PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killing

ABSTRACT Non-typhoidal Salmonella serovars, such as Salmonella enterica serovar Typhimurium (STm), are a leading cause of inflammatory diarrhea in otherwise healthy individuals. Among children, the elderly, and immunocompromised individuals, STm can spread to systemic sites and cause potentially let...

Full description

Saved in:
Bibliographic Details
Main Authors: Michael H. Lee, Araceli Perez-Lopez, Leigh A. Knodler, Grace Nguyen, Gregory T. Walker, Judith Behnsen, Steven Silva, Jean Celli, Melissa A. Tamin, Michael H. Liang, Karine Melchior, Felix A. Argueta, Sean-Paul Nuccio, Manuela Raffatellu
Format: Article
Language:English
Published: American Society for Microbiology 2025-08-01
Series:mBio
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/mbio.03802-24
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849407809144225792
author Michael H. Lee
Araceli Perez-Lopez
Leigh A. Knodler
Grace Nguyen
Gregory T. Walker
Judith Behnsen
Steven Silva
Jean Celli
Melissa A. Tamin
Michael H. Liang
Karine Melchior
Felix A. Argueta
Sean-Paul Nuccio
Manuela Raffatellu
author_facet Michael H. Lee
Araceli Perez-Lopez
Leigh A. Knodler
Grace Nguyen
Gregory T. Walker
Judith Behnsen
Steven Silva
Jean Celli
Melissa A. Tamin
Michael H. Liang
Karine Melchior
Felix A. Argueta
Sean-Paul Nuccio
Manuela Raffatellu
author_sort Michael H. Lee
collection DOAJ
description ABSTRACT Non-typhoidal Salmonella serovars, such as Salmonella enterica serovar Typhimurium (STm), are a leading cause of inflammatory diarrhea in otherwise healthy individuals. Among children, the elderly, and immunocompromised individuals, STm can spread to systemic sites and cause potentially lethal bacteremia. Phagocytic cells and the immune complement system are pivotal to preventing the dissemination of STm. PgtE, an STm outer membrane protease, has been previously described to cleave over a dozen mammalian protein substrates in vitro, including complement protein C3. However, these activities have mostly been observed with mutant, avirulent strains with a truncated O-antigen that renders bacteria sensitive to complement killing. Here, we report that virulent STm utilizes PgtE to evade complement-mediated killing in vivo. The wild-type pathogen increases pgtE expression and PgtE proteolytic function within macrophages and in macrophage-like in vitro growth conditions, concomitant with physiologic O-antigen truncation in these environments. Furthermore, we found that wild-type STm’s resistance to complement-mediated serum and neutrophil killing is PgtE-dependent. We propose that PgtE promotes the systemic spread of STm by acting as a second line of defense against complement when STm escapes from a macrophage.IMPORTANCENon-typhoidal Salmonella serovars primarily cause gastrointestinal infections but can also lead to bacteremia through mechanisms that are not completely elucidated. Here we show that the outer membrane protease PgtE enables virulent Salmonella to evade complement-mediated killing in vivo, thereby promoting bacteremia. We also demonstrate that pgtE expression and PgtE proteolytic function are increased within macrophages and under macrophage-like growth conditions. Upon escaping from macrophages, PgtE protects against complement-mediated killing by serum and neutrophils, promoting the systemic spread of the pathogen. These findings highlight PgtE as a potential therapeutic target for preventing Salmonella bacteremia.
format Article
id doaj-art-5185356e7ff244669d298c0f42e161a9
institution Kabale University
issn 2150-7511
language English
publishDate 2025-08-01
publisher American Society for Microbiology
record_format Article
series mBio
spelling doaj-art-5185356e7ff244669d298c0f42e161a92025-08-20T03:35:57ZengAmerican Society for MicrobiologymBio2150-75112025-08-0116810.1128/mbio.03802-24PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killingMichael H. Lee0Araceli Perez-Lopez1Leigh A. Knodler2Grace Nguyen3Gregory T. Walker4Judith Behnsen5Steven Silva6Jean Celli7Melissa A. Tamin8Michael H. Liang9Karine Melchior10Felix A. Argueta11Sean-Paul Nuccio12Manuela Raffatellu13Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USAPaul G. Allen School for Global Health, College of Veterinary Medicine, Washington State University, Pullman, Washington, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADepartment of Microbiology and Immunology, University of Illinois