Dynamics of the blood plasma proteome during hyperacute HIV-1 infection

Abstract The complex dynamics of protein expression in plasma during hyperacute HIV-1 infection and its relation to acute retroviral syndrome, viral control, and disease progression are largely unknown. Here, we quantify 1293 blood plasma proteins from 157 longitudinally linked plasma samples collec...

Full description

Saved in:
Bibliographic Details
Main Authors: Jamirah Nazziwa, Eva Freyhult, Mun-Gwan Hong, Emil Johansson, Filip Årman, Jonathan Hare, Kamini Gounder, Melinda Rezeli, Tirthankar Mohanty, Sven Kjellström, Anatoli Kamali, Etienne Karita, William Kilembe, Matt A. Price, Pontiano Kaleebu, Susan Allen, Eric Hunter, Thumbi Ndung’u, Jill Gilmour, Sarah L. Rowland-Jones, Eduard Sanders, Amin S. Hassan, Joakim Esbjörnsson
Format: Article
Language:English
Published: Nature Portfolio 2024-12-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-54848-0
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850169114263289856
author Jamirah Nazziwa
Eva Freyhult
Mun-Gwan Hong
Emil Johansson
Filip Årman
Jonathan Hare
Kamini Gounder
Melinda Rezeli
Tirthankar Mohanty
Sven Kjellström
Anatoli Kamali
Etienne Karita
William Kilembe
Matt A. Price
Pontiano Kaleebu
Susan Allen
Eric Hunter
Thumbi Ndung’u
Jill Gilmour
Sarah L. Rowland-Jones
Eduard Sanders
Amin S. Hassan
Joakim Esbjörnsson
author_facet Jamirah Nazziwa
Eva Freyhult
Mun-Gwan Hong
Emil Johansson
Filip Årman
Jonathan Hare
Kamini Gounder
Melinda Rezeli
Tirthankar Mohanty
Sven Kjellström
Anatoli Kamali
Etienne Karita
William Kilembe
Matt A. Price
Pontiano Kaleebu
Susan Allen
Eric Hunter
Thumbi Ndung’u
Jill Gilmour
Sarah L. Rowland-Jones
Eduard Sanders
Amin S. Hassan
Joakim Esbjörnsson
author_sort Jamirah Nazziwa
collection DOAJ
description Abstract The complex dynamics of protein expression in plasma during hyperacute HIV-1 infection and its relation to acute retroviral syndrome, viral control, and disease progression are largely unknown. Here, we quantify 1293 blood plasma proteins from 157 longitudinally linked plasma samples collected before, during, and after hyperacute HIV-1 infection of 54 participants from four sub-Saharan African countries. Six distinct longitudinal expression profiles are identified, of which four demonstrate a consistent decrease in protein levels following HIV-1 infection. Proteins involved in inflammatory responses, immune regulation, and cell motility are significantly altered during the transition from pre-infection to one month post-infection. Specifically, decreased ZYX and SCGB1A1 levels, and increased LILRA3 levels are associated with increased risk of acute retroviral syndrome; increased NAPA and RAN levels, and decreased ITIH4 levels with viral control; and increased HPN, PRKCB, and ITGB3 levels with increased risk of disease progression. Overall, this study provides insight into early host responses in hyperacute HIV-1 infection, and present potential biomarkers and mechanisms linked to HIV-1 disease progression and viral load.
format Article
id doaj-art-dcf2b3c1e62f45ceb50912141a3bb216
institution OA Journals
issn 2041-1723
language English
publishDate 2024-12-01
publisher Nature Portfolio
record_format Article
series Nature Communications
spelling doaj-art-dcf2b3c1e62f45ceb50912141a3bb2162025-08-20T02:20:48ZengNature PortfolioNature Communications2041-17232024-12-0115111410.1038/s41467-024-54848-0Dynamics of the blood plasma proteome during hyperacute HIV-1 infectionJamirah Nazziwa0Eva Freyhult1Mun-Gwan Hong2Emil Johansson3Filip Årman4Jonathan Hare5Kamini Gounder6Melinda Rezeli7Tirthankar Mohanty8Sven Kjellström9Anatoli Kamali10Etienne Karita11William Kilembe12Matt A. Price13Pontiano Kaleebu14Susan Allen15Eric Hunter16Thumbi Ndung’u17Jill Gilmour18Sarah L. Rowland-Jones19Eduard Sanders20Amin S. Hassan21Joakim Esbjörnsson22Department of Translational Medicine, Lund UniversityNational Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Department of Cell and Molecular Biology, Uppsala UniversityNational Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm UniversityDepartment of Translational Medicine, Lund UniversityBioMS−Swedish National Infrastructure for Biological Mass Spectrometry, Lund UniversityIAVI Human Immunology Laboratory, Imperial CollegeAfrica Health Research InstituteBioMS−Swedish National Infrastructure for Biological Mass Spectrometry, Lund UniversityDivision of Infection Medicine, Department of Clinical Sciences Lund, Faculty of Medicine, Lund UniversityBioMS−Swedish National Infrastructure for Biological Mass