Evidence map›Paper›PMID 34370795›Full record

ArticlePLoS pathogens2021

Cuban history of CRF19 recombinant subtype of HIV-1.

Anna Zhukova, Jakub Voznica, Miraine Dávila Felipe, Thu-Hien To, Lissette Pérez, Yenisleidys Martínez, Yanet Pintos, Melissa Méndez, Olivier Gascuel, Vivian Kouri

Erratum issuedAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Anna ZhukovaUnité Bioinformatique Evolutive, Département de Biologie Computationelle, Institut Pasteur, Paris, France.ORCID 0000-0003-2200-7935
Jakub VoznicaUnité Bioinformatique Evolutive, Département de Biologie Computationelle, Institut Pasteur, Paris, France.
Miraine Dávila FelipeUnité Bioinformatique Evolutive, Département de Biologie Computationelle, Institut Pasteur, Paris, France.ORCID 0000-0002-3013-2958
Thu-Hien ToCentre for Integrative Genetics (CIGENE), Department of Animal and Aquacultural Sciences, Faculty of Biosciences, Norwegian University of Life Sciences, Ås, Norway.
Lissette PérezInstitute of Tropical Medicine Pedro Kourí, Virology Department, Havana City, Cuba.
Yenisleidys MartínezInstitute of Tropical Medicine Pedro Kourí, Virology Department, Havana City, Cuba.ORCID 0000-0001-8183-3685
Yanet PintosInstitute of Tropical Medicine Pedro Kourí, Virology Department, Havana City, Cuba.
Melissa MéndezInstitute of Tropical Medicine Pedro Kourí, Virology Department, Havana City, Cuba.
Olivier GascuelUnité Bioinformatique Evolutive, Département de Biologie Computationelle, Institut Pasteur, Paris, France.
Vivian KouriInstitute of Tropical Medicine Pedro Kourí, Virology Department, Havana City, Cuba.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CRF19 is a recombinant form of HIV-1 subtypes D, A1 and G, which was first sampled in Cuba in 1999, but was already present there in 1980s. CRF19 was reported almost uniquely in Cuba, where it accounts for ∼25% of new HIV-positive patients and causes rapid progression to AIDS (∼3 years). We analyzed a large data set comprising ∼350 pol and env sequences sampled in Cuba over the last 15 years and ∼350 from Los Alamos database. This data set contained both CRF19 (∼315), and A1, D and G sequences. We performed and combined analyses for the three A1, G and D regions, using fast maximum likelihood approaches, including: (1) phylogeny reconstruction, (2) spatio-temporal analysis of the virus spread, and ancestral character reconstruction for (3) transmission mode and (4) drug resistance mutations (DRMs). We verified these results with a Bayesian approach. This allowed us to acquire new insights on the CRF19 origin and transmission patterns. We showed that CRF19 recombined between 1966 and 1977, most likely in Cuban community stationed in Congo region. We further investigated CRF19 spread on the Cuban province level, and discovered that the epidemic started in 1970s, most probably in Villa Clara, that it was at first carried by heterosexual transmissions, and then quickly spread in the 1980s within the "men having sex with men" (MSM) community, with multiple transmissions back to heterosexuals. The analysis of the transmission patterns of common DRMs found very few resistance transmission clusters. Our results show a very early introduction of CRF19 in Cuba, which could explain its local epidemiological success. Ignited by a major founder event, the epidemic then followed a similar pattern as other subtypes and CRFs in Cuba. The reason for the short time to AIDS remains to be understood and requires specific surveillance, in Cuba and elsewhere.

Indexed as

Genetic VariationPhylogenyBayes TheoremCubaDisease Transmission, InfectiousFemaleHIV-1HIV InfectionsHumansMale

Identifiers

PMID34370795
PMCPMC8376097

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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.