Increased resistance in the rat to Nippostrongylus brasiliensis following immunization against Trichinella spiralis

1975 ◽  
Vol 1 (2) ◽  
pp. 165-174 ◽  
Author(s):  
Kevin R. Kazacos
Keyword(s):  
Trichinella Spiralis ◽  
Nippostrongylus Brasiliensis

scholarly journals Intestinal epithelial cell secretion of RELM-β protects against gastrointestinal worm infection

2009 ◽  
Vol 206 (13) ◽  
pp. 2947-2957 ◽  
Author(s):  
De'Broski R. Herbert ◽  
Jun-Qi Yang ◽  
Simon P. Hogan ◽  
Kathryn Groschwitz ◽  
Marat Khodoun ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Trichinella Spiralis ◽  
Intestinal Lumen ◽  
Th2 Cells ◽  
Nippostrongylus Brasiliensis ◽  
Intestinal Epithelial ◽  
Cell Secretion ◽  
Heligmosomoides Polygyrus ◽  
Parasitic Helminths

Th2 cells drive protective immunity against most parasitic helminths, but few mechanisms have been demonstrated that facilitate pathogen clearance. We show that IL-4 and IL-13 protect against intestinal lumen-dwelling worms primarily by inducing intestinal epithelial cells (IECs) to differentiate into goblet cells that secrete resistin-like molecule (RELM) β. RELM-β is essential for normal spontaneous expulsion and IL-4–induced expulsion of Nippostrongylus brasiliensis and Heligmosomoides polygyrus, which both live in the intestinal lumen, but it does not contribute to immunity against Trichinella spiralis, which lives within IEC. RELM-β is nontoxic for H. polygyrus in vitro but directly inhibits the ability of worms to feed on host tissues during infection. This decreases H. polygyrus adenosine triphosphate content and fecundity. Importantly, RELM-β–driven immunity does not require T or B cells, alternative macrophage activation, or increased gut permeability. Thus, we demonstrate a novel mechanism for host protection at the mucosal interface that explains how stimulation of epithelial cells by IL-4 and IL-13 contributes to protection against parasitic helminthes that dwell in the intestinal lumen.

Host–parasite interactions in rodent nematode infections

2003 ◽  
Vol 77 (2) ◽  
pp. 125-131 ◽  
Author(s):  
Y.R. Mahida
Keyword(s):  
Neutralizing Antibodies ◽  
Host Response ◽  
Trichinella Spiralis ◽  
Host Responses ◽  
Nippostrongylus Brasiliensis ◽  
Trichuris Muris ◽  
Epithelial Phenotype ◽  
Worm Expulsion ◽  
Genetically Manipulated ◽  
Host Parasite

AbstractIn rodents,Trichinella spiralisandNippostrongylus brasiliensisinfect the small intestine andTrichuris murisresides in the colon. The intestinal host response in these animals is characterized by changes in mucosal architecture and inflammation and is associated with worm expulsion. The requirement of T cell-mediated host response in worm expulsion has been demonstrated over many years. Subsequent studies have shown that Th2-type, but not Th1-type, responses mediate resistance to the nematodes. Investigations using neutralizing antibodies and genetically manipulated mice have characterized the contribution of individual Th2-type cytokines in not only worm expulsion, but also specific cellular changes that occur in the mucosa, such as alterations in epithelial phenotype and smooth muscle. There is also increasing appreciation of the contribution of non-bone marrow-derived cells in innate and adaptive host responses in these models.

Effect of dietary condensed tannins on gastrointestinal nematodes

2001 ◽  
Vol 137 (4) ◽  
pp. 461-469 ◽  
Author(s):  
N. L. BUTTER ◽  
J. M. DAWSON ◽  
D. WAKELIN ◽  
P. J. BUTTERY
Keyword(s):  
Condensed Tannins ◽  
Trichinella Spiralis ◽  
Condensed Tannin ◽  
Intestinal Lumen ◽  
Parasitic Nematodes ◽  
Nippostrongylus Brasiliensis ◽  
Small Intestinal Mucosa ◽  
Quebracho Tannin ◽  
Small Intestinal

