Engineering Mycoplasma pneumoniae to bypass the association with Guillain-Barré syndrome

A non-pathogenic Mycoplasma pneumoniae-based chassis is leading the development of live biotherapeutic products (LBPs) for respiratory diseases. However, reports connecting Guillain-Barré syndrome (GBS) cases to prior M. pneumoniae infections represent a concern for exploiting such a chassis. Galact...

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Detalhes bibliográficos
Autores: Broto, Alicia, Piñero-Lambea, Carlos, Segura-Morales, Carolina, Tio-Gillen, Anne P., Unger, Wendy W. J., Burgos, Raul, Mazzolini, Rocco, Miravet Verde, Samuel, 1992-, Jacobs, Bart C., Casas, Josefina, Huizinga, Ruth, Lluch-Senar, Maria 1982-, Serrano Pubull, Luis, 1982-
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10230/61028
Acesso em linha:http://hdl.handle.net/10230/61028
http://dx.doi.org/10.1016/j.micinf.2024.105342
Access Level:acceso abierto
Palavra-chave:Galactocerebrosides
Glycolipids
Glycosyltransferases
Immune response
Molecular mimicry
Mycoplasma pneumoniae
Descrição
Resumo:A non-pathogenic Mycoplasma pneumoniae-based chassis is leading the development of live biotherapeutic products (LBPs) for respiratory diseases. However, reports connecting Guillain-Barré syndrome (GBS) cases to prior M. pneumoniae infections represent a concern for exploiting such a chassis. Galactolipids, especially galactocerebroside (GalCer), are considered the most likely M. pneumoniae antigens triggering autoimmune responses associated with GBS development. In this work, we generated different strains lacking genes involved in galactolipids biosynthesis. Glycolipid profiling of the strains demonstrated that some mutants show a complete lack of galactolipids. Cross-reactivity assays with sera from GBS patients with prior M. pneumoniae infection showed that certain engineered strains exhibit reduced antibody recognition. However, correlation analyses of these results with the glycolipid profile of the engineered strains suggest that other factors different from GalCer contribute to sera recognition, including total ceramide levels, dihexosylceramide (DHCer), and diglycosyldiacylglycerol (DGDAG). Finally, we discuss the best candidate strains as potential GBS-free Mycoplasma chassis.