Cited by 197Salmonella and Campylobacter epidemiologyEscherichia coli research studiesImmune Response and Inflammation

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Life in the inflamed intestine, Salmonella style

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Santos, Renato L., Raffatellu, Manuela, Bevins, Charles L., Adams, L. Garry, Tükel, Çagla, Tsolis, Renée M., Bäumler, Andreas J.·2009·Trends in Microbiology

DOI 10.1016/j.tim.2009.08.008PMC PMC3235402

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Abstract

The lower gastrointestinal tract is densely populated with resident microbial communities (microbiota), which do not elicit overt host responses but rather provide benefit to the host, including niche protection from pathogens. However, introduction of bacteria into the underlying tissue evokes acute inflammation. Non-typhoidal Salmonella serotypes (NTS) elicit this stereotypic host response by actively penetrating the intestinal epithelium and surviving in tissue macrophages. Initial responses generated by bacterial host cell interaction are amplified in tissue through the interleukin (IL)-18/interferon-gamma and IL-23/IL-17 axes, resulting in the activation of mucosal barrier functions against NTS dissemination. However, the pathogen is adapted to survive antimicrobial defenses encountered in the lumen of the inflamed intestine. This strategy enables NTS to exploit inflammation to outcompete the intestinal microbiota, and promotes the Salmonella transmission by the fecal/oral route.

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Gillis, C. C., Winter, M. G., Chanin, R. B., Zhu, W., Spiga, L., & Winter, S. (2019) · Infection and Immunity · doi:10.1128/iai.00773-18 · Cited by 35
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Silva, M. T., & Pestana, N. (2012) · Immunobiology · doi:10.1016/j.imbio.2012.05.011 · Cited by 36
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Byndloss, M. X., Rivera-Chávez, F., Tsolis, R. M., & Bäumler, A. J. (2016) · Current Opinion in Microbiology · doi:10.1016/j.mib.2016.08.007 · Cited by 32
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Yang, Y., Wan, C., Xu, H., Aguilar, Z. P., Tan, Q., Xu, F., Lai, W., Xiong, Y., & Wei, H. (2013) · Microbes and Infection · doi:10.1016/j.micinf.2013.02.005 · Cited by 26
Salmonella
Graziani, C., Losasso, C., Luzzi, I., Ricci, A., Scavia, G., & Pasquali, P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-385007-2.00005-x · Cited by 25
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Yang, Y., Wan, C., Xu, H., & Wei, H. (2013) · Vaccine · doi:10.1016/j.vaccine.2013.04.044 · Cited by 25
Transient Loss of Protection Afforded by a Live Attenuated Non-typhoidal Salmonella Vaccine in Mice Co-infected with Malaria
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Pseudogenization of sopA and sopE2 is functionally linked and contributes to virulence of Salmonella enterica serovar Typhi
Valenzuela, L. M., Hidalgo, A. A., Rodríguez, L. M., Urrutia, Í. M., Ortega, A., Villagra, N. A., Paredes‐Sabja, D., Calderón, I. L., Gil, F., Saavedra, C. P., et al. (2015) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2015.04.021 · Cited by 25
Multicopy Single-Stranded DNA Directs Intestinal Colonization of Enteric Pathogens
Elfenbein, J. R., Knodler, L. A., Nakayasu, E. S., Ansong, C. K., Brewer, H. M., Bogomolnaya, L. M., Adams, L. G., McClelland, M., Adkins, J., & Andrews‐Polymenis, H. L. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005472 · Cited by 23
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Wang, H., Zeng, X., Mo, Y., He, B., Lin, H., & Lin, J. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.00358-19 · Cited by 22

Authors: Santos, R. L., Raffatellu, M., Bevins, C. L., Adams, L. G., Tükel, Ç., Tsolis, R. M., & Bäumler, A. J.
Affiliations: Universidade Federal de Minas Gerais (BR)
University of California, Irvine (US)
University of California, Davis (US)
Texas A&M University (US)
Corresponding author: Bäumler, Andreas J.
ORCID: Santos, Renato L.
Raffatellu, Manuela
Bevins, Charles L.
Adams, L. Garry
Tsolis, Renée M.
Bäumler, Andreas J.
Venue: Trends in Microbiology
Publisher: Elsevier BV
Published: 2009-11
Volume: 17
Issue: 11
Pages: 498-506
ISSN: 0966-842X (ISSN-L)
DOI: 10.1016/j.tim.2009.08.008
PMC: PMC3235402
OpenAlex: W2075058732
Cited by: 197
References: 100
Citations by year: 2026: 5 · 2025: 8 · 2024: 3 · 2023: 10 · 2022: 11 · 2021: 8 · 2020: 10 · 2019: 13 · 2018: 8 · 2017: 12 · 2016: 15 · 2015: 15 · 2014: 12 · 2013: 19 · 2012: 17
FWCI: 2.13
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Trends in Microbiology (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Funders: National Institute of Allergy and Infectious Diseases (R01AI044170, AI 040124, AI044170, AI079173, R21AI079173, R01AI032738, R29AI040124, R01AI050843, R01AI076246, R01AI040124, R01AI050553, AI050553, AI076246, R37AI032738)
Topics: Life Sciences › Agricultural and Biological Sciences › Food Science › Salmonella and Campylobacter epidemiology
Life Sciences › Immunology and Microbiology › Microbiology › Escherichia coli research studies
Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
Keywords: non-typhoidal Salmonella, intestinal inflammation, host-pathogen interaction, gut microbiota, tissue macrophages, IL-23/IL-17 axis, mucosal barrier, antimicrobial resistance, fecal-oral transmission
MeSH terms: Animals, Humans, Intestinal Mucosa, Intestines, Macrophages, Models, Biological, Salmonella, Salmonella Infections, Cytokines

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