scholarly journals THE TRANSMISSION OF THE VIRUS OF LYMPHOCYTIC CHORIOMENINGITIS BY TRICHINELLA SPIRALIS

1947 ◽  
Vol 85 (6) ◽  
pp. 759-769 ◽  
Author(s):  
J. T. Syverton ◽  
O. R. McCoy ◽  
J. Koomen
Keyword(s):  
Outer Surface ◽  
Guinea Pigs ◽  
Parasitic Nematode ◽  
Trichinella Spiralis ◽  
Lymphocytic Choriomeningitis

In experiments in which guinea pigs were infected concurrently with the virus of lymphocytic choriomeningitis and the parasitic nematode, Trichinella spiralis, proof was obtained that trichinella larvae, after maturation in the muscles, had acquired the virus and were capable of transmitting it to new susceptible hosts. Transmission resulted both when living larvae were fed to normal guinea pigs and when triturated dead larvae were injected subcutaneously. Control experiments and other tests made plain that transmission of the virus was not due to mere adherence of it to the outer surface of the larvae but that these actually harbored it. The significance of these experiments in relation to natural transmission of the virus of lymphocytic choriomeningitis remains to be determined.

scholarly journals A SOLUBLE ANTIGEN OF LYMPHOCYTIC CHORIOMENINGITIS

1940 ◽  
Vol 72 (4) ◽  
pp. 389-405 ◽  
Author(s):  
J. E. Smadel ◽  
M. J. Wall
Keyword(s):  
Guinea Pig ◽  
Guinea Pigs ◽  
Lymphocytic Choriomeningitis ◽  
The Other ◽  
Soluble Antigen ◽  
Soluble Substance ◽  
Other Hand ◽  
The Times

Anti-soluble substance antibodies and neutralizing substances, which develop following infection with the virus of lymphocytic choriomeningitis, appear to be separate entities. The times of appearance and regression of the two antibodies are different in both man and the guinea pig; the antisoluble substance antibodies appear earlier and remain a shorter time. Moreover, mice develop them but no demonstrable neutralizing substances. Injection of formalin-treated, virus-free extracts containing considerable amounts of soluble antigen fails to elicit anti-soluble substance antibodies and to induce immunity in normal guinea pigs; administration of such preparations to immune pigs, however, is followed by a marked increase in the titer of anti-soluble substance antibodies in their serum. On the other hand, suspensions of formolized washed virus are effective in normal guinea pigs in stimulating both anti-soluble substance antibodies and protective substances, and in inducing immunity to infection.

Reactivity and Specificity of Trichinella spiralis Fractions in Cutaneous and Serological Tests

1977 ◽  
Vol 6 (3) ◽  
pp. 274-279
Author(s):  
Omar O. Barriga
Keyword(s):  
Guinea Pigs ◽  
Trichinella Spiralis ◽  
Chronic Phase ◽  
Epidemiological Studies ◽  
Cross Reactivity ◽  
Serological Tests ◽  
Specific Diagnosis ◽  
Diethylaminoethyl Cellulose ◽  
Cutaneous Reactions ◽  
Healthy Persons

Six diethylaminoethyl-cellulose fractions of a larval Trichinella spiralis extract, an Ascaris suum extract, and a nonrelated protein were used for cutaneous tests in guinea pigs with 8-, 14-, and 73-day-old T. spiralis infections, in guinea pigs with 13-day-old A. suum infections, and in normal guinea pigs. A selected T. spiralis fraction was used in hemagglutination (HA) tests with sera of 8 T. spiralis -infected rabbits, 41 sera of trichinellosis patients positive by bentonite agglutination tests, and 50 sera of clinically healthy persons. Immediate-type cutