Changes in macromolecular transport appear early in Caco-2 cells infected with a human rotavirus

References

• Parashar U, Gibson C, Bresee J, Glass RI. Rotavirus and severe childhood diarrhea. Emerg Infect Dis 2006; 12: 304–6
   PubMed Web of Science ®Google Scholar
• Superti F, Ammendolia MG, Tinari A, Bucci B, Giammarioli AM, Rainaldi G, et al. Induction of apoptosis in HT-29 cells infected with SA-11 rotavirus. J Med Virol 1996; 50: 325–34
   PubMedGoogle Scholar
• Burke B, Desselberger U. Rotavirus pathogenicity. Virology 1996; 218: 299–305
   PubMed Web of Science ®Google Scholar
• Salim AF, Phillips AD, Walker-Smith JA, Farthing MJ. Sequential changes in small intestinal structure and function during rotavirus infection in neonatal rats. Gut 1995; 36: 231–8
   PubMedGoogle Scholar
• Davidson GP, Barnes GL. Structural and functional abnormalities of the small intestine in infants and young children with rotavirus enteritis. Acta Paediatr Scand 1979; 68: 181–6
   PubMed Web of Science ®Google Scholar
• Barnes GL, Townley RR. Duodenal mucosal damage in 31 infants with gastroenteritis. Arch Dis Child 1973; 48: 343–9
   PubMed Web of Science ®Google Scholar
• Dong Y, Zeng CQ, Ball JM, Estes MK, Morris AP. The rotavirus enterotoxin NSP4 mobilizes intracellular calcium in human intestinal cells by stimulating phospholipase C-mediated inositol 1,4,5-trisphosphate production. Proc Natl Acad Sci USA 1997; 94: 3960–5
   PubMed Web of Science ®Google Scholar
• Casola A, Estes MK, Crawford SE, Ogra PL, Ernst PB, Garofalo RP. Rotavirus infection of cultured intestinal epithelial cells induces secretion of CXC and CC chemokines. Gastroenterology 1998; 114: 947–55
   PubMedGoogle Scholar
• Jalonen T, Isolauri E, Heyman M, Crain-Denoyelle AM, Sillanaukee P, Koivula T. Increased beta-lactoglobulin absorption during rotavirus enteritis in infants: relationship to sugar permeability. Pediatr Res 1991; 30: 290–3
   PubMedGoogle Scholar
• Dickman KG, Hempson SJ, Anderson J, Lippe S, Zhao L, Burakoff R. Rotavirus alters paracellular permeability and energy metabolism in Caco–2 cells. Am J Physiol Gastrointest Liver Physiol 2000; 279: G757–66
   PubMed Web of Science ®Google Scholar
• Obert G, Peiffer I, Servin AL. Rotavirus-induced structural and functional alterations in tight junctions of polarized intestinal Caco-2 cell monolayers. J Virol 2000; 74: 4645–51
   PubMed Web of Science ®Google Scholar
• Nava P, Lopez S, Arias CF, Islas S, Gonzalez-Mariscal L. The rotavirus surface protein VP8 modulates the gate and fence function of tight junctions in epithelial cells. J Cell Sci 2004; 117: 5509–19
   PubMed Web of Science ®Google Scholar
• Ahmed T, Sumazaki R, Shin K, Nagai Y, Shibasaki M, Fuchs GJ, et al. Humoral immune and clinical responses to food antigens following acute diarrhoea in children. J Paediatr Child Health 1998; 34: 229–32
   PubMedGoogle Scholar
• Davidson GP, Gall DG, Petric M, Butler DG, Hamilton JR. Human rotavirus enteritis induced in conventional piglets. Intestinal structure and transport. J Clin Invest 1977; 60: 1402–9
   PubMed Web of Science ®Google Scholar
• Jourdan N, Maurice M, Delautier D, Quero AM, Servin AL, Trugnan G. Rotavirus is released from the apical surface of cultured human intestinal cells through nonconventional vesicular transport that bypasses the Golgi apparatus. J Virol 1997; 71: 8268–78
   PubMed Web of Science ®Google Scholar
• Sambuy Y, De Angelis I, Ranaldi G, Scarino ML, Stammati A, Zucco F. The Caco-2 cell line as a model of the intestinal barrier: influence of cell and culture-related factors on Caco-2 cell functional characteristics. Cell Biol Toxicol 2005; 21: 1–26
   PubMed Web of Science ®Google Scholar
• Jourdan N, Brunet JP, Sapin C, Blais A, Cotte-Laffitte J, Forestier F. Rotavirus infection reduces sucrase-isomaltase expression in human intestinal epithelial cells by perturbing protein targeting and organization of microvillar cytoskeleton. J Virol 1998; 72: 7228–36
   PubMed Web of Science ®Google Scholar
• Coulson BS, Fowler KJ, Bishop RF, Cotton RG. Neutralizing monoclonal antibodies to human rotavirus and indications of antigenic drift among strains from neonates. J Virol 1985; 54: 14–20
   PubMed Web of Science ®Google Scholar
