Virulence traits of a serogroup C Meningococcus and isogenic cssA mutant, defective in surface-exposed sialic acid, in a murine model of meningitis
Autor: | Laura Paragliola, Chiara Pagliuca, Pietro Alifano, Fabrizio Farina, Gianni Pozzi, Ilias Masouris, Roberta Colicchio, Susanna Ricci, Paola Salvatore, Giuseppe Mantova, Caterina Pagliarulo, Uwe Koedel, Stephen L. Leib, Elena Scaglione, Denis Grandgirard |
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Přispěvatelé: | Colicchio, R., Pagliuca, C., Ricci, S., Scaglione, E., Grandgirard, D., Masouris, I., Farina, F., Pagliarulo, C., Mantova, G., Paragliol, L., Leib, S. L., Koedel, U., Pozzi, G., Alifano, P., Salvatorea, P., Colicchio, Roberta, Pagliuca, Chiara, Ricci, Susanna, Scaglione, Elena, Grandgirard, Deni, Masouris, Ilia, Farina, Fabrizio, Pagliarulo, Caterina, Mantova, Giuseppe, Laura, Paragliola, Leib Stephen, L., Koedel, Uwe, Pozzi, Gianni, Alifano, Pietro, Salvatore, Paola |
Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Mutant Neisseria meningitidis Serogroup C Neisseria meningitidis medicine.disease_cause corpus callosum Gene Knockout Techniques chemistry.chemical_compound Mice 0302 clinical medicine Capsule Mice Inbred BALB C Virulence LOS Gene Knockout Technique Meningoencephalitis Brain meningitis mouse models meningoencephalitis Bacterial Infections Infectious Diseases sialic acid Meningitis mouse model Female Meningitis Human capsule Corpus callosum Immunology Bacterial Protein Biology Carbohydrate Epimerase Meningitis Meningococcal Microbiology 03 medical and health sciences Bacterial Proteins medicine Neisseria meningitidi Animals Humans Tropism Animal Wild type medicine.disease Sialic acid N-Acetylneuraminic Acid Disease Models Animal 030104 developmental biology chemistry Parasitology Carbohydrate Epimerases 030217 neurology & neurosurgery Meningoencephaliti |
Popis: | In serogroup C Neisseria meningitidis, the cssA (siaA) gene codes for an UDP-N-acetylglucosamine 2-epimerase that catalyzes the conversion of UDP-N-acetyl-alpha-D-glucosamine into N-acetyl-D-mannosamine and UDP in the first step in sialic acid biosynthesis. This enzyme is required for the biosynthesis of the (alpha 2 -> 9)-linked polysialic acid capsule and for lipooligosaccharide (LOS) sialylation. In this study, we have used a reference serogroup C meningococcal strain and an isogenic cssA knockout mutant to investigate the pathogenetic role of surface-exposed sialic acids in a model of meningitis based on intracisternal inoculation of BALB/c mice. Results confirmed the key role of surface-exposed sialic acids in meningococcal pathogenesis. The 50% lethal dose (LD50) of the wild-type strain 93/4286 was about four orders of magnitude lower than that of the cssA mutant. Compared to the wild-type strain, the ability of this mutant to replicate in brain and spread systemically was severely impaired. Evaluation of brain damage evidenced a significant reduction in cerebral hemorrhages in mice infected with the mutant in comparison with the levels in those challenged with the wild-type strain. Histological analysis showed the typical features of bacterial meningitis, including inflammatory cells in the subarachnoid, perivascular, and ventricular spaces especially in animals infected with the wild type. Noticeably, 80% of mice infected with the wild-type strain presented with massive bacterial localization and accompanying inflammatory infiltrate in the corpus callosum, indicating high tropism of meningococci exposing sialic acids toward this brain structure and a specific involvement of the corpus callosum in the mouse model of meningococcal meningitis. |
Databáze: | OpenAIRE |
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