Evidence map›Paper›PMID 31409874›Full record

ArticleScientific reports2019

Novel clinical and dual infection by Histoplasma capsulatum genotypes in HIV patients from Northeastern, Brazil.

Lisandra Serra Damasceno, Marcus de Melo Teixeira, Bridget Marie Barker, Marcos Abreu Almeida, Mauro de Medeiros Muniz, Cláudia Vera Pizzini, Jacó Ricarte Lima Mesquita, Gabriela Rodríguez-Arellanes, José Antonio Ramírez, Tania Vite-Garín and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-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

15 citing papers in PubMed, 23 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

14 authors at 6 institutions in 3 countries.

Lisandra Serra DamascenoHospital São José de Doenças Infecciosas - Secretaria de Saúde do Ceará, Fortaleza, Ceará, Brazil. lisainfecto@gmail.com.ORCID http://orcid.org/0000-0003-1425-5912
Marcus de Melo TeixeiraNúcleo de Medicina Tropical, Faculdade de Medicina, Universidade de Brasília, Brasília, Distrito Federal, Brazil.ORCID http://orcid.org/0000-0003-1763-3464
Bridget Marie BarkerNúcleo de Medicina Tropical, Faculdade de Medicina, Universidade de Brasília, Brasília, Distrito Federal, Brazil.ORCID http://orcid.org/0000-0002-3439-4517
Marcos Abreu AlmeidaInstituto Nacional de Infectologia Evandro Chagas (INI), FIOCRUZ - Fundação Oswaldo Cruz, Laboratório de Micologia, 21045-900, Rio de Janeiro, RJ, Brazil.
Mauro de Medeiros MunizPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Cláudia Vera PizziniPathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Jacó Ricarte Lima MesquitaHospital São José de Doenças Infecciosas - Secretaria de Saúde do Ceará, Fortaleza, Ceará, Brazil.
Gabriela Rodríguez-ArellanesFacultad de Medicina, UNAM - Universidad Nacional Autónoma de México, Departamento de Microbiología y Parasitología, Laboratorio de Inmunología de Hongos, 04510, Ciudad de México, Mexico.
José Antonio RamírezFacultad de Medicina, UNAM - Universidad Nacional Autónoma de México, Departamento de Microbiología y Parasitología, Laboratorio de Inmunología de Hongos, 04510, Ciudad de México, Mexico.
Tania Vite-GarínFacultad de Medicina, UNAM - Universidad Nacional Autónoma de México, Departamento de Microbiología y Parasitología, Laboratorio de Inmunología de Hongos, 04510, Ciudad de México, Mexico.
Terezinha do Menino Jesus Silva LeitãoHospital São José de Doenças Infecciosas - Secretaria de Saúde do Ceará, Fortaleza, Ceará, Brazil.
Maria Lucia TaylorFacultad de Medicina, UNAM - Universidad Nacional Autónoma de México, Departamento de Microbiología y Parasitología, Laboratorio de Inmunología de Hongos, 04510, Ciudad de México, Mexico.
Rodrigo Almeida-PaesInstituto Nacional de Infectologia Evandro Chagas (INI), FIOCRUZ - Fundação Oswaldo Cruz, Laboratório de Micologia, 21045-900, Rio de Janeiro, RJ, Brazil.
Rosely Maria Zancopé-OliveiraInstituto Nacional de Infectologia Evandro Chagas (INI), FIOCRUZ - Fundação Oswaldo Cruz, Laboratório de Micologia, 21045-900, Rio de Janeiro, RJ, Brazil.
Universidad Nacional Autónoma de México · MXFundação Oswaldo Cruz · BRHospital Geral de Fortaleza · BRNorthern Arizona University · USUniversidade de Brasília · BRUniversidade Federal do Ceará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histoplasmosis is a worldwide-distributed deep mycosis that affects healthy and immunocompromised hosts. Severe and disseminated disease is especially common in HIV-infected patients. At least 11 phylogenetic species are recognized and the majority of diversity is found in Latin America. The northeastern region of Brazil has one of the highest HIV/AIDS prevalence in Latin America and Ceará State has one of the highest death rates due to histoplasmosis in the world, where the mortality rate varies between 33-42%. The phylogenetic distribution and population genetic structure of 51 clinical isolates from Northeast Brazil was studied. For that morphological characteristics, exoantigens profile, and fungal mating types were evaluated. The genotypes were deduced by a MSLT in order to define local population structure of this fungal pathogen. In addition, the relationships of H. capsulatum genotypes with clinically relevant phenotypes and clinical aspects were investigated. The results suggest two cryptic species, herein named population Northeast BR1 and population Northeast BR2. These populations are recombining, exhibit a high level of haplotype diversity, and contain different ratios of mating types MAT1-1 and MAT1-2. However, differences in phenotypes or clinical aspects were not observed within these new cryptic species. A HIV patient can be co-infected by two or more genotypes from Northeast BR1 and/or Northeast BR2, which may have significant impact on disease progression due to the impaired immune response. We hypothesize that co-infections could be the result of multiple exposure events and may indicate higher risk of disseminated histoplasmosis, especially in HIV infected patients.

Indexed as

PhylogenyAdultBrazilFemaleGenetic VariationGenotypeHaplotypesHistoplasmaHistoplasmosisHIVHIV InfectionsHumansMaleMiddle AgedYoung Adult

Identifiers

PMID31409874
PMCPMC6692370
OpenAlexW2967976977

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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.