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Rotavirus NSP4114-135 peptide has no direct, specific effect on chloride transport in rabbit brush-border membrane
Virology Journal volume 3, Article number: 94 (2006)
The direct effect of the rotavirus NSP4114-135 and Norovirus NV464-483 peptides on 36Cl uptake was studied by using villus cell brush border membrane (BBM) isolated from young rabbits. Both peptides inhibited the Cl-/H+ symport activity about equally and partially. The interaction involved one peptide-binding site per carrier unit. Whereas in vitro NSP4114-135 caused nonspecific inhibition of the Cl-/H+ symporter, the situation in vivo is different. Because rotavirus infection in young rabbits accelerated both Cl- influx and Cl- efflux rates across villi BBM without stimulating Cl- transport in crypt BBM, we conclude that the NSP4114-135 peptide, which causes diarrhea in young rodents, did not have any direct, specific effect on either intestinal absorption or secretion of chloride. The lack of direct effect of NSP4 on chloride transport strengthens the hypothesis that NSP4 would trigger signal transduction pathways to enhance net chloride secretion at the onset of rotavirus diarrhea.
Rotavirus is the major cause of infantile gastroenteritis and each year causes 611000 deaths worldwide. A rotavirus nonstructural glycoprotein, NSP4, and a synthetic peptide, NSP4114-135, corresponding to residues 114 to 135 of this protein, both have been shown to induce diarrhea in young rodents, unaccompanied by any histological lesions . But despite considerable research over several decades, the mechanisms underlying the diarrheal illness remain unclear [2, 3].
The rotavirus NSP4114-135 peptide has been shown to interact with small unilamellar phospholipid vesicles characterized by highly curved membrane regions . However, it is unknown whether such interaction of NSP4 with a putative membrane receptor may be important for its biological activity. Tian et al. reported that NSP4 and NSP4114-135 caused membrane destabilization activity . This seems to be true for liposomes and endoplasmic reticulum vesicles, but not for plasma membrane vesicles such as intestinal brush border membrane vesicles (BBM). On the other hand, the NSP4114-135 peptide has been shown to directly and specifically inhibit the SGLT1-mediated Na+-D-glucose symport activity in villi BBM of rabbit intestine . In contrast, the Norovirus NV464-483 and mNSP4131K (NSP4114-135 having an L-lysine residue substituting for the L-tyrosine at position 131) peptides neither cause diarrhea nor inhibit SGLT1. The selective and strong inhibition caused in vitro by NSP4114-135 on SGLT1 suggests that, during rotavirus infection in vivo, the newly synthesized glycoprotein NSP4 is released into the intestinal lumen and acts on the SGLT1 protein, hence, directly causing glucose malabsorption and a concomitant inhibition of water reabsorption .
The observation that addition of either NSP4 or carbachol (a cholinergic agonist that mobilizes Ca2+) to neonatal mouse intestinal mucosal sheets induced transient, small and almost identical increases in Cl- secretory currents was interpreted as indicating that NSP4 induced a Ca2+-dependent Cl- secretory mechanism . However, the cellular and molecular bases by which rotavirus and NSP4 induce a moderate net chloride secretion remain unclear. Recently, Lorrot et al. reported that rotavirus infection in vivo in young rabbits failed to stimulate the Cl- transport activities at the crypt level, but not at the villus level, questioning, therefore, the origin of net chloride secretion at the onset of diarrhea [8, 9]. Because rotavirus stimulated both Cl- influx and Cl- efflux in villi, Lorrot et al. proposed that the Cl-/H+ symporter might function in both normal (absorption) and reversed (secretion) modes, depending on the direction of the chloride electrochemical gradient resulting from rotavirus infection .
In the present study, we examined whether or not the ability of rotavirus to stimulate chloride transport across rabbit villus cell BBM might be due to the direct activity of NSP4114-135. The Norovirus NV464-483 peptide was tested as a possible control since this peptide, unlike NSP4114-135, does not cause diarrhea even though its amphipathic score is practically identical to that of NSP4114-135 .
Both peptides were the gift of Dr. J. M. Ball (College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas) and Dr. M. K. Estes (Baylor College of Medicine, Houston, Texas). Because of peptide solubility and the inevitable carry-over of a quantity of peptide from the preincubation to the incubation media (in the proportion of 1/10), the maximum peptide concentration that could be reached in the incubation mixtures was 0.55 mM . The NSP4 protein action could not be demonstrated in the present paper, mainly because the maximum concentration of 0.5 μM was found to be too low to significantly affect chloride uptake . Intestinal villi BBM vesicles were prepared from specific pathogen-free, four-week-old New Zealand albino hybrid rabbit by using the magnesium precipitation method as described [6–10]. They were suspended at about 20 mg of membrane protein/ml in membrane buffer (20 mM Hepes/40 mM citric acid/100 mM Tris gluconate/0.02% LiN3, supplemented to a total osmolarity of 560 mOsM with sorbitol and adjusted to pH 7.5 with Tris base) and stored in liquid nitrogen until the day of transport assay, as described [6–9]. Chloride transport was assayed by using 36Cl and a rapid filtration technique as described [8, 9, 11]. To test the effect of a peptide on proton-coupled Cl- transport, BBM vesicles were mixed in the appropriate volume of membrane buffer in either the absence or presence of a given peptide. After preincubation for 5 min at 22°C, 5 μl aliquots were used to perform uptake measurements by mixing with 45 μl of transport buffer formed by the membrane buffer supplemented with 15 mM cis 36Cl, the amount of sorbitol necessary to obtain a total osmolarity of 660 mOsM, and adjusted to pH 5.0 with Tris base (final concentrations and pH in the incubation mixtures). Uncorrected initial (4 sec) uptake rates as a function of the inhibitor concentration (v = f [I] at constant substrate concentration) were fitted by non-linear least-squares regression analysis to Hill's equation. To perform each fit, the procedure of Fletcher and Powell as modified by van Melle and Robinson  was used. To test the fit of data to Hill's equation, we used the commercial program Stata (Integral Software, Paris, France). For statistical evaluation, fits were compared either within each given condition (F test) or between pairs of conditions (F' test), as described .
We earlier showed that an alkaline-inside pH gradient can furnish the energy necessary for the uphill transport of Cl- across intestinal villi BBM purified from four week-old rabbits, indicating the presence of a Cl-/H+ symporter in these vesicles [8, 9]. To investigate the possible direct effect of each of these peptides on chloride influx, the initial Cl- entry rates were quantified by using the v = f [I] approach in the presence of a pHo/pHi = 5.0/7.5 gradient (o (out) and i (in) indicate the extra- and intravesicular spaces, respectively). As illustrated in figure 1, both the NSP4114-135 and NV464-483 peptides caused a practically identical inhibition of proton-coupled Cl- uptake across the BBM, approaching 55 % and 40 % inhibition, respectively, at 0.5 mM peptide. Analysis of the chloride results according to Hill's equation revealed that the two peptides gave statistically indistinguishable data (see F' test in Table 1). Therefore, the data were pooled and fitted again to obtain the overall fit given in Table 1 (line 3). To find the best integer value of the Hill number, the data were further fitted by fixing the ni value to either 1 or 2. According to the F value, one peptide-binding site per carrier unit is involved in the interaction with BBM (Table 1).
Taken together, the whole set of available results for peptide concentrations from 0.015 to 0.55 mM strongly supports the conclusion that the rotavirus NSP4114-135 peptide caused in vitro nonspecific inhibition of the Cl-/H+ symporter across villus cell BBM. Similar conclusions have been reached with the rabbit BBM Na+-L-leucine symporter, further confirming nonspecific, lipophilic interactions of the amphipathic peptides with the membrane . Clearly, the results indicate the existence of NSP4-lipid interactions with biological membranes, as could be expected from the presence of regions of high curvatures in intestinal BBM . However, the interactions appear to be unimportant for the direct biological effects of NSP4, at least as concerns the rabbit BBM Cl-/H+ and Na+-L-leucine symporters at the villus cell level. Whereas in vitro NSP4114-135 inhibits the Cl-/H+ symporter, the situation in vivo is different. Because rotavirus accelerated both Cl- influx and Cl- efflux rates across villi BBM whereas it failed to stimulate Cl- transport in crypt BBM [8, 9], we conclude that NSP4 has no direct effect on either intestinal absorption or secretion of chloride.
Interestingly, the lack of direct effect of NSP4 on the BBM Cl-/H+ symporter strengthens the hypothesis that NSP4 would trigger signal transduction pathways to enhance net chloride secretion at the onset of diarrhea [2, 3, 14]. Whether NSP4 or its cleavage product, NSP4112-175, after it is released from virus-infected cells , binds to an apical membrane receptor in villus enterocytes or crypt cells, or both, to activate intracellular second messengers is not known. Furthermore, the possibility that the secreted NSP4 – as most luminal enterotoxins – may reach the crypt region would seem to be unlikely . Using human intestinal epithelial HT-29 cells, it was shown that exogenous addition of NSP4 induced intracellular calcium mobilization through phospholipase C (PLC) signaling . The same signaling pathway was also found in rotavirus-infected Caco-2 cells . Such PLC activation can lead to transient chloride secretion [18, 19]. Also, NSP4-mediated Ca2+ mobilization can lead to an activation of the nervous system (ENS) in the intestinal wall, and hence stimulated intestinal chloride secretion . However, many details regarding the ENS-linked hypothesis of rotavirus-induced secretory diarrhea remain to be elucidated . Obviously, more work will need to be performed before a clear understanding of the regulatory mechanisms of intestinal net chloride secretion during rotavirus and NSP4-mediated diarrhea can be achieved.
Ball JM, Tian P, Zeng CQ, Morris AP, Estes MK: Age-dependent diarrhea induced by a rotaviral nonstructural glycoprotein. Science 1996, 272: 101-104. 10.1126/science.272.5258.101
Lundgren O, Svensson L: Pathogenesis of Rotavirus diarrhea. Microbes Infect 2001, 3: 1145-1156. 10.1016/S1286-4579(01)01475-7
Ramig RF: Pathogenesis of intestinal and systemic rotavirus infection. J Virol 2004, 78: 10213-10220. 10.1128/JVI.78.19.10213-10220.2004
Huang H, Schroeder F, Zeng C, Estes MK, Schoer JK, Ball JM: Membrane interactions of a novel viral enterotoxin: rotavirus nonstructural glycoprotein NSP4. Biochemistry 2001, 40: 4169-4180. 10.1021/bi002346s
Tian P, Ball JM, Zeng CQ, Estes MK: The rotavirus nonstructural glycoprotein NSP4 possesses membrane destabilization activity. J Virol 1996, 70: 6973-6981.
Halaihel N, Lievin V, Ball JM, Estes MK, Alvarado F, Vasseur M: Direct inhibitory effect of rotavirus NSP4(114-135) peptide on the Na(+)-D-glucose symporter of rabbit intestinal brush border membrane. J Virol 2000, 74: 9464-9470. 10.1128/JVI.74.20.9464-9470.2000
Halaihel N, Lievin V, Alvarado F, Vasseur M: Rotavirus infection impairs intestinal brush-border membrane Na(+)- solute cotransport activities in young rabbits. Am J Physiol Gastrointest Liver Physiol 2000, 279: G587-G596.
Lorrot M, Martin S, Vasseur M: Rotavirus infection stimulates the Cl- reabsorption process across the intestinal brush-border membrane of young rabbits. J Virol 2003, 77: 9305-9311. 10.1128/JVI.77.17.9305-9311.2003
Lorrot M, Benhamadouche-Casari H, Vasseur M: Mechanisms of net chloride secretion during rotavirus diarrhea in young rabbits : do intestinal villi secrete chloride? Cell Physiol Biochem 2006, 18: 103-112. 10.1159/000095174
Hauser H, Howell K, Dawson RM, Bowyer DE: Rabbit small intestinal brush border membrane preparation and lipid composition. Biochim Biophys Acta 1980, 602: 567-577. 10.1016/0005-2736(80)90335-1
Vasseur M, Cauzac M, Alvarado F: Electroneutral, HCO3(-)-independent, pH gradient-dependent uphill transport of Cl- by ileal brush-border membrane vesicles. Possible role in the pathogenesis of chloridorrhea. Biochem J 1989, 263: 775-784.
van Melle G, Robinson JW: A systematic approach to the analysis of intestinal transport kinetics. J Physiol (Paris) 1981, 77: 1011-1016.
Lipka G, Schulthess G, Thurnhofer H, Wacker H, Wehrli E, Zeman K, Weber FE, Hauser H: Characterization of lipid exchange proteins isolated from small intestinal brush border membrane. J Biol Chem 1995, 270: 5917-5925. 10.1074/jbc.270.11.5917
Ball JM, Mitchell DM, Gibbons TF, Parr RD: Rotavirus NSP4: a multifunctional viral enterotoxin. Viral Immunol 2005, 18: 27-40. 10.1089/vim.2005.18.27
Zhang M, Zeng CQ, Morris AP, Estes MK: A functional NSP4 enterotoxin peptide secreted from rotavirus-infected cells. J Virol 2000, 74: 11663-11670. 10.1128/JVI.74.24.11663-11670.2000
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 U S A 1997, 94: 3960-3965. 10.1073/pnas.94.8.3960
Brunet JP, Cotte-Laffitte J, Linxe C, Quero AM, Geniteau-Legendre M, Servin A: Rotavirus infection induces an increase in intracellular calcium concentration in human intestinal epithelial cells: role in microvillar actin alteration. J Virol 2000, 74: 2323-2332. 10.1128/JVI.74.5.2323-2332.2000
Barrett KE: Bowditch lecture. Integrated regulation of intestinal epithelial transport: intercellular and intracellular pathways. Am J Physiol 1997, 272: C1069-76.
Barrett KE, Keely SJ:Chloride secretion by the intestinal epithelium: molecular basis and regulatory aspects. Annu Rev Physiol 2000, 62: 535-572. 10.1146/annurev.physiol.62.1.535
We thank Sheila Carrodus for help preparing the manuscript. This work was supported in part by the Institut National de la Santé et de la Recherche Médicale (INSERM); by the Fondation pour la Recherche Médicale, Paris; by the INCO Program of the European Economic Community (grant ERB 3514 PL 950019) and the Ministère Français de l'Education nationale, de la Recherche et de la Technologie (grant MENRT-PRFMMIP).
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