Evaluation of CHROMagar Staph, aureus, a new chromogenic medium, for isolation and presumptive identification of Staphylococcus aureus from human clinical specimens

被引:72
作者
Gaillot, O [1 ]
Wetsch, M [1 ]
Fortineau, N [1 ]
Berche, P [1 ]
机构
[1] Hop Necker Enfants Malad, Lab Bacteriol Virol, F-75730 Paris 15, France
关键词
D O I
10.1128/JCM.38.4.1587-1591.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
CHROMagar Staph, aureus (CSA) is a new chromogenic medium for presumptive identification of Staphylococcus aureus as mauve colonies after 24 h of incubation. We conducted a preliminary study with 100 S. aureus and 45 coagulase-negative Staphylococcus (CoNS) stock isolates plated on CSA, All S, aureus isolates yielded mauve colonies after 24 h of incubation at 37 degrees C, while CoNS isolates grew as blue, white, or beige colonies. Culture on CSA was then prospectively compared to a conventional laboratory method, i.e., culture on 5% horse blood agar (HBA), catalase test, and latex agglutination test (HBA-catalase-latex), for isolation and presumptive identification of S. aureus from 2,000 consecutive clinical samples. Among the 310 S. aureus isolates recovered by at least one of the two methods, 296 grew as typical mauve colonies on CSA, while only 254 yielded catalase-positive, latex-positive colonies on HBA. The sensitivity of CSA was significantly higher than that of the conventional method (95.5 and 81.9%, respectively; P < 0.001) and allowed the recovery of important clinical isolates that were undetected on blood agar, The specificities of the two methods were not significantly different, although that of CSA was slightly higher (99.4% versus 98.9% for HBA-catalase-latex; P = 0.08). On the basis of its excellent sensitivity and specificity, ease of identification of positive colonies, and absence of complementary testing, CSA can be recommended as a routine plating medium for presumptive identification of S. aureus in clinical specimens.
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页码:1587 / 1591
页数:5
相关论文
共 12 条
  • [1] MEDIA USED IN THE DETECTION AND ENUMERATION OF STAPHYLOCOCCUS-AUREUS
    BAIRD, RM
    LEE, WH
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1995, 26 (01) : 15 - 24
  • [2] BLAIR EB, 1967, AM J CLIN PATHOL, V47, P30
  • [3] DETECTION OF STAPHYLOCOCCUS-AUREUS BY POLYMERASE CHAIN-REACTION AMPLIFICATION OF THE NUC GENE
    BRAKSTAD, OG
    AASBAKK, K
    MAELAND, JA
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (07) : 1654 - 1660
  • [4] THE SIGNIFICANCE OF SODIUM CHLORIDE IN STUDIES OF STAPHYLOCOCCI
    CHAPMAN, GH
    [J]. JOURNAL OF BACTERIOLOGY, 1945, 50 (02) : 201 - 203
  • [5] DIRECT IDENTIFICATION OF BACTERIAL ISOLATES IN BLOOD CULTURES BY USING A DNA PROBE
    DAVIS, TE
    FULLER, DD
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (10) : 2193 - 2196
  • [6] FELTEN A, 1995, PATHOL BIOL, V43, P471
  • [7] NEW LATEX REAGENT USING MONOCLONAL-ANTIBODIES TO CAPSULAR POLYSACCHARIDE FOR RELIABLE IDENTIFICATION OF BOTH OXACILLIN-SUSCEPTIBLE AND OXACILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS
    FOURNIER, JM
    BOUVET, A
    MATHIEU, D
    NATO, F
    BOUTONNIER, A
    GERBAL, R
    BRUNENGO, P
    SAULNIER, C
    SAGOT, N
    SLIZEWICZ, B
    MAZIE, JC
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (05) : 1342 - 1344
  • [8] GUNN BA, 1972, AM J CLIN PATHOL, V57, P230
  • [9] GUZMAN CA, 1992, J CLIN MICROBIOL, V30, P1194
  • [10] Salt tolerance of EMRSA-16 and its effect on the sensitivity of screening cultures
    Jones, EM
    Bowker, KE
    Cooke, R
    Marshall, RJ
    Reeves, DS
    MacGowan, AP
    [J]. JOURNAL OF HOSPITAL INFECTION, 1997, 35 (01) : 59 - 62