• Title of article

    Identification of Listeria monocytogenes Virulence Factors in Women With Abortion by Polymerase Chain Reaction

  • Author/Authors

    Eslami، Gita نويسنده , , Goudarzi، Hossein نويسنده Shahid Beheshti University of Medical Sciences , , Ohadi، Elnaz نويسنده Department of Microbiology, International Branch of Shahid Beheshti University of Medical Sciences, Tehran, IR Iran Ohadi, Elnaz , Taherpour، Arezou نويسنده Department of Microbiology, Kurdistan University of Medical Sciences, Taherpour, Arezou , Pourkaveh، Bita نويسنده Infectious Disease and Tropical Medicine Research Center, Shahid Beheshti University of Medical Sciences. Pourkaveh, Bita , Taheri، Soudabeh نويسنده ,

  • Issue Information
    فصلنامه با شماره پیاپی سال 2014
  • Pages
    5
  • From page
    1
  • To page
    5
  • Abstract
    Background: Listeria monocytogenes, as one of the foodborne pathogens, is a causative agent of listeriosis. The transfer of L. monocytogenes bacteremia in pregnant women occurs as self-limited flu-like symptoms, but it may result in abortion, stillbirth or premature birth of the infected baby. One of the best methods for detection of this bacterium is polymerase chain reaction (PCR). Objectives: The purpose of this study was detection of virulence factors (hlyA and plcA) of L. monocytogenes in women with abortion, using PCR. Patients and Methods: In this pilot and cross-sectional study, 96 patients with abortion admitted in educational university, Tehran, Iran were surveyed for L. monocytogenes by PCR and culture methods. Some variants like age, occupation, history of abortion and education were considered for all patients. Vaginal swabs and secretions were transferred to trypticase soy broth as the transport media and then all the samples were transferred to a microbiology laboratory. The tubes were incubated in 4 ?C and the specimens were cultured on PALCAM media. The isolates were verified by Gram staining, catalase and oxidase test, methyl red-Voges-Proskauer (MR-VP), sugar fermentations and motility in 20-25?C. Then, PCR was performed for the extracted DNAs. Data were analyzed by SPSS software version 17, and ?2 (Chisquare test). Results: Out of 96 samples, 16 isolates of L. monocytogenes by PCR (plcA and hlyA) and four isolates by culture were identified. There was a significant difference between PCR and culture methods (P = 0.003). The results of this study showed that PCR was more sensitive and specific than culture method. There was also a significant association between the bacteria and hlyA and plcA genes and human abortion and between patients with abortion precedence and education. Conclusions: Based on our study, plcA and hlyA played a key role in the virulence determination of L. monocytogenes. Data analysis also showed that L. monocytogenes could be a causative agent of abortion in pregnant women
  • Journal title
    Archives of Clinical Infectious Diseases
  • Serial Year
    2014
  • Journal title
    Archives of Clinical Infectious Diseases
  • Record number

    1886036