Liu Zhen, Tang Hao, Xu Huaming, Lu Guoping, Yang Wensu, Xia Zhaoxin, Zhu Yi, Ni Shenwang, Men Wanqi, Shen Jilu
The Fourth Affiliated Hospital of Anhui Medical University Laboratory Department, Hefei, People's Republic of China.
Laboratory Department of Fuyang Hospital Affiliated to Anhui Medical University, Fuyang, Anhui, 236000, People's Republic of China.
Infect Drug Resist. 2022 Mar 31;15:1391-1397. doi: 10.2147/IDR.S356045. eCollection 2022.
To reduce the inspection time for urinary tract pathogens and provide a rapid and effective therapeutic plan for clinical anti-infection treatment, this study developed a rapid identification (ID) and antimicrobial sensitivity test (AST) method by DOT-MGA.
We grouped midstream urine samples with single bacteria according to the number of bacteria (≤5/5-15/≥ 15) under per oil microscope after Gram staining. Then we adopted differential centrifugation to process the grouped samples to collect precipitate. MALDI-TOF MS was performed using precipitate directly or after short-term culture. If succeed, we resuspended the precipitate into droplets with or without antibiotics at a MALDI target. Four hours later, mass spectrometer (MS) was used to identify the culture on the target and to analyse AST.
Samples (count ≥ 15), which precipitate can be directly identified by MS; otherwise, the precipitate need a short-term cultured for 3-6 h before ID. The consistency of the ID results between conventional culture and the precipitate is 100%. Compared with broth microdilution method, DOT-MGA for predicting AST had a high consistency. EA and CA for IPM, LEV, CAZ, NIT, and FOT were 100%/100%, 98%/90%, 98%/92%, 100%/90%, 98%/94%, respectively. No VME was observed in all tests. Besides, MIC50 for the five antibiotics by DOT-MGA and broth microdilution method were ≤1/≤0.5,>2/2,≤4/≤2,≤32/≤16,≤64/≤32 and MIC90 were ≤1/≤0.5, >2/>4, 16/16, 128/128, 128/64.
This study can shorten the ID time (minimum 0.5h) and AST (minimum 4h) of the main pathogens of urinary tract infection to 5-10 hours, which greatly reduce the inspection time and provide substantial help for the rapid diagnosis and treatment of patients with urinary tract infection.
为缩短尿路病原体检测时间,为临床抗感染治疗提供快速有效的治疗方案,本研究开发了一种基于点杂交-基质辅助激光解吸电离飞行时间质谱(DOT-MGA)的快速鉴定(ID)和抗菌药敏试验(AST)方法。
革兰染色后,在每油镜下根据细菌数量(≤5/5 - 15/≥15)对单一细菌的中段尿样本进行分组。然后采用差速离心法对分组后的样本进行处理以收集沉淀。直接对沉淀或短期培养后的沉淀进行基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)检测。若成功,将沉淀在MALDI靶板上重悬于含或不含抗生素的液滴中。4小时后,使用质谱仪(MS)对靶板上的培养物进行鉴定并分析AST。
样本(菌落计数≥15),其沉淀可直接通过MS鉴定;否则,沉淀在进行ID前需短期培养3 - 6小时。常规培养与沉淀的ID结果一致性为100%。与肉汤微量稀释法相比,DOT-MGA预测AST具有较高的一致性。对于亚胺培南(IPM)、左氧氟沙星(LEV)、头孢他啶(CAZ)、呋喃妥因(NIT)和福提霉素(FOT),大肠埃希菌(EA)和肺炎克雷伯菌(CA)的一致性分别为100%/100%、98%/90%、98%/92%、100%/90%、98%/94%。所有测试中均未观察到VME。此外,DOT-MGA和肉汤微量稀释法对五种抗生素的MIC50分别为≤1/≤0.5、>2/2、≤4/≤2、≤32/≤16、≤64/≤32,MIC90分别为≤1/≤0.5、>2/>4、16/16、128/128、128/64。
本研究可将尿路感染主要病原体的ID时间(最短0.5小时)和AST时间(最短4小时)缩短至5 - 10小时,大大减少了检测时间,为尿路感染患者的快速诊断和治疗提供了有力帮助。