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在德国北部的一项田间研究中,使用PathoProof实时聚合酶链反应检测法与传统细菌培养法对奶牛乳腺炎进行诊断的比较

Mastitis diagnosis in dairy cows using PathoProof real-time polymerase chain reaction assay in comparison with conventional bacterial culture in a Northern German field study.

作者信息

Spittel Susanne, Hoedemaker Martina

机构信息

Production Medicine Unit, Clinic for Cattle, University of Veterinary Medicine, Hannover, Germany.

出版信息

Berl Munch Tierarztl Wochenschr. 2012 Nov-Dec;125(11-12):494-502.

Abstract

In the following field study, the commercial PathoProof Mastitis PCR Assay, a real-time PCR for identifying eleven mastitis pathogens and the staphylococcal beta-lactamase gene, was compared with conventional bacterial culture. For this purpose, 681 udder quarter samples from 173 clinically healthy cows with varying somatic cell count from four dairy herds in the region of Osnabrück, Lower Saxony, Germany, were collected between July 2010 and February 2011 and subjected to PCR and bacterial culture. The frequency of positive pathogen signals was markedly higher with PCR compared with culture (70.6% vs. 32.2%). This was accompanied by a substantial higher percentage of multiple pathogen identifications and a lower percentage of single identifications in the PCR compared with bacterial culture. Using bacterial culture as gold standard, moderate to high sensitivities (76.9-100%) and specificities (63.3-98.7%) were calculated for six out of seven pathogens with sufficient detection numbers. For Enterococcus spp, the sensitivity was only 9.1%. When the PCR results of pooled udder quarter samples of the 173 cows were compared with the single udder quarter samples, in 72% of the cases, major pathogen DNA was either not found in both types of samples, or in the case of a positive pool sample, the respective pathogens were found in at least one udder quarter sample. With both methods, the most frequently detected mastitis pathogens were coryneform bacteria (PCR: Corynebacterium bovis), coagulase-negative staphylococci (CNS) and Staphylococcus (S.) aureus, followed by Arcanobacterium pyogenes/Peptoniphilus indolicus with PCR, and then with both methods, Streptococcus uberis. The staphylococcal beta-lactamase gene was found in 27.7% of the S. aureus and in 37.0% of the CNS identifications.

摘要

在以下现场研究中,将商业化的PathoProof乳腺炎PCR检测法(一种用于鉴定11种乳腺炎病原体和葡萄球菌β-内酰胺酶基因的实时PCR方法)与传统细菌培养法进行了比较。为此,在2010年7月至2011年2月期间,从德国下萨克森州奥斯纳布吕克地区四个奶牛场的173头临床健康、体细胞计数各异的奶牛身上采集了681份乳腺象限样本,并进行了PCR和细菌培养。与培养法相比,PCR检测到的病原体阳性信号频率明显更高(70.6%对32.2%)。这伴随着PCR检测中多重病原体鉴定的百分比大幅提高,而单一鉴定的百分比低于细菌培养法。以细菌培养为金标准,对七种病原体中检测数量充足的六种病原体计算出了中度至高度的敏感性(76.9 - 100%)和特异性(63.3 - 98.7%)。对于肠球菌属,敏感性仅为9.1%。当将173头奶牛的乳腺象限混合样本的PCR结果与单个乳腺象限样本的结果进行比较时,在72%的病例中,两种类型的样本中要么都未检测到主要病原体DNA,要么在混合样本呈阳性的情况下,至少在一个乳腺象限样本中发现了相应的病原体。两种方法检测到的最常见乳腺炎病原体都是棒状杆菌(PCR检测为牛棒状杆菌)、凝固酶阴性葡萄球菌(CNS)和金黄色葡萄球菌(S. aureus),其次是PCR检测到的化脓隐秘杆菌/产吲哚普雷沃菌,然后两种方法都检测到的是乳房链球菌。在27.7%的金黄色葡萄球菌鉴定结果和37.0%的CNS鉴定结果中发现了葡萄球菌β-内酰胺酶基因。

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