Literature DB >> 9232620

Multiplex PCR for avian pathogenic mycoplasmas.

H Wang1, A A Fadl, M I Khan.   

Abstract

Mycoplasma infections are of great concern in avian medicine, because they cause economic losses in commercial poultry production. A multiplex polymerase chain reaction (PCR) was optimized to simultaneously detect four pathogenic species of avian mycoplasmas. Four sets of oligonucleotide primers specific for Mycoplasma gallisepticum (MG), M. synoviae (MS), M. meleagridis (MM) and M. iowae (MI) were used in the test. By using agarose gel electrophoreses for detection of the PCR-amplified DNA products, the sensitivity of detection was between 1 pg for MG, 1 pg for MS, 100 fg for MM and 100 pg for MI after 35 cycles of PCR. Similar sensitivity of these primers was achieved with broth cultures of these four organisms.

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Year:  1997        PMID: 9232620     DOI: 10.1006/mcpr.1997.0108

Source DB:  PubMed          Journal:  Mol Cell Probes        ISSN: 0890-8508            Impact factor:   2.365


  3 in total

Review 1.  Specificity and performance of PCR detection assays for microbial pathogens.

Authors:  Konrad Sachse
Journal:  Mol Biotechnol       Date:  2004-01       Impact factor: 2.695

2.  Diagnosis and differentiation of Mycoplasma hyopneumoniae and Mycoplasma hyorhinis infections in pigs by PCR amplification of the p36 and p46 genes.

Authors:  J Caron; M Ouardani; S Dea
Journal:  J Clin Microbiol       Date:  2000-04       Impact factor: 5.948

3.  Real-time Loop-mediated Isothermal Amplification (LAMP) of mgc2 Gene of Mycoplasma Gallisepticum.

Authors:  Syed Ehtisham-Ul-Haque; Madiha Kiran; Usman Waheed; Muhammad Younus
Journal:  J Vet Res       Date:  2017-12-27       Impact factor: 1.744

  3 in total

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