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头孢喹肟对健康犬肠道菌群的影响。

Effect of cefovecin on the fecal flora of healthy dogs.

机构信息

Department of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USA.

出版信息

Vet J. 2013 Oct;198(1):259-66. doi: 10.1016/j.tvjl.2013.04.010. Epub 2013 May 20.

DOI:10.1016/j.tvjl.2013.04.010
PMID:23702279
Abstract

Cefovecin is an extended-spectrum long-acting third generation cephalosporin used to treat canine infections. The study objective was to determine the effect of cefovecin on the absolute number and antimicrobial susceptibility of fecal enteric bacteria in healthy dogs. Fourteen Beagles were randomly assigned to a treated (n=7, 8 mg/kg cefovecin subcutaneously on day 1) or untreated (n=7) group. LC/MS was used to determine plasma cefovecin concentration on day 14. E. coli, enterococci, and Salmonella were isolated and enumerated from fecal samples collected on days 0, 3, 7, 14, and 28. Antimicrobial resistance was determined using disc diffusion, MIC, and detected using PCR for the blaCMY-2 gene on select isolates. Mean plasma concentration of cefovecin on day 14 was 9.59 μg/mL in treated dogs; untreated dogs had no measurable plasma cefovecin. The absolute number of E. coli was lower in treated dogs on day 3 (P ≤ 0.0001), and the absolute number of cefovecin-resistant E. coli was higher in treated dogs on days 7 (P=0.002), 14 (P=0.004) and 28 (P ≤ 0.0001), compared to untreated dogs. Enterococci increased and were higher in the treatment group on day 7 (P=0.0226). Isolation of Salmonella was rare. After cefovecin treatment, beta-lactam resistance was more common in fecal E. coli from treated dogs than untreated dogs, while resistance of enterococci was not altered. On day 28, treated dogs were 3.25 times more likely to carry the blaCMY-2 gene than untreated dogs (95% CI 1.27 - 8.35). The implications of these findings in clinically ill patients require further research.

摘要

头孢噻肟是一种用于治疗犬感染的第三代长效广谱头孢菌素。本研究的目的是确定头孢噻肟对健康犬粪便肠道细菌绝对数量和抗菌敏感性的影响。14 只比格犬随机分为治疗组(n=7,皮下注射 8mg/kg 头孢噻肟,第 1 天)和未治疗组(n=7)。第 14 天采用 LC/MS 法测定血浆头孢噻肟浓度。第 0、3、7、14 和 28 天采集粪便样本,分离并计数大肠杆菌、肠球菌和沙门氏菌。采用纸片扩散法、微量肉汤稀释法测定抗菌药物敏感性,对部分分离株采用 PCR 法检测 blaCMY-2 基因。治疗组第 14 天的平均血浆头孢噻肟浓度为 9.59μg/ml;未治疗组无可测量的血浆头孢噻肟浓度。治疗组第 3 天大肠杆菌的绝对数量较低(P≤0.0001),第 7、14 和 28 天头孢噻肟耐药大肠杆菌的绝对数量较高(P=0.002、0.004 和 P≤0.0001)。治疗组第 7 天肠球菌增加,且高于未治疗组(P=0.0226)。沙门氏菌分离少见。头孢噻肟治疗后,治疗组粪便大肠杆菌的β-内酰胺类耐药性较未治疗组更为常见,而肠球菌的耐药性未改变。第 28 天,治疗组携带 blaCMY-2 基因的可能性是未治疗组的 3.25 倍(95%CI 1.27-8.35)。这些发现对临床感染患者的影响需要进一步研究。

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