Jaglal Prenika, Velaphi Sithembiso Christopher, Menezes Colin Nigel, Swe Swe-Han Khine
Department of Clinical Microbiology and Infectious Diseases, National Health Laboratory Service and Faculty of Health Sciences, University of Witwatersrand, Johannesburg 2050, South Africa.
Department of Paediatrics and Child Health, Chris Hani Baragwanath Academic Hospital, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2050, South Africa.
Antibiotics (Basel). 2025 Jun 20;14(7):630. doi: 10.3390/antibiotics14070630.
: In vitro synergy testing (ST) is a useful means to gauge the performance ofantibiotic combinations against multidrug-resistant (MDR) Gram-negative bacteria (GNB). This study aimed to determine synergy of antibiotics against paediatric bloodstream (BS) carbapenem-resistant Enterobacterales (CRE) and extremely drug-resistant (XDR) species. : This cross-sectional study was conducted at a public tertiary hospital in South Africa, from January 2023 to December 2023. Sixty-eight isolates from children with bloodstream infections (BSI), comprising 55.9% (38/68) CRE and 44.1% (30/68) XDR species, were performed ST using the fixed-ratio Epsilometer-test method. Combinations of colistin and meropenem, colistin and fosfomycin, colistin and tigecycline, meropenem and fosfomycin, meropenem and tigecycline, and fosfomycin and tigecycline were tested. : In vitro synergy for CRE was best demonstrated with tigecycline and meropenem, at 92.1% (35/38), and fosfomycin and meropenem at 73.7% (28/38). Among the XDR species, the highest rates of synergy of 76.7% (23/30) were observed with tigecycline and meropenem. The absence of synergy was noted with colistin and meropenem for the CRE, with many displaying indifference and antagonism at rates of 65.8% and 22%. Most XDR species (56.7%; 17/30) expressed indifference to colistin and meropenem with synergy and antagonism displayed in 23.3% and 10% of isolates. : This study highlights tigecycline and meropenem displaying impressive in vitro synergy when compared to the in-use colistin and meropenem for CRE and XDR species. Tigecycline and meropenem may be a viable salvage therapeutic option for MDR Gram-negative paediatric infections. Future research is warranted to confirm in vivo synergy clinically.
体外协同试验(ST)是评估抗生素联合用药对多重耐药(MDR)革兰氏阴性菌(GNB)疗效的一种有用方法。本研究旨在确定抗生素对儿童血流(BS)碳青霉烯耐药肠杆菌科细菌(CRE)和极耐药(XDR)菌株的协同作用。 :本横断面研究于2023年1月至2023年12月在南非一家公立三级医院进行。对68例血流感染(BSI)儿童的分离株进行ST,采用固定比例梯度扩散法,其中碳青霉烯耐药肠杆菌科细菌(CRE)占55.9%(38/68),极耐药(XDR)菌株占44.1%(30/68)。测试了黏菌素和美罗培南、黏菌素和磷霉素、黏菌素和替加环素、美罗培南和磷霉素、美罗培南和替加环素以及磷霉素和替加环素的联合用药。 :对于碳青霉烯耐药肠杆菌科细菌(CRE),替加环素和美罗培南的体外协同作用最佳,为92.1%(35/38),磷霉素和美罗培南为73.7%(28/38)。在极耐药(XDR)菌株中,替加环素和美罗培南的协同率最高,为76.7%(23/30)。碳青霉烯耐药肠杆菌科细菌(CRE)中黏菌素和美罗培南无协同作用,许多表现为无关作用和拮抗作用,发生率分别为65.8%和22%。大多数极耐药(XDR)菌株(56.7%;17/30)对黏菌素和美罗培南表现为无关作用,23.3%的分离株表现为协同作用,10%表现为拮抗作用。 :本研究强调,与目前使用的黏菌素和美罗培南相比,替加环素和美罗培南对碳青霉烯耐药肠杆菌科细菌(CRE)和极耐药(XDR)菌株显示出令人印象深刻的体外协同作用。替加环素和美罗培南可能是治疗多重耐药革兰氏阴性菌儿科感染的一种可行的挽救治疗选择。有必要进行进一步研究以临床证实体内协同作用。