Analytical and clinical validation of diagnostic tests for the detection of leucospermia in beef bulls

IF 2.4 2区 农林科学 Q3 REPRODUCTIVE BIOLOGY
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Abstract

The objectives of this study were to validate diagnostic tests to detect polymorphonuclear cells (PMNs) in bull semen, and to determine the prevalence of leucospermia in beef bulls with varying semen quality. We hypothesized that all tests have comparable diagnostic value, and that leucospermia is more prevalent in unsatisfactory breeders in association with poor semen quality. For the analytical validation, one ejaculate was obtained from five bulls. Aliquots of 50 × 106 purified sperm were incubated in triplicate with six concentrations of purified bovine PMNs: 1) no PMNs, 2) 0.25 × 106 PMN/ml, 3) 0.5 × 106 PMN/ml, 4) 2.5 × 106 PMN/ml, 5) 5 × 106 PMN/ml, 6) 10 × 106 PMN/ml. The PMNs were quantified using a hemacytometer, cytology, a leucocyte esterase dipstick test (LEDT), a peroxidase test, and CD45 immunolabeling. The number of leucocytes detected with the LEDT differed among treatments (P < 0.0001). The quantitative tests detected differences with the control treatment at a PMN concentration of ≥2.5 × 106 PMN/ml (P < 0.0001). Sperm motion parameters after 4 h of incubation at 38 °C were lower in samples with ≥5 × 106 PMN/ml (P < 0.05). For the clinical validation, semen samples from 305 beef bulls were evaluated. Unsatisfactory breeders (n = 83) had more CD45-positive cells (P = 0.016) and positive LEDT results (P = 0.008) than satisfactory breeders (n = 222). With CD45 immunostaining as the gold standard, the hemacytometer count had the highest clinical sensitivity (64.3 %) but the lowest specificity (73.3 %). A higher specificity was obtained with the peroxidase test (95.1 %) or semen cytology (98.8 %). In conclusion, the presence of ≥5 × 106 PMN/ml was associated with decreased semen quality in beef bulls. The hemacytometer count was the most sensitive bull-side test. But due to the low specificity, positive hemacytometer counts should be confirmed with the identification of peroxidase-positive cells or morphological identification of leucocytes on semen cytology. The CD45 immunostaining is the gold standard for the diagnosis of leucospermia in bulls.

检测肉牛白精子症的诊断测试的分析和临床验证
本研究的目的是验证检测公牛精液中多形核细胞(PMN)的诊断测试,并确定不同精液质量的肉用公牛白精症的发病率。我们假设所有检测方法都具有相当的诊断价值,而在精液质量较差的不合格种公牛中,白精子症更为普遍。为了进行分析验证,我们从五头公牛身上提取了一份精液。将 50 × 106 个纯化精子的等分试样与六种浓度的纯化牛 PMN 一起孵育,每种浓度的试样一式三份:1) 无 PMN,2) 0.25 × 106 PMN/ml,3) 0.5 × 106 PMN/ml,4) 2.5 × 106 PMN/ml,5) 5 × 106 PMN/ml,6) 10 × 106 PMN/ml。使用血细胞计数器、细胞学、白细胞酯酶滴定测试(LEDT)、过氧化物酶测试和 CD45 免疫标记法对 PMN 进行定量。LEDT 检测到的白细胞数量在不同处理之间存在差异(P < 0.0001)。定量检测发现,在 PMN 浓度≥2.5×106 PMN/ml 时,与对照处理存在差异(P < 0.0001)。38 °C下培养4小时后,PMN浓度≥5 × 106 PMN/ml的样本精子运动参数较低(P <0.05)。为了进行临床验证,对 305 头肉用公牛的精液样本进行了评估。不合格种公牛(n = 83)比合格种公牛(n = 222)有更多的 CD45 阳性细胞(P = 0.016)和 LEDT 阳性结果(P = 0.008)。以 CD45 免疫染色为金标准,血细胞计数器计数的临床灵敏度最高(64.3%),但特异性最低(73.3%)。过氧化物酶检测(95.1%)或精液细胞学检测(98.8%)的特异性更高。总之,PMN ≥5 × 106/ml与肉用公牛精液质量下降有关。血细胞计数器计数是最灵敏的公牛侧检测方法。但由于特异性较低,血细胞计数阳性应通过过氧化物酶阳性细胞鉴定或精液细胞学白细胞形态鉴定来确认。CD45 免疫染色是诊断公牛白精子症的金标准。
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来源期刊
Theriogenology
Theriogenology 农林科学-生殖生物学
CiteScore
5.50
自引率
14.30%
发文量
387
审稿时长
72 days
期刊介绍: Theriogenology provides an international forum for researchers, clinicians, and industry professionals in animal reproductive biology. This acclaimed journal publishes articles on a wide range of topics in reproductive and developmental biology, of domestic mammal, avian, and aquatic species as well as wild species which are the object of veterinary care in research or conservation programs.
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