It has been previously shown in this laboratory that feeding a model condensed tannin, quebracho tannin, reduces the small intestinal nematode burden in sheep and rats. The aim of the current programme was to determine whether this occurs through direct toxicity against the parasites. Both in vivo and in vitro studies were conducted. The first study compared the effect of dietary quebracho tannin (40 g/kg) on the establishment of the parasitic nematodes Nippostrongylus brasiliensis and Trichinella spiralis in the rat small intestine. The burden of N. brasiliensis, which, although closely associated with the mucosa, actually dwells within the small intestinal lumen, was significantly reduced (P<0·001) by dietary quebracho tannin. In contrast, T. spiralis, which penetrates into the small intestinal mucosa, was unaffected (>0·05) by the dietary inclusion of quebracho tannin. The second study involved monitoring the survival of adult N. brasiliensis and T. spiralis when incubated in vitro in varying concentrations of quebracho tannin in Hanks’ balanced salt solution. The survival of N. brasiliensis was compromised at concentrations as low as 0·01% (w/v) quebracho tannin but improved with the addition of 0·1% (w/v) polyethylene glycol, which binds to, and inactivates, tannin. T. spiralis was similarly affected, but much more rapidly. These results suggest that dietary quebracho tannin may reduce nematode worm burdens through a toxic effect that requires direct contact between parasite and tannin. This raises the possibility that feeding locally available plant material containing condensed tannins may be an alternative method for controlling parasite infections, especially in areas such as the tropics and subtropics.

Use of cortisone derivatives to inhibit resistance to Nippostrongylus brasiliensis and to study the fate of parasites in resistant hosts

Parasitology ◽  
1965 ◽  
Vol 55 (4) ◽  
pp. 723-730 ◽  
Author(s):  
Bridget M. Ogilvie
Keyword(s):  
Cellular Response ◽  
Marked Effect ◽  
Trichinella Spiralis ◽  
Early Stage ◽  
Acquired Resistance ◽  
Challenge Infection ◽  
Cortisone Acetate ◽  
Nippostrongylus Brasiliensis ◽  
Initial Infection ◽  
Nematode Parasites

Acquired resistance to some nematode parasites can be suppressed by daily administration of cortisone acetate to the host. Cortisone treatment completely suppressed previously acquired resistance of mice to Trichinella spiralis (Coker, 1956) and suppressed, at least partially, the acquisition of resistance to T. spiralis by rats during initial infection (Markell & Lewis, 1957).A previous report (Weinstein, 1955) suggested cortisone acetate treatment was less effective in the suppression of acquired resistance of rats to Nippostrongylus brasiliensis. Weinstein showed that daily treatment with 2 mg cortisone acetate throughout five immunizing infections and continued during the challenge infection increased the number of worms in the intestine and had a marked effect on the cellular response in the skin and lungs. However, there was no significant effect when daily cortisone treatment commenced only on the fifth day before the challenge infection. This result suggested that acquisition of immunity to N. brasiliensis was partially overcome by cortisone treatment, but the same level of drug treatment had no effect on immunity already acquired.In the experiments reported here, previously acquired resistance to N. brasiliensis was suppressed completely and the initiation of immunity stopped, either completely or at a very early stage, by treatment with the cortisone derivatives prednisolone or betamethasone. The complete suspension of all manifestations of acquired resistance obtained by treatment with these drugs was used to investigate the fate of larvae migrating in an immune host.The rats and strain of parasite, and the methods of handling them, have been described previously (Ogilvie, 1965).

scholarly journals Rapid purification and characterization of l-dopachrome-methyl ester tautomerase (macrophage-migration-inhibitory factor) from Trichinella spiralis, Trichuris muris and Brugia pahangi

1998 ◽  
Vol 335 (3) ◽  
pp. 495-498 ◽  
Author(s):  
Joanne L. PENNOCK ◽  
Jerzy M. BEHNKE ◽  
Quentin D. BICKLE ◽  
Eileen DEVANEY ◽  
Richard K. GRENCIS ◽  
...  
Keyword(s):  
Methyl Ester ◽  
Soluble Fraction ◽  
Trichinella Spiralis ◽  
Hymenolepis Diminuta ◽  
Nippostrongylus Brasiliensis ◽  
Macrophage Migration ◽  
Trichuris Muris ◽  
Brugia Pahangi ◽  
Dopachrome Tautomerase ◽  
Parasitic Helminths

Macrophage-migration-inhibition factor (MIF) is an essential stimulator of mammalian T-lymphocyte-dependent adaptive immunity, hence MIF orthologues might be expressed by infectious organisms as an immunosubversive stratagem. Since MIF actively catalyses the tautomerization of the methyl ester of l-dopachrome (using dopachrome tautomerase), the occurrence of MIF orthologues in several parasitic helminths was investigated by assaying and characterizing such activity. Evidence of MIF orthologues (dopachrome tautomerase) was found in the soluble fraction of the nematodes Trichinella spiralis (stage 4 larvae) and Trichuris muris (adults), and the filarial nematode Brugia pahangi (adults). The MIF orthologues of Tr. muris(TmMIF) and B. pahangi (BpMIF) were purified to homogeneity using phenyl-agarose chromatography, that of T. spiralis (TsMIF) required a further step: cation-exchange FPLC. Retention time on reverse-phase HPLC and Mr on SDS/PAGE of the nematode MIFs were similar to those of human MIF. N-terminal sequences (19 residues) of TsMIF and TmMIF showed 47 and 36% identity, respectively, with human MIF. The N-terminal sequence of BpMIF (14 residues) was identical to that of an MIF orthologue in the genome of B. malayi (Swiss-Prot, P91850) and showed 43% identity to either human or TsMIF. TsMIF had 10-fold higher dopachrome tautomerase activity than MIF from the other sources. The enzyme activities of TsMIF, BpMIF and TmMIF were less sensitive to inhibition by haematin (I50: > 15 µM, > 15 µM and 2.6 µM, respectively) than that of human MIF (I50 0.2 µM). Significant dopachrome tautomerase or phenyl-agarose-purifiable MIF-like protein was not detected in the soluble fraction of the nematodes Heligmosomoides polygyrus and Nippostrongylus brasiliensis, the cestode Hymenolepis diminuta, or the trematodes Schistosoma mansoni, S. japonicum and S. haematobium, or the free-living nematode, Caenorhabditis elegans, which does contain an MIF-related gene.

Antigen-induced contraction of jejunal smooth muscle in the sensitized rat

1988 ◽  
Vol 255 (6) ◽  
pp. G701-G708 ◽  
Author(s):  
D. L. Vermillion ◽  
P. B. Ernst ◽  
R. Scicchitano ◽  
S. M. Collins
Keyword(s):  
Mast Cell ◽  
Smooth Muscle ◽  
Receptor Antagonist ◽  
Immunoglobulin E ◽  
Trichinella Spiralis ◽  
Cell Number ◽  
Nippostrongylus Brasiliensis ◽  
H2 Receptor Antagonist ◽  
Synthase Inhibitor ◽  
H1 Receptor Antagonist

We examined contractility of longitudinal muscle strips of jejunum from control rats and rats infected 34-85 days previously with Trichinella spiralis. Antigen prepared from T. spiralis larvae contracted muscle from previously infected but not control rats. Contraction was specific for the sensitizing agent because antigen from Nippostrongylus brasiliensis did not induce contraction. Contraction was resistant to atropine or tetrodotoxin but was inhibited by the 5-hydroxytryptamine (5-HT) antagonist cyproheptadine and by 5-HT desensitization. Neither histamine antagonists, diphenhydramine (H1-receptor antagonist) or ranitidine (H2-receptor antagonist), nor indomethacin, a prostaglandin synthase inhibitor, influenced the antigen response. In Trichinella-infected rats there was a significant increase in mast cell number in the muscle layers, and the contraction induced by T. spiralis antigen was inhibited by the mast cell stabilizer doxantrazole. In addition, anti-rat immunoglobulin E serum, compound 48/80, and concanavalin A each contracted muscles from rats previously infected with T. spiralis. These results are consistent with the hypothesis that T. spiralis infection leads to mast cell proliferation in the muscle layers and that subsequent exposure to antigen results in mast cell degranulation, 5-HT release, and contraction of smooth muscle.