Spectrometry, Lund UniversityIAVICenter for Family Health ResearchCenter for Family Health ResearchIAVIUganda Research Unit, Medical Research Council/Uganda Virus Research Institute and London School of Hygiene and Tropical MedicineCenter for Family Health ResearchCenter for Family Health ResearchAfrica Health Research InstituteDepartment of Infectious Diseases, Infection and Immunity, Faculty of Medicine, Imperial CollegeNuffield Department of Medicine, University of OxfordSir William Dunn School of Pathology, University of OxfordDepartment of Translational Medicine, Lund UniversityDepartment of Translational Medicine, Lund UniversityAbstract The complex dynamics of protein expression in plasma during hyperacute HIV-1 infection and its relation to acute retroviral syndrome, viral control, and disease progression are largely unknown. Here, we quantify 1293 blood plasma proteins from 157 longitudinally linked plasma samples collected before, during, and after hyperacute HIV-1 infection of 54 participants from four sub-Saharan African countries. Six distinct longitudinal expression profiles are identified, of which four demonstrate a consistent decrease in protein levels following HIV-1 infection. Proteins involved in inflammatory responses, immune regulation, and cell motility are significantly altered during the transition from pre-infection to one month post-infection. Specifically, decreased ZYX and SCGB1A1 levels, and increased LILRA3 levels are associated with increased risk of acute retroviral syndrome; increased NAPA and RAN levels, and decreased ITIH4 levels with viral control; and increased HPN, PRKCB, and ITGB3 levels with increased risk of disease progression. Overall, this study provides insight into early host responses in hyperacute HIV-1 infection, and present potential biomarkers and mechanisms linked to HIV-1 disease progression and viral load.https://doi.org/10.1038/s41467-024-54848-0
spellingShingle Jamirah Nazziwa
Eva Freyhult
Mun-Gwan Hong
Emil Johansson
Filip Årman
Jonathan Hare
Kamini Gounder
Melinda Rezeli
Tirthankar Mohanty
Sven Kjellström
Anatoli Kamali
Etienne Karita
William Kilembe
Matt A. Price
Pontiano Kaleebu
Susan Allen
Eric Hunter
Thumbi Ndung’u
Jill Gilmour
Sarah L. Rowland-Jones
Eduard Sanders
Amin S. Hassan
Joakim Esbjörnsson
Dynamics of the blood plasma proteome during hyperacute HIV-1 infection
Nature Communications
title Dynamics of the blood plasma proteome during hyperacute HIV-1 infection
title_full Dynamics of the blood plasma proteome during hyperacute HIV-1 infection
title_fullStr Dynamics of the blood plasma proteome during hyperacute HIV-1 infection
title_full_unstemmed Dynamics of the blood plasma proteome during hyperacute HIV-1 infection
title_short Dynamics of the blood plasma proteome during hyperacute HIV-1 infection
title_sort dynamics of the blood plasma proteome during hyperacute hiv 1 infection
url https://doi.org/10.1038/s41467-024-54848-0
work_keys_str_mv AT jamirahnazziwa dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT evafreyhult dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT mungwanhong dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT emiljohansson dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT filiparman dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT jonathanhare dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT kaminigounder dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT melindarezeli dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT tirthankarmohanty dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT svenkjellstrom dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT anatolikamali dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT etiennekarita dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT williamkilembe dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT mattaprice dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT pontianokaleebu dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT susanallen dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT erichunter dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT thumbindungu dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT jillgilmour dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT sarahlrowlandjones dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT eduardsanders dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT aminshassan dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection
AT joakimesbjornsson dynamicsofthebloodplasmaproteomeduringhyperacutehiv1infection