Identification of Bartonella using PCR; genus and species-specific primer sets

被引:20
作者
Minnick, MF [1 ]
Barbian, KD [1 ]
机构
[1] Univ Montana, Div Biol Sci, Missoula, MT 59812 USA
关键词
Bartonella; PCR; rapid method; identification;
D O I
10.1016/S0167-7012(97)00083-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Four Bartonella species cause a variety of emerging infectious diseases in humans that can be difficult to diagnose. A PCR-based identification system using amplimers designed from internal portions of the 16S-23S intergenic spacer (ITS) region is described. A genus-specific primer set can distinguish Bartonella species from Escherichia coli or closely-related alpha-Proteobacteria including Brucella abortus, Agrobacterium tumefaciens and Rhizobium meliloti. Species-specific primer sets for bartonellae that cause human disease (B. bacilliformis, B. elizabethae, B. henselae and B. quintana) produce single, unique amplicons from their respective target and do not react with DNA from other Bartonella species, close bacterial relatives, or E. coli. The described system streamlines current PCR-based identification of pathogenic bartonellae by generating genus- or species-specific amplicons, obviating the need for subsequent RFLP or sequence analysis of the PCR product. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:51 / 57
页数:7
相关论文
共 50 条
[31]   Development of a Species-Specific PCR Assay for Aerococcus urinaeequi Using Whole Genome Sequencing [J].
Wang, Hailong ;
Li, Haixia ;
Lu, Zhenxiang ;
Li, Wenchao ;
Guo, Weina .
PATHOGENS, 2025, 14 (07)
[32]   Rapid identification of the species of the Bacteroides fragilis group by multiplex PCR assays using group- and species-specific primers [J].
Liu, CX ;
Song, YL ;
McTeague, M ;
Vu, AW ;
Wexler, H ;
Finegold, SM .
FEMS MICROBIOLOGY LETTERS, 2003, 222 (01) :9-16
[33]   Molecular identification of lactic acid bacteria in Chinese rice wine using species-specific multiplex PCR [J].
Ke, Leqin ;
Wang, Liling ;
Li, Haibo ;
Lin, Haiping ;
Zhao, Li .
EUROPEAN FOOD RESEARCH AND TECHNOLOGY, 2014, 239 (01) :59-65
[34]   Detection of Enterocytozoon bieneusi (Microsporidia) by polymerase chain reaction (PCR) using species-specific primer in stool samples of HIV patients [J].
Kumar, SS ;
Ananthan, S ;
Joyee, AG .
INDIAN JOURNAL OF MEDICAL RESEARCH, 2005, 121 (04) :215-219
[35]   Identification of Fel ursi and Cattle and Pig Bile Juices by species-specific PCR and PCR-RFLP [J].
Kwon, Ki-Rok ;
Baek, Seung-Il ;
Choi, Suk Ho .
JOURNAL OF PHARMACOPUNCTURE, 2009, 12 (01) :13-20
[36]   Development of the primer sets for identification of a rice cultivar, Koshihikari, by PCR [J].
Ohtsubo, K ;
Nakamura, S ;
Imamura, T .
NIPPON NOGEIKAGAKU KAISHI-JOURNAL OF THE JAPAN SOCIETY FOR BIOSCIENCE BIOTECHNOLOGY AND AGROCHEMISTRY, 2002, 76 (04) :388-397
[37]   Simultaneous detection and identification of the Xanthomonas species complex associated with tomato bacterial spot using species-specific primers and multiplex PCR [J].
Araujo, E. R. ;
Costa, J. R. ;
Ferreira, M. A. S. V. ;
Quezado-Duval, A. M. .
JOURNAL OF APPLIED MICROBIOLOGY, 2012, 113 (06) :1479-1490
[38]   Development of two species-specific primer sets to detect the cereal cyst nematodes Heterodera avenae and Heterodera filipjevi [J].
Fateh Toumi ;
Lieven Waeyenberge ;
Nicole Viaene ;
Amer Dababat ;
Julie M. Nicol ;
Francis Ogbonnaya ;
Maurice Moens .
European Journal of Plant Pathology, 2013, 136 :613-624
[39]   Identification of respiratory isolates of Stenotrophomonas maltophilia by commercial biochemical systems and species-specific PCR [J].
Giordano, A ;
Magni, A ;
Trancassini, M ;
Varesi, P ;
Turner, R ;
Mancini, C .
JOURNAL OF MICROBIOLOGICAL METHODS, 2006, 64 (01) :135-138
[40]   Optimisation of a species-specific primer set to quantify the soybean cyst nematode, Heterodera glycines, in soil using real-time PCR [J].
Shirai, Sayo ;
Toyota, Koki .
NEMATOLOGY, 2019, 21 (10) :1037-1042