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:

322
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

143
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

2

Information Journal Paper

Title

THE FREQUENCY OF EXOTOXIN A AND EXOENZYMES S AND U GENES AMONG CLINICAL ISOLATES OF PSEUDOMONAS AERUGINOSA IN SHIRAZ, IRAN

Pages

  167-173

Abstract

PSEUDOMONAS AERUGINOSA as an opportunistic pathogen produces several virulence factors. The most important of these factors are EXOTOXIN A and type III secretion system (T3SS). The aim of this study was to determine the frequency of toxA, exoU and exoS genes among clinical isolates of P. aeruginosa. In this cross-sectional study from September 2011 to February 2012, 156 P. aeruginosa isolates were recovered from different clinical samples. Susceptibility testing against 10 antibiotics was performed on individual isolates by the disc diffusion method according to CLSI guidelines. Extracted DNA was subjected to PCR assay for determining the presence of toxA, exoU and exoS genes. Overall, the frequency of toxA, exoU and exoS genes were 90.4%, 66.7% and 65.4%, respectively. All of the abdominal and eye isolates were exoS+. The frequency of exoS+/exoU- and exoS-/exoU+ genotypes was estimated 19.2% and 16.2%, respectively. Indeed, genotypes exoS+/exoU+ and exoS-/exoU were found with frequencies of 48.7% and 15.3%, respectively. The highest and lowest antibiotic resistance rate was seen against azteroenam (94.2%) and amikacin (44.9%), respectively. Fluoroqinolone-resistant isolates were isolated with frequency of 45.8%. Multi-drug resistant (MDR) isolates were detected in 62.8% of isolates. The resistance rate in exoU+ isolates was 86% compared to 66% in exoS+ isolates. The high frequencies of virulence genes detected in our clinical isolates with notable antibiotic resistance rates indicate the potential risk of these isolates in nosocomial infections.

Cites

References

  • No record.
  • Cite

    APA: Copy

    YOUSEFI AVARVAND, ARSHID, KHASHEI, REZA, SEDIGH EBRAHIM SARAIE, HADI, EMAMI, AMIR, ZOMORODIAN, KAMIAR, & MOTAMEDIFAR, MOHAMMAD. (2015). THE FREQUENCY OF EXOTOXIN A AND EXOENZYMES S AND U GENES AMONG CLINICAL ISOLATES OF PSEUDOMONAS AERUGINOSA IN SHIRAZ, IRAN. INTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE, 4(3), 167-173. SID. https://sid.ir/paper/332131/en

    Vancouver: Copy

    YOUSEFI AVARVAND ARSHID, KHASHEI REZA, SEDIGH EBRAHIM SARAIE HADI, EMAMI AMIR, ZOMORODIAN KAMIAR, MOTAMEDIFAR MOHAMMAD. THE FREQUENCY OF EXOTOXIN A AND EXOENZYMES S AND U GENES AMONG CLINICAL ISOLATES OF PSEUDOMONAS AERUGINOSA IN SHIRAZ, IRAN. INTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE[Internet]. 2015;4(3):167-173. Available from: https://sid.ir/paper/332131/en

    IEEE: Copy

    ARSHID YOUSEFI AVARVAND, REZA KHASHEI, HADI SEDIGH EBRAHIM SARAIE, AMIR EMAMI, KAMIAR ZOMORODIAN, and MOHAMMAD MOTAMEDIFAR, “THE FREQUENCY OF EXOTOXIN A AND EXOENZYMES S AND U GENES AMONG CLINICAL ISOLATES OF PSEUDOMONAS AERUGINOSA IN SHIRAZ, IRAN,” INTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE, vol. 4, no. 3, pp. 167–173, 2015, [Online]. Available: https://sid.ir/paper/332131/en

    Related Journal Papers

  • No record.
  • 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