Thapa Eliza, Knauss Hanna M, Colvin Benjamin A, Fischer Benjamin A, Weyand Nathan J
Department of Biological Sciences, Ohio University, Athens, Ohio, USA.
Department of Biological Sciences, Ohio University, Athens, Ohio, USA
Antimicrob Agents Chemother. 2020 Jul 22;64(8). doi: 10.1128/AAC.02232-19.
Pharyngeal infections by are often asymptomatic, making them difficult to treat. However, animal modeling of human pharyngeal infections by pathogenic species is challenging due to numerous host tropism barriers. We have relied on rhesus macaques to investigate pharyngeal persistence of naturally occurring species in response to antibiotics. These species include , , and a species unique to macaques. Four animals previously treated intramuscularly with the fluoroquinolone enrofloxacin for 2 weeks were monitored for persistence of their preexisting populations for a period of 10 weeks. Enrofloxacin exposure did not eliminate preexisting flora from two of the four animals. Characterization of a collection of macaque isolates supported the hypothesis that pharyngeal persistence was linked to reduced enrofloxacin susceptibility conferred by mutations in either or Interestingly, we observed a change in neisserial population dynamics for several weeks following enrofloxacin exposure. Enrofloxacin appeared to promote competition between strains for dominance in the pharyngeal niche. Specifically, following enrofloxacin treatment, strains bearing single mutations and low MICs persisted long-term. In contrast, strains with both and mutations and high MICs became culturally undetectable, consistent with the hypothesis that they were less fit. Our study has provided insight into pharyngeal persistence dynamics of species bearing fluoroquinolone resistance determinants. The rhesus macaque provides a valuable host animal that may be used in the future to simulate treatment failures associated with the presence of antimicrobial-resistant spp. in the human pharynx.
由[病原体名称]引起的咽部感染通常没有症状,这使得它们难以治疗。然而,由于众多宿主嗜性障碍,对人类咽部感染进行[病原体名称]致病物种的动物建模具有挑战性。我们依靠恒河猴来研究天然存在的[病原体名称]物种在抗生素作用下在咽部的持续存在情况。这些物种包括[具体物种1]、[具体物种2]以及恒河猴特有的一个物种。对四只先前肌肉注射氟喹诺酮恩诺沙星两周的动物进行了为期10周的监测,以观察其原有[病原体名称]菌群的持续存在情况。恩诺沙星暴露并未清除四只动物中两只动物体内原有的菌群。对一组恒河猴[病原体名称]分离株的特征分析支持了这样一种假设,即咽部持续存在与[相关基因1]或[相关基因2]突变导致的恩诺沙星敏感性降低有关。有趣的是,我们观察到恩诺沙星暴露后几周内奈瑟菌种群动态发生了变化。恩诺沙星似乎促进了菌株之间在咽部生态位中争夺优势的竞争。具体而言,恩诺沙星治疗后,携带单个[相关基因1]突变且最低抑菌浓度低的菌株长期持续存在。相比之下,同时具有[相关基因1]和[相关基因2]突变且最低抑菌浓度高的菌株在培养中无法检测到,这与它们适应性较差的假设一致。我们的研究深入了解了携带氟喹诺酮耐药决定因素的[病原体名称]物种的咽部持续存在动态。恒河猴提供了一种有价值的宿主动物,未来可用于模拟与人类咽部存在耐抗菌药物的[病原体名称]物种相关的治疗失败情况。