scholarly journals MALDI-TOF mass spectrometry identification of yeast-form fungi: a comparison between methods

2019 ◽  
Vol 39 (2) ◽  
pp. 128-135
Author(s):  
Max Roberto Batista Araújo ◽  
Luisa Ferreira Seabra ◽  
Mireille Ângela Bernardes Sousa
Mycoses ◽  
2013 ◽  
Vol 57 (3) ◽  
pp. 135-140 ◽  
Author(s):  
Stéphane Ranque ◽  
Anne-Cécile Normand ◽  
Carole Cassagne ◽  
Jean-Benjamin Murat ◽  
Nathalie Bourgeois ◽  
...  

2012 ◽  
Vol 159 (3-4) ◽  
pp. 544 ◽  
Author(s):  
Zoheira Djelouadji ◽  
Véronique Roux ◽  
Didier Raoult ◽  
Angeli Kodjo ◽  
Michel Drancourt

Author(s):  
Yu. A. Tyurin ◽  
R. S. Fassakhov ◽  
T. V. Grigorieva ◽  
I. G. Mustafin

Aim. Study transformation of skin microflora during development of atopic dermatitis. Materials and methods. 45 patients with various forms of atopic dermatitis (AtD) were examined. Control group consisted of 26 healthy individuals. The strains were cultivated on elective nutrient media. Identification of the isolated strains was carried out by MALDI-TOF mass-spectrometry method. Results. A low frequency of occurrence of taxon Staphylococcus epidermidis on face skin and high frequency of occurrence of Staphylococcus aureus on upper and lower limb skin was established for AtD patients compared with healthy individuals. The frequency of occurrence of proteolytically active isolates of S. aureus in AtD patients was 3 times higher than in healthy carriers of this taxon. Taxons of microorganisms not inherent to healthy individuals such as Bacillus mycoides, Pseudomonas putida, Pseudomonas radiobacter were isolated on lower limb and neck skin of AtD patients. A high frequency of occurrence of Cryptococcus satoi, Candida albicans, Malassezia globosa fungi was noted. Conclusion. A decrease of barrier functions of skin during AtD facilitates contamination of patients’ skin with rare bacterial taxons and fungi. One of the possible mechanisms of suppression of immune competent cell functions could be proteolytic enzymes of S. aureus.


2016 ◽  
Vol 115 (11) ◽  
pp. 4199-4210 ◽  
Author(s):  
Bersissa Kumsa ◽  
Maureen Laroche ◽  
Lionel Almeras ◽  
Oleg Mediannikov ◽  
Didier Raoult ◽  
...  

Anaerobe ◽  
2012 ◽  
Vol 18 (3) ◽  
pp. 294-297 ◽  
Author(s):  
Rémi Fournier ◽  
Frédéric Wallet ◽  
Bruno Grandbastien ◽  
Luc Dubreuil ◽  
René Courcol ◽  
...  

2016 ◽  
Vol 26 (5) ◽  
pp. 69-73
Author(s):  
Lina Savickaitė ◽  
Jelena Kopeykinienė

Rapid identification of the infecting organism may aid in choosing appropriate antimicrobial therapy. We used MALDI-TOF mass spectrometry to identify bacteria directly from the positive blood culture samples (n=21). 85,71 percent of these results was identified using of MALDI-TOF mass spectrometry. Identification time of bacteria directly from the blood culture takes more than 1 hour for 27,8 percent results.


2020 ◽  
Vol 8 (8) ◽  
pp. 1143
Author(s):  
Sofiane Regoui ◽  
Aurélie Hennebique ◽  
Thomas Girard ◽  
Sandrine Boisset ◽  
Yvan Caspar ◽  
...  

Francisella tularensis is a tier 1 agent causing the zoonosis tularemia. This highly infectious Gram-negative bacterium is occasionally isolated from human samples (especially blood samples) in routine clinical microbiology laboratories. A rapid and accurate method for identifying this pathogen is needed in order to optimize the infected patient’s healthcare management and prevent contamination of the laboratory personnel. MALDI TOF mass spectrometry has become the gold standard for the rapid identification of most human pathogens. However, F. tularensis identification using such technology and commercially available databases is currently considered unreliable. Real-time PCR-based methods for rapid detection and accurate identification of F. tularensis are not available in many laboratories. As a national reference center for tularemia, we developed a MALDI TOF database allowing accurate identification of the species F. tularensis and its differentiation from the closely related neighbor species F. tularensis subsp. novicida and F. philomiragia. The sensitivity and specificity of this database were validated by testing 71 F. tularensis strains and 165 strains from 63 species not belonging to the Francisella genus. We obtained accurate identification at the species level and differentiation of all the tested bacterial strains. In particular, F. tularensis could be accurately differentiated from other small Gram-negative bacilli occasionally isolated from human samples, including species of the HACEK group and Brucella melitensis.


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