Chicago, Chicago, Illinois, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USAPaul G. Allen School for Global Health, College of Veterinary Medicine, Washington State University, Pullman, Washington, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USADivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, California, USAABSTRACT Non-typhoidal Salmonella serovars, such as Salmonella enterica serovar Typhimurium (STm), are a leading cause of inflammatory diarrhea in otherwise healthy individuals. Among children, the elderly, and immunocompromised individuals, STm can spread to systemic sites and cause potentially lethal bacteremia. Phagocytic cells and the immune complement system are pivotal to preventing the dissemination of STm. PgtE, an STm outer membrane protease, has been previously described to cleave over a dozen mammalian protein substrates in vitro, including complement protein C3. However, these activities have mostly been observed with mutant, avirulent strains with a truncated O-antigen that renders bacteria sensitive to complement killing. Here, we report that virulent STm utilizes PgtE to evade complement-mediated killing in vivo. The wild-type pathogen increases pgtE expression and PgtE proteolytic function within macrophages and in macrophage-like in vitro growth conditions, concomitant with physiologic O-antigen truncation in these environments. Furthermore, we found that wild-type STm’s resistance to complement-mediated serum and neutrophil killing is PgtE-dependent. We propose that PgtE promotes the systemic spread of STm by acting as a second line of defense against complement when STm escapes from a macrophage.IMPORTANCENon-typhoidal Salmonella serovars primarily cause gastrointestinal infections but can also lead to bacteremia through mechanisms that are not completely elucidated. Here we show that the outer membrane protease PgtE enables virulent Salmonella to evade complement-mediated killing in vivo, thereby promoting bacteremia. We also demonstrate that pgtE expression and PgtE proteolytic function are increased within macrophages and under macrophage-like growth conditions. Upon escaping from macrophages, PgtE protects against complement-mediated killing by serum and neutrophils, promoting the systemic spread of the pathogen. These findings highlight PgtE as a potential therapeutic target for preventing Salmonella bacteremia.https://journals.asm.org/doi/10.1128/mbio.03802-24Salmonellacomplementneutrophilsmacrophagesproteasesbacteremia
spellingShingle Michael H. Lee
Araceli Perez-Lopez
Leigh A. Knodler
Grace Nguyen
Gregory T. Walker
Judith Behnsen
Steven Silva
Jean Celli
Melissa A. Tamin
Michael H. Liang
Karine Melchior
Felix A. Argueta
Sean-Paul Nuccio
Manuela Raffatellu
PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killing
mBio
Salmonella
complement
neutrophils
macrophages
proteases
bacteremia
title PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killing
title_full PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killing
title_fullStr PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killing
title_full_unstemmed PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killing
title_short PgtE protease enables virulent Salmonella to evade C3-mediated serum and neutrophil killing
title_sort pgte protease enables virulent salmonella to evade c3 mediated serum and neutrophil killing
topic Salmonella
complement
neutrophils
macrophages
proteases
bacteremia
url https://journals.asm.org/doi/10.1128/mbio.03802-24
work_keys_str_mv AT michaelhlee pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT araceliperezlopez pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT leighaknodler pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT gracenguyen pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT gregorytwalker pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT judithbehnsen pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT stevensilva pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT jeancelli pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT melissaatamin pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT michaelhliang pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT karinemelchior pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT felixaargueta pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT seanpaulnuccio pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling
AT manuelaraffatellu pgteproteaseenablesvirulentsalmonellatoevadec3mediatedserumandneutrophilkilling