• Messer M, Dahlqvist A. A one-step ultramicro method for the assay of intestinal disaccharidases. Anal Biochem 1966; 14: 376–92
   PubMed Web of Science ®Google Scholar
• Dawson D. Principles of membrane transport. Intestinal absorption and secretion, M Field, R Frizzell. American Physiological Society, Bethesda, Md 1991; 1–44
   Google Scholar
• Bos ES, van der Doelen AA, van Rooy N, Schuurs AH. 3,3′,5,5′ – Tetramethylbenzidine as an Ames test negative chromogen for horse-radish peroxidase in enzyme-immunoassay. J Immunoassay 1981; 2: 187–204
   PubMedGoogle Scholar
• Sapin C, Baricault L, Trugnan G. PKC-dependent long-term effect of PMA on protein cell surface expression in Caco-2 cells. Exp Cell Res 1997; 231: 308–18
   PubMedGoogle Scholar
• Lundgren O, Svensson L. Pathogenesis of rotavirus diarrhea. Microbes Infect 2001; 3: 1145–56
   PubMed Web of Science ®Google Scholar
• Ciarlet M, Estes MK. Interactions between rotavirus and gastrointestinal cells. Curr Opin Microbiol 2001; 4: 435–41
   PubMedGoogle Scholar
• Ruiz MC, Cohen J, Michelangeli F. Role of Ca2+ in the replication and pathogenesis of rotavirus and other viral infections. Cell Calcium 2000; 28: 137–49
   PubMedGoogle Scholar
• Gardet A, Breton M, Fontanges P, Trugnan G, Chwetzoff S. Rotavirus spike protein VP4 binds to and remodels actin bundles of the epithelial brush border into actin bodies. J Virol 2006; 80: 3947–56
   PubMedGoogle Scholar
• Berkova Z, Crawford SE, Blutt SE, Morris AP, Estes MK. Expression of rotavirus NSP4 alters the actin network organization through the actin remodeling protein cofilin. J Virol 2007; 81: 3545–53
   PubMed Web of Science ®Google Scholar
• Ball JM, Tian P, Zeng CQ, Morris AP, Estes MK. Age-dependent diarrhea induced by a rotaviral nonstructural glycoprotein. Science 1996; 272: 101–4
   PubMed Web of Science ®Google Scholar
• Zhang M, Zeng CQ, Dong Y, Ball JM, Saif LJ, Morris AP, et al. Mutations in rotavirus nonstructural glycoprotein NSP4 are associated with altered virus virulence. J Virol 1998; 72: 3666–72
   PubMed Web of Science ®Google Scholar
• Kirkwood CD, Coulson BS, Bishop RF. G3P2 rotaviruses causing diarrhoeal disease in neonates differ in VP4, VP7 and NSP4 sequence from G3P2 strains causing asymptomatic neonatal infection. Arch Virol 1996; 141: 1661–76
   PubMed Web of Science ®Google Scholar
• Veiga E, Cossart P. The role of clathrin-dependent endocytosis in bacterial internalization. Trends Cell Biol 2006; 16: 499–504
   PubMedGoogle Scholar
• Smythe E, Ayscough KR. Actin regulation in endocytosis. J Cell Sci 2006; 119: 4589–98
   PubMed Web of Science ®Google Scholar
• Zhang Y, Gu Y, Li H, Lucas MJ, Wang Y. Increased endothelial monolayer permeability is induced by serum from women with preeclampsia but not by serum from women with normal pregnancy or that are not pregnant. Hypertension 2003; 22: 99–108
   Google Scholar
• Kiliaan AJ, Scholten G, Bijlsma PB, Dekker K, Groot JA. Influence of forskolin and carbachol on intestinal absorption of horseradish peroxidase in the goldfish (Carassius auratus). Cell Tissue Res 1996; 285: 51–6
   PubMed Web of Science ®Google Scholar
• Shurety W, Bright NA, Luzio JP. The effects of cytochalasin D and phorbol myristate acetate on the apical endocytosis of ricin in polarised Caco-2 cells. J Cell Sci 1996; 109: 2927–35
   PubMedGoogle Scholar
• Holm PK, Eker P, Sandvig K, van Deurs B. Phorbol myristate acetate selectively stimulates apical endocytosis via protein kinase C in polarized MDCK cells. Exp Cell Res 1995; 217: 157–68
   PubMed Web of Science ®Google Scholar
• Bass DM. Interferon gamma and interleukin 1, but not interferon alpha, inhibit rotavirus entry into human intestinal cell lines. Gastroenterology 1997; 113: 81–9
   PubMed Web of Science ®Google Scholar
• Hocini H, Bomsel M. Infectious human immunodeficiency virus can rapidly penetrate a tight human epithelial barrier by transcytosis in a process impaired by mucosal immunoglobulins. J Infect Dis 1999; 179(Suppl 3)S448–53
   Google Scholar
• Schwartz-Cornil I, Benureau Y, Greenberg H, Hendrickson BA, Cohen J. Heterologous protection induced by the inner capsid proteins of rotavirus requires transcytosis of mucosal immunoglobulins. J Virol 2002; 76: 8110–17
   PubMedGoogle Scholar