Department of Veterinary Medicine and Animal Sciences, University of Milan, Lodi, Italy.
Laboratory of Animal Infectious Diseases (MiLab), University of Milan, Lodi, Italy.
BMC Vet Res. 2024 Oct 3;20(1):447. doi: 10.1186/s12917-024-04014-x.
Dairy cow milking practices require cleaning and disinfection of the teat skin before and after milking to ensure the safety and quality of milk and prevent intramammary infections. Antimicrobial proteins of natural origin can be valuable alternatives to traditional disinfectants. In a recent field trial, we demonstrated that a teat dip based on a nisin A-producing Lactococcus cremoris (L) had comparable efficacy to conventional iodophor dip (C) in preventing dairy cow mastitis. Here, we present the differential shotgun proteomics investigation of the milk collected during the trial.
Four groups of quarter milk samples with low (LSCC) and high somatic cell count (HSCC) collected at the beginning (T0) and end (TF) of the trial were analyzed for a total of 28 LSCC (14 LSCC T0 and 14 LSCC TF) and 12 HSCC (6 HSCC T0 and 6 HSCC TF) samples. Milk proteins were digested into peptides, separated by nanoHPLC, and analyzed by tandem mass spectrometry (LC-MS/MS) on an Orbitrap Fusion Tribrid mass spectrometer. The proteins were identified with MaxQuant and interaction networks of the differential proteins were investigated with STRING. The proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD045030.
In healthy milk (LSCC), we detected 90 and 80 differential proteins at T0 and TF, respectively. At TF, the Lactococcus group showed higher levels of antimicrobial proteins. In mastitis milk (HSCC), we detected 88 and 106 differential proteins at T0 and TF, respectively. In the Lactococcus group, 14 proteins with antimicrobial and immune defense functions were enriched at TF vs. 4 proteins at T0. Cathelicidins were among the most relevant enriched proteins. Western immunoblotting validation confirmed the differential abundance.
At T0, the proteomic differences observed in healthy milk of the two groups were most likely dependent on physiological variation. On the other hand, antimicrobial and immune defense functions were higher in the milk of cows with mammary gland inflammation of the Lactococcus-treated group. Among other factors, the immunostimulatory action of nisin A might be considered as a contributor.
奶牛挤奶操作需要在挤奶前后对乳头皮肤进行清洗和消毒,以确保牛奶的安全和质量,并防止乳房感染。天然来源的抗菌蛋白可以作为传统消毒剂的有价值替代品。在最近的一项田间试验中,我们证明了一种基于产乳链球Nisin A 的奶头浸液(L)在预防奶牛乳腺炎方面与传统的碘伏浸液(C)具有相当的功效。在这里,我们介绍了该试验中收集的牛奶的差异 shotgun 蛋白质组学研究。
共分析了四组低体细胞计数(LSCC)和高体细胞计数(HSCC)的四分奶样,每组 14 个 LSCC (14 个 LSCC T0 和 14 个 LSCC TF)和 6 个 HSCC (6 个 HSCC T0 和 6 个 HSCC TF)。将牛奶蛋白消化成肽,通过纳升 HPLC 分离,并在 Orbitrap Fusion Tribrid 质谱仪上进行串联质谱(LC-MS/MS)分析。使用 MaxQuant 鉴定蛋白质,并使用 STRING 研究差异蛋白的相互作用网络。蛋白质组学数据已通过 PRIDE 合作伙伴知识库通过 ProteomeXchange 联盟进行了存储,数据集标识符为 PXD045030。
在健康牛奶(LSCC)中,我们分别在 T0 和 TF 时检测到 90 种和 80 种差异蛋白。在 TF 时,乳球菌组显示出更高水平的抗菌蛋白。在乳腺炎牛奶(HSCC)中,我们分别在 T0 和 TF 时检测到 88 种和 106 种差异蛋白。在乳球菌组中,在 TF 时,14 种具有抗菌和免疫防御功能的蛋白比在 T0 时的 4 种蛋白更丰富。抗菌肽是最相关的富集蛋白之一。Western 免疫印迹验证证实了差异丰度。
在 T0,两组健康牛奶中观察到的蛋白质组差异很可能取决于生理变化。另一方面,在乳球菌处理组的乳腺炎奶牛的牛奶中,抗菌和免疫防御功能更高。在其他因素中,乳链菌肽 A 的免疫刺激作用可以被认为是一个贡献因素。