The Molecular Approaches and Challenges of Streptococcus pneumoniae Serotyping for Epidemiological Surveillance in the Vaccine Era.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Nurul Asyikin Abdul Rahman, Mohd Nasir Mohd Desa, Siti Norbaya Masri, Niazlin Mohd Taib, Nurshahira Sulaiman, Hazmin Hazman, James John
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引用次数: 2

Abstract

Streptococcus pneumoniae (pneumococcus) belongs to the Gram-positive cocci. This bacterium typically colonizes the nasopharyngeal region of healthy individuals. It has a distinct polysaccharide capsule - a virulence factor allowing the bacteria to elude the immune defense mechanisms. Consequently, it might trigger aggressive conditions like septicemia and meningitis in immunocompromised or older individuals. Moreover, children below five years of age are at risk of morbidity and mortality. Studies have found 101 S. pneumoniae capsular serotypes, of which several correlate with clinical and carriage isolates with distinct disease aggressiveness. Introducing pneumococcal conjugate vaccines (PCV) targets the most common disease-associated serotypes. Nevertheless, vaccine selection pressure leads to replacing the formerly dominant vaccine serotypes (VTs) by non-vaccine types (NVTs). Therefore, serotyping must be conducted for epidemiological surveillance and vaccine assessment. Serotyping can be performed using numerous techniques, either by the conventional antisera-based (Quellung and latex agglutination) or molecular-based approaches (sequetyping, multiplex PCR, real-time PCR, and PCR-RFLP). A cost-effective and practical approach must be used to enhance serotyping accuracy to monitor the prevalence of VTs and NVTs. Therefore, dependable pneumococcal serotyping techniques are essential to precisely monitor virulent lineages, NVT emergence, and genetic associations of isolates. This review discusses the principles, associated benefits, and drawbacks of the respective available conventional and molecular approaches, and potentially the whole genome sequencing (WGS) to be directed for future exploration.

疫苗时代肺炎链球菌血清分型在流行病学监测中的分子途径和挑战。
肺炎链球菌(肺炎球菌)属于革兰氏阳性球菌。这种细菌通常在健康人的鼻咽区定植。它有一个独特的多糖胶囊-一种毒力因子,使细菌逃避免疫防御机制。因此,它可能在免疫功能低下或老年人中引发败血症和脑膜炎等侵袭性疾病。此外,五岁以下儿童面临发病和死亡的风险。研究发现了101种荚膜肺炎链球菌血清型,其中几种与临床和携带分离株相关,具有明显的疾病侵袭性。引入肺炎球菌结合疫苗(PCV)针对最常见的疾病相关血清型。然而,疫苗选择压力导致以前占主导地位的疫苗血清型(VTs)被非疫苗血清型(NVTs)取代。因此,必须进行血清分型以进行流行病学监测和疫苗评估。血清分型可以使用多种技术进行,无论是通过传统的基于抗血清的方法(Quellung和乳胶凝集)还是基于分子的方法(序列分型,多重PCR,实时PCR和PCR- rflp)。必须采用一种具有成本效益和实用的方法来提高血清分型准确性,以监测室性血管病和非室性血管病的流行情况。因此,可靠的肺炎球菌血清分型技术对于精确监测毒株、NVT的出现和分离株的遗传关联至关重要。本文综述了现有的常规方法和分子方法的原理、优缺点,以及全基因组测序(WGS)在未来的研究方向。
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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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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