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Strain-specific virulence phenotypes of Streptococcus pneumoniae assessed using the Chinchilla laniger model of otitis media
Journal article   Open access

Strain-specific virulence phenotypes of Streptococcus pneumoniae assessed using the Chinchilla laniger model of otitis media

Michael L Forbes, Edward Horsey, N Luisa Hiller, Farrel J Buchinsky, Jay D Hayes, James M Compliment, Todd Hillman, Suzanne Ezzo, Kai Shen, Randy Keefe, …
PloS one, v 3(4), pp e1969-e1969
09 Apr 2008
PMID: 18398481
url
https://doi.org/10.1371/journal.pone.0001969View
Published, Version of Record (VoR) Open

Abstract

Species Specificity Humans Virulence Pneumococcal Infections - diagnosis Stem Cells Phenotype Animals Streptococcus pneumoniae - pathogenicity Chinchilla - microbiology Streptococcus pneumoniae - genetics Otitis Media - genetics Pneumococcal Infections - microbiology Antigens, Bacterial - metabolism Disease Models, Animal
Streptococcus pneumoniae [Sp] infection is associated with local and systemic disease. Our current understanding of the differential contributions of genetic strain variation, serotype, and host response to disease phenotype is incomplete. Using the chinchilla model of otitis media [OM] we investigated the disease phenotype generated by the laboratory strain TIGR4 and each of thirteen clinical strains (BS68-75, BS290, BS291, BS293, BS436 and BS437); eleven of the thirteen strains have been genomically sequenced. For each strain 100 colony forming units were injected bilaterally into the tympanic bullae of 6 young adult chinchillas under general anesthesia. All animals were examined daily for local and systemic disease by a blinded observer. Pneumatic otoscopy was used to evaluate local disease, and behavioral assessments served as the measure of systemic disease. Virulence scoring was performed using a 4-point scale to assess four clinical parameters [severity and rapidity of local disease onset; and severity and rapidity of systemic disease onset] during a 10-day evaluation period. Highly significant variation was observed among the strains in their ability to cause disease and moribundity. As expected, there was a significant correlation between the rapidity of systemic disease onset and severity of systemic disease; however, there was little correlation between the severity of otoscopic changes and severity of systemic disease. Importantly, it was observed that different strains of the same serotype produced as broad an array of disease phenotypes as did strains of different serotypes. We attribute these phenotypic differences among the strains to the high degree of genomic plasticity that we have previously documented.

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Collaboration types
Domestic collaboration
Web of Science research areas
Immunology
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