RARE SPECIES IN THE STRUCTURE OF ACID-RESISTANT MEMBERS OF THE ORDER ACTINOMYCETALES ISOLATED FROM CLINICAL MATERIAL

2020 ◽  
Vol 65 (2) ◽  
pp. 111-115
Author(s):  
Artem Viktorovich Lyamin

The article presents data on the structure of acid-resistant members of the order Actinomycetales and rare species that have been isolated and identified using various methods. The study included strains of non-tuberculous mycobacteria (NTM) isolated from clinical material during examination for tuberculosis in the period from 2016 to 2019. The total number of samples with signs of NTMs growth that were included in the study was 316 samples. Primary isolation on Levenshtein-Jensen, Finn II, and MGIT media and NTMs identification by DNA-hybridization. All strains that were not identified prior to the species and culture, identified as microorganisms with a high G+C content (High GC GR +) were re-identified using a MALDI-ToF Microflex LT mass spectrometer (Bruker®). By the method of DNA-hybridization, 188 strains isolated by NTM were successfully identified to form 58.5% of all selected cultures. Among the selected species, representatives of slowly growing NTMs (M. avium complex, M. gordonae, M. kansasii) predominated, which amounted to 67.0% of all NTM strains identified to the species. Among the cultures for which DNA hybridization failed to carry out acceptable identification, predominantly NTMs were found, among which M. gordonae, M. avium, M. kansasii dominated. A number of NTMs were represented by rare species: M. iranicum and M. pseudoshottsii. Among this group of microorganisms, other acid-resistant aerobic actinomycetes were isolated, including those of potential clinical significance: Gordonia spp., Tsukamurella spp., Rhodococcus spp., Nocardia spp. When identifying cultures containing high concentrations of G+C, the maximum number of microbial associations was revealed, including those consisting of two types of NTMs (M. monacense + M. flavescens, M. avium + M. kansasii), as well as associations of M. gordonae with staphylococci. The same group included rare NTM species: M. fredericbergense, M. szulgai, M. malmoense, M. bohemicum, M. septicum, as well as representatives of the genera Nocardia, Gordonia, Tsukamurella.

2003 ◽  
Vol 75 (24) ◽  
pp. 6886-6893 ◽  
Author(s):  
Robert D. English ◽  
Bettina Warscheid ◽  
Catherine Fenselau ◽  
Robert J. Cotter

2004 ◽  
Vol 76 (8) ◽  
pp. 2343-2354 ◽  
Author(s):  
Elaine Stephens ◽  
Sarah L. Maslen ◽  
Luke G. Green ◽  
Dudley H. Williams

Author(s):  
A. Brian Mochon ◽  
Den Sussland ◽  
Michael A. Saubolle

2012 ◽  
Vol 29 ◽  
pp. S160-S161
Author(s):  
Piotr A. Baran ◽  
Anna Bierczyńska-Krzysik ◽  
Michał Odrowąż-Sypniewski
Keyword(s):  

2015 ◽  
Vol 54 (2) ◽  
pp. 376-384 ◽  
Author(s):  
S. P. Buckwalter ◽  
S. L. Olson ◽  
B. J. Connelly ◽  
B. C. Lucas ◽  
A. A. Rodning ◽  
...  

The value of matrix-assisted laser desorption ionization−time of flight mass spectrometry (MALDI-TOF MS) for the identification of bacteria and yeasts is well documented in the literature. Its utility for the identification of mycobacteria andNocardiaspp. has also been reported in a limited scope. In this work, we report the specificity of MALDI-TOF MS for the identification of 162Mycobacteriumspecies and subspecies, 53Nocardiaspecies, and 13 genera (totaling 43 species) of other aerobic actinomycetes using both the MALDI-TOF MS manufacturer's supplied database(s) and a custom database generated in our laboratory. The performance of a simplified processing and extraction procedure was also evaluated, and, similar to the results in an earlier literature report, our viability studies confirmed the ability of this process to inactivateMycobacterium tuberculosisprior to analysis. Following library construction and the specificity study, the performance of MALDI-TOF MS was directly compared with that of 16S rRNA gene sequencing for the evaluation of 297 mycobacteria isolates, 148Nocardiaspecies isolates, and 61 other aerobic actinomycetes isolates under routine clinical laboratory working conditions over a 6-month period. MALDI-TOF MS is a valuable tool for the identification of these groups of organisms. Limitations in the databases and in the ability of MALDI-TOF MS to rapidly identify slowly growing mycobacteria are discussed.


2016 ◽  
Vol 4 (4) ◽  
Author(s):  
A. Brian Mochon ◽  
Den Sussland ◽  
Michael A. Saubolle

Sign in / Sign up

Export Citation Format

Share Document