The lack of specificity of <i>sodC</i> -based PCR for the detection of <i>Neisseria meningitidis</i> carriage in pharyngeal swabs from adolescents

The utility of the superoxide dismutase C (<i>sodC</i>) gene for detecting <i>Neisseria meningitidis</i> carriage in pharyngeal swab samples is unclear. While it has been explored as an alternative to the capsule transport A gene for detecting invasive strains, its potential as the sole target for real-time PCR in meningococcal carriage screening remains unexplored. This study aimed to assess the utility of using <i>sodC</i> as a target for detecting invasive and non-invasive strains of <i>Neisseria meningitidis</i> in pharyngeal swabs. Oropharyngeal swab samples collected from adolescents (approximately 15-18 years of age) enrolled in the "B-Part-of-It" cluster-randomized controlled trial (NCT03089086) were selected for this study. Samples were initially screened for the presence of specific <i>N meningitidis</i> porin A gene (<i>porA</i>) using PCR and then preserved by freezing at -80°C. An assay targeting the <i>sodC</i> gene was developed using the locked nucleic acid probe-based method. Upon optimization of the <i>sodC</i> assay, 1,092 samples were retested using this assay and compared against the results from the <i>porA</i> assays to determine concordance. Out of 1,092 samples tested, 965 (88.4%) were <i>sodC</i> positive, with 100% sensitivity and 13% specificity compared to <i>porA</i>. The positive predictive values and negative predictive values for the <i>sod</i>C assay were 12% and 100%, respectively. When compared to <i>porA</i> PCR as the gold standard, the <i>sodC</i> assay lacks sufficient specificity to serve as a stand-alone screening assay for the detection of <i>Neisseria meningitidis</i> carriage in pharyngeal samples from adolescents.IMPORTANCEWhile the <i>sodC</i> assay successfully detects <i>N. meningitidis</i>, we identified a limitation in its specificity due to potential cross-reactivity with other organisms, including <i>Haemophilus</i> spp., which can result in false positives. This limitation highlights the need for careful interpretation of <i>Neisseria meningitidis</i> carriage results, especially in epidemiological studies.

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Publication Details

Journal
Microbiology Spectrum
Published
2025-04-08
DOI
https://doi.org/10.1128/spectrum.02779-24
Citations
2
Primary Topic
Bacterial Infections and Vaccines
Type
article
Field-Weighted Citation Impact
2.37
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article

The lack of specificity of sodC -based PCR for the detection of Neisseria meningitidis carriage in pharyngeal swabs from adolescents

Andrew J. Lawrence, Mark McMillan, Adam Finn, Dan Duy Pham-Tran et al.
2 citations
Microbiology Spectrum
Bacterial Infections and Vaccines
2.37
article

The lack of specificity of sodC -based PCR for the detection of Neisseria meningitidis carriage in pharyngeal swabs from adolescents

Andrew J. Lawrence, Mark McMillan, Adam Finn, Dan Duy Pham-Tran, Lex E. X. Leong, Hassen Mohammed, Helen Siobhan Marshall
article en
2 citations

Abstract

The utility of the superoxide dismutase C (<i>sodC</i>) gene for detecting <i>Neisseria meningitidis</i> carriage in pharyngeal swab samples is unclear. While it has been explored as an alternative to the capsule transport A gene for detecting invasive strains, its potential as the sole target for real-time PCR in meningococcal carriage screening remains unexplored. This study aimed to assess the utility of using <i>sodC</i> as a target for detecting invasive and non-invasive strains of <i>Neisseria meningitidis</i> in pharyngeal swabs. Oropharyngeal swab samples collected from adolescents (approximately 15-18 years of age) enrolled in the "B-Part-of-It" cluster-randomized controlled trial (NCT03089086) were selected for this study. Samples were initially screened for the presence of specific <i>N meningitidis</i> porin A gene (<i>porA</i>) using PCR and then preserved by freezing at -80°C. An assay targeting the <i>sodC</i> gene was developed using the locked nucleic acid probe-based method. Upon optimization of the <i>sodC</i> assay, 1,092 samples were retested using this assay and compared against the results from the <i>porA</i> assays to determine concordance. Out of 1,092 samples tested, 965 (88.4%) were <i>sodC</i> positive, with 100% sensitivity and 13% specificity compared to <i>porA</i>. The positive predictive values and negative predictive values for the <i>sod</i>C assay were 12% and 100%, respectively. When compared to <i>porA</i> PCR as the gold standard, the <i>sodC</i> assay lacks sufficient specificity to serve as a stand-alone screening assay for the detection of <i>Neisseria meningitidis</i> carriage in pharyngeal samples from adolescents.IMPORTANCEWhile the <i>sodC</i> assay successfully detects <i>N. meningitidis</i>, we identified a limitation in its specificity due to potential cross-reactivity with other organisms, including <i>Haemophilus</i> spp., which can result in false positives. This limitation highlights the need for careful interpretation of <i>Neisseria meningitidis</i> carriage results, especially in epidemiological studies.

Microbiology SpectrumVol. 13(5)
South Australia Pathology (AU), University of Bristol (GB), Women's and Children's Health Network (AU), The University of Adelaide (AU)
Good health and well-being
Openalex Percentile: Top 13%
Bacterial Infections and Vaccines
2.37
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