Zeineldin Mohamed M, Lehman Kimberly, Camp Patrick, Farrell David, Thacker Tyler C
National Veterinary Services Laboratories, Veterinary Services, Animal and Plant Health Inspection Service, United States Department of Agriculture, Ames, IA 50010, USA.
Pathogens. 2023 Jul 25;12(8):972. doi: 10.3390/pathogens12080972.
The ability of () to survive in bovine milk has emerged as a serious public health concern. The first objective of this study was to evaluate the diagnostic utility of IS1081-targeted real-time PCR for the detection of DNA in different fractions of bovine milk. In a model study, bovine milk samples were spiked with serially diluted BCG to investigate the detection limit of DNA in whole milk and milk fractions (cream, pellet, and pellet + cream combined) using IS1081 real-time PCR. The assay was then used to detect DNA in whole milk and milk fractions from naturally infected animals. The results showed that the IS1081 real-time PCR was more sensitive when detecting DNA in the cream layer alone and cream + pellet combined compared to whole milk or the pellet alone. While PCR-based diagnostic assays for the detection of in milk samples provide a quicker diagnostic tool for bovine tuberculosis, safe processing, and handling of -infected milk samples remain a challenge and pose a human health risk. PrimeStore Molecular Transport Medium (MTM) has been shown to rapidly inactivate infected specimens while preserving nucleic acid for subsequent Molecular analysis. Therefore, the secondary objective of this study was to evaluate the ability of MTM to inactivate BCG in spiked milk samples as well as its ability to preserve BCG DNA for the PCR assay. The results showed that MTM can successfully inactivate BCG alone or in spiked milk samples while preserving DNA for the PCR assay. The CT values of BCG alone and spiked milk samples aliquoted in MTM and without MTM were similar at various dilutions. Taken together, our results indicate that using DNA extracted from the milk cream fraction alone or combined milk cream and pellet improved the recovery rate of DNA in bovine milk samples. MTM has the potential to provide a safe and rapid sample processing tool for inactivation in milk samples and preserve DNA for molecular diagnostics.
()在牛乳中存活的能力已成为一个严重的公共卫生问题。本研究的首要目标是评估靶向IS1081的实时荧光定量PCR检测牛乳不同组分中()DNA的诊断效用。在一项模型研究中,向牛乳样品中加入系列稀释的卡介苗,以使用IS1081实时荧光定量PCR研究全脂牛奶及牛奶各组分(奶油、沉淀以及沉淀+奶油混合物)中()DNA的检测限。然后该检测方法用于检测自然感染动物的全脂牛奶及牛奶各组分中的()DNA。结果表明,与全脂牛奶或单独的沉淀相比,IS1081实时荧光定量PCR在单独检测奶油层以及奶油+沉淀混合物中的()DNA时更为灵敏。虽然基于PCR的诊断检测方法可用于检测牛奶样品中的(),为牛结核病提供了一种更快的诊断工具,但安全处理和处理感染()的牛奶样品仍然是一项挑战,并对人类健康构成风险。PrimeStore分子转运培养基(MTM)已被证明能快速使感染样本失活,同时保留核酸用于后续分子分析。因此,本研究的次要目标是评估MTM使加样牛奶样品中的卡介苗失活的能力及其为PCR检测保留卡介苗DNA的能力。结果表明,MTM可成功使单独的卡介苗或加样牛奶样品失活,同时保留用于PCR检测的DNA。在不同稀释度下,单独的卡介苗以及加样到MTM中和未加MTM的牛奶样品中的卡介苗的CT值相似。综上所述,我们的结果表明,仅使用从牛奶奶油组分中提取的DNA或奶油与沉淀的混合DNA可提高牛乳样品中()DNA的回收率。MTM有潜力为牛奶样品中()的失活提供一种安全快速的样品处理工具,并保留用于分子诊断的DNA。