2019
DOI: 10.1007/s10096-019-03758-x
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Assessment of VITEK® MS IVD database V3.0 for identification of Nocardia spp. using two culture media and comparing direct smear and protein extraction procedures

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Cited by 17 publications
(13 citation statements)
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“…Due to the large number of Nocardia species, biochemical methods are insufficient to identify the clinically relevant species [ 4 ]. MALDI-TOF MS can rapidly identify the frequently encountered Nocardia species, but it is limited by the database and distinguishing closely related species [ 10 ]. The 16S rRNA gene sequencing is robust for accurate identification of Nocardia species, but it is also limited by discriminating closely related species due to high conservation [ 12 ].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Due to the large number of Nocardia species, biochemical methods are insufficient to identify the clinically relevant species [ 4 ]. MALDI-TOF MS can rapidly identify the frequently encountered Nocardia species, but it is limited by the database and distinguishing closely related species [ 10 ]. The 16S rRNA gene sequencing is robust for accurate identification of Nocardia species, but it is also limited by discriminating closely related species due to high conservation [ 12 ].…”
Section: Discussionmentioning
confidence: 99%
“…With the development of matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS), the common clinical Nocardia species (e.g., N. cyriacigeorgica and N. farcinica ) can be identified rapidly. However, the available database of MALDI-TOF MS is limited for Nocardia strains leading to some uncommon isolates with no or false identification [ 10 , 11 ]. The 16S rRNA gene sequencing is generally considered as the primary means for accurate identification of the clinically encountered Nocardia isolates [ 12 ], but it cannot discriminate closely related species due to high conservation, unless it combines with a housekeeping gene, such as gyrB or rpoB [ 13 ].…”
Section: Introductionmentioning
confidence: 99%
“…[40][41][42] A preliminary step of protein extraction (with glass beads and ethanol, followed by formic acid) and repeated spotting of different extracts is frequently required to increase the likelihood of identification. 43,44 complexes. When identified by MALDI-TOF MS, these species should therefore be referred to as "N. nova complex" or "N. abscessus complex" and/or should be analyzed using molecular biology (see earlier).…”
Section: Figurementioning
confidence: 99%
“…Durand et al evaluated the performance of VITEK ® MS (V3.0) for the identification of Nocardia spp. The identification rates at the species level can be improved by using repeat or new extracts [ 9 ].…”
Section: Accuracy For Microbial Identification and Other Applicationmentioning
confidence: 99%
“…MALDI-TOF MS is not limited to identifying strains cultured on solid media but can also directly identify them from the blood culture, cerebrospinal fluid, and urine [ 1 , 2 , 3 , 4 , 5 ]. MALDI-TOF MS identification has been used to identify gram-negative and gram-positive bacteria, aerobes, anaerobes, mycobacteria, Nocardia , yeasts, filamentous fungi and viruses [ 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 ].…”
Section: Introductionmentioning
confidence: 99%