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1 to oxacillin (based on amplification of the mecA gene).
2 ssette chromosome (SCC) elements without the mecA gene.
3 e methicillin resistant and positive for the mecA gene.
4 the results of PCR for the detection of the mecA gene.
5 is emerged as the preeminent carriers of the mecA gene.
6 studied by LightCycler PCR for the sa442 and mecA genes.
7 s-specific (nuc) and methicillin resistance (mecA) genes.
8 acilities were analyzed for the conventional mecA gene and mecC homologue by using standard PCR-based
9 ntification was based on the presence of the mecA gene and S. aureus-specific femA-SA gene, with abse
11 c sensitivity was 1 CFU per reaction for the mecA gene and was 1 to 250 CFU per reaction depending on
12 had virtually identical DNA sequences in the mecA gene and were similar in genetic organization in th
13 time PCR assays against novel targets in the mecA gene as an adjunct to routine susceptibility testin
14 were evaluated by using the presence of the mecA gene, as detected by PCR, as the "gold standard." T
16 of bacteremia from isolates that carried the mecA gene but were susceptible to oxacillin (oxacillin-s
17 icrodilution method and the detection of the mecA gene by PCR ("gold standard" reference result) were
18 crodilution method, and the detection of the mecA gene by PCR were compared with the commercial produ
20 o suggest that acquisition of PBP2a-encoding mecA gene can impart an additional regulatory layer for
22 However, six of these MSSA isolates had the mecA gene confirmed by PCR and sequencing (99.8% sensiti
23 to those generated by two reference methods: mecA gene detection and MICs of oxacillin previously det
25 for 48 h (one isolate that did not carry the mecA gene did not grow, and the sensitivity was 100%).
26 to the genus level and the detection of the mecA gene directly from a positive blood culture bottle.
27 enicillin-binding protein 2A (encoded by the mecA gene), directly contributes to pathogenicity during
30 esistance arose around this period, when the mecA gene encoding methicillin resistance carried on an
32 eus is dependent upon the acquisition of the mecA gene encoding penicillin-binding protein 2a (PBP2a)
34 strains of S. aureus that have acquired the mecA gene for PBP2a are designated as methicillin-resist
37 trip) was developed for the detection of the mecA gene from methicillin-resistant Staphylococcus aure
38 ce analysis of a 2.1-kb gene fragment of the mecA gene from the susceptible isolate revealed a one-ba
46 PCR detected the methicillin resistance (mecA) gene in all three culture-confirmed methicillin-re
47 ologue of the acquired Staphylococcus aureus mecA gene is present as a native gene in Staphylococcus
49 We synthesized, cloned, and expressed the mecA gene of S. sciuri in Escherichia coli, and the prot
50 attempt to activate the apparently "silent" mecA gene of S. sciuri, a methicillin-resistant derivati
52 immobilizing probe DNA complementary to the mecA gene on the internal walls of the nanopipette, the
55 el electrophoretic pattern, carried the same mecA gene polymorph type II, were free of the transposon
57 tection of a clinically relevant target, the mecA gene present in methicillin-resistant Staphylococcu
58 strains, 1 strain was unable to express the mecA gene product after induction and was not included i
64 ant, while introduction of the plasmid-borne mecA gene, the genetic determinant of the beta-lactam re
71 bility test results and the detection of the mecA gene was observed for Staphylococcus aureus, S. epi
72 tes with oxacillin resistance related to the mecA gene were detected when 0 or 2% NaCl agar supplemen
74 most commonly mediated by acquisition of the mecA gene, which encodes an altered penicillin binding p
77 heated prior to amplification of the nuc and mecA genes with isothermal helicase-dependent amplificat
78 taphylococcus epidermidis is mediated by the mecA gene, with resistance reported to be as high as 90%