Herpes simplex encephalitis in adult patients with MASP-2 deficiency
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Stéphanie Bibert aff001; Jocelyne Piret aff002; Mathieu Quinodoz aff003; Emilie Collinet aff001; Vincent Zoete aff004; Olivier Michielin aff004; Rafik Menasria aff002; Pascal Meylan aff001; Titus Bihl aff008; Véronique Erard aff008; Florence Fellmann aff009; Carlo Rivolta aff003; Guy Boivin aff002; Pierre-Yves Bochud aff001
Působiště autorů:
Infectious Diseases Service, Department of Medicine, University Hospital and University of Lausanne, Lausanne, Switzerland
aff001; Research center in Infectious Diseases, CHU of Quebec and Laval University, Quebec city, Canada
aff002; Department of Computational Biology, Unit of Medical Genetics, University of Lausanne, Lausanne Switzerland
aff003; Ludwig Institute for Cancer research, University of Lausanne, Lausanne, Switzerland
aff004; Molecular Modeling Group, Swiss Institute of Bioinformatics, Quartier Sorge, Génopode, Lausanne, Switzerland
aff005; Department of Oncology, University Hospital and University of Lausanne, Lausanne, Switzerland
aff006; Institute of Microbiology, Department of Laboratory Medicine, University Hospital and University of Lausanne, Lausanne, Switzerland
aff007; Canton Hospital of Fribourg, Fribourg, Switzerland
aff008; Department of Genetics, Laboratoire National de Santé, Dudelange, Luxembourg
aff009; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom
aff010
Vyšlo v časopise:
Herpes simplex encephalitis in adult patients with MASP-2 deficiency. PLoS Pathog 15(12): e32767. doi:10.1371/journal.ppat.1008168
Kategorie:
Research Article
doi:
https://doi.org/10.1371/journal.ppat.1008168
Souhrn
We report here two cases of Herpes simplex virus encephalitis (HSE) in adult patients with very rare, previously uncharacterized, non synonymous heterozygous G634R and R203W substitution in mannan-binding lectin serine protease 2 (MASP2), a gene encoding a key protease of the lectin pathway of the complement system. None of the 2 patients had variants in genes involved in the TLR3-interferon signaling pathway. Both MASP2 variants induced functional defects in vitro, including a reduced (R203W) or abolished (G634R) protein secretion, a lost capability to cleave MASP-2 precursor into its active form (G634R) and an in vivo reduced antiviral activity (G634R). In a murine model of HSE, animals deficient in mannose binding lectins (MBL, the main pattern recognition molecule associated with MASP-2) had a decreased survival rate and an increased brain burden of HSV-1 compared to WT C57BL/6J mice. Altogether, these data suggest that MASP-2 deficiency can increase susceptibility to adult HSE.
Klíčová slova:
Alleles – Complement system – Cytokines – Chemokines – Molecular dynamics – Mouse models – Sequence motif analysis – Lectins
Zdroje
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Štítky
Hygiena a epidemiologie Infekční lékařství LaboratořČlánek vyšel v časopise
PLOS Pathogens
2019 Číslo 12
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