Evidence map›Paper›PMID 37283922›Full record

ArticleFrontiers in microbiology2023

Utility of MF-non coding region for measles molecular surveillance during post-elimination phase, Spain, 2017-2020.

Camille Jacqueline, Ana María Gavilán, Noemí López-Perea, Ana Raquel Penedos, Josefa Masa-Calles, Juan E Echevarría, Aurora Fernández-García, MMR Study Group

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. What's going on with measles?Journal of virology · 2024
    Review
  3. Article
  4. Article
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

8 authors at 4 institutions in 2 countries.

Camille JacquelineCentro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Majadahonda, Spain.
Ana María GavilánCentro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Majadahonda, Spain.
Noemí López-PereaCIBER de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Ana Raquel PenedosUnited Kingdom Health Security Agency, London, United Kingdom.
Josefa Masa-CallesCIBER de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Juan E EchevarríaCentro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Majadahonda, Spain.
Aurora Fernández-GarcíaCentro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Majadahonda, Spain.
MMR Study Group
Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública · ESCentro Nacional de Epidemiología · ESCentro Nacional de Microbiologia · ESInstituto de Salud Carlos III · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In countries entering the post-elimination phase for measles, the study of variants by sequencing of 450 nucleotides of the N gene (N450) does not always allow the tracing of chains of transmission. Indeed, between 2017 and 2020, most measles virus sequences belonged to either the MVs/Dublin.IRL/8.16 (B3-Dublin) or the MVs/Gir Somnath.IND/42.16 (D8-Gir Somnath) variants. We evaluated the additional use of a non-coding region (MF-NCR) as a tool to enhance resolution and infer case origin, chains of transmission and characterize outbreaks. Methods: We obtained 115 high-quality MF-NCR sequences from strains collected from Spanish patients infected with either B3-Dublin or D8-Gir Somnath variants between 2017 and 2020, performed epidemiological, phylogenetic and phylodynamic analyses and applied a mathematical model to determine relatedness among identified clades. Results: Applying this model allowed us to identify phylogenetic clades potentially derived from concomitant importations of the virus rather than single chain of transmission, inferred based on only N450 and epidemiology data. In a third outbreak, we found two related clades that corresponded to two chains of transmission. Discussion: Our results show the ability of the proposed method to improve identification of simultaneous importations in the same region which could trigger enhanced contact tracing. Moreover, the identification of further transmission chains indicates that the size of import-related outbreaks was smaller than previously found, supporting the interpretation that endemic measles transmission was absent in Spain between 2017 and 2020. We suggest considering the use of the MF-NCR region in conjunction with the study of N450 variants in future WHO recommendations for measles surveillance.

Indexed as

B3 genotypeD8 genotypemathematical modeloutbreaksphylodynamic analysesphylogenetic analysis

Identifiers

PMID37283922
PMCPMC10240958
OpenAlexW4377290590

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.