Three-Dimensional Tissue Assemblies: Novel Models for the Study of Salmonella enterica Serovar Typhimurium Pathogenesis

ABSTRACT The lack of readily available experimental systems has limited knowledge pertaining to the development ofSalmonella-induced gastroenteritis and diarrheal disease in humans. We used a novel low-shear stress cell culture system developed at the National Aeronautics and Space Administration in conjunction with cultivation of three-dimensional (3-D) aggregates of human intestinal tissue to study the infectivity of Salmonella enterica serovar Typhimurium for human intestinal epithelium. Immunohistochemical characterization and microscopic analysis of 3-D aggregates of the human intestinal epithelial cell line Int-407 revealed that the 3-D cells more accurately modeled human in vivo differentiated tissues than did conventional monolayer cultures of the same cells. Results from infectivity studies showed thatSalmonella established infection of the 3-D cells in a much different manner than that observed for monolayers. Following the same time course of infection with Salmonella, 3-D Int-407 cells displayed minimal loss of structural integrity compared to that of Int-407 monolayers. Furthermore, Salmonella exhibited significantly lower abilities to adhere to, invade, and induce apoptosis of 3-D Int-407 cells than it did for infected Int-407 monolayers. Analysis of cytokine expression profiles of 3-D Int-407 cells and monolayers following infection with Salmonellarevealed significant differences in expression of interleukin 1α (IL-1α), IL-1β, IL-6, IL-1Ra, and tumor necrosis factor alpha mRNAs between the two cultures. In addition, uninfected 3-D Int-407 cells constitutively expressed higher levels of transforming growth factor β1 mRNA and prostaglandin E2 than did uninfected Int-407 monolayers. By more accurately modeling many aspects of human in vivo tissues, the 3-D intestinal cell model generated in this study offers a novel approach for studying microbial infectivity from the perspective of the host-pathogen interaction.

[1]  S. Colgan,et al.  Apical secretion of a pathogen-elicited epithelial chemoattractant activity in response to surface colonization of intestinal epithelia by Salmonella typhimurium. , 1998, Journal of immunology.

[2]  Iushchuk Nd,et al.  Pathogenesis of salmonellosis , 1980 .

[3]  T. Wallis,et al.  Characterization of intestinal invasion by Salmonella typhimurium and Salmonella dublin and effect of a mutation in the invH gene , 1995, Infection and immunity.

[4]  M. Zafari,et al.  Signaling through the lymphotoxin beta receptor induces the death of some adenocarcinoma tumor lines , 1996, The Journal of experimental medicine.

[5]  M. Kasuga,et al.  Induction of cyclooxygenase 2 in gastric mucosal lesions and its inhibition by the specific antagonist delays healing in mice. , 1997, Gastroenterology.

[6]  E. Lennox,et al.  Transduction of linked genetic characters of the host by bacteriophage P1. , 1955, Virology.

[7]  R. Curtiss,et al.  Plasmid-associated virulence of Salmonella typhimurium , 1987, Infection and immunity.

[8]  J. Galán,et al.  Salmonella spp. are cytotoxic for cultured macrophages , 1996, Molecular microbiology.

[9]  P. Mullan,et al.  A secreted effector protein of Salmonella dublin is translocated into eukaryotic cells and mediates inflammation and fluid secretion in infected ileal mucosa , 1997, Molecular microbiology.

[10]  R. Gots,et al.  Pathogenesis of Salmonella-mediated intestinal fluid secretion. Activation of adenylate cyclase and inhibition by indomethacin. , 1975, Gastroenterology.

[11]  D. Pl A sensitive microplate assay for glycoproteins that utilizes an immunological digoxigenin-based detection system. , 1992 .

[12]  V. L. Miller,et al.  Tissue-culture invasion: fact or artefact? , 1995, Trends in microbiology.

[13]  H. Collins,et al.  Pathogenesis of salmonellosis. Studies of fluid secretion, mucosal invasion, and morphologic reaction in the rabbit ileum. , 1973, The Journal of clinical investigation.

[14]  K. Darwin,et al.  Molecular Basis of the Interaction ofSalmonella with the Intestinal Mucosa , 1999, Clinical Microbiology Reviews.

[15]  G. Henle,et al.  The establishment of strains of human cells in tissue culture. , 1957, Journal of immunology.

[16]  S. Miller,et al.  Salmonella typhimurium attachment to human intestinal epithelial monolayers: transcellular signalling to subepithelial neutrophils , 1993, The Journal of cell biology.

[17]  C. Vanderburg,et al.  E-cadherin transforms embryonic corneal fibroblasts to stratified epithelium with desmosomes. , 1996, Acta anatomica.

[18]  T. Ficht,et al.  Contribution of Salmonella typhimuriumVirulence Factors to Diarrheal Disease in Calves , 1999, Infection and Immunity.

