Species identification of staphylococci by amplification and sequencing of the tuf gene compared to the gap gene and by matrix-assisted laser desorption ionization time-of-flight mass spectrometry

被引:57
作者
Bergeron, M. [2 ]
Dauwalder, O. [2 ,3 ,4 ]
Gouy, M. [5 ]
Freydiere, A-M [2 ]
Bes, M. [2 ,3 ,4 ]
Meugnier, H. [2 ,3 ,4 ]
Benito, Y. [2 ,3 ,4 ]
Etienne, J. [2 ,3 ,4 ]
Lina, G. [2 ,3 ,4 ]
Vandenesch, F. [2 ,3 ,4 ]
Boisset, S. [1 ,2 ,3 ,4 ]
机构
[1] Ctr Natl Reference Staphylocoques, Bacteriol Lab, F-69677 Bron, France
[2] Hosp Civils Lyon, Ctr Biol & Pathol Est, Bacteriol Lab, Bron, France
[3] Univ Lyon 1, Ctr Natl Reference Staphylocoques, F-69365 Lyon, France
[4] INSERM, U851, IFR128, F-69008 Lyon, France
[5] Univ Lyon, CNRS, UMR 5558, Lab Biometrie & Biol Evolut, F-69622 Villeurbanne, France
关键词
COAGULASE-NEGATIVE STAPHYLOCOCCI; FRAGMENT LENGTH POLYMORPHISM; DEHYDROGENASE-ENCODING GENE; 16S RIBOSOMAL-RNA; SUBSP-NOV; PHYLOGENETIC-RELATIONSHIPS; MICROBIOLOGY LABORATORIES; RAPID IDENTIFICATION; LEVEL IDENTIFICATION; CLINICAL SPECIMENS;
D O I
10.1007/s10096-010-1091-z
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Staphylococcal species, notably, coagulase-negative staphylococci (CoNS), are frequently misidentified using phenotypic methods. The partial nucleotide sequences of the tuf and gap genes were determined in 47 reference strains to assess their suitability, practicability, and discriminatory power as target molecules for staphylococcal identification. The partial tuf gene sequence was selected and further assessed with a collection of 186 strains, including 35 species and subspecies. Then, to evaluate the efficacy of this genotyping method versus the technology of matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS), the 186 strains were identified using MALDI-TOF-MS (AximaA (R) Shimadzu) coupled to the SARAMISA (R) database (AnagnosTec). The French National Reference Center for Staphylococci identification method was used as a reference. One hundred and eighty-four strains (98.9%) were correctly identified by tuf gene sequencing. Only one strain was misidentified and one was unidentified. MALDI-TOF-MS identified correctly 138 isolates (74.2%). Four strains were misidentified, 39 were unidentified, five were identified at the group (hominis/warneri) level, and one strain was identified at the genus level. These results confirm the value of MALDI-TOF-MS identification for common species in clinical laboratory practice and the value of the partial tuf gene sequence for the identification of all staphylococcal species as required in a reference laboratory.
引用
收藏
页码:343 / 354
页数:12
相关论文
共 53 条
[11]   Genetic classification and distinguishing of Staphylococcus species based on different partial gap, 16S rRNA, hsp60, rpoB, sodA, and tuf gene sequences [J].
Ghebremedhin, B. ;
Layer, F. ;
Koenig, W. ;
Koenig, B. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (03) :1019-1025
[12]   WSP60 gene sequences as universal targets for microbial species identification: Studies with coagulase-negative staphylococci [J].
Goh, SH ;
Potter, S ;
Wood, JO ;
Hemmingsen, SM ;
Reynolds, RP ;
Chow, AW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :818-823
[13]   SeaView Version 4: A Multiplatform Graphical User Interface for Sequence Alignment and Phylogenetic Tree Building [J].
Gouy, Manolo ;
Guindon, Stephane ;
Gascuel, Olivier .
MOLECULAR BIOLOGY AND EVOLUTION, 2010, 27 (02) :221-224
[14]   Rapid identification by specific PCR of coagulase-negative staphylococcal species important in hospital infection [J].
Gribaldo, S ;
Cookson, B ;
Saunders, N ;
Marples, R ;
Stanley, J .
JOURNAL OF MEDICAL MICROBIOLOGY, 1997, 46 (01) :45-53
[15]   Staphylococcus saprophyticus subsp, bovis subsp nov, isolated from bovine nostrils [J].
Hajek, V ;
Meugnier, H ;
Bes, M ;
Brun, Y ;
Fiedler, F ;
Chmela, Z ;
Lasne, Y ;
Fleurette, J ;
Freney, J .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1996, 46 (03) :792-796
[16]   Staphylococcus stepanovicii sp nov., a novel novobiocin-resistant oxidase-positive staphylococcal species isolated from wild small mammals [J].
Hauschild, Tomasz ;
Stepanovic, Srdjan ;
Zakrzewska-Czerwinska, Jolanta .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 2010, 33 (04) :183-187
[17]   Comparison of genotypic and phenotypic methods for species-level identification of clinical isolates of coagulase-negative staphylococci [J].
Heikens, E ;
Fleer, A ;
Paauw, A ;
Florijn, A ;
Fluit, AC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (05) :2286-2290
[18]   STAPHYLOCOCCUS-SCHLEIFERI SUBSP COAGULANS SUBSP-NOV, ISOLATED FROM THE EXTERNAL AUDITORY MEATUS OF DOGS WITH EXTERNAL EAR OTITIS [J].
IGIMI, S ;
TAKAHASHI, E ;
MITSUOKA, T .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1990, 40 (04) :409-411
[19]   Relationships between Staphylococcus aureus genetic background, virulence factors, agr groups (Alleles), and human disease [J].
Jarraud, S ;
Mougel, C ;
Thioulouse, J ;
Lina, G ;
Meugnier, H ;
Forey, F ;
Nesme, X ;
Etienne, J ;
Vandenesch, F .
INFECTION AND IMMUNITY, 2002, 70 (02) :631-641
[20]   Development of a PCR assay for rapid detection of enterococci [J].
Ke, DB ;
Picard, FJ ;
Martineau, F ;
Ménard, C ;
Roy, PH ;
Ouellette, M ;
Bergeron, MG .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (11) :3497-3503