Advanced SearchSearch Tips
Development of Rapid Detection Method for Bacillus Anthrax and Brucella Abortus
facebook(new window)  Pirnt(new window) E-mail(new window) Excel Download
 Title & Authors
Development of Rapid Detection Method for Bacillus Anthrax and Brucella Abortus
Choi, Jae-Gu;
  PDF(new window)
The livestocks are sometimes infected with pathogenic microorganisms such as bird influenza, brucellosis, pig cholerae, and salmonella. However, it is difficult to predict the outcome of these diseases because the livestocks are mostly raised in the rural areas. Efficient systems for detecting and alerting the onset of livestock diseases are urgently required. In these studies, the fluorescent analysis method, luminescent analysis method, and frequently used gene amplification method (polymerase chain reaction) have been developed in order to detect the pathogenic microbes in the early stages of disease progression. By using these developed systems, damages due to the livestock diseases induced by microbes can be minimized. If we can detect livestock diseases in the early stage, the costs for diagnosis and treatment will be reduced, and the livestock can be quickly recovered.
bird influenza;brucellosis;pig cholerae;salmonella;fluorescent analysis;
 Cited by
Yagupsky, P. : Detection of brucellae in blood cultures. Journal of Clinical Microbiology, 37, 3437-3442, 1999

Eamon, C., Donnacha O'., Orla, F., Rory, O'., Mark, R., Frances, Q., John, E. and John, G. : Study of restriction fragment length polymorphism analysis and spoligotyping for epidemiological investigation of Mycobacterium bovis infection. Journal of Clinical Microbiology, 36, 3217-3222, 1998

Matthew, D. E., Axel, Cloeckaert, and Philip, H. E. : Brucella species lacking the major outer membrane protein Omp25 are attenuated in mice and protect against Brucella melitensis and Brucella ovis. Veterinary Microbiology, 88, 205-221, 2002 crossref(new window)

Lizzie, J. and Einsele, H. : Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation. Journal of Clinical Microbiology, 33, 1847-1850, 1995

Michael, J. Brumlik : Use of long-range repetitive element polymorphism-PCR to differentiate Bacillus anthracis strains. Applied and Environmental Microbiology, 61, 3021-3028, 2001

송주희, 민진영, 조경아, 윤영희, 백남원 : 서울시 일부 종합병원의 공기 중 미생물 농도 분포. 한국환경보건학회지, 33(2), 104-114, 2007 crossref(new window)

이항, 오영희, 최성민, 박석기 : 어패류에서 분리한 장비브리오균의 분포 및 항상제 감수성. 한국환경보건학회지, 33(1), 16-20, 2007 crossref(new window)

김기연, 장규엽, 박재범, 김치년, 이경종 : 배지 종류 및 저장 조건에 따른 impactor의 부유세균 시료 채취 효율 평가. 한국환경보건학회지, 33(2), 145-149, 2007 crossref(new window)

Isalell, E. T. : Characterization of the Bacillus anthracis S-Layer: cloning and sequencing of the structural gene. Journal of Bacteriology, 177, 614-620, 1995 crossref(new window)

Nielsen, K. : Serological relationship between cattle exposed to Brucella abortus, Yersinia enterocolitica O:9 and Escherichia coli O157:H7. Veterinary Microbiology, 100, 25-30, 2004 crossref(new window)

Maria Isabel Queipo-Ortun, and Miguel Angel Garcia-Ordon : PCR-DIG ELISA with biotinylated primers is unsuitable for use in whole blood samples from patients with brucellosis. Molecular and Cellular Probes, 18, 243-250, 2004 crossref(new window)

Zahra Fayazi, Ali Ghadersohi and Robert, G. : Development of a Brucella suis specific hybridisation probe and PCR which distinguishes B. suis from Brucella abortus. HirstVeterinary Microbiology, 84, 253-261, 2002

Navarro, E. and Escribano, J. : Comparison of three different PCR methods for detection of Brucella spp in human blood samples. FEMS Immunology and Medical Microbiology, 34, 147-151, 2002 crossref(new window)

Redkar, R., Rose, S., Bricker, B. and Del Vecchio, V. : Real-time detection of Brucella abortus, Brucella melitensis and Brucella suis. Molecular and Cellular Probes, 15, 43-52, 2001 crossref(new window)

Smith, K. L. : Bacillus anthracis diversity in kruger national park. Journal of Clinical Microbilogy, 38, 3780-3784, 2000

Shively, L. and Chang, L. : Real-time PCR assay for quantitative mismatch detection. BioTechniques 34, 498-504, 2003

Alessandra Ciervo and L o renzo C icero ni : R apid detection and differentiation of Bartonella spp. by a single-run real-time PCR. Molecular and Cellular Probes, 18, 307-312, 2004 crossref(new window)

Dixon, T. J., Taggart, J. B. and George, S. G. : Application of real time PCR determination to assess interanimal variabilities in CYP1A induction in the European flounder (Platichthys flesus). Marine Environmental Research, 54, 267-270, 2002 crossref(new window)

Nicola C. Elviss, Andrew J. Lawson, Robert, J. Owen : Application of 3-mismatched reverse primer PCR compared with real-time PCR and PCR-RFLP for the rapid detection of 23S rDNA mutations associated with clarithromycin resistance in Helicobacter pylori. International Journal of Antimicrobia, 23, 349-355, 2004 crossref(new window)

Bell, A., S. and Ranford-Cartwright. L. C. : International Journal for Parasitology, 34, 795-802, 2004 crossref(new window)

Jim O'Mahony and Colin Hill. : A real time PCR assay for the detection and quantitation of Mycobacterium avium subsp. paratuberculosis using SYBR Green and the Light Cycler. Journal of Microbiological Methods, 51, 283-293, 2002 crossref(new window)

Stuart N. Peirson, Jason N. Butler and Russell G. Foster : Experimental validation of novel and conventional approaches to quantitative real-time PCR data analysis. Nucleic Acids Research, 31, e73, 2003 crossref(new window)

Carole A. Foy, Helen C. Parkes : Emerging homogeneous DNA-based technologies in the clinical laboratory. Clinical Chemistry, 47, 990-1000, 2001

Jessica L. Dang, Karen Heroux, John Kearney, Ameneh Arasteh, Mark Gostomsi and Peter A. Emanuel : Bacillus spore inactivation methods affect detection assays. Applied and Environmental Microbiology, 67, 3665-3670, 2001 crossref(new window)