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Molecular Design Real Time Loop-Mediated Isothermal Amplification Method for Rapid Detection of Neisseria Meningitidis; [Метод Молекулярного Конструирования Петлевой Изотермической Амплификации В Реальном Времени Для Быстрого Обнаружения Neisseria Meningitidis] Publisher Pubmed



Soleimani M1 ; Morovvati A2 ; Majidzadeha K3
Authors
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Authors Affiliations
  1. 1. Department of Microbiology, Faculty of Medicine, AJA University of Medical Sciences, Tasnim Biotechnology Research Center, Tehran, Iran
  2. 2. Department of Microbiology, Qom Branch, Islamic Azad University, Qom, Iran
  3. 3. Tasnim Biotechnology Research Center, Faculty of Medicine, AJA University of Medical Sciences, Academic Center for Culture, Education & Research, Breast Cancer Research Center, Tehran, Iran

Source: Folia Medica Published:2021


Abstract

Introduction: Detecting Neisseria meningitides using conventional methods is time consuming and laborious. Development of a reliable, rapid method for prompt control and prevention of meningococcal disease is required. Although PCR and real time PCR methods have been developed, they require electrophoresis or expensive devices. Loop-mediated isothermal amplification (LAMP) method is a simple gene amplification method which can be performed at a single temperature without the need for thermal cycling. Aim: We aimed to develop a quantitative real-time LAMP assay for detection of N. meningitides and accurate quantification of the bacterial load in patients with meningococcal disease. Materials and methods: LAMP reaction was set up and optimized by four primers. Amplification results were assessed by obtaining real time turbidity graphs from each LAMP reaction tube using real time turbidimeter apparatus. A standard curve was generated from turbidity graphs corresponding to ten-fold serial dilution of crgA gene containing recombinant plasmid. Results: LAMP assay could isolate only N. meningitides, whereas no amplification was obtained with negative control isolates, which indicates 100% specificity. The limit of detection (LOD) of our LAMP assay was found to be ~ 5 copies of crgA gene per reaction. REAL LAMP analysis of the standard curve revealed excellent linear correlation between gene copy number and time threshold, with a correlation coefficient equal to 0.92. Conclusions: The REAL LAMP assay is a rapid, simple, cost-effective, sensitive, specific method for detection of N. meningitides. It has the potential of finding application in epidemiological studies and biodefense situations. © Folia Medica.