Classification of GenusPseudomonasby MALDI-TOF MS Based on Ribosomal Protein Coding inS10−spc−alphaOperon at Strain Level

2010 ◽  
Vol 9 (12) ◽  
pp. 6722-6728 ◽  
Author(s):  
Yudai Hotta ◽  
Kanae Teramoto ◽  
Hiroaki Sato ◽  
Hiromichi Yoshikawa ◽  
Akifumi Hosoda ◽  
...  
2021 ◽  
Vol 9 (3) ◽  
pp. 661
Author(s):  
Adriana Calderaro ◽  
Mirko Buttrini ◽  
Monica Martinelli ◽  
Benedetta Farina ◽  
Tiziano Moro ◽  
...  

Typing methods are needed for epidemiological tracking of new emerging and hypervirulent strains because of the growing incidence, severity and mortality of Clostridioides difficile infections (CDI). The aim of this study was the evaluation of a typing Matrix-Assisted Desorption/Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS (T-MALDI)) method for the rapid classification of the circulating C. difficile strains in comparison with polymerase chain reaction (PCR)-ribotyping results. Among 95 C. difficile strains, 10 ribotypes (PR1–PR10) were identified by PCR-ribotyping. In particular, 93.7% of the isolates (89/95) were grouped in five ribotypes (PR1–PR5). For T-MALDI, two classifying algorithm models (CAM) were tested: the first CAM involved all 10 ribotypes whereas the second one only the PR1–PR5 ribotypes. Better performance was obtained using the second CAM: recognition capability of 100%, cross-validation of 96.6% and agreement of 98.4% (60 correctly typed strains, limited to PR1–PR5 classification, out of 61 examined strains) with PCR-ribotyping results. T-MALDI seems to represent an alternative to PCR-ribotyping in terms of reproducibility, set up time and costs, as well as a useful tool in epidemiological investigation for the detection of C. difficile clusters (either among CAM included ribotypes or out-of-CAM ribotypes) involved in outbreaks.


2006 ◽  
Vol 66 (3) ◽  
pp. 399-409 ◽  
Author(s):  
Márta Vargha ◽  
Zoltán Takáts ◽  
Allan Konopka ◽  
Cindy H. Nakatsu
Keyword(s):  

2018 ◽  
Author(s):  
Wenfa Ng

Ribosomes are the protein synthesis factories of a cell and thus are evolutionary conserved in structure and function. Comprising a large and small subunit, the ribosome is further made up of ribosomal proteins that give structure and function to different parts of the macromolecular complex. Current methods for isolating the ribosome include density gradient ultracentrifugation that separates the ribosome into the large and small subunit. Separation of the various ribosomal proteins that comprise each of the subunit would require a solubilization step followed by the use of sodium dodecyl sulphate and polyacrylamide gel electrophoresis (SDS-PAGE). However, possibility exists for the use of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) to profile the set of ribosomal proteins that could be solubilized from each ribosome subunit. Using ribosomal protein amino acid sequence information from Kyoto Encyclopaedia of Genes and Genomes (KEGG), the molecular weight of each ribosomal protein from Pseudomonas aeruginosa PAO1 was calculated in this report. Obtained results revealed that each ribosomal protein had a unique mass that could be detected by mid-range MALDI-TOF MS instruments. More importantly, the mass of ribosomal proteins constitutes a unique mass fingerprint of each ribosome subunit, which accounts for the different structure and functions of the large and small ribosome subunit. Overall, current mass resolution of MALDI-TOF MS instruments could resolve ribosomal proteins and thus provides a tool for profiling the set of ribosomal proteins that constitute the large and small subunit of the ribosome.


2011 ◽  
Vol 59 (10) ◽  
pp. 5222-5230 ◽  
Author(s):  
Yudai Hotta ◽  
Jun Sato ◽  
Hiroaki Sato ◽  
Akifumi Hosoda ◽  
Hiroto Tamura

2015 ◽  
Vol 99 (13) ◽  
pp. 5547-5562 ◽  
Author(s):  
Dominik Ziegler ◽  
Joël F. Pothier ◽  
Julie Ardley ◽  
Romain Kouakou Fossou ◽  
Valentin Pflüger ◽  
...  

