % of gilts were pubertal and 48.2 % were prepubertal. Pubertal gilts had significantly higher serum progesterone levels than prepubertal gilts (30.8 ± 11.4 vs. 0.8 ± 0.8 ng/ml; P < 0.001). The LFAs correctly identified 98.2 % of pubertal gilts and 94.4 % of prepubertal gilts, yielding a sensitivity of 98.2 % and specificity of 94.4 %. In conclusion, the progesterone strip test demonstrated high accuracy and shows strong potential for on-farm use in identifying pubertal gilts based on serum progesterone concentration.
KW - Gilts
KW - Progesterone
KW - Puberty
KW - Serum
KW - Strip test
UR - https://www.scopus.com/pages/publications/105012459995
UR - https://www.scopus.com/pages/publications/105012459995#tab=citedBy
U2 - 10.1016/j.theriogenology.2025.117627
DO - 10.1016/j.theriogenology.2025.117627
M3 - Article
C2 - 40780065
AN - SCOPUS:105012459995
SN - 0093-691X
VL - 248
JO - Theriogenology
JF - Theriogenology
M1 - 117627
ER -