مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

991
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

CLONING AND SEQUENCING OF PARTIAL PLB1 GENE OF ASPERGILLUS FUMIGATUS

Author(s)

KAZEMI A. | Issue Writer Certificate 

Pages

  47-54

Abstract

 Background and Objectives: Aspergillus species are primarily opportunistic pathogens and, with a few exceptions, cause invasive disease only in an immunocompromised hosts. During last two decades, the importance of fungal disease has been increased dramatically due to an increased occurrence of tuberculosis, chemotherapy-induced neutropenia, AIDS, open chest surgery and use of antibiotics and immunosuppressive therapy. The production of extracellular phospholipases by pathogenic fungi such as A. fumigatus are involved in the degradation of target cell membrane phospholipids in invaded tissues. Materials and Methods: Using degenerate primers based on homologous amino acid sequences of fungal PHOSPHOLIPASE B (plb) gene, PCR products of 545bp were generated. Sequence analysis revealed that the sequence had a high homology to published plb sequences sharing highest homology to Aspergillus oryzae PLB (76% identity). Inverse PCR was used to attempt to clone the entire plb1 genes. Initially, genomic DNA was digested with selected restriction enzymes and self-ligated with T4 DNA ligase to give circular DNA for inverse PCR (IPCR) for afplb1. IPCR with Xho I self-ligated digest gave product of 1.8 Kb for afplb1 and was found to encode the 3 ends of gene and using CAP assembly software this sequence was assembled with 545 bp sequence. Results: BLST X and GeneFinder analysis revealed that the first 960 bp of assembled total 2197 bp (after deletion of similar bp from both sequences) encoded the 3 end of afplb1 gene.Conclusion: The sequence availability of partial afplb1 gene and after that full sequence of this gene represents a major breakthrough in the study of this opportunistic pathogen and function of plb gene in pathogenesis of A. fumigatus. Also phylogenic tree analysis of afplb1 gene shows that plbs and potential plb analogues are contained in a large cluster of the plb family. A. fumigatus is more closely related to A. oryzae, A.niger, P.notatum, and N. crassa plb than other fungi.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    KAZEMI, A.. (2004). CLONING AND SEQUENCING OF PARTIAL PLB1 GENE OF ASPERGILLUS FUMIGATUS. MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, 38(62), 47-54. SID. https://sid.ir/paper/46683/en

    Vancouver: Copy

    KAZEMI A.. CLONING AND SEQUENCING OF PARTIAL PLB1 GENE OF ASPERGILLUS FUMIGATUS. MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2004;38(62):47-54. Available from: https://sid.ir/paper/46683/en

    IEEE: Copy

    A. KAZEMI, “CLONING AND SEQUENCING OF PARTIAL PLB1 GENE OF ASPERGILLUS FUMIGATUS,” MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, vol. 38, no. 62, pp. 47–54, 2004, [Online]. Available: https://sid.ir/paper/46683/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button