Fast and Accurate Bacterial Species Identification in Urine Specimens Using LC-MS/MS Mass Spectrometry and Machine Learning

被引:49
作者
Roux-Dalvai, Florence [1 ]
Gotti, Clarisse [1 ]
Leclercq, Mickael [2 ]
Helie, Marie-Claude [4 ]
Boissinot, Maurice [4 ]
Arrey, Tabiwang N. [6 ]
Dauly, Claire [6 ]
Fournier, Frederic [1 ]
Kelly, Isabelle [1 ]
Marcoux, Judith [1 ]
Bestman-Smith, Julie [7 ]
Bergeron, Michel G. [4 ,5 ]
Droit, Arnaud [1 ,2 ,3 ]
机构
[1] Univ Laval, Res Ctr, CHU Quebec, Prote Platform, Quebec City, PQ, Canada
[2] Univ Laval, Res Ctr, CHU Quebec, Computat Biol Lab, Quebec City, PQ, Canada
[3] Univ Laval, Fac Med, Dept Mol Med, Quebec City, PQ, Canada
[4] Univ Laval, CHU Quebec, Axe Malad Infect & Immunitaires, Ctr Rech,Ctr Rech Infectiol, Quebec City, PQ, Canada
[5] Univ Laval, Fac Med, Dept Microbiol Infectiol & Immunol, Quebec City, PQ, Canada
[6] Thermo Fisher Sci, Bremen, Germany
[7] Univ Laval, CHU Quebec, Lab Microbiol Infectiol, Pavillon Hop Enfant Jesus, Quebec City, PQ, Canada
关键词
Microbiology; bacteria; SWATH-MS; tandem mass spectrometry; targeted mass spectrometry; urine analysis; LC-MS; MS; machine learning; DESORPTION IONIZATION-TIME; BLOOD CULTURE BOTTLES; MALDI-TOF MS; CLINICAL MICROBIOLOGY; RAPID IDENTIFICATION; EPIDEMIOLOGY; CENTRIFUGATION; ANTIMICROBIALS; INFECTIONS; VALIDATION;
D O I
10.1074/mcp.TIR119.001559
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fast identification of microbial species in clinical samples is essential to provide an appropriate antibiotherapy to the patient and reduce the prescription of broad-spectrum antimicrobials leading to antibioresistances. MALDI-TOF-MS technology has become a tool of choice for microbial identification but has several drawbacks: it requires a long step of bacterial culture before analysis (?24 h), has a low specificity and is not quantitative. We developed a new strategy for identifying bacterial species in urine using specific LC-MS/MS peptidic signatures. In the first training step, libraries of peptides are obtained on pure bacterial colonies in DDA mode, their detection in urine is then verified in DIA mode, followed by the use of machine learning classifiers (NaiveBayes, BayesNet and Hoeffding tree) to define a peptidic signature to distinguish each bacterial species from the others. Then, in the second step, this signature is monitored in unknown urine samples using targeted proteomics. This method, allowing bacterial identification in less than 4 h, has been applied to fifteen species representing 84% of all Urinary Tract Infections. More than 31,000 peptides in 190 samples were quantified by DIA and classified by machine learning to determine an 82 peptides signature and build a prediction model. This signature was validated for its use in routine using Parallel Reaction Monitoring on two different instruments. Linearity and reproducibility of the method were demonstrated as well as its accuracy on donor specimens. Within 4h and without bacterial culture, our method was able to predict the predominant bacteria infecting a sample in 97% of cases and 100% above the standard threshold. This work demonstrates the efficiency of our method for the rapid and specific identification of the bacterial species causing UTI and could be extended in the future to other biological specimens and to bacteria having specific virulence or resistance factors. We have developed a new method for the identification of bacterial species causing Urinary Tract Infections. The first training step used DIA analysis on multiple replicates of bacterial inoculates to define a peptide signature by machine learning classifiers. In a second identification step, the signature is monitored by targeted proteomics on unknown samples. This fast, culture-free and accurate method paves the way of the development of new diagnostic approaches limiting the emergence of antimicrobial resistances.
引用
收藏
页码:2492 / 2505
页数:14
相关论文
共 81 条
[1]   The genetic background of antibiotic resistance among clinical uropathogenic Escherichia coli strains [J].
Adamus-Bialek, Wioletta ;
Baraniak, Anna ;
Wawszczak, Monika ;
Gluszek, Stanislaw ;
Gad, Beata ;
Wrobel, Klaudia ;
Bator, Paulina ;
Majchrzak, Marta ;
Parniewski, Pawel .
MOLECULAR BIOLOGY REPORTS, 2018, 45 (05) :1055-1065
[2]   Matrix assisted laser desorption time of flight mass spectrometry (MALDI-TOF MS) in clinical microbiology [J].
Angeletti, Silvia .
JOURNAL OF MICROBIOLOGICAL METHODS, 2017, 138 :20-29
[3]  
[Anonymous], 7 ACM SIGKDD INT C K
[4]  
[Anonymous], 2018, MOL CELL PROTEOMICS, DOI DOI 10.1074/mcp.TIR118.000853
[5]  
[Anonymous], 2017, GLOB HEALTH EPIDEM G, DOI DOI 10.1017/gheg.2017.4
[6]  
[Anonymous], MICROBES CONCEPTS AP
[7]  
[Anonymous], 2014, ANTIMICROBIAL RESIST
[8]  
[Anonymous], EV THREAT ANT RES
[9]   From Theory to Practice: Translating Whole-Genome Sequencing (WGS) into the Clinic [J].
Balloux, Francois ;
Brynildsrud, Ola Bronstad ;
van Dorp, Lucy ;
Shaw, Liam P. ;
Chen, Hongbin ;
Harris, Kathryn A. ;
Wang, Hui ;
Eldholm, Vegard .
TRENDS IN MICROBIOLOGY, 2018, 26 (12) :1035-1048
[10]   DETECTION OF BACTERIA IN BLOOD BY CENTRIFUGATION AND FILTRATION [J].
BERNHARDT, M ;
PENNELL, DR ;
ALMER, LS ;
SCHELL, RF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (03) :422-425