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肉桂油对从患肺炎的绵羊和山羊中分离出的多重耐药菌的抗菌及抗生物膜活性

Antibacterial and Anti-Biofilm Activities of Cinnamon Oil against Multidrug-Resistant Isolated from Pneumonic Sheep and Goats.

作者信息

Mahrous Sara H, El-Balkemy Farouk A, Abo-Zeid Naser Z, El-Mekkawy Mamdouh F, El Damaty Hend M, Elsohaby Ibrahim

机构信息

Infectious Diseases, Department of Animal Medicine, Faculty of Veterinary Medicine, Zagazig University, Zagazig City 44511, Egypt.

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Hong Kong SAR 999077, China.

出版信息

Pathogens. 2023 Sep 6;12(9):1138. doi: 10.3390/pathogens12091138.

Abstract

The primary objectives were to isolate and identify (), and determine the antimicrobial resistance patterns and biofilm formation abilities of the isolates. Additionally, the study aimed to investigate the antimicrobial and anti-biofilm effects of cinnamon oil against isolates. A cross-sectional study was conducted from March 2022 to April 2023 to collect 200 samples (including 156 nasal swabs and 44 lung specimens) from pneumonic sheep and goats admitted to the Veterinary Teaching Hospital of Zagazig University, Egypt. was isolated from a total of 72 (36%) samples, with 53 (73.6%) isolates recovered from nasal swabs and 19 (26.4%) from lung samples. Among the samples, 52 (36.9%) were from sheep and 20 (33.9%) were from goats. Antimicrobial susceptibility testing of the 72 isolates to 18 antimicrobials revealed that all isolates were resistant to ampicillin, amoxicillin/clavulanic acid, cefotaxime, ceftriaxone, tetracycline, colistin, fosfomycin, and trimethoprim/sulphamethoxazole. None of the isolates were resistant to amikacin, imipenem, and norfloxacin. Multidrug resistance (MDR) was observed in all isolates recovered from sheep and goats. The average MAR index was 0.71, ranging from 0.50 to 0.83. Regarding biofilm formation, among the isolates with a high MAR index (n = 30), 10% exhibited strong formation, 40% showed moderate formation, 43.3% displayed weak formation, and 6.7% did not form biofilms. Additionally, the biofilm-forming genes and were present in all 28 biofilm-forming isolates, while the gene was detected in 15 (53.6%) of the 28 isolates. MDR isolates with strong biofilm formation abilities were treated with cinnamon oil at varying concentrations (100%, 75%, 50%, and 25%). This treatment resulted in inhibition zone diameters ranging from 35 to 45 mm. Cinnamon oil exhibited lower minimum inhibitory concentration and minimum bactericidal concentration values compared to norfloxacin for all isolates. Additionally, cinnamon oil significantly reduced the expression of biofilm-associated genes (, , and ) when compared to isolates treated with norfloxacin or untreated. In conclusion, this study identified a high level of MDR with strong and moderate biofilm formation abilities in pneumonic sheep and goats in Sharika Governorate, Egypt. Although cinnamon oil demonstrated potential antibacterial and anti-biofilm properties against , further research is required to investigate its effectiveness in treating infections in pneumonic sheep and goats.

摘要

主要目标是分离和鉴定(),并确定分离株的抗菌药物耐药模式和生物膜形成能力。此外,该研究旨在调查肉桂油对分离株的抗菌和抗生物膜作用。于2022年3月至2023年4月进行了一项横断面研究,从埃及扎加齐格大学兽医教学医院收治的患肺炎的绵羊和山羊中收集了200份样本(包括156份鼻拭子和44份肺标本)。从总共72份(36%)样本中分离出(),其中53份(73.6%)分离株从鼻拭子中回收,19份(26.4%)从肺样本中回收。在这些样本中,52份(36.9%)来自绵羊,20份(33.9%)来自山羊。对72株()分离株进行的18种抗菌药物敏感性测试显示,所有分离株均对氨苄西林、阿莫西林/克拉维酸、头孢噻肟、头孢曲松、四环素、黏菌素、磷霉素和甲氧苄啶/磺胺甲恶唑耐药。没有分离株对阿米卡星、亚胺培南和诺氟沙星耐药。在从绵羊和山羊中回收的所有()分离株中均观察到多重耐药(MDR)。平均多重耐药指数(MAR)为0.71,范围为0.50至0.83。关于生物膜形成,在MAR指数高的()分离株(n = 30)中,10%表现出强形成,40%表现出中等形成,43.3%表现出弱形成,6.7%未形成生物膜。此外,在所有28株形成生物膜的()分离株中均存在生物膜形成基因()和(),而在28株分离株中的15株(53.6%)中检测到()基因。对具有强生物膜形成能力的MDR()分离株用不同浓度(100%、75%、50%和25%)的肉桂油进行处理。该处理导致抑菌圈直径范围为35至45毫米。与诺氟沙星相比,肉桂油对所有分离株的最低抑菌浓度和最低杀菌浓度值更低。此外,与用诺氟沙星处理或未处理的分离株相比,肉桂油显著降低了生物膜相关基因()、()和()的表达。总之,本研究在埃及沙里卡省患肺炎的绵羊和山羊中发现了高水平的具有强和中等生物膜形成能力的MDR()。尽管肉桂油对()显示出潜在的抗菌和抗生物膜特性,但需要进一步研究以调查其在治疗患肺炎的绵羊和山羊的()感染中的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d642/10536549/05ed3fcb5dd4/pathogens-12-01138-g001.jpg

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