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
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