Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/164614
Título: The exception that proves the rule
Autor: Wichers-Misterek, Jan Stephan
Krumkamp, Ralf
Held, Jana
von Thien, Heidrun
Wittmann, Irene
Höppner, Yannick Daniel
Ruge, Julia M.
Moser, Kara
Dara, Antoine
Strauss, Jan
Esen, Meral
Fendel, Rolf
Sulyok, Zita
Jeninga, Myriam D.
Kremsner, Peter G.
Sim, B. Kim Lee
Hoffman, Stephen L.
Duffy, Michael F.
Otto, Thomas D.
Gilberger, Tim Wolf
Silva, Joana C.
Mordmüller, Benjamin
Petter, Michaela
Bachmann, Anna
Palavras-chave: RA Public aspects of medicine
QR Microbiology
Parasitology
Microbiology
Immunology
Molecular Biology
Genetics
Infectious Diseases
SDG 3 - Good Health and Well-being
Data: Jun-2023
Resumo: Controlled human malaria infections (CHMI) are a valuable tool to study parasite gene expression in vivo under defined conditions. In previous studies, virulence gene expression was analyzed in samples from volunteers infected with the Plasmodium falciparum (Pf) NF54 isolate, which is of African origin. Here, we provide an in-depth investigation of parasite virulence gene expression in malaria-naïve European volunteers undergoing CHMI with the genetically distinct Pf 7G8 clone, originating in Brazil. Differential expression of var genes, encoding major virulence factors of Pf, PfEMP1s, was assessed in ex vivo parasite samples as well as in parasites from the in vitro cell bank culture that was used to generate the sporozoites (SPZ) for CHMI (Sanaria PfSPZ Challenge (7G8)). We report broad activation of mainly B-type subtelomeric located var genes at the onset of a 7G8 blood stage infection in naïve volunteers, mirroring the NF54 expression study and suggesting that the expression of virulence-associated genes is generally reset during transmission from the mosquito to the human host. However, in 7G8 parasites, we additionally detected a continuously expressed single C-type variant, Pf7G8_040025600, that was most highly expressed in both pre-mosquito cell bank and volunteer samples, suggesting that 7G8, unlike NF54, maintains expression of some previously expressed var variants during transmission. This suggests that in a new host, the parasite may preferentially express the variants that previously allowed successful infection and transmission.  Trial registration: ClinicalTrials.gov NCT02704533; 2018-004523-36.
Descrição: 323759012). Manufacture of the Sanaria PfSPZ vaccine, PfSPZ challenge (NF54), and PfSPZ challenge (7G8) was funded in part by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under SLH's SBIR award numbers SLH 5R44AI058375 and 5R44AI055229. JCS, KAM and AD were funded by awards U19 AI110820 and R01 AI141900, from the National Institute for Allergy and Infectious Diseases, National Institutes of Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank all volunteers who participated in the trials at the Institute of Tropical Medicine in Tübingen, Germany, and the entire study team. We thank Sanaria Inc. for providing the 7G8 working cell bank parasites and the PfSPZ Challenge (7G8) used in the CHMI trials and Balázs Horváth for his help with data analysis, mapping and variant calling. The following reagents were obtained through BEI Resources, NIAID, NIH: Plasmodium falciparum, Strain 7G8, MRA-152, contributed by David Walliker, MRA-154, contributed by Dennis E. Kyle and MRA-926, contributed by Karen Hayton and Tom Wellems. Publisher Copyright: Copyright: © 2023 Wichers-Misterek et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Peer review: yes
URI: http://hdl.handle.net/10362/164614
DOI: https://doi.org/10.1371/journal.ppat.1011468
ISSN: 1553-7366
Aparece nas colecções:Home collection (IHMT)

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