Fujian Key Laboratory of Traditional Chinese Veterinary Medicine and Animal Health, College of Animal Sciences (College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Fujian Key Laboratory of Traditional Chinese Veterinary Medicine and Animal Health, College of Animal Sciences (College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
J Therm Biol. 2024 Feb;120:103786. doi: 10.1016/j.jtherbio.2024.103786. Epub 2024 Jan 28.
Heat stress is a common environmental factor in livestock breeding that has been shown to impact the development of antibiotic resistance within the gut microbiota of both human and animals. However, studies investigating the effect of temperature on antibiotic resistance in Enterococcus isolates remain limited. In this study, specific pathogen free (SPF) mice were divided into a control group maintained at normal temperature and an experimental group subjected to daily 1-h heat stress at 38 °C, respectively. Gene expression analysis was conducted to evaluate the activation of heat shock responsive genes in the liver of mice. Additionally, the antibiotic-resistant profile and antibiotic resistant genes (ARGs) in fecal samples from mice were analyzed. The results showed an upregulation of heat-inducible proteins HSP27, HSP70 and HSP90 following heat stress exposure, indicating successful induction of cellular stress within the mice. Furthermore, heat stress resulted in an increase in the proportion of erythromycin-resistant Enterococcus isolates, escalating from 0 % to 0.23 % over a 30-day duration of heat stress. The resistance of Enterococcus isolates to erythromycin also had a 128-fold increase in minimum inhibitory concentration (MIC) within the heated-stressed group compared to the control group. Additionally, a 2∼8-fold rise in chloramphenicol MIC was observed among these erythromycin-resistant Enterococcus isolates. The acquisition of ermB genes was predominantly responsible for mediating the erythromycin resistance in these Enterococcus isolates. Moreover, the abundance of macrolide, lincosamide and streptogramin (MLS) resistant-related genes in the fecal samples from the heat-stressed group exhibited a significant elevation compared to the control group, primarily driven by changes in bacterial community composition, especially Enterococcaceae and Planococcaceae, and the transfer of mobile genetic elements (MGEs), particularly insertion elements. Collectively, these results highlight the role of environmental heat stress in promoting antibiotic resistance in Enterococcus isolates and partly explain the increasing prevalence of erythromycin-resistant Enterococcus isolates observed among animals in recent years.
热应激是家畜养殖中常见的环境因素,已被证明会影响人类和动物肠道微生物群中抗生素耐药性的发展。然而,研究温度对肠球菌分离株抗生素耐药性影响的研究仍然有限。在这项研究中,无菌(SPF)小鼠分为对照组,维持在正常温度,实验组每天在 38°C 下进行 1 小时热应激,分别。进行基因表达分析以评估小鼠肝脏中热休克反应基因的激活情况。此外,还分析了来自小鼠粪便样本中的抗生素耐药谱和抗生素耐药基因(ARGs)。结果表明,热应激暴露后热诱导蛋白 HSP27、HSP70 和 HSP90 的表达上调,表明细胞应激在小鼠体内成功诱导。此外,热应激导致红霉素耐药肠球菌分离株的比例增加,在 30 天的热应激期间,从 0%增加到 0.23%。与对照组相比,加热应激组肠球菌分离株对红霉素的耐药性也使最低抑菌浓度(MIC)增加了 128 倍。此外,这些红霉素耐药肠球菌分离株的氯霉素 MIC 增加了 2∼8 倍。ermB 基因的获得主要负责介导这些肠球菌分离株对红霉素的耐药性。此外,与对照组相比,热应激组粪便样本中大环内酯、林可酰胺和链阳性菌素(MLS)耐药相关基因的丰度显著升高,主要是由于细菌群落组成的变化,特别是肠球菌科和片球菌科,以及移动遗传元件(MGEs)的转移,特别是插入元件。总之,这些结果强调了环境热应激在促进肠球菌分离株抗生素耐药性方面的作用,并部分解释了近年来动物中红霉素耐药肠球菌分离株日益增多的原因。