[19]  P. Devine A sensitive microplate assay for glycoproteins that utilizes an immunological digoxigenin-based detection system. , 1992, BioTechniques.

[20]  M. Kagnoff,et al.  Epithelial cells secrete the chemokine interleukin-8 in response to bacterial entry , 1993, Infection and immunity.

[21]  E. Metcalf,et al.  Differential Early Interactions betweenSalmonella enterica Serovar Typhi and Two Other PathogenicSalmonella Serovars with Intestinal Epithelial Cells , 1998, Infection and Immunity.

[22]  T. Strom,et al.  Prostaglandins posttranscriptionally inhibit monocyte expression of interleukin 1 activity by increasing intracellular cyclic adenosine monophosphate. , 1986, Journal of immunology.

[23]  John Paul,et al.  Tissue culture. Methods and applications. , 1974 .

[24]  S. Miller,et al.  Transepithelial signaling to neutrophils by salmonellae: a novel virulence mechanism for gastroenteritis , 1995, Infection and immunity.

[25]  W. R. Rout,et al.  Effect of indomethacin on intestinal water transport in salmonella-infected rhesus monkeys , 1977, Infection and immunity.

[26]  L. Reimer Principles and practice of infectious diseases , 1987 .

[27]  M. Neutra,et al.  Human Intestinal M Cells Display the Sialyl Lewis A Antigen , 1999, Infection and Immunity.

[28]  R. Curtiss,et al.  Role of sigma factor RpoS in initial stages of Salmonella typhimurium infection , 1997, Infection and immunity.

[29]  John E. Bennett,et al.  Principles and practice of infectious diseases. Vols 1 and 2. , 1979 .

[30]  J. Galán,et al.  The invasion‐associated type III system of Salmonella typhimurium directs the translocation of Sip proteins into the host cell , 1997, Molecular microbiology.

[31]  J. Bliska,et al.  Cross-talk between bacterial pathogens and their host cells. , 1996, Annual review of cell and developmental biology.

[32]  Seamus J. Martin,et al.  Suppression of TNF-α-Induced Apoptosis by NF-κB , 1996, Science.

[33]  P. Scheurich,et al.  TNF receptors TR60 and TR80 can mediate apoptosis via induction of distinct signal pathways. , 1994, Journal of immunology.

[34]  T S Wallis,et al.  Molecular basis of Salmonella‐induced enteritis , 2000, Molecular microbiology.

[35]  M. Kagnoff,et al.  A distinct array of proinflammatory cytokines is expressed in human colon epithelial cells in response to bacterial invasion. , 1995, The Journal of clinical investigation.

[36]  B. Finlay,et al.  Salmonella typhimurium invasion of epithelial cells: role of induced host cell tyrosine protein phosphorylation , 1994, Infection and immunity.

[37]  S. Falkow,et al.  Salmonella typhimurium invasion induces apoptosis in infected macrophages. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[38]  D. Green,et al.  Suppression of TNF-alpha-induced apoptosis by NF-kappaB. , 1996, Science.

[39]  B. McCormick,et al.  A secreted Salmonella protein induces a proinflammatory response in epithelial cells, which promotes neutrophil migration. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[40]  E. Heyderman Histotechnology. A self‐instructional text , 1992 .

[41]  J. Bard Tissue culture, methods and applications , 1974 .

[42]  P. Lelkes,et al.  Growing tissues in microgravity , 1998, Nature Medicine.

[43]  S. Targan,et al.  Divergent induction of apoptosis and IL-8 secretion in HT-29 cells in response to TNF-alpha and ligation of Fas antigen. , 1995, Journal of immunology.

[44]  J. R. Smith,et al.  Role of intestinal epithelial cells in the host secretory response to infection by invasive bacteria. Bacterial entry induces epithelial prostaglandin h synthase-2 expression and prostaglandin E2 and F2alpha production. , 1997, The Journal of clinical investigation.

[45]  D. Frank Culture of Animal Cells: A Manual of Basic Technique , 1984, The Yale Journal of Biology and Medicine.

[46]  T G Hammond,et al.  Optimized suspension culture: the rotating-wall vessel. , 2001, American journal of physiology. Renal physiology.

[47]  J. Wallace,et al.  Exacerbation of inflammation-associated colonic injury in rat through inhibition of cyclooxygenase-2. , 1996, The Journal of clinical investigation.

[48]  M. Moyer,et al.  Rotating-Wall Vessel Coculture of Small Intestine as a Prelude to Tissue Modeling: Aspects of Simulated Microgravity , 1993, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[49]  J. M. Kim,et al.  Apoptosis of human intestinal epithelial cells after bacterial invasion. , 1998, The Journal of clinical investigation.