scholarly journals Pseudomonas Species Diversity Along the Danube River Assessed by rpoD Gene Sequence and MALDI-TOF MS Analyses of Cultivated Strains

2020 ◽  
Vol 11 ◽  
Author(s):  
Magdalena Mulet ◽  
María Montaner ◽  
Daniela Román ◽  
Margarita Gomila ◽  
Clemens Kittinger ◽  
...  
2020 ◽  
Vol 8 (7) ◽  
pp. 1057 ◽  
Author(s):  
Johanna Burtscher ◽  
Franziska Küller ◽  
Matthias Dreier ◽  
Emmanuelle Arias-Roth ◽  
David Drissner ◽  
...  

Clostridium tyrobutyricum is well known as one of the main causative agents of severe cheese spoilage. The metabolism of this anaerobic bacterium during ripening leads to textural and sensory defects in cheese and consequential loss of product value. The potential to induce cheese spoilage, however, may vary among different strains of the same species. Therefore, a better understanding of the intra-species diversity of C. tyrobutyricum may be of practical relevance for the dairy industry. In the present study, we compared the ability of three typing techniques to differentiate 95 C. tyrobutyricum strains on the subspecies level: (1) repetitive element palindromic PCR (rep-PCR) fingerprinting combined with conventional agarose gel electrophoresis, (2) hexaplex-PCR followed by an automated capillary electrophoresis and (3) matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) typing. MALDI-TOF MS fingerprinting provided only moderate reproducibility and low discriminatory power. Both PCR-based methods were highly reproducible and discriminative, with hexaplex-PCR fingerprinting being slightly more discriminative than rep-PCR typing. Overall, a high intra-species diversity was observed among the tested strains, indicating that further investigations on the strain level may be of interest.


2019 ◽  
Vol 132 ◽  
pp. 313-318 ◽  
Author(s):  
Miroslava Kačániová ◽  
Alīna Klūga ◽  
Attila Kántor ◽  
Juraj Medo ◽  
Jana Žiarovská ◽  
...  

2013 ◽  
Vol 13 (5) ◽  
pp. 1383-1389 ◽  
Author(s):  
Maja Taučer-Kapteijn ◽  
Gertjan Medema ◽  
Wim Hoogenboezem

Matrix-Assisted Laser Desorption Ionisation–Time of Flight Mass Spectrometry (MALDI–TOF MS) has increasingly been used for rapid and reliable identification of clinically relevant micro-organisms. To establish the applicability of this technique in (drinking) water quality analysis, the MALDI–TOF MS identification results for Enterococcus spp. isolated from various water environments were compared with those obtained using the commercial Rapid 32 ID Strep system. One hundred and one bacterial isolates were isolated from various types of water and determined as enterococci on the basis of their growth on Slanetz-Bartley agar in typical colonies. The isolates were identified by MALDI–TOF MS and the commercial biochemical test Rapid 32 ID Strep. Isolates yielding in discrepant identifications were genotyped using 16S rRNA gene sequence analysis. For 86 isolates (85%), the results of Rapid ID 32 Strep were identical to those obtained with MALDI–TOF MS. Six isolates were impossible to be classified by means of the Rapid 32 ID Strep test. And for eight out of a total of nine discrepant results (89%), the 16S analyses confirmed the MALDI–TOF MS identification. MALDI–TOF MS produced highly reproducible results. These results indicated that the use of two different culture media had no effect on the identification. In addition, no significant differences (p = 0.32; n = 20) were evident between the scores obtained from a 20-fold measurement of the same isolate. The results of this study showed that MALDI–TOF MS identification (Bruker) is a reliable method for identifying E. faecium, E. faecalis, E. durans, E. hirae and E. casseliflavus isolated from water samples. E. mundtii and E. moraviensis were not included in the Rapid 32 ID Strep database and could therefore not be identified using that test set. However, MALDI–TOF MS and 16S identified all six isolates as members of these species.


2007 ◽  
Vol 177 (4S) ◽  
pp. 297-297
Author(s):  
Kristina Schwamborn ◽  
Rene Krieg ◽  
Ruth Knüchel-Clarke ◽  
Joachim Grosse ◽  
Gerhard Jakse

Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
L Fougère ◽  
D Da Silva ◽  
E Destandau ◽  
C Elfakir
Keyword(s):  

2017 ◽  
Author(s):  
M Erhard ◽  
M Metzner ◽  
D Köhler-Repp ◽  
B Köhler ◽  
R Storandt
Keyword(s):  

2019 ◽  
Author(s):  
M Hooshyari ◽  
H Rezadoost ◽  
P Ghezellou ◽  
A Ghassempour

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