Abstract

By the example of Martin Christ Epsilon 2-6D device carried out was assessment of the possibility to use freeze-dryers of the chamber type for conservation of pathogenic microorganisms collection strains. Elaborated was algorithm of lyophilisation of the III-IV pathogenicity groups bacteria, which incorporated conditions of freeze-drying and biological safety provision of this process. Indices of viability and survivability were defined for freeze-dried cells of pathogenic bacteria strains. Using thermostability test calculated were predicted timelines of storage of collection strains preparations freeze-dried in the flasks in Martin Christ Epsilon 2-6D. It was determined that in the collections of pathogenic microorganisms freeze-dryers of the chamber type could be used most prospectively for the III-IV pathogenicity groups bacteria conservation requiring mass reproduction and not intended for long storage. At the same time their application for freeze-drying of the strains of the I-II pathogenicity groups bacteria intended for a long storage, requires further adaptation of these devices as regards biological safety provision and prolongation of the shelf life.

Highlights

  • By the example of Martin Christ Epsilon 2-6D device carried out was assessment of the possibility to use freeze-dryers of the chamber type for conservation of pathogenic microorganisms collection strains

  • Indices of viability and survivability were defined for freeze-dried cells of pathogenic bacteria strains

  • At the same time their application for freeze-drying of the strains of the I–II pathogenicity groups bacteria intended for a long storage, requires further adaptation of these devices as regards biological safety provision and prolongation of the shelf life

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Summary

Материалы и методы

В работе использовано восемь тест-штаммов микроорганизмов III–IV групп патогенности: Escherichia coli 18 и 675, Shigella flexneri 17, 58573, 8516, Shigella sonnei «S-форма», Staphylococcus aureus ATCC 6538 (209-P), Enterococcus faecalis ATCC 29212. Выращивание микроорганизмов проводили на агаре Хоттингера с соблюдением необходимых условий, требующихся для нормального роста вышеуказанных видов бактерий. Лиофилизацию культур осуществляли на сублимационной установке камерного типа фирмы Martin Christ Epsilon 2-6D согласно ее правилам эксплуатации. Жизнеспособность микробов определяли путем высева их на питательные среды с последующим подсчетом к первоначальному числу жизнеспособных клеток (до начала хранения), принятому за 100 %. Для определения возможного времени хранения при 4 °С использовали ускоренный тест прогнозирования выживаемости лиофилизированных культур бактерий (тест термостабильности) [5, 9]. Статистическая обработка данных осуществлялась с помощью методов вариационной статистики. Определяли среднюю арифметическую (М), стандартную ошибку (m) [3]

Результаты и обсуждение
После лиофилизации
Количество клеток жизнеспособных бактерий
Full Text
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