Literature DB >> 29105571

Accuracy of PCR targeting different markers for Staphylococcus aureus identification: a comparative study using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry as the gold standard.

Mauro M Saraiva1,2,3,4,5, Candice M De Leon1,2,3,4,5, Silvana C Santos1,2,3,4,5, Danilo T Stipp1,2,3,4,5, Miliane M Souza1,2,3,4,5, Lauro Santos Filho1,2,3,4,5, Wondwossen A Gebreyes1,2,3,4,5, Celso J Oliveira1,2,3,4,5.   

Abstract

Staphylococcus aureus is considered a major pathogen in veterinary and human medicine, and the emergence of multidrug-resistant strains, such as livestock-associated methicillin-resistant S. aureus, means that reliable, inexpensive, and fast methods are required to identify S. aureus obtained from animal sources. We tested the accuracy of a PCR targeting the genes femA, nuc, and coa in identifying S. aureus from animals. A total of 157 Staphylococcus spp. isolates were examined by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry; 18 different Staphylococcus species were identified. Of 68 S. aureus isolates, the genes femA, nuc, and coa were found in 61, 53, and 32 isolates, respectively. Considering MALDI-TOF as the gold standard, the PCR assays targeting all 3 genes showed 100% specificity; the sensitivity values were 89.7, 77.9, and 47.0% for femA, nuc, and coa, respectively. Sensitivity was 100% when femA and nuc markers were targeted simultaneously. These results confirm PCR as an accurate method to identify S. aureus species from animal sources and strongly suggest the simultaneous use of primers targeting femA and nuc genes.

Entities:  

Keywords:  MALDI-TOF; coa; femA; molecular identification; nuc

Mesh:

Year:  2017        PMID: 29105571      PMCID: PMC6505873          DOI: 10.1177/1040638717732370

Source DB:  PubMed          Journal:  J Vet Diagn Invest        ISSN: 1040-6387            Impact factor:   1.279


  4 in total

1.  Colorimetric detection of Staphylococcus aureus using gold nanorods labeled with yolk immunoglobulin and urease, magnetic beads, and a phenolphthalein impregnated test paper.

Authors:  Bo Pang; Yan Zheng; Juan Wang; Yushen Liu; Xiuling Song; Jinhua Li; Shuo Yao; Kaiyue Fu; Kun Xu; Chao Zhao; Juan Li
Journal:  Mikrochim Acta       Date:  2019-08-08       Impact factor: 5.833

2.  Evaluation of the MRSA/SA ELITe MGB Assay for the Detection of Staphylococcus aureus in Bone and Joint Infections.

Authors:  R Labetoulle; J Rigaill; P O Verhoeven; A Carricajo; M Lleres-Vadeboin; F Grattard; B Pozzetto; C Cazorla; E Botelho-Nevers; B Boyer; C Dupieux-Chabert; F Laurent
Journal:  J Clin Microbiol       Date:  2021-11-17       Impact factor: 11.677

3.  Predominance of t355/ST152/SCCmec V clonal type among PVL-positive MRSA isolates in a tertiary care hospital in Belgrade, Serbia.

Authors:  Bojan Rakonjac; Zorica Lepšanović; Vesna Šuljagić; Branko Jovčić; Milan Kojić; Anders Rhod Larsen; Momčilo Đurić; Ivana Ćirković
Journal:  PLoS One       Date:  2022-09-08       Impact factor: 3.752

4.  Occurrence of foodborne pathogens in Italian soft artisanal cheeses displaying different intra- and inter-batch variability of physicochemical and microbiological parameters.

Authors:  Frédérique Pasquali; Antonio Valero; Arícia Possas; Alex Lucchi; Cecilia Crippa; Lucia Gambi; Gerardo Manfreda; Alessandra De Cesare
Journal:  Front Microbiol       Date:  2022-08-25       Impact factor: 6.064

  4 in total

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