2015 ◽  
Vol 26 (2) ◽  
pp. 69-80 ◽  
Author(s):  
Anna Petri ◽  
Andreas Rabenstein ◽  
Jan Kuever ◽  
Helmut König
Keyword(s):  

2013 ◽  
Vol 2013 ◽  
pp. 1-15
Author(s):  
Ting Yu Wang ◽  
Hua Zhou ◽  
Yuen Fan Wong ◽  
Pui Kei Wu ◽  
Wen-Luan Wendy Hsiao ◽  
...  

Qingfu Guanjieshu (QFGJS) is an herbal preparation for treating rheumatoid arthritis (RA). Previous studies revealed that QFGJS significantly inhibited experimental arthritis and acute inflammation, accompanied by reduction of proinflammatory cytokines and elevation of anti-inflammatory cytokines. This study aims to identify the targeted proteins and predict the proteomic network associated with the drug action of QFGJS by using 2D gel and MALDI-TOF-MS/MS techniques. Thirty female Wistar rats were evenly grouped as normal and vehicle- and QFGJS-treated CIA rats. The antiarthritic effect of QFGJS was examined with a 19-day treatment course, and the knee synovial tissues of animals from each group were obtained for 2D gel and MALDI-TOF-MS/MS analysis. Results showed that QFGJS significantly ameliorated collagen II-induced arthritis when administrated at 2.8 g/kg body weight for 19 days. 2D gel image analysis revealed 89 differentially expressed proteins in the synovial tissues among the normal and vehicle- and QFGJS-treated CIA rats from over 1000 proteins of which 63 proteins were identified by MALDI-TOF-MS/MS analysis, and 32 proteins were included for classification of functions using Gene Ontology (GO) method. Finally, 14 proteins were analyzed using bioinformatics, and a predicted proteomic network related to the anti-arthritic effect of QFGJS was established, and Pgk1 plays a central role.


PLoS ONE ◽  
2011 ◽  
Vol 6 (2) ◽  
pp. e17319 ◽  
Author(s):  
Thi-Nguyen-Ny Tran ◽  
Gérard Aboudharam ◽  
Armelle Gardeisen ◽  
Bernard Davoust ◽  
Jean-Pierre Bocquet-Appel ◽  
...  
Keyword(s):  

2020 ◽  
Vol 21 (8) ◽  
pp. 2694 ◽  
Author(s):  
Piotr Jarocki ◽  
Elwira Komoń-Janczara ◽  
Agnieszka Glibowska ◽  
Michał Dworniczak ◽  
Monika Pytka ◽  
...  

The genus Lactobacillus includes, among others, Lactobacillus casei, Lactobacillus paracasei and Lactobacillus rhamnosus, species that are collectively referred to as the Lactobacillus casei group. Many studies have shown that strains belonging to this group may decrease lactose intolerance, the effects of inflammatory bowel disease, diarrhea, constipation, food allergies and even colon cancer. Moreover, evidences exists of positive effects of these bacteria on mucosal immunity and blood cholesterol level. Because of their beneficial influence on human health, many of them are used as food additives and probiotic pharmaceuticals. It should be stressed that health-promoting properties are not attributed at the species level, but to specific strains. Therefore, procedures are necessary to allow specific identification at each phylogenetic level—genus, species and strain. In this paper we present a practical overview of molecular methods for the identification and differentiation of L. casei bacteria. The research included 30 bacterial strains belonging to three species: L.casei, L. paracasei and L. rhamnosus. Among the tested procedures were genus- and species-specific PCR, multiplex-PCR, Real-Time HRM analysis, RFLP-PCR, rep-PCR, RAPD-PCR, AFLP-PCR, and proteomic methods such as MALDI-TOF MS typing and SDS-PAGE fingerprinting. The obtained results showed that multiplex-PCR and MALDI-TOF MS turned out to be the most useful methods to identify the tested bacteria at the species level. At the strain level, the AFLP-PCR method showed the highest discriminatory power. We hope that the presented results will allow for the easy selection of an appropriate procedure, depending on the experiment conducted and the equipment capabilities of any given laboratory.


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