Literature DB >> 17337057

Porcine differential gene expression in response to Salmonella enterica serovars Choleraesuis and Typhimurium.

Jolita J Uthe1, Atabak Royaee, Joan K Lunney, Thomas J Stabel, Shu-Hong Zhao, Christopher K Tuggle, Shawn M D Bearson.   

Abstract

An investigation of the porcine response to gastrointestinal infection with Salmonella enterica serovars Choleraesuis (narrow host range) and Typhimurium (broad host range) revealed markedly different transcriptional profiles. Seven genes identified by suppression subtractive hybridization as up-regulated in the mesenteric lymph nodes at 24h (h) post-inoculation (p.i.) in serovar Choleraesuis-infected pigs (ARPC2, CCT7, HSPH1, LCP1, PTMA, SDCBP, VCP) and three genes in serovar Typhimurium-infected pigs (CD47/IAP, CXCL10, SCARB2) were analyzed by real-time PCR at 8h, 24 h, 48 h, 7 days (d) and 21 d p.i. A comparison between the two Salmonella infections revealed significant differences in transcriptional induction early in the infection (8-24h) for the serovar Typhimurium-infected pigs, whereas the serovar Choleraesuis-infected pigs exhibited significantly higher levels of gene expression at the later time points (48h-21 d), except for HSPH1. A similar gene expression trend was observed for immune-related genes involved in innate immunity and the inflammatory T helper 1 (Th1) response. Initial repression of gene expression in the serovar Choleraesuis-infected pigs from 8 to 48h p.i. (IFNG, IL12A, IL4, IL8, CSF2) coincided with extended transcriptional activation throughout the 21 d infection (IFNG, INDO, SOCS1, STAT1, IL1B, IL6, IL8, SLC11A1). The serovar Typhimurium-infected swine presented a more transient induction of immune-related genes (IFNG, INDO, IRF1, SOCS1, STAT1, IL1B, IL8, SLC11A1) early in the infection (24-48 h) followed by a significant repression of IL12A, IL12B, IL4, IL8 and CSF2. Collectively, these data reveal specific porcine genes with differences in gene expression kinetics that may be responsible for the variation in disease progression observed in swine infected with Typhimurium compared to Choleraesuis.

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Year:  2007        PMID: 17337057     DOI: 10.1016/j.molimm.2007.01.016

Source DB:  PubMed          Journal:  Mol Immunol        ISSN: 0161-5890            Impact factor:   4.407


  13 in total

1.  Salmonella enterica Serovar Typhimurium Temporally Modulates the Enteric Microbiota and Host Responses To Overcome Colonization Resistance in Swine.

Authors:  Danisa M Bescucci; Paul E Moote; Rodrigo Ortega Polo; Richard R E Uwiera; G Douglas Inglis
Journal:  Appl Environ Microbiol       Date:  2020-10-15       Impact factor: 4.792

Review 2.  Methods for transcriptomic analyses of the porcine host immune response: application to Salmonella infection using microarrays.

Authors:  C K Tuggle; S M D Bearson; J J Uthe; T H Huang; O P Couture; Y F Wang; D Kuhar; J K Lunney; V Honavar
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3.  Distinct peripheral blood RNA responses to Salmonella in pigs differing in Salmonella shedding levels: intersection of IFNG, TLR and miRNA pathways.

Authors:  Ting-Hua Huang; Jolita J Uthe; Shawn M D Bearson; Cumhur Yusuf Demirkale; Dan Nettleton; Susan Knetter; Curtis Christian; Amanda E Ramer-Tait; Michael J Wannemuehler; Christopher K Tuggle
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4.  Early immune response following Salmonella enterica subspecies enterica serovar Typhimurium infection in porcine jejunal gut loops.

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5.  Immunogenomics for identification of disease resistance genes in pigs: a review focusing on Gram-negative bacilli.

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Journal:  J Anim Sci Biotechnol       Date:  2012-11-08

6.  Analysis of porcine transcriptional response to Salmonella enterica serovar Choleraesuis suggests novel targets of NFkappaB are activated in the mesenteric lymph node.

Authors:  Yanfang Wang; Oliver P Couture; Long Qu; Jolita J Uthe; Shawn M D Bearson; Daniel Kuhar; Joan K Lunney; Dan Nettleton; Jack C M Dekkers; Christopher K Tuggle
Journal:  BMC Genomics       Date:  2008-09-23       Impact factor: 3.969

7.  Pyroptosis and adaptive immunity mechanisms are promptly engendered in mesenteric lymph-nodes during pig infections with Salmonella enterica serovar Typhimurium.

Authors:  Rodrigo Prado Martins; Carmen Aguilar; James E Graham; Ana Carvajal; Rocío Bautista; M Gonzalo Claros; Juan J Garrido
Journal:  Vet Res       Date:  2013-12-05       Impact factor: 3.683

8.  Gene co-expression network analysis identifies porcine genes associated with variation in Salmonella shedding.

Authors:  Arun Kommadath; Hua Bao; Adriano S Arantes; Graham S Plastow; Christopher K Tuggle; Shawn M D Bearson; Le Luo Guan; Paul Stothard
Journal:  BMC Genomics       Date:  2014-06-09       Impact factor: 3.969

9.  Dissecting clinical outcome of porcine circovirus type 2 with in vivo derived transcriptomic signatures of host tissue responses.

Authors:  Nicolaas Van Renne; Ruifang Wei; Nathalie Pochet; Hans J Nauwynck
Journal:  BMC Genomics       Date:  2018-11-20       Impact factor: 3.969

10.  Net replication of Salmonella enterica serovars Typhimurium and Choleraesuis in porcine intestinal mucosa and nodes is associated with their differential virulence.

Authors:  Susan M Paulin; Aparna Jagannathan; June Campbell; Timothy S Wallis; Mark P Stevens
Journal:  Infect Immun       Date:  2007-06-04       Impact factor: 3.441

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