Literature DB >> 28254444

Comparison of growth on mannitol salt agar, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, VITEK® 2 with partial sequencing of 16S rRNA gene for identification of coagulase-negative staphylococci.

Funmilola A Ayeni1, Camilla Andersen2, Niels Nørskov-Lauritsen3.   

Abstract

Mannitol salt agar (MSA) is often used in resources' limited laboratories for identification of S. aureus however, coagulase-negative staphylococci (CoNS) grows and ferments mannitol on MSA. 171 strains of CoNS which have been previously misidentified as S. aureus due to growth on MSA were collected from different locations in Nigeria and two methods for identification of CoNS were compared i.e. ViTEK 2 and MALDI-TOF MS with partial 16S rRNA gene sequencing as gold standard. Partial tuf gene sequencing was used for contradicting identification. All 171 strains (13 species) grew on MSA and ferments mannitol. All tested strains of S. epidermidis, S. haemolyticus, S. nepalensis, S. pasteuri, S. sciuri,, S. warneri, S. xylosus, S. capitis were correctly identified by MALDI-TOF while variable identification were observed in S. saprophyticus and S. cohnii (90%, 81%). There was low identification of S. arlettae (14%) while all strains of S. kloosii and S. gallinarum were misidentified. There is absence of S. gallinarum in the MALDI-TOF database at the period of this study. All tested strains of S. epidermidis, S. gallinarum, S. haemolyticus, S. sciuri,, S. warneri, S. xylosus and S. capitis were correctly identified by ViTEK while variable identification were observed in S. saprophyticus, S. arlettae, S. cohnii, S. kloosii, (84%, 86%, 75%, 60%) and misidentification of S. nepalensis, S. pasteuri. Partial sequencing of 16S rRNA gene was used as gold standard for most strains except S. capitis and S. xylosus where the two species were misidentified by partial sequencing of 16S rRNA contrary to MALDI-TOF and ViTEK identification. Tuf gene sequencing was used for correct identification. Characteristic growth on MSA for CoNS is also identical to S. aureus growth on the media and therefore, MSA could not differentiate between S. aureus and CoNS. The percentage accuracy of ViTEK was better than MALDI-TOF in identification of CoNS. Although partial sequencing of 16S rRNA gene was used as gold standard in this study, it could not correctly identify S. capitis and S. xylosus.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Coagulase negative staphylococci; Identification; MALDI-TOF; Mannitol salt agar; VITEK

Mesh:

Substances:

Year:  2017        PMID: 28254444     DOI: 10.1016/j.micpath.2017.02.034

Source DB:  PubMed          Journal:  Microb Pathog        ISSN: 0882-4010            Impact factor:   3.738


  10 in total

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Journal:  Front Cell Infect Microbiol       Date:  2019-08-07       Impact factor: 5.293

Review 4.  Coagulase-negative staphylococci (CoNS) as a significant etiological factor of laryngological infections: a review.

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7.  Molecular characterization of clonal lineage and staphylococcal toxin genes from S. aureus in Southern Nigeria.

Authors:  Funmilola A Ayeni; Werner Ruppitsch; Franz Allerberger
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9.  Additional Bacteriological Examinations Might be Required for the Correct Identification of Staphylococcus warneri.

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Journal:  Intern Med       Date:  2020-09-30       Impact factor: 1.271

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Journal:  Intern Med       Date:  2020-09-30       Impact factor: 1.271

  10 in total

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