Development of a Loop-Mediated Isothermal Amplification Assay for Rapid, Sensitive and Specific Detection of a Campylobacter jejuni Clone
Author:
Affiliation:
1. Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, Iowa 50011, U.S.A.
2. Laboratory of Microbiology, Dujiangyan Campus, Sichuan Agricultural University, Dujiangyan 611830 China
Publisher
Japanese Society of Veterinary Science
Subject
General Veterinary
Link
https://www.jstage.jst.go.jp/article/jvms/74/5/74_11-0462/_pdf
Reference19 articles.
1. 1.Baqar, S., Bourgeois, A. L., Applebee, L. A., Mourad, A. S., Kleinosky, M. T., Mohran, Z. and Murphy, J. R. 1996. Murine intranasal challenge model for the study of Campylobacter pathogenesis and immunity. Infect. Immun. 64: 4933-4939.
2. Pathogenicity of an emergent, ovine abortifacientCampylobacter jejuniclone orally inoculated into pregnant guinea pigs
3. 3.Fu, S. J., Qu, G. G., Guo, S. J., Ma, L., Zhang, N., Zhang, S. L., Gao, S. Y. and Shen, Z. Q. 2011. Applications of Loop-Mediated Isothermal DNA Amplification. Appl. Biochem. Biotechnol. 163: 845-850.
4. Unique Features of a Highly Pathogenic Campylobacter jejuni Strain
5. 5.Logan, J. M. J., Edwards, K. J., Saunders, N. A. and Stanley, J. 2001. Rapid identification of Campylobacter spp. by melting peak analysis of biprobes in real-time PCR. J. Clin. Microbiol. 39: 2227-2232.
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