Hao Haihong, Gokulan Kuppan, Piñeiro Silvia A, Williams Katherine M, Yuan Zonghui, Cerniglia Carl E, Khare Sangeeta
Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, 3900 NCTR Rd, Jefferson, AR 72079, USA.
National Reference Laboratory of Veterinary Drug Residues (HZAU), College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.
Microorganisms. 2019 Sep 6;7(9):325. doi: 10.3390/microorganisms7090325.
Residual concentrations of erythromycin in food could result in gastrointestinal tract exposure that potentially poses a health-hazard to the consumer, affecting intestinal epithelial permeability, barrier function, microbiota composition, and antimicrobial resistance. We investigated the effects of erythromycin after acute (48 h single treatment with 0.03 μg/mL to 300 μg/mL) or chronic (repeated treatment with 0.3 µg/mL and 300 µg/mL erythromycin for five days) exposures on the permeability of human colonic epithelial cells, a model that mimics a susceptible intestinal surface devoid of commensal microbiota. Transepithelial electrical resistance (TER) measurements indicated that erythromycin above 0.3 µg/mL may compromise the epithelial barrier. Acute exposure increased cytotoxicity, while chronic exposure decreased the cytotoxicity. Quantitative PCR analysis revealed that only (intercellular adhesion molecule 1) was up-regulated during 0.3 μg/mL acute-exposure, while , (junctional adhesion molecule 3), and (integrin alpha 8), were over-expressed in the 300 μg/mL acute treatment group. However, during chronic exposure, no change in the mRNA expression was observed at 0.3 μg/mL, and only was significantly up-regulated after 300 μg/mL. and are known to be involved in the formation of extracellular matrices. These gene expression changes may be related to the immunoregulatory activity of erythromycin, or a compensatory mechanism of the epithelial cells to overcome the distress caused by erythromycin due to increased permeability.
食物中残留的红霉素浓度可能导致胃肠道接触,这可能对消费者构成健康危害,影响肠道上皮通透性、屏障功能、微生物群组成和抗菌药物耐药性。我们研究了急性(48小时单次用0.03μg/mL至300μg/mL处理)或慢性(用0.3μg/mL和300μg/mL红霉素重复处理五天)暴露后红霉素对人结肠上皮细胞通透性的影响,该模型模拟了一个缺乏共生微生物群的易感肠道表面。跨上皮电阻(TER)测量表明,高于0.3μg/mL的红霉素可能会损害上皮屏障。急性暴露增加细胞毒性,而慢性暴露降低细胞毒性。定量PCR分析显示,在0.3μg/mL急性暴露期间,只有细胞间黏附分子1(ICAM-1)上调,而在300μg/mL急性处理组中,紧密连接蛋白1(ZO-1)、连接黏附分子3(JAM-3)和整合素α8(ITGA8)均过表达。然而,在慢性暴露期间,0.3μg/mL时mRNA表达未观察到变化,300μg/mL后只有ICAM-1显著上调。已知ZO-1和JAM-3参与细胞外基质的形成。这些基因表达变化可能与红霉素的免疫调节活性有关,或者是上皮细胞为克服因通透性增加而由红霉素引起的应激的一种代偿机制。