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

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

Open Access
|Jun 2023

Figures & Tables

Serotyping methods with associated benefits and challenges_

TechniqueTarget areasBenefitsDrawbacksReferences
QuellungPneumococcal capsular polysaccharides
  • Straightforward

  • High sensitivity and specificity

  • Rapid outcomes

  • Time, cost, and labor intensive

  • Cannot detect multiple serotypes using one sample

  • Inconvenient for larger samples

  • Extensive skills are required

  • Henrichsen 1979

  • Sørenson 1993

  • Lalitha et al. 1999

  • Jauneikaite et al. 2015

  • Jin et al. 2016

Latex agglutinationPneumococcal capsular polysaccharides
  • Straightforward

  • Easy

  • Rapid outcomes

  • Appropriate for resource-poor conditions

  • Needs the least expertise

  • Cost-intensive

  • Questionable accuracy

  • Culture-negative isolate might be missed

  • Slotved et al. 2004

  • Ortika et al. 2013

  • Porter et al. 2014

  • Swarthout et al. 2021

Multiplex PCRGlycosyltransferase gene
  • Economical

  • Rapid outcomes

  • Versatile

  • Accurate

  • Sensitive

  • Several primers

  • Several steps

  • Limited serotypes supported

  • Lack of internal control for specific serotypes

  • Emerging NVTs remain unexploited

  • Lawrence et al. 2003

  • Carvalho et al. 2010

  • Jin et al. 2016

  • Zhou et al. 2021

SequetypingCpsB gene
  • Straightforward and economical

  • Single PCR amplification

  • Single-step PCR

  • Needs one primer set

  • Restricted to single isolate detection

  • Some isolates exhibit high homology of the cpsB gene across different serotypes

  • Needs sequencing facilities or services

  • Leung et al. 2012

  • Jin et al. 2016

  • Nagaraj et al. 2017

  • Zhou et al. 2021

Real-time PCRPneumococcal capsular polysaccharides
  • High sensitivity

  • Able to replicate DNA in low copy number

  • Serotyping from culture-negative samples

  • No sample manipulation is needed after the amplification

  • Need specialised equipment

  • Costly PCR probes

  • Emerging NVTs remain unexploited

  • Tarragó et al. 2008

  • Azzari et al. 2010

  • Pimenta et al. 2013

  • Pernica et al. 2014

  • Kralik et al. 2017

PCR-RFLPcps genes
  • Straightforward

  • Fast

  • Cost-effective

  • Versatile

  • Reproducible

  • Needs targeted restriction enzymes

  • Needs several restriction enzymes

  • Cannot assess mutation type

  • Time-intensive

  • Batt et al. 2005

  • Camargo et al. 2015

  • Dai and Long 2015

  • Garcia Suarez et al. 2019

Whole genome sequencing (WGS)Pneumococcal capsular polysaccharides
  • High accuracy

  • Greater resolution

  • Comprehensive analysis

  • Reduced turnaround time

  • Cost-intensive

  • Needs an advanced bioinformatic tool

  • Requires technical expertise and skill

  • Kapatai et al. 2016

  • Mauffrey et al. 2017

  • Epping et al. 2018

  • Knight et al. 2021

  • Sheppard et al. 2022

DOI: https://doi.org/10.33073/pjm-2023-023 | Journal eISSN: 2544-4646 | Journal ISSN: 1733-1331
Language: English
Page range: 103 - 115
Submitted on: Jan 27, 2023
|
Accepted on: May 9, 2023
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Published on: Jun 14, 2023
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2023 Nurul Asyikin Abdul Rahman, Mohd Nasir Mohd Desa, Siti Norbaya Masri, Niazlin Mohd Taib, Nurshahira Sulaiman, Hazmin Hazman, James John, published by Polish Society of Microbiologists
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.