Abstract

Currently, the identity of measles, mumps and rubella virus vaccines is determined during certification testing by a labour-consuming, lengthy and costly neutralisation test using cell cultures. The identity of the virus contained in such vaccines is established based on neutralisation of cytopathic effect of viruses in sensitive RK-13 and Vero cell cultures using a specific immune serum. An urgent challenge is to simplify and reduce the cost of controlling the identity of commercial batches of measles, mumps and rubella vaccines using polymerase chain reaction (PCR) tests. The aim of the study was to determine the possibility of viral ribonucleic acid (RNA) detection in these vaccines using reagent kits from different manufacturers for detection of measles, mumps and rubella viruses in clinical material by real-time reverse transcription-PCR (RT-PCR). The article presents the results of the study, which assessed the possibility of using the real-time RT-PCR for testing the identity of measles, mumps and rubella viruses in vaccines. The authors of the study analysed domestically produced and foreign reagent kits intended for detection of measles, mumps and rubella viruses in clinical material. All the studied reagent kits were able to detect RNAs of the above-mentioned viruses in vaccine products. All the reagent kits demonstrated high specificity and could be used to confirm the identity of the measles, mumps and rubella viruses in all the studied vaccines. Commercial domestic reagent kits can be used to determine the identity of rubella vaccines by RT-PCR. However, it is advisable to develop domestic reagent kits for checking the identity of measles and mumps vaccines by RT-PCR. The acceptability of the test results was assessed using the industry reference standards of measles, mumps and rubella viruses activity with certified stable activity values.

Highlights

  • Использование наборов реагентов для обратной транскрипцией в реальном времени (ОТ-ПЦР) в реальном времени для оценки подлинности вакцин против кори, паротита и краснухи

  • The aim of the study was to determine the possibility of viral ribonucleic acid (RNA) detection in these vaccines using reagent kits from different manufacturers for detection of measles, mumps and rubella viruses in clinical material by real-time reverse transcription-polymerase chain reaction (PCR) (RT-PCR)

  • The article presents the results of the study, which assessed the possibility of using the real-time RT-PCR for testing the identity of measles, mumps and БИОпрепараты

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Summary

Материалы и методы

Объектом исследования были коммерческие диагностические наборы отечественного и зарубежного производства для выявления вирусов кори, паротита и краснухи в клиническом материале для ОТ-ПЦР в режиме реального времени. Выделение РНК вирусов кори, паротита и краснухи для последующей работы с набором АмплиСенс® и наборами зарубежного производства проводили с помощью комплекта реагентов для выделения РНК/ДНК из клинического материала РИБО-преп производства ООО «ИнтерЛабСервис» (РУ No ФСР 2008/03147). - вакцина против краснухи культуральная живая (штамм вируса краснухи RA-27/3) — 10 серий;. - вакцина паротитно-коревая культуральная живая (штамм вируса кори Ленинград-16, штамм вируса паротита Ленинград-3) — 2 серии. Использование наборов реагентов для ОТ-ПЦР в реальном времени для оценки подлинности вакцин против кори, паротита и краснухи Using Real-Time RT-PCR Reagent Kits for Identity Testing of Measles, Mumps and Rubella Vaccines. Статистическая обработка полученных результатов была проведена общепринятыми методами [4], расчеты проведены с помощью программы Microsoft Office Excel 2007

Результаты и обсуждение
Циклирование с
Элонгация с
Денатурация Элонгация с
Стандартное отклонение
Значение порогового цикла
Статистические показатели оценки порогового цикла
Об авторах
Full Text
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