Evidence map›Paper›PMID 40799787›Full record

ArticleOpen forum infectious diseases2025

High Propensity for Multidrug-Resistant Pneumococcal Shedding Among Adults Living With HIV on Stable Antiretroviral Therapy in Malawi.

Lusako L Sibale, Newton Kalata, Ndaona Mitole, Tinashe K Nyazika, Joseph A Phiri, Alice Kusakala, Mercy Khwiya, Gift Sagawa, Stephanie W Lo, Chrispin Chaguza and 10 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

20 authors.

Lusako L SibaleInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.ORCID https://orcid.org/0000-0001-5378-3561
Newton KalataInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Ndaona MitoleInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Tinashe K NyazikaDepartment of Biomedical Sciences and Physiology, School of Life Sciences, Faculty of Science and Engineering, University of Wolverhampton, Wolverhampton, UK.
Joseph A PhiriInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Alice KusakalaInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Mercy KhwiyaInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Gift SagawaInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Stephanie W LoParasites and Microbes, Wellcome Sanger Institute, Cambridge, UK.
Chrispin ChaguzaResearch Department of Infection, Division of Infection and Immunity, University College London, London, UK.
Deus ThindwaInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Todd D SwarthoutResearch Department of Infection, Division of Infection and Immunity, University College London, London, UK.
Neil FrenchInstitute of Infection Veterinary & Ecological Science, University of Liverpool, Liverpool, UK.ORCID https://orcid.org/0000-0003-4814-8293
Ken MalisitaLighthouse, Queen Elizabeth Hospital and Gateway Health Centre, Blantyre District Health Office, Blantyre, Malawi.
Arox Kamng'onaSchool of Life Science and Allied Health Professions, Kamuzu University of Health Sciences, Blantyre, Malawi.ORCID https://orcid.org/0000-0002-0841-7586
Daniela M FerreiraDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Stephen D BentleyParasites and Microbes, Wellcome Sanger Institute, Cambridge, UK.
Robert S HeydermanResearch Department of Infection, Division of Infection and Immunity, University College London, London, UK.ORCID https://orcid.org/0000-0003-4573-449X
Brenda A Kwambana-AdamsInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Kondwani C JamboInfection and Immunity Research Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.ORCID https://orcid.org/0000-0002-3195-2210

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: People living with human immunodeficiency virus (HIV; PLHIV) on antiretroviral therapy (ART) are still at risk of pneumococcal disease and have over 2-fold higher pneumococcal carriage prevalence than HIV-uninfected (HIV-) adults). Carriage is a risk factor for pneumococcal disease, antimicrobial resistance (AMR) emergence, and transmission. Therefore, we tested whether the high prevalence of pneumococcal carriage in PLHIV on ART is associated with increased bacterial density, shedding, and AMR. Methods: We recruited asymptomatic PLHIV on ART for >1 year (PLHIV-ART>1y) and HIV- adults. Nasopharyngeal swab samples were collected on days 3, 7, 14, 21, and 28, followed by monthly collections for 12 months, while shedding samples were collected on days 3, 21, and 28. Peripheral blood samples were collected on day 3 to measure CD4 cell count and HIV viral load. Pneumococcal carriage density and shedding were assessed using standard bacterial culture, multiple carriage was detected using whole-plate sweep sequencing, and AMR profiling was conducted using disk diffusion and Etest. Results: PLHIV-ART>1y had a higher propensity for high-density carriage (adjusted odds ratio, 1.67 [95% confidence interval (CI), 1.07-2.60]; Conclusions: These findings indicate that PLHIV-ART>1y remain at high risk of pneumococcal disease and could also be an important reservoir for shedding multidrug-resistant pneumococci.

Indexed as

AMRARTcarriageHIVStreptococcus pneumoniae

Identifiers

PMID40799787
PMCPMC12343114

What Socratic 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 Socratic graph.