Evidence map›Paper›PMID 34757832›Full record

ArticleJournal of clinical microbiology2022

Streamlined Whole-Genome Sequencing of Mumps Virus for High-Resolution Outbreak Analysis.

Patrick Bryant, Haley Caldwell, Daryl M Lamson, Tugba Yildirim, Kirsten St George

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Patrick BryantLaboratory of Viral Diseases, Wadsworth Centergrid.465543.5, New York State Department of Health, Albany, New York, USA.ORCID 0000-0003-0651-0274
Haley CaldwellLaboratory of Viral Diseases, Wadsworth Centergrid.465543.5, New York State Department of Health, Albany, New York, USA.
Daryl M LamsonLaboratory of Viral Diseases, Wadsworth Centergrid.465543.5, New York State Department of Health, Albany, New York, USA.ORCID 0000-0002-6497-917X
Tugba YildirimLaboratory of Viral Diseases, Wadsworth Centergrid.465543.5, New York State Department of Health, Albany, New York, USA.
Kirsten St GeorgeLaboratory of Viral Diseases, Wadsworth Centergrid.465543.5, New York State Department of Health, Albany, New York, USA.ORCID 0000-0001-5168-763X
New York State Department of Health · US

Funding

CDC HHS NU60OE000104
6 · The paper itself

Abstract

Since 2015, the United States has experienced a resurgence in the number of mumps cases and outbreaks in fully vaccinated populations. These outbreaks have occurred predominantly in close-quarter settings, such as camps, colleges, and detention centers. Phylogenetic analysis of 758 mumps-positive samples from outbreaks across the United States identified 743 (98%) as genotype G based on sequence analysis of the mumps small hydrophobic (SH) gene. Additionally, SH sequences in the genotype G samples showed almost no sequence diversity, with 675 (91%) of them having identical sequences or only one nucleotide difference. This uniformity of circulating genotype and strain created complications for epidemiologic investigations and necessitated the development of a system for rapidly generating mumps whole-genome sequences for more detailed analysis. In this study, we report a novel and streamlined assay for whole-genome sequencing (WGS) of mumps virus genotype G. The WGS procedure successfully generated 318 high-quality WGS sequences on nucleic acid from genotype G-positive respiratory samples collected during several mumps outbreaks in the United States between 2016 and 2019. Sequencing was performed by a rapid and highly sensitive custom Ion AmpliSeq mumps genotype G panel, with sample preparation performed on an Ion Chef and sequencing on an Ion S5. The WGS data generated by the AmpliSeq panel provided enhanced genomic resolution for epidemiological outbreak investigations. Translation and protein sequence analysis also identified several potentially important epitope changes in the circulating mumps genotype G strains compared to the Jeryl-Lynn strain (JL5) used in vaccines in the United States, which could explain the current level of vaccine escapes.

Indexed as

MumpsMumps virusDisease OutbreaksGenotypeHumansPhylogenyWhole Genome SequencingAmpliSeqgenotypingmolecular epidemiologymumpsvaccinewhole-genome sequencing

Identifiers

PMID34757832
PMCPMC8769722
OpenAlexW3212036756

What OpenQuestion holds

Textmetadata
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.