Evidence map›Paper›PMID 33261551›Full record

ArticleBMC microbiology2020

MALDI-TOF mass spectrometry for sub-typing of Streptococcus pneumoniae.

Sivkheng Kann, Sena Sao, Chanleakhena Phoeung, Youlet By, Juliet Bryant, Florence Komurian-Pradel, Vonthanak Saphonn, Monidarin Chou, Paul Turner

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  6. Rapid, Simple, and Highly Specific Detection ofFrontiers in cellular and infection microbiology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Sivkheng KannRodolphe Mérieux Laboratory, University of Health Sciences, Phnom Penh, Cambodia.
Sena SaoCambodia Oxford Medical Research Unit, Angkor Hospital for Children, PO Box 50, Siem Reap, Cambodia.
Chanleakhena PhoeungRodolphe Mérieux Laboratory, University of Health Sciences, Phnom Penh, Cambodia.
Youlet ByRodolphe Mérieux Laboratory, University of Health Sciences, Phnom Penh, Cambodia.
Juliet BryantFondation Mérieux and Centre International de Recherche en Infectiologie (CIRI), INSERM, Lyon, France.
Florence Komurian-PradelFondation Mérieux and Centre International de Recherche en Infectiologie (CIRI), INSERM, Lyon, France.
Vonthanak SaphonnUniversity of Health Sciences, Phnom Penh, Cambodia.
Monidarin ChouRodolphe Mérieux Laboratory, University of Health Sciences, Phnom Penh, Cambodia.
Paul TurnerCambodia Oxford Medical Research Unit, Angkor Hospital for Children, PO Box 50, Siem Reap, Cambodia. pault@tropmedres.ac.ORCID 0000-0002-1013-7815
University of Health Science · KHAngkor Hospital for Children · KHUniversité Claude Bernard Lyon 1 · FR

Funding

Wellcome Trust 106698/Z/14/Z
6 · The paper itself

Abstract

backgroundSerotyping of Streptococcus pneumoniae is important for monitoring of vaccine impact. Unfortunately, conventional and molecular serotyping is expensive and technically demanding. This study aimed to determine the ability of matrix-assisted laser desorption-ionisation time-of-flight (MALDI-TOF) mass spectrometry to discriminate between pneumococcal serotypes and genotypes (defined by global pneumococcal sequence cluster, GPSC). In this study, MALDI-TOF mass spectra were generated for a diverse panel of whole genome sequenced pneumococcal isolates using the bioMerieux VITEK MS in clinical diagnostic (IVD) mode. Discriminatory mass peaks were identified and hierarchical clustering was performed to visually assess discriminatory ability. Random forest and classification and regression tree (CART) algorithms were used to formally determine how well serotypes and genotypes were identified by MALDI-TOF mass spectrum.

resultsOne hundred and ninety-nine pneumococci, comprising 16 serotypes and non-typeable isolates from 46 GPSC, were analysed. In the primary experiment, hierarchical clustering revealed poor congruence between MALDI-TOF mass spectrum and serotype. The correct serotype was identified from MALDI-TOF mass spectrum in just 14.6% (random forest) or 35.4% (CART) of 130 isolates. Restricting the dataset to the nine dominant GPSC (61 isolates / 13 serotypes), discriminatory ability improved slightly: the correct serotype was identified in 21.3% (random forest) and 41.0% (CART). Finally, analysis of 69 isolates of three dominant serotype-genotype pairs (6B-GPSC1, 19F-GPSC23, 23F-GPSC624) resulted in the correct serotype identification in 81.1% (random forest) and 94.2% (CART) of isolates.

conclusionsThis work suggests that MALDI-TOF is not a useful technique for determination of pneumococcal serotype. MALDI-TOF mass spectra appear more associated with isolate genotype, which may still have utility for future pneumococcal surveillance activities.

Indexed as

SerotypingSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationCluster AnalysisGenotypeHumansSerogroupStreptococcus pneumoniaeGenotypeMALDI-TOFMass spectrometrySerotypeStreptococcus pneumoniae

Identifiers

PMID33261551
PMCPMC7709296
OpenAlexW3108292984

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.