Infectious Disease Translational Research, Ochsner Clinic Foundation, New Orleans, Louisiana, USA.
Infectious Disease Translational Research, Ochsner Clinic Foundation, New Orleans, Louisiana, USA
J Investig Med. 2021 Jan;69(1):96-99. doi: 10.1136/jim-2020-001552. Epub 2020 Nov 18.
was discovered in 2009 and has rapidly emerged as a serious public health threat with cases reported in over 20 countries worldwide. As of May 8, 2020, the Centers for Disease Control and Prevention reported a total of 1122 US cases. is often multidrug resistant, leaving few options for treatment. Sulfonamides are known to inhibit a bacterial enzyme involved in folate synthesis and may also inhibit yeast organisms by a similar mechanism. The combination of trimethoprim and sulfamethoxazole is more commonly used than either drug alone. The objective of this study was to evaluate the combination of fluconazole and trimethoprim-sulfamethoxazole against Minimum inhibitory concentrations (MICs) of fluconazole and trimethoprim-sulfamethoxazole were determined by ETEST and broth microdilution for 11 strains. Fluconazole MICs (µg/mL) were 4->256 by ETEST and 2->256 by broth microdilution (73% resistant); trimethoprim-sulfamethoxazole MICs were >32 by ETEST and 32->128 by broth microdilution (no interpretive guidelines for ). Using our MIC: MIC ETEST method and a checkerboard method, we investigated the interaction of fluconazole and trimethoprim-sulfamethoxazole against all isolates. These interactions were analyzed by calculating the summation fractional inhibitory concentration with synergyof ≤0.5, additivity of >0.5-1.0, indifference of >1-4, and antagonism of >4. The combination of fluconazole and trimethoprim-sulfamethoxazole revealed synergy with three (27%) and additivity with one (9%) isolate. Indifference was found for the remaining seven (64%) isolates. With the checkerboard method, synergy was seen in 1/11 (9%) isolates with fluconazole (½ MIC) plus trimethoprim-sulfamethoxazole (1/64 MIC); additivity, in 7/11 (64%) isolates with fluconazole (1/8 MIC-1×MIC) plus trimethoprim-sulfamethoxazole (1/128 MIC-½ MIC); and indifference in 3/11 (27%) isolates. Regardless, in vitro interactions may or may not correlate with clinical outcomes. Synergy testing with additional drug combinations and isolates should be performed.
该病毒于 2009 年被发现,迅速成为严重的公共卫生威胁,全球 20 多个国家报告了病例。截至 2020 年 5 月 8 日,美国疾病控制与预防中心报告了总共 1122 例美国病例。通常具有多重耐药性,治疗选择有限。磺胺类药物已知可抑制叶酸合成中涉及的细菌酶,也可能通过类似机制抑制酵母生物。甲氧苄啶-磺胺甲恶唑的联合使用比单独使用任何一种药物更为常见。本研究的目的是评估氟康唑和甲氧苄啶-磺胺甲恶唑联合用药对 11 株 的疗效。通过 ETEST 和肉汤微量稀释法测定氟康唑和甲氧苄啶-磺胺甲恶唑的最低抑菌浓度 (MIC)。氟康唑 MICs (µg/mL) 通过 ETEST 为 4->256,通过肉汤微量稀释法为 2->256(73%耐药);甲氧苄啶-磺胺甲恶唑 MICs 通过 ETEST 为 >32,通过肉汤微量稀释法为 32->128(无磺胺甲恶唑的解释性指南)。使用我们的 MIC:MIC ETEST 方法和棋盘法,我们研究了氟康唑和甲氧苄啶-磺胺甲恶唑联合用药对所有分离株的相互作用。通过计算抑菌浓度总和分数,协同作用≤0.5、相加作用>0.5-1.0、无关作用>1-4、拮抗作用>4,分析这些相互作用。氟康唑和甲氧苄啶-磺胺甲恶唑联合用药对 3 株(27%)分离株表现出协同作用,对 1 株(9%)分离株表现出相加作用。对其余 7 株(64%)分离株发现无关作用。通过棋盘法,在 1/11(9%)氟康唑(½MIC)加甲氧苄啶-磺胺甲恶唑(1/64MIC)的分离株中发现协同作用;在 7/11(64%)氟康唑(1/8MIC-1×MIC)加甲氧苄啶-磺胺甲恶唑(1/128MIC-½MIC)的分离株中发现相加作用;在 3/11(27%)的分离株中发现无关作用。无论如何,体外相互作用可能与临床结果相关,也可能不相关。应进行协同试验和其他药物组合及分离株的测试。