The Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia

ABSTRACT The Spl proteases are a group of six serine proteases that are encoded on the νSaβ pathogenicity island and are unique to Staphylococcus aureus. Despite their interesting biochemistry, their biological substrates and functions in virulence have been difficult to elucidate. We found that an...

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Autores principales: Alexandra E. Paharik, Wilmara Salgado-Pabon, David K. Meyerholz, Mark J. White, Patrick M. Schlievert, Alexander R. Horswill
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Publicado: American Society for Microbiology 2016
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spelling oai:doaj.org-article:12e10c29758d4e8abac34b089f61f88d2021-11-15T15:21:29ZThe Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia10.1128/mSphere.00208-162379-5042https://doaj.org/article/12e10c29758d4e8abac34b089f61f88d2016-10-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00208-16https://doaj.org/toc/2379-5042ABSTRACT The Spl proteases are a group of six serine proteases that are encoded on the νSaβ pathogenicity island and are unique to Staphylococcus aureus. Despite their interesting biochemistry, their biological substrates and functions in virulence have been difficult to elucidate. We found that an spl operon mutant of the community-associated methicillin-resistant S. aureus USA300 strain LAC induced localized lung damage in a rabbit model of pneumonia, characterized by bronchopneumonia observed histologically. Disease in the mutant-infected rabbits was restricted in distribution compared to that in wild-type USA300-infected rabbits. We also found that SplA is able to cleave the mucin 16 glycoprotein from the surface of the CalU-3 lung cell line, suggesting a possible mechanism for wild-type USA300 spreading pneumonia to both lungs. Investigation of the secreted and surface proteomes of wild-type USA300 and the spl mutant revealed multiple alterations in metabolic proteins and virulence factors. This study demonstrates that the Spls modulate S. aureus physiology and virulence, identifies a human target of SplA, and suggests potential S. aureus targets of the Spl proteases. IMPORTANCE Staphylococcus aureus is a versatile human pathogen that produces an array of virulence factors, including several proteases. Of these, six proteases called the Spls are the least characterized. Previous evidence suggests that the Spls are expressed during human infection; however, their function is unknown. Our study shows that the Spls are required for S. aureus to cause disseminated lung damage during pneumonia. Further, we present the first example of a human protein cut by an Spl protease. Although the Spls were predicted not to cut staphylococcal proteins, we also show that an spl mutant has altered abundance of both secreted and surface-associated proteins. This work provides novel insight into the function of Spls during infection and their potential ability to degrade both staphylococcal and human proteins.Alexandra E. PaharikWilmara Salgado-PabonDavid K. MeyerholzMark J. WhitePatrick M. SchlievertAlexander R. HorswillAmerican Society for MicrobiologyarticleStaphylococcus aureusmucinpneumoniaproteasesSplvirulence factorsMicrobiologyQR1-502ENmSphere, Vol 1, Iss 5 (2016)
institution DOAJ
collection DOAJ
language EN
topic Staphylococcus aureus
mucin
pneumonia
proteases
Spl
virulence factors
Microbiology
QR1-502
spellingShingle Staphylococcus aureus
mucin
pneumonia
proteases
Spl
virulence factors
Microbiology
QR1-502
Alexandra E. Paharik
Wilmara Salgado-Pabon
David K. Meyerholz
Mark J. White
Patrick M. Schlievert
Alexander R. Horswill
The Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia
description ABSTRACT The Spl proteases are a group of six serine proteases that are encoded on the νSaβ pathogenicity island and are unique to Staphylococcus aureus. Despite their interesting biochemistry, their biological substrates and functions in virulence have been difficult to elucidate. We found that an spl operon mutant of the community-associated methicillin-resistant S. aureus USA300 strain LAC induced localized lung damage in a rabbit model of pneumonia, characterized by bronchopneumonia observed histologically. Disease in the mutant-infected rabbits was restricted in distribution compared to that in wild-type USA300-infected rabbits. We also found that SplA is able to cleave the mucin 16 glycoprotein from the surface of the CalU-3 lung cell line, suggesting a possible mechanism for wild-type USA300 spreading pneumonia to both lungs. Investigation of the secreted and surface proteomes of wild-type USA300 and the spl mutant revealed multiple alterations in metabolic proteins and virulence factors. This study demonstrates that the Spls modulate S. aureus physiology and virulence, identifies a human target of SplA, and suggests potential S. aureus targets of the Spl proteases. IMPORTANCE Staphylococcus aureus is a versatile human pathogen that produces an array of virulence factors, including several proteases. Of these, six proteases called the Spls are the least characterized. Previous evidence suggests that the Spls are expressed during human infection; however, their function is unknown. Our study shows that the Spls are required for S. aureus to cause disseminated lung damage during pneumonia. Further, we present the first example of a human protein cut by an Spl protease. Although the Spls were predicted not to cut staphylococcal proteins, we also show that an spl mutant has altered abundance of both secreted and surface-associated proteins. This work provides novel insight into the function of Spls during infection and their potential ability to degrade both staphylococcal and human proteins.
format article
author Alexandra E. Paharik
Wilmara Salgado-Pabon
David K. Meyerholz
Mark J. White
Patrick M. Schlievert
Alexander R. Horswill
author_facet Alexandra E. Paharik
Wilmara Salgado-Pabon
David K. Meyerholz
Mark J. White
Patrick M. Schlievert
Alexander R. Horswill
author_sort Alexandra E. Paharik
title The Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia
title_short The Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia
title_full The Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia
title_fullStr The Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia
title_full_unstemmed The Spl Serine Proteases Modulate <named-content content-type="genus-species">Staphylococcus aureus</named-content> Protein Production and Virulence in a Rabbit Model of Pneumonia
title_sort spl serine proteases modulate <named-content content-type="genus-species">staphylococcus aureus</named-content> protein production and virulence in a rabbit model of pneumonia
publisher American Society for Microbiology
publishDate 2016
url https://doaj.org/article/12e10c29758d4e8abac34b089f61f88d
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