Manzulli Viviana, Fasanella Antonio, Parisi Antonio, Serrecchia Luigina, Donatiello Adelia, Rondinone Valeria, Caruso Marta, Zange Sabine, Tscherne Alina, Decaro Nicola, Pedarra Carmine, Galante Domenico
Anthrax Reference Institute of Italy, Experimental Zooprophylactic Institute of Puglia and Basilicata Regions, Foggia 71121, Italy.
Bundeswehr Institute of Microbiology, Munich 80937, Germany.
J Vet Sci. 2019 Jan 31;20(1):58-62. doi: 10.4142/jvs.2019.20.1.58.
Anthrax, caused by , is a non-contagious infectious disease that affects a wide range of animal species (primarily ruminants) including humans. Due to the often-fatal outcome in humans, quick administration of definitely effective antimicrobials is crucial either as prophylaxis or as a clinical case therapy. In this study, 110 strains, temporally, geographically, and genetically different, isolated during anthrax outbreaks in Italy from 1984 to 2017, were screened using a broth microdilution method to determine their susceptibility to 16 clinically relevant antimicrobial agents. The strains were isolated from various matrices (human, animal, and environmental samples) and were representative of thirty distinct genotypes previously identified by 15-loci multiple-locus variable-number of tandem repeats analysis. The antimicrobials tested were gentamicin, ceftriaxone, streptomycin, penicillin G, clindamycin, chloramphenicol, vancomycin, linezolid, cefotaxime, tetracycline, erythromycin, rifampin, amoxicillin, ciprofloxacin, doxycycline, and trimethoprim. All isolates were susceptible to most of the tested antimicrobials, with the exception of trimethoprim for which all of them showed high minimal inhibitory concentration values. An intermediate level of susceptibility was recorded for ceftriaxone and cefotaxime. Although the Centers for Disease Control and Prevention recommend the use of doxycycline, ciprofloxacin, penicillin G, and amoxicillin for treatment of human cases and for post-exposure prophylaxis to anthrax spores, this study shows a high degree of susceptibility of to many other antimicrobials, suggesting the possibility of an alternative choice for prophylaxis and therapy.
炭疽病由[未提及的病原体]引起,是一种非传染性传染病,可影响包括人类在内的多种动物物种(主要是反刍动物)。由于人类感染后往往会导致致命后果,因此迅速给予绝对有效的抗菌药物作为预防措施或临床病例治疗至关重要。在本研究中,使用肉汤微量稀释法对1984年至2017年期间在意大利炭疽疫情爆发期间分离出的110株菌株进行了筛选,这些菌株在时间、地理和基因上均有差异,以确定它们对16种临床相关抗菌药物的敏感性。这些菌株从各种基质(人类、动物和环境样本)中分离出来,代表了先前通过15个位点多位点可变串联重复序列分析确定的30种不同基因型。所测试的抗菌药物有庆大霉素、头孢曲松、链霉素、青霉素G、克林霉素、氯霉素、万古霉素、利奈唑胺、头孢噻肟、四环素、红霉素、利福平、阿莫西林、环丙沙星、强力霉素和甲氧苄啶。除甲氧苄啶外,所有分离株对大多数测试抗菌药物敏感,所有分离株对甲氧苄啶均显示出高最低抑菌浓度值。头孢曲松和头孢噻肟记录为中度敏感性。尽管疾病控制与预防中心建议使用强力霉素、环丙沙星、青霉素G和阿莫西林治疗人类病例以及预防接触炭疽孢子,但本研究表明[未提及的病原体]对许多其他抗菌药物具有高度敏感性,这表明预防和治疗可能有其他选择。