Potential of Treatment-Specific Protein Biomarker Profiles for Detection of Hormone Abuse in Cattle

被引:16
作者
Ludwig, Susann Katrina Julie [1 ]
Smits, Nathalie Gabrielle Esther [1 ]
Cannizzo, Francesca Tiziana [2 ]
Nielen, Michel Wilhelmus Franciscus [1 ,3 ]
机构
[1] RIKILT Wageningen UR, NL-6700 AE Wageningen, Netherlands
[2] Univ Turin, Dipartimento Patol Anim, Sez Anat Patol, I-10095 Turin, Italy
[3] Wageningen Univ, Lab Organ Chem, NL-6700 EG Wageningen, Netherlands
关键词
biomarker; hormone abuse; veterinary control; multiplex; binding assay; steroids; RECOMBINANT BOVINE SOMATOTROPIN; IGF-BINDING PROTEINS; FLOW-CYTOMETRIC IMMUNOASSAY; GROWTH-FACTOR-I; DEXAMETHASONE TREATMENT; ANTIBODY-FORMATION; INSULIN; SERUM; OSTEOCALCIN; CALVES;
D O I
10.1021/jf4004972
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Targeted protein biomarker profiling is suggested as a fast screening approach for detection of illegal hormone treatment in meat production. The advantage of using biomarkers is that they mark the biological response and, thus, are responsive to a panel of substances with similar effects. In a preliminary feasibility study, a 4-plex protein biomarker flow cytometric immunoassay (FCIA) previously developed for the detection of recombinant bovine somatotropin (rbST) was applied to cattle treated with steroids, such as estradiol, dexamethasone, and prednisolone. Each treatment resulted in a specific plasma biomarker profile for insulin-like growth factor-1 (IGF-1), IGF binding protein 2, osteocalcin, and anti-rbST antibodies, which could be distinguished from the profile of untreated animals. In summary, the 4-plex biomarker FCIA is, apart from rbST, also capable of detecting treatment with other growth-promoting agents and therefore clearly shows the potential of biomarker profiling as a screening method in veterinary control. It is proposed to perform additional validation studies covering high numbers of treated and untreated animals to support inclusion or adaptation of protein biomarker approaches in future monitoring regulations.
引用
收藏
页码:4514 / 4519
页数:6
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