PCR and Infectious Diseases

D. Zauli
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引用次数: 7

Abstract

Since the 1950s, the medical community has been faced with infectious diseases, which have brought significant public health and financial challenges. Currently, rou-tine testing for the laboratory diagnosis for infectious agents is based on cell culture, serological, and molecular methods. However, cell culture-based methods are used mainly in research laboratories and are less sensitive methods when compared with serological and molecular methods. The diagnosis of infectious diseases has been revolutionized by the development of molecular techniques, mainly with the applications of polymerase chain reaction (PCR). The high sensitivity, specificity, and ease with which the PCR can be used to detect genetic sequences known have led to your wide application in science. A great number of qualitative and quantitative molecular assays are mostly based on what have been described such as real-time PCR, multiplex PCR, LAMP-PCR, and digital PCR. These assays could identify active infection by detecting infectious agents and nucleic acid in various clinical conditions including arboviruses, sexually transmitted infections, and bacterial infections. Further advancement of molecular technology is needed to improve the capacity to detect infectious agents in order to control the spread of infectious diseases and lead to appropriate actions which help to benefit patients and health-care workers themselves.
聚合酶链反应与传染病
自20世纪50年代以来,医学界一直面临着传染病,这给公共卫生和财政带来了重大挑战。目前,实验室诊断传染性病原体的常规检测是基于细胞培养、血清学和分子方法。然而,基于细胞培养的方法主要用于研究实验室,与血清学和分子方法相比,灵敏度较低。随着分子技术的发展,主要是聚合酶链反应(PCR)的应用,传染病的诊断已经发生了革命性的变化。PCR检测已知基因序列的高灵敏度、特异性和易用性使其在科学领域得到广泛应用。大量的定性和定量分子分析大多基于已经描述的,如实时PCR,多重PCR, LAMP-PCR和数字PCR。这些检测方法通过检测虫媒病毒、性传播感染和细菌感染等各种临床情况下的感染因子和核酸来识别活动性感染。需要进一步提高分子技术,以提高检测传染因子的能力,从而控制传染病的传播,并采取有助于病人和保健工作者本身受益的适当行动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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