Evidence map›Paper›PMID 36851588›Full record

ArticleViruses2023

SARS-CoV-2 Genome Variations in Viral Shedding of an Immunocompromised Patient with Non-Hodgkin's Lymphoma.

Rodrigo Villaseñor-Echavarri, Laura Gomez-Romero, Alexandra Martin-Onraet, Luis A Herrera, Marco A Escobar-Arrazola, Oscar A Ramirez-Vega, Corazón Barrientos-Flores, Alfredo Mendoza-Vargas, Alfredo Hidalgo-Miranda, Diana Vilar-Compte and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Viruses, 2023. 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
1.6field-weighted citation impact, top 19% 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, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
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

11 authors at 3 institutions in 1 country.

Rodrigo Villaseñor-EchavarriDepartment of Infectious Diseases, Instituto Nacional de Cancerología, Mexico City 14080, Mexico.ORCID 0000-0001-5750-884X
Laura Gomez-RomeroInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0001-9685-6492
Alexandra Martin-OnraetSchool of Medicine, Universidad Panamericana, Mexico City 03920, Mexico.ORCID 0000-0002-8627-404X
Luis A HerreraInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0003-3998-9306
Marco A Escobar-ArrazolaInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0003-3834-4709
Oscar A Ramirez-VegaInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0002-2246-4485
Corazón Barrientos-FloresDepartment of Infectious Diseases, Instituto Nacional de Cancerología, Mexico City 14080, Mexico.ORCID 0000-0002-7449-5961
Alfredo Mendoza-VargasInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.
Alfredo Hidalgo-MirandaInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0003-2315-3977
Diana Vilar-CompteDepartment of Infectious Diseases, Instituto Nacional de Cancerología, Mexico City 14080, Mexico.ORCID 0000-0001-8564-8735
Alberto Cedro-TandaInstituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.ORCID 0000-0001-8708-462X
National Institute of Genomic Medicine · MXInstituto Nacional de Cancerología · MXUniversidad Panamericana · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing coronavirus disease 2019 (COVID-19) is the most transmissible ß-coronavirus in history, affecting all population groups. Immunocompromised patients, particularly cancer patients, have been highlighted as a reservoir to promote accumulation of viral mutations throughout persistent infection. CASE PRESENTATION: We aimed to describe the clinical course and SARS-CoV-2 mutation profile for 102 days in an immunocompromised patient with non-Hodgkin's lymphoma and COVID-19. We used RT-qPCR to quantify SARS-CoV-2 viral load over time and whole-virus genome sequencing to identify viral lineage and mutation profile. The patient presented with a persistent infection through 102 days while being treated with cytotoxic chemotherapy for non-Hodgkin's lymphoma and received targeted therapy for COVID-19 with remdesivir and hyperimmune plasma. All sequenced samples belonged to the BA.1.1 lineage. We detected nine amino acid substitutions in five viral genes (Nucleocapsid, ORF1a, ORF1b, ORF13a, and ORF9b), grouped in two clusters: the first cluster with amino acid substitutions only detected on days 39 and 87 of sample collection, and the second cluster with amino acid substitutions only detected on day 95 of sample collection. The Spike gene remained unchanged in all samples. Viral load was dynamic but consistent with the disease flares.

conclusionsThis report shows that the multiple mutations that occur in an immunocompromised patient with persistent COVID-19 could provide information regarding viral evolution and emergence of new SARS-CoV-2 variants.

Indexed as

COVID-19Lymphoma, Non-HodgkinHumansImmunocompromised HostPersistent InfectionSARS-CoV-2Virus SheddingCOVID-19mutational landscapenon-Hodgkin’s lymphomaSARS-CoV-2

Identifiers

PMID36851588
PMCPMC9962578
OpenAlexW4318478736

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.