Evidence map›Paper›PMID 29970133›Full record

ArticleParasites & vectors2018

Competitive suppression of dengue virus replication occurs in chikungunya and dengue co-infected Mexican infants.

Mussaret B Zaidi, Julio Garcia-Cordero, Ricardo Rivero-Gomez, Josselin Corzo-Gomez, María Elena González Y Almeida, Raúl Bonilla-Moreno, José Bustos-Arriaga, Nicolás Villegas-Sepulveda, Leopoldo Flores-Romo, Leticia Cedillo-Barron

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 17 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

10 authors at 3 institutions in 2 countries.

Mussaret B ZaidiInfectious Diseases Research Unit, Hospital General O'Horan, Merida, Mexico.
Julio Garcia-CorderoDepartment of Molecular Biomedicine, CINVESTAV-IPN, México City, México.
Ricardo Rivero-GomezInfectious Diseases Research Unit, Hospital General O'Horan, Merida, Mexico.
Josselin Corzo-GomezDepartment of Molecular Biomedicine, CINVESTAV-IPN, México City, México.
María Elena González Y AlmeidaInfectious Diseases Research Unit, Hospital General O'Horan, Merida, Mexico.
Raúl Bonilla-MorenoDepartment of Molecular Biomedicine, CINVESTAV-IPN, México City, México.
José Bustos-ArriagaMolecular Biology and Arbovirus Immunology UBIMED FES Iztacala, Mexican National Autonomous University, Edo de Mexico, Mexico.
Nicolás Villegas-SepulvedaDepartment of Molecular Biomedicine, CINVESTAV-IPN, México City, México.
Leopoldo Flores-RomoDepartment of Cell Biology, CINVESTAV-IPN, Mexico City, Mexico.
Leticia Cedillo-BarronDepartment of Molecular Biomedicine, CINVESTAV-IPN, México City, México. lcedillo@cinvestav.mx.
Center for Research and Advanced Studies of the National Polytechnic Institute · MXMichigan State University · USUniversidad Nacional Autónoma de México · MX

Funding

CONACYT FONSEC0 2014-1-233347Mexican Foundation for Health, Peninsular Chapter S/N
6 · The paper itself

Abstract

backgroundCo-circulation of dengue virus (DENV) and chikungunya virus (CHIKV) is increasing worldwide but information on the viral dynamics and immune response to DENV-CHIKV co-infection, particularly in young infants, is scant.

methodsBlood samples were collected from 24 patients, aged 2 months to 82 years, during a CHIKV outbreak in Mexico. DENV and CHIKV were identified by RT-PCR; ELISA was used to detect IgM and IgG antibodies. CHIKV PCR products were cloned, sequenced and subjected to BLAST analysis. To address serological findings, HMEC-1 and Vero cells were inoculated with DENV-1, DENV-2 and CHIKV alone and in combination (DENV-2-CHIKV and DENV-1-CHIKV); viral titers were measured at 24, 48 and 72 h.

resultsNine patients (38%) presented co-infection, of who eight were children. None of the patients presented severe illness. Sequence analysis showed that the circulating CHIKV virus belonged to the Asian lineage. Seroconversion to both viruses was only observed in the four patients five years or older, while the five infants under two years of age only seroconverted to CHIKV. Viral titers in the CHIKV mono-infected cells were greater than in the DENV-1 and DENV-2 mono-infected cells. Furthermore, we observed significantly increased CHIKV progeny and reduction of DENV progeny in the co-infected cells.

conclusionsIn our population, DENV-CHIKV co-infection was not associated with increased clinical severity. Our in vitro assay findings strongly suggest that the lack of DENV IgG conversion in the co-infected infants is due to suppression of DENV replication by the Asian lineage CHIKV. The presence of maternal antibody and immature immune responses in the young infants may also play a role.

Indexed as

Virus ReplicationAdolescentAdultAgedAged, 80 and overAnimalsAntibodies, ViralChikungunya FeverChikungunya virusChildChild, PreschoolChlorocebus aethiopsCoinfectionDengueDengue VirusDisease OutbreaksAntibodies, ViralImmunoglobulin GImmunoglobulin MChikungunya virusCo-infectionDengue virusDisease severityMaternal antibodiesSeroconversionViral competition

Identifiers

PMID29970133
PMCPMC6029041
OpenAlexW2811289118

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Registered trials

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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.