Laboratory of Veterinary Pharmacokinetics and Pharmacodynamics, Institute for Veterinary Biomedical Science, College of Veterinary Medicine, Kyungpook National University, Daegu, 41566, Republic of Korea.
Institute for Tuberculosis Research, College of Pharmacy, University of Illinois Chicago, 833 S Wood St, Chicago, IL, 60612, USA.
Sci Rep. 2024 Aug 12;14(1):18670. doi: 10.1038/s41598-024-69566-2.
Tylosin, an antibiotic with a long history in treating respiratory bacterial infections, has unknown effects on the gut microbiota of healthy and infected pigs. The study aimed to investigate the effect of a therapeutic dose of tylosin on swine gut microbiota and explored the relationship between this effect and tylosin pharmacokinetics (PK). We also assessed whether changes in gut microbiota after tylosin administration differ between healthy animals (n = 7) and animals intranasally co-infected (n = 7) with Actinobacillus pleuropneumoniae and Pasteurella multocida. Both groups were intramuscularly administered with tylosin (20 mg/kg). The 16S rRNA gene analyses revealed a significantly lower species richness and diversity, after tylosin treatment, in the infected than the healthy pigs, with infected pigs having lower levels of Bacteroidetes and Firmicutes and higher levels of Proteobacteria. Greater tylosin exposure (greater area under curve (AUC) and maximum plasma concentration (C), and slower elimination (longer terminal half-life, T) were observed in healthy than infected pigs. Relative abundance of Lactobacillus, Oscillibacter, Prevotella, and Sporobacter was positively and significantly correlated with AUC and C, whereas the abundance of Acinetobacter, Alishewanella, and Pseudomonas was positively and significantly correlated with T and mean residence time (MRT) of tylosin. Our findings, for the first time, demonstrated significant changes in swine gut microbiota after a single therapeutic dose of tylosin was administered, whereas the effect of these changes on tylosin PK was not evident.
泰乐菌素是一种治疗呼吸道细菌感染的抗生素,其对健康和感染猪的肠道微生物群的影响尚不清楚。本研究旨在研究治疗剂量的泰乐菌素对猪肠道微生物群的影响,并探讨这种影响与泰乐菌素药代动力学(PK)之间的关系。我们还评估了在泰乐菌素给药后,健康动物(n=7)和猪传染性胸膜肺炎放线杆菌和多杀性巴氏杆菌鼻内共感染动物(n=7)的肠道微生物群变化是否不同。两组均肌肉注射泰乐菌素(20mg/kg)。16S rRNA 基因分析显示,与健康猪相比,感染猪在泰乐菌素治疗后物种丰富度和多样性显著降低,感染猪的拟杆菌门和厚壁菌门水平较低,变形菌门水平较高。与感染猪相比,健康猪的泰乐菌素暴露量更大(曲线下面积(AUC)和最大血浆浓度(C)更大,消除速度更慢(半衰期(T)更长)。与 AUC 和 C 呈正相关且显著相关的乳杆菌、 Oscillibacter、普雷沃氏菌和 Sporobacter 的相对丰度增加,而不动杆菌、Alishewanella 和铜绿假单胞菌的丰度与 T 和泰乐菌素的平均驻留时间(MRT)呈正相关且显著相关。我们的研究结果首次表明,猪单次给予治疗剂量的泰乐菌素后,肠道微生物群发生了显著变化,但这些变化对泰乐菌素 PK 的影响尚不清楚。