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In Vitro Antimicrobial Susceptibility Testing of Bacterial Enteropathogens Causing Travelers Diarrhea in Four Geographic Regions

机译:在四个地理区域引起旅行者腹泻的细菌性肠病原菌的体外抗菌药敏试验

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摘要

The emergence of resistant enteropathogens has been reported worldwide. Few data are available on the contemporary in vitro activities of commonly used antimicrobial agents against enteropathogens causing traveler's diarrhea (TD). The susceptibility patterns of antimicrobial agents currently available or under evaluation against pathogens causing TD in four different areas of the world were evaluated. Pathogens were identified in stool samples from U.S., Canadian, or European adults (18 years of age or older) with TD during 1997, visiting India, Mexico, Jamaica, or Kenya. MICs of 11different antimicrobials were determined against 284 bacterial enteropathogens by the agar dilution method. Ciprofloxacin, levofloxacin, ceftriaxone, and azithromycin were highly active in vitro against the enteropathogens, while traditional antimicrobials such as ampicillin, trimethoprim, and trimethoprim/sulfamethoxazole showed high levels and high frequencies of resistance. Rifaximin, a promising and poorly absorbable drug, had an MIC at which 90% of the strains tested were inhibited of 32 μg/ml, 250 times lower than the concentration of this drug in the stools. Amdinocillin, nalidixic acid, and doxycycline showed moderate activity. Fluoroquinolones are still the drugs of choice for TD in most regions of the world, although our study has a limitation due to the lack of Escherichia coli samples from Kenya and possible bias in selection of the patients for evaluation. Azithromycin and rifaximin should be considered as promising new agents. The widespread in vitro resistance of the traditional antimicrobial agents reported since the 1980s and the new finding of resistance to fluoroquinolones in Southeast Asia are the main reasons for monitoring carefully the antimicrobial susceptibility patterns worldwide and for developing and evaluating new antimicrobial agents for the treatment of TD.
机译:耐药性肠病原菌的出现已在世界范围内报道。关于常用抗微生物剂对引起旅行者腹泻(TD)的肠病原菌的当代体外活性的可用数据很少。评估了目前可用或正在评估中的抗微生物剂对世界上四个不同地区引起TD的病原体的敏感性模式。在1997年期间访问印度,墨西哥,牙买加或肯尼亚的美国,加拿大或欧洲成年人(18岁以上)的粪便样本中鉴定出病原体。通过琼脂稀释法确定了针对284种细菌性肠病原菌的11种不同抗菌药物的MIC。环丙沙星,左氧氟沙星,头孢曲松和阿奇霉素在体外对肠病原体具有很高的活性,而传统的抗菌药物(如氨苄青霉素,甲氧苄氨嘧啶和甲氧苄氨嘧啶/磺胺甲恶唑)显示出高水平和高频率的耐药性。利福昔明是一种有前途且难以吸收的药物,其MIC抑制率为90%,测试菌株的抑制率为32μg/ ml,比粪便中该药物的浓度低250倍。 Amdinocillin,萘啶酸和强力霉素显示中等活性。氟喹诺酮类药物在世界上大多数地区仍然是TD的首选药物,尽管我们的研究由于缺乏来自肯尼亚的大肠杆菌样本以及在选择患者进行评估方面存在偏见而受到限制。阿奇霉素和利福昔明应被视为有希望的新药。自1980年代以来报道的传统抗微生物剂广泛的体外耐药性以及东南亚地区对氟喹诺酮类耐药性的新发现是在全球范围内仔细监测抗菌药敏感性模式以及开发和评估用于治疗TD的新抗菌剂的主要原因。

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