MALDI-TOF MS database expansion for identification of Bacillus and related genera isolated from a pharmaceutical facility

rpoB公司 生物 管家基因 16S核糖体RNA 芽孢杆菌(形态) 微生物学 基质辅助激光解吸/电离 系统发育树 核糖体RNA 细菌 基因 遗传学 化学 基因表达 吸附 解吸 有机化学
作者
Luciana Veloso da Costa,Rebeca Vitória da Silva Lage de Miranda,Cristhiane Moura Falavina dos Reis,Joyce Modesto de Andrade,Fernanda Ventura Cruz,Adriana Marques Frazão,Érica Louro da Fonseca,Juliana Nunes Ramos,Marcelo Luiz Lima Brandão,Verônica Viana Vieira
出处
期刊:Journal of Microbiological Methods [Elsevier BV]
卷期号:203: 106625-106625 被引量:23
标识
DOI:10.1016/j.mimet.2022.106625
摘要

Bacillus and related genera are among the main bacterial groups isolated from pharmaceutical production areas. The identification of Bacillus species and related genera by classical methods is particularly difficult, due to similarities between closely related species. The Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS) is one of the most promising techniques for chemotaxonomic characterization of microorganisms, being an alternative to genotypic methods. This study aimed to identify Bacillus strains and related genera isolated from immunobiological production areas by phylogenetic analysis of housekeeping genes and expand the database associated with MALDI-TOF MS to improve their identification. In a previous study, 97 aerobic endospore-forming bacteria isolated from a pharmaceutical facility were analyzed by MALDI-TOF MS and 16S rRNA gene full-length sequencing. All strains were identified as Bacillus and related genera by the latest methodology. Among the 97 strains, 22 were unidentified and 2 strains were misidentified by MALDI-TOF MS. In the present study, these 24 strains were subjected to 16S rRNA gene phylogenetic analysis. Strains not identified at species level by this methodology were submitted to rpoB gene phylogenetic analysis. After identifying the strains, 19 of the 24 strains were incubated for 24, 48, and 72 h on Tryptic Soy Agar and Sheep Blood Agar and subjected to analysis by MALDI-TOF MS. A SuperSpectrum for each strain was created and entered into the equipment database. Finally, the 24 strains were again submitted to proteomic analysis by MALDI-TOF MS, and, at this time, all were correctly identified. The genotypic identification of in-house isolated strains and the introduction of these spectra in MALDI-TOF MS, in order to obtain a customized database, proved to be an extremely effective tool in the identification of Bacillus and related genera from pharmaceutical industry origin.

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