Coombs Geoffrey W, Yee Nicholas W T, Daley Denise, Bennett Catherine M, Robinson James O, Stegger Marc, Shoby Princy, Mowlaboccus Shakeel
Antimicrobial Resistance and Infectious Diseases (AMRID) Research Laboratory, Murdoch University, Murdoch, WA 6150, Australia.
Department of Microbiology, PathWest Laboratory Medicine-WA, Fiona Stanley Hospital, Murdoch, WA 6150, Australia.
Microorganisms. 2022 Aug 15;10(8):1650. doi: 10.3390/microorganisms10081650.
Defined by the emergence of antibiotic resistant strains, is a priority bacterial species with high antibiotic resistance. However, a rise in the prevalence of penicillin-susceptible (PSSA) bloodstream infections has recently been observed worldwide, including in Australia, where the proportion of methicillin-susceptible causing bacteremia identified phenotypically as penicillin-susceptible has increased by over 35%, from 17.5% in 2013 to 23.7% in 2020.
To determine the population structure of PSSA causing community- and hospital-onset bacteremia in Australia and to evaluate routine phenotypic antimicrobial susceptibility methods to reliably confirm penicillin resistance on -positive initially classified as penicillin-susceptible by the Vitek 2 automated microbiology system.
Whole genome sequencing on 470 PSSA collected in the 2020 Australian Group on Antimicrobial Resistance Australian Sepsis Outcome Programme identified 84 multilocus sequence types (STs), of which 79 (463 isolates) were grouped into 22 clonal complexes (CCs). The dominant CCs included CC5 (31.9%), CC97 (10.2%), CC45 (10.0%), CC15 (8.7%), and CC188 (4.9%). Many of the CCs had multiple STs and types and, based on the immune evasion cluster type, isolates within a CC could be classified into different strains harboring a range of virulence and resistance genes. Phylogenetic analyses of the isolates showed most CCs were represented by one clade. The gene was identified in 45 (9.6%) PSSA. Although multiclonal, approximately 50% of -positive PSSA were from CC15 and were found to be genetically distant from the -negative CC15 PSSA. The broth microdilution, Etest and cefinase, performed poorly; however, when the appearance of the zone edge was considered; as per the EUCAST and CLSI criteria, disc diffusion detected 100% of -positive PSSA.
In Australia, PSSA bacteremia is not caused by the expansion of a single clone. Approximately 10% of classified as penicillin-susceptible by the Vitek 2 harbored . Consequently, we recommend that confirmation of Vitek 2 PSSA be performed using an alternative method, such as disc diffusion with careful interpretation of the zone edge.
以抗生素耐药菌株的出现为特征,是具有高抗生素耐药性的重点细菌物种。然而,最近在全球范围内观察到对青霉素敏感的(PSSA)血流感染的患病率有所上升,包括在澳大利亚,其中表型鉴定为对青霉素敏感的甲氧西林敏感引起菌血症的比例增加了超过35%,从2013年的17.5%增至2020年的23.7%。
确定在澳大利亚引起社区和医院获得性菌血症的PSSA的种群结构,并评估常规表型抗菌药物敏感性方法,以可靠地确认最初由Vitek 2自动化微生物系统分类为对青霉素敏感的阳性上的青霉素耐药性。
对2020年澳大利亚抗菌药物耐药性澳大利亚脓毒症结果计划收集的470株PSSA进行全基因组测序,确定了84种多位点序列类型(STs),其中79种(463株分离株)被归为22个克隆复合体(CCs)。主要的CCs包括CC5(31.9%)、CC97(10.2%)、CC45(10.0%)、CC15(8.7%)和CC188(4.9%)。许多CCs有多个STs和类型,并且基于免疫逃避簇类型,一个CC内的分离株可被分类为携带一系列毒力和耐药基因的不同菌株。对分离株的系统发育分析表明,大多数CCs由一个进化枝代表。在45株(9.6%)PSSA中鉴定出基因。尽管是多克隆的,但约50%的阳性PSSA来自CC15,并且发现与阴性CC15 PSSA在基因上距离较远。肉汤微量稀释法、Etest法和头孢菌素酶法表现不佳;然而,根据欧盟CAST和CLSI标准,当考虑抑菌圈边缘的外观时,纸片扩散法检测到100%的阳性PSSA。
在澳大利亚,PSSA菌血症不是由单个克隆的扩张引起的。约10%被Vitek 2分类为对青霉素敏感的携带。因此,我们建议使用替代方法,如仔细解读抑菌圈边缘的纸片扩散法,对Vitek 2 PSSA进行确认。