Sudan Sudhanshu, Zhan Xiaoshu, Li Julang
Department of Animal Biosciences, University of Guelphgrid.34429.38, Guelph, Ontario, Canada.
Microbiol Spectr. 2022 Aug 31;10(4):e0125721. doi: 10.1128/spectrum.01257-21. Epub 2022 Jun 23.
Enteric infections caused by enterotoxic Escherichia coli (ETEC) negatively impact the growth performance of piglets during weaning, resulting in significant economic losses for the producers. With the ban on antibiotic usage in livestock production, probiotics have gained a lot of attention as a potential alternative. However, strain specificity and limited knowledge on the host-specific targets limit their efficacy in preventing ETEC-related postweaning enteric infections. We recently isolated and characterized a novel probiotic Bacillus subtilis bacterium (CP9) that demonstrated antimicrobial activity. Here, we report anti-ETEC properties of CP9 and its impact on metabolic activity of swine intestinal epithelial (IPEC-J2) cells. Our results showed that pre- or coincubation with CP9 protected IPEC-J2 cells from ETEC-induced cytotoxicity. CP9 significantly attenuated ETEC-induced inflammatory response by reducing ETEC-induced nitric oxide production and relative mRNA expression of the Toll-like receptors (TLRs; TLR2, TLR4, and TLR9), proinflammatory tumor necrosis factor alpha, interleukins (ILs; IL-6 and IL-8), augmenting anti-inflammatory granulocyte-macrophage colony-stimulating factor and host defense peptide mucin 1 (MUC1) mRNA levels. We also show that CP9 significantly (<0.05) reduced caspase-3 activity, reinstated cell proliferation and increased relative expression of tight junction genes, claudin-1, occludin, and zona occludens-1 in ETEC-infected cells. Finally, metabolomic analysis revealed that CP9 exposure induced metabolic modulation in IPEC J2 cells with the greatest impact seen in alanine, aspartate, and glutamate metabolism; pyrimidine metabolism; nicotinate and nicotinamide metabolism; glutathione metabolism; the citrate cycle (TCA cycle); and arginine and proline metabolism. Our study shows that CP9 incubation attenuated ETEC-induced cytotoxicity in IPEC-J2 cells and offers insight into potential application of this probiotic for ETEC infection control. ETEC remains one of the leading causes of postweaning diarrhea and mortality in swine production. Due to the rising concerns with the antibiotic use in livestock, alternative interventions need to be developed. In this study, we analyzed the cytoprotective effect of a novel probiotic strain in combating ETEC infection in swine intestinal cells, along with assessing its mechanism of action. To our knowledge, this is also the first study to analyze the metabolic impact of a probiotic on intestinal cells. Results from this study should provide effective cues in developing a probiotic intervention for ameliorating ETEC infection and improving overall gut health in swine production.
肠毒素性大肠杆菌(ETEC)引起的肠道感染会对仔猪断奶后的生长性能产生负面影响,给养殖户造成重大经济损失。随着畜牧业生产中抗生素使用的禁令出台,益生菌作为一种潜在的替代品受到了广泛关注。然而,菌株特异性以及对宿主特异性靶点的了解有限,限制了它们在预防与ETEC相关的断奶后肠道感染中的功效。我们最近分离并鉴定了一种具有抗菌活性的新型益生菌枯草芽孢杆菌(CP9)。在此,我们报告CP9的抗ETEC特性及其对猪肠上皮(IPEC-J2)细胞代谢活性的影响。我们的结果表明,与CP9预孵育或同时孵育可保护IPEC-J2细胞免受ETEC诱导的细胞毒性。CP9通过降低ETEC诱导的一氧化氮产生以及Toll样受体(TLRs;TLR2、TLR4和TLR9)、促炎肿瘤坏死因子α、白细胞介素(ILs;IL-6和IL-8)的相对mRNA表达,显著减轻了ETEC诱导的炎症反应,同时增加了抗炎粒细胞-巨噬细胞集落刺激因子和宿主防御肽粘蛋白1(MUC1)的mRNA水平。我们还表明,CP9显著(<0.05)降低了caspase-3活性,恢复了细胞增殖,并增加了ETEC感染细胞中紧密连接基因claudin-1、occludin和zonula occludens-1的相对表达。最后,代谢组学分析表明,CP9处理可诱导IPEC J2细胞的代谢调节,其中对丙氨酸、天冬氨酸和谷氨酸代谢;嘧啶代谢;烟酸和烟酰胺代谢;谷胱甘肽代谢;柠檬酸循环(TCA循环);以及精氨酸和脯氨酸代谢的影响最大。我们的研究表明,CP9孵育可减轻ETEC诱导的IPEC-J2细胞毒性,并为这种益生菌在控制ETEC感染中的潜在应用提供了见解。ETEC仍然是猪生产中断奶后腹泻和死亡的主要原因之一。由于对畜牧业中抗生素使用的担忧日益增加,需要开发替代干预措施。在本研究中,我们分析了一种新型益生菌菌株在对抗猪肠道细胞中ETEC感染时的细胞保护作用,并评估了其作用机制。据我们所知,这也是第一项分析益生菌对肠道细胞代谢影响的研究。本研究的结果应为开发益生菌干预措施以改善ETEC感染和提高猪生产中的整体肠道健康提供有效线索。