Alternative Molecular Tests for Virological Diagnosis

被引:16
作者
Sidoti, Francesca [1 ]
Bergallo, Massimiliano [1 ]
Costa, Cristina [1 ]
Cavallo, Rossana [1 ]
机构
[1] Univ Turin, Univ Hosp San Giovanni Battista Torino, Dept Publ Hlth & Microbiol, Virol Unit, I-10126 Turin, Italy
关键词
LAMP; NASBA; HDA; Isothermal amplification; Virological diagnosis; MEDIATED ISOTHERMAL AMPLIFICATION; SEQUENCE-BASED-AMPLIFICATION; HELICASE-DEPENDENT AMPLIFICATION; REAL-TIME PCR; HERPES-SIMPLEX-VIRUS; JAPANESE ENCEPHALITIS-VIRUS; NUCLEIC-ACID AMPLIFICATION; REVERSE TRANSCRIPTION-PCR; NUCLISENS(R) BASIC KIT; RAPID DETECTION;
D O I
10.1007/s12033-012-9533-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several nucleic acid amplification techniques (NAATs), particularly PCR and real-time PCR, are currently used in the routine clinical laboratories. Such approaches have allowed rapid diagnosis with a high degree of sensitivity and specificity. However, conventional PCR methods have several intrinsic disadvantages such as the requirement for temperature cycling apparatus, and sophisticated and costly analytical equipments. Therefore, amplification at a constant temperature is an attractive alternative method to avoid these requirements. A new generation of isothermal amplification techniques are gaining a wide popularity as diagnostic tools due to their simple operation, rapid reaction and easy detection. The main isothermal methods reviewed here include loop-mediated isothermal amplification, nucleic acid sequence-based amplification, and helicase-dependent amplification. In this review, design criteria, potential of amplification, and application of these alternative molecular tests will be discussed and compared to conventional NAATs.
引用
收藏
页码:352 / 362
页数:11
相关论文
共 100 条
[1]   An oligomeric form of E-coli UvrD is required for optimal helicase activity [J].
Ail, JA ;
Maluf, NK ;
Lohman, TM .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 293 (04) :815-834
[2]   Characterization of a thermostable UvrD helicase and its participation in helicase-dependent amplification [J].
An, LX ;
Tang, W ;
Ranalli, TA ;
Kim, HJ ;
Wytiaz, J ;
Kong, HM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (32) :28952-28958
[3]   Helicase-dependent amplification: use in OnChip amplification and potential for point-of-care diagnostics [J].
Andresen, Dennie ;
von Nickisch-Rosenegk, Markus ;
Bier, Frank F. .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2009, 9 (07) :645-650
[4]   Helicase dependent OnChip-amplification and its use in multiplex pathogen detection [J].
Andresen, Dennie ;
von Nickisch-Rosenegk, Markus ;
Bier, Frank F. .
CLINICA CHIMICA ACTA, 2009, 403 (1-2) :244-248
[5]  
Annaka Toshimitsu, 2003, Rinsho Biseibutshu Jinsoku Shindan Kenkyukai Shi, V14, P25
[6]  
BERNSTEIN JA, 1989, J BIOL CHEM, V264, P13066
[7]   Development of a loop-mediated isothermal amplification assay for rapid detection of BK virus [J].
Bista, Bipin Raj ;
Ishwad, Chandra ;
Wadowsky, Robert M. ;
Manna, Pradip ;
Randhawa, Parmjeet Singh ;
Gupta, Gaurav ;
Adhikari, Meena ;
Tyagi, Rakhi ;
Gasper, Gina ;
Vats, Abhay .
JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (05) :1581-1587
[8]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[9]   BACTERIOPHAGE-T4 GENE-32 PROTEIN - MODULATION OF PROTEIN-NUCLEIC ACID AND PROTEIN-PROTEIN ASSOCIATION BY STRUCTURAL DOMAINS [J].
CASASFINET, JR ;
KARPEL, RL .
BIOCHEMISTRY, 1993, 32 (37) :9735-9744
[10]   A sensitive and robust method for measles RNA detection [J].
Chadwick, N ;
Bruce, I ;
Davies, M ;
van Gemen, B ;
Schukkink, R ;
Khan, K ;
Pounder, R ;
Wakefield, A .
JOURNAL OF VIROLOGICAL METHODS, 1998, 70 (01) :59-70