Direct identification of mycobacteria from smear-positive sputum samples using an improved multiplex polymerase chain reaction assay

被引:9
|
作者
Chia, Ju-Hsin [1 ,2 ]
Wu, Tsu-Lan [1 ,2 ]
Su, Lin-Hui [1 ,2 ]
Kuo, An-Jing [1 ,2 ]
Lai, Hsin-Chih [1 ]
机构
[1] Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Tao Yuan, Taiwan
[2] Chang Gung Mem Hosp, Dept Lab Med, Tao Yuan, Taiwan
关键词
Multiplex PCR assay; Mycobacterium; Direct identification; REAL-TIME PCR; TUBERCULOSIS COMPLEX MEMBERS; NONTUBERCULOUS MYCOBACTERIA; CLINICAL-SIGNIFICANCE; RAPID IDENTIFICATION; DIFFERENTIATION; EPIDEMIOLOGY; INFECTION; SPECIMENS;
D O I
10.1016/j.diagmicrobio.2011.12.008
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The rapid identification of mycobacteria from smear-positive sputum samples is very important. To identify the Mycobacterium tuberculosis complex (MTBC) and frequently isolated nontuberculous mycobacteria strains directly from smear-positive sputum samples, an improved multiplex polymerase chain reaction (PCR) assay was developed. Nine pairs of primers targeting the 16S-23S rDNA internal transcribed spacer-1, hsp65, and the early secretory antigen (ESAT-6) gene sequences were developed, and their efficacy was evaluated in comparison to traditional culturing and 16S rRNA gene sequencing methods. A total of 200 smear- and culture-positive sputum specimens collected between November 2005 and May 2006 were used for the analysis. The results of the assay showed an accurate identification rate for acid-fast bacilli (AFB) 3+, AFB 2+, and AFB rare/1+ samples of 98%, 95%, and 53%, respectively. The improved multiplex PCR method saves time and has advantages for identifying mycobacteria from AFB 2+ and 3+ sputum samples. The method is suitable for use in countries with a high MTBC prevalence rate. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:340 / 349
页数:10
相关论文
共 50 条
  • [31] DETECTION OF ASTROVIRUSES FROM STOOL SAMPLES IN JAPAN USING REVERSE TRANSCRIPTION AND POLYMERASE CHAIN-REACTION AMPLIFICATION
    SAITO, K
    USHIJIMA, H
    NISHIO, O
    OSETO, MK
    MOTOHIRO, H
    UEDA, Y
    TAKAGI, M
    NAKAYA, S
    ANDO, T
    GLASS, R
    ZAIMAN, K
    MICROBIOLOGY AND IMMUNOLOGY, 1995, 39 (10) : 825 - 828
  • [32] Identification of bacteria in culture negative and polymerase chain reaction (PCR) positive intraocular specimen from patients with infectious endopthalmitis
    Aarthi, Pasupathi
    Harini, Rajagopal
    Sowmiya, Murali
    Malathi, Jambulingam
    Therese, K. Lily
    Madhavan, Hajib N.
    JOURNAL OF MICROBIOLOGICAL METHODS, 2011, 85 (01) : 47 - 52
  • [33] Detection of herpes simplex virus type 1 in addition to Epstein-Bar virus in tonsils using a new multiplex polymerase chain reaction assay
    Sahin, Fikret
    Gerceker, Devran
    Karasartova, Djursun
    Ozsan, T. Murat
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2007, 57 (01) : 47 - 51
  • [34] Detection of Rickettsia rickettsii, Rickettsia parkeri, and Rickettsia akari in Skin Biopsy Specimens Using a Multiplex Real-time Polymerase Chain Reaction Assay
    Denison, Amy M.
    Amin, Bijal D.
    Nicholson, William L.
    Paddock, Christopher D.
    CLINICAL INFECTIOUS DISEASES, 2014, 59 (05) : 635 - 642
  • [35] Evaluation of multiplex Polymerase chain reaction utilising multiple targets in Mycobacterium tuberculosis direct test negative but culture positive cases: A potential method for enhancing the diagnosis of tuberculosis
    Sharma, K.
    Ashkin, D.
    Fiorella, P.
    Willis, D.
    Dean, S.
    Sharma, A.
    Singh, K. K.
    Lee, Y.
    Pedrosa, M.
    Singh, G.
    Sharma, M.
    Laal, S.
    INDIAN JOURNAL OF MEDICAL MICROBIOLOGY, 2013, 31 (04) : 370 - 373
  • [36] Screening for Aspergillus spp. using polymerase chain reaction of whole blood samples from patients with haematological malignancies
    Lass-Flörl, C
    Aigner, J
    Gunsilius, E
    Petzer, A
    Nachbaur, D
    Gastl, G
    Einsele, H
    Löffler, R
    Dierich, MP
    Würzner, R
    BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (01) : 180 - 184
  • [37] Comparative study of direct polymerase chain reaction, microscopic examination and culture-based morphological methods for detection and identification of dermatophytes in nail and skin samples
    Uchida, Takao
    Makimura, Koichi
    Ishihara, Katsuhito
    Goto, Hideaki
    Tajiri, Yoshito
    Okuma, Mariko
    Fujisaki, Ryuichi
    Uchida, Katsuhisa
    Abe, Sigeru
    Iijima, Masafumi
    JOURNAL OF DERMATOLOGY, 2009, 36 (04) : 202 - 208
  • [38] Detection and serotype-specific differentiation of vesicular stomatitis virus using a multiplex, real-time, reverse transcription-polymerase chain reaction assay
    Hole, K
    Clavijo, A
    Pineda, LA
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2006, 18 (02) : 139 - 146
  • [39] Detection of Mycoplasma pneumoniae and Chlamydophila pneumoniae directly from respiratory clinical specimens using a rapid real-time polymerase chain reaction assay
    Diaz, Maureen H.
    Winchell, Jonas M.
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2012, 73 (03) : 278 - 280
  • [40] A multiplex real-time polymerase chain reaction assay with two internal controls for the detection of Brucella species in tissues, blood, and feces from marine mammals
    Sidor, Inga F.
    Dunn, J. Lawrence
    Tsongalis, Gregory J.
    Carlson, Jolene
    Frasca, Salvatore, Jr.
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2013, 25 (01) : 72 - 81