Department of Pathology and Microbiology, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, QC, J2S 2M2, Canada.
Groupe de Recherche et d'Enseignement en Salubrité Alimentaire (GRESA), Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, QC, J2S 2M2, Canada.
BMC Vet Res. 2024 Oct 29;20(1):492. doi: 10.1186/s12917-024-04329-9.
Antimicrobial resistance (AMR) is a global concern impacting both humans, animals and their environment. The use of oral antimicrobials in livestock, particularly in pigs, has been identified as a driver in the selection of AMR bacteria. The aim of the present study was to evaluate the effects of a single intramuscular (IM) dose of marbofloxacin (8 mg/kg) on Enterobacteriaceae and E. coli populations, as well as on fluoroquinolone resistance within the fecal microbiota of pigs. Twenty healthy pigs, 60-days old, were divided into two groups: a treated group (n = 13) and a control group (n = 7) and were monitored over a 28-day experimental period. Fecal samples were collected from all animals for the isolation of E. coli and Salmonella strains. The minimum inhibitory concentration (MIC) of marbofloxacin for the isolates recovered on MacConkey agar supplemented with 1 or 4 µg/mL of marbofloxacin and for some generic E. coli isolates (recovered from MacConkey agar not supplemented with marbofloxacin) was determined using the broth microdilution method. Genomic DNA was extracted from the confirmed bacterial strains and sequenced using the Sanger method to identify mutations in the quinolone resistance determining regions (QRDRs) of the gyrA and parC genes.
The single IM administration of marbofloxacin resulted in a significant decrease in Enterobacteriaceae and E. coli fecal populations from days 1 to 3 post- treatment. No Salmonella isolates were detected in either group, and no marbofloxacin-resistant E. coli isolates were identified. The MIC of the selected generic E. coli strains (n = 100) showed an increase to up to 0.5 µg/mL between days 1 and 3 post-treatment but remained below the clinical breakpoint of marbofloxacin resistance (4 µg/mL). Sequencing of these isolates revealed no mutations in gyrA and parC genes.
The present study showed that this dosing regimen of marbofloxacin significantly decreases the fecal shedding of Enterobacteriaceae and E. coli populations in pigs, while limiting the selection of marbofloxacin-resistant E. coli isolates. These findings warrant validation in sick pigs to support the selective use of this antibiotic solely in cases of clinical disease, thereby minimizing the reliance on conventional (metaphylactic) group treatments in pigs.
抗菌药物耐药性(AMR)是一个全球性问题,影响着人类、动物及其环境。在畜牧业中使用口服抗菌药物,特别是在猪中,已被确定为选择 AMR 细菌的驱动因素。本研究的目的是评估单肌内(IM)剂量马波沙星(8mg/kg)对猪肠道菌和大肠杆菌种群以及粪便微生物群中氟喹诺酮耐药性的影响。20 头 60 天大的健康猪被分为两组:治疗组(n=13)和对照组(n=7),并在 28 天的实验期间进行监测。所有动物的粪便样本均用于分离大肠杆菌和沙门氏菌菌株。从补充了 1 或 4µg/ml 马波沙星的 MacConkey 琼脂上回收的分离物以及从未补充马波沙星的 MacConkey 琼脂上回收的一些通用大肠杆菌分离物的最小抑菌浓度(MIC)使用肉汤微量稀释法确定。从确认的细菌株中提取基因组 DNA,并使用 Sanger 法测序,以鉴定 gyrA 和 parC 基因中喹诺酮耐药决定区(QRDR)的突变。
单次肌内注射马波沙星可导致治疗后 1 至 3 天粪便中肠杆菌科和大肠杆菌数量显著减少。两组均未检测到沙门氏菌分离株,也未鉴定出马波沙星耐药的大肠杆菌分离株。所选通用大肠杆菌株(n=100)的 MIC 在治疗后 1 至 3 天内增加至高达 0.5µg/ml,但仍低于马波沙星耐药的临床临界值(4µg/ml)。对这些分离株的测序未发现 gyrA 和 parC 基因的突变。
本研究表明,这种马波沙星剂量方案可显著降低猪肠道菌和大肠杆菌种群的粪便脱落,同时限制马波沙星耐药大肠杆菌分离株的选择。这些发现需要在患病猪中进行验证,以支持仅在临床疾病的情况下选择性使用这种抗生素,从而最大限度地减少猪中常规(预防)群体治疗的依赖。