Comparison different methods of long-term maintenance and survival of Streptococcus pneumoniae isolates
Publish place: Iranian Journal of Medical Microbiology، Vol: 10، Issue: 6
Publish Year: 1395
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
JR_IJMM-10-6_010
تاریخ نمایه سازی: 16 مرداد 1402
Abstract:
Background and Aim: One of the major problems for the isolation and detection of S. pneumoniae from clinical specimens, high sensitivity, rapid autolysis and thus the inability to hold isolates of pneumococcus. So, it is essential to use specific techniques for the preservation of the organism. In this study several different cultures for S. pneumoniae isolates were compared and evaluated.
Materials and Methods: In ۲۰۱۴, ۲ ATCC standard , ۳۰ clinical, and ۳۰ normal flora pneumococcal available isolates were selected from a previous study. Dorset egg medium was prepared for midterm preservation, three storage environments, including Skim milk-Tryptone-Glucose-Glycerin (STGG), nutrient broth enriched and Todd Hewitt Broth (THB) was constructed to long-term preservation, and their performance on maintenance pneumococcal isolates was assessed.
Results and Conclusions: ۹۵% of the isolates cultured on Dorset after ۷۰ days and ۸۰% after four months later had the ability to grow. All three long-term storage environment, had a good performance for one year but enriched nutrient broth could keep bacteria with but better-quality up to ۲ years. There is no difference between isolates from the patients and isolates from normal flora to survive in the environment. Also aggressive origin of iclinical isolates had no effect on their survival rate. Dorset egg (DE) medium can be considered as a simple, low cost and efficient, medium for midterm preservation and enriched nutrient broth for long term storage of pneumococcal isolates in clinical laboratories.
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Authors
Ali Ahmadi
Molecular Biology Research Center, Baqiatallah University of Medical Sciences, Tehran, Iran
Malihe Talebi
Department of Microbiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
Elnaz Parvizi
Department of Microbiology, Science and Research Branch, Islamic Azad University, Fars, Iran
Gholamreza Irajian
Department of Microbiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
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