Distribution of mast cells in intestinal muscle of nematode-sensitized rats

1992 ◽  
Vol 262 (3) ◽  
pp. G477-G482 ◽  
Author(s):  
L. Marzio ◽  
P. Blennerhassett ◽  
D. Vermillion ◽  
S. Chiverton ◽  
S. Collins
Keyword(s):  
Mast Cell ◽  
Mast Cells ◽  
Connective Tissue ◽  
Longitudinal Muscle ◽  
Trichinella Spiralis ◽  
Maximum Response ◽  
Nippostrongylus Brasiliensis ◽  
Cell Numbers ◽  
Mast Cell Stabilizer ◽  
Functional Integrity

We examined the distribution and functional integrity of mast cells in intestinal longitudinal muscle in rats sensitized by two previous infections with Trichinella spiralis. A segment of jejunum was excluded from the gut before infection, and the remainder of the gut was anastomosed. Few mast cells were seen in muscle of noninfected control rats except in the region of the jejunal anastomosis. In rats sensitized by T. spiralis infection, mast cells were increased in number in the jejunum and the number of mast cells followed an aboral gradient down the entire length of the gut in continuity. In addition, mast cells were present in muscle of the excluded segment of sensitized rats. All mast cells were stained red with safranin. Functional integrity was assessed by the ability of mast cells to induce contraction after degranulation by antigen. In muscle from sensitized rats, contraction was induced in each region after exposure to T. spiralis antigen but not Nippostrongylus brasiliensis antigen. Contraction was inhibited by the mast cell stabilizer doxantrazole and the 5-hydroxytryptamine (5-HT) antagonist cyproheptadine. When antigen-induced contraction was expressed as a percentage of the maximum response of the tissue to exogenous 5-HT, the magnitude of contraction decreased along an aboral gradient down the intestine and correlated well (r2 = 0.878) with mast cell numbers. These results suggest that the increase in connective tissue mast cells in gut muscle after T. spiralis infection involves both local and systemic mechanisms.

Immunologically mediated, non-specific interactions between the intestinal phases of Trichinella spiralis and Nippostrongylus brasiliensis in the mouse

Parasitology ◽  
1980 ◽  
Vol 80 (1) ◽  
pp. 61-72 ◽  
Author(s):  
M. W. Kennedy
Keyword(s):  
Immune Response ◽  
Environmental Changes ◽  
Trichinella Spiralis ◽  
Single Species ◽  
Species Interaction ◽  
Nippostrongylus Brasiliensis ◽  
Specific Effects ◽  
Heterologous Challenge ◽  
Direct Cross ◽  
Concurrent Infections

SummaryInteractions between infections of Trichinella spiralis and Nippostrongylus brasiliensis were studied in the NIH strain of mouse which is known to react strongly to T. spiralis. The course of N. brasiliensis infection in this strain of mouse is described and expulsion is shown to be accelerated in immunized mice and inhibited in cortisone-treated mice. There was no evidence of inter-specific competition between the two species of worm in concurrent infections; the number and location of adults of both species were normal and T. spiralis was able to grow and reproduce normally. No evidence was found of direct immunological cross-reaction between N. brasiliensis and T. spiralis as assessed by the kinetics of adult worm numbers on heterologous challenge of immunized mice 90 days after the initiation of the last of 3 immunizing infections. Interaction was observed only when the timing of concurrent infections was such that one species was established in the intestine immediately before the beginning of expulsion of the second species. Interaction was manifested as a premature loss of worms and, in addition, as impairment of growth and fecundity of T. spiralis. These effects on T. spiralis were similar to those observed as a consequence of a specific immune response to T. spiralis. The rapidity of appearance of these effects and the lack of direct cross-immunity between the two species of worm suggest that the events involved in interaction were non-specific in action and possibly due to environmental changes in the gut caused by the immune response. These non-specific effects are therefore analogous, but not necessarily homologous, to the expulsion of these parasites in single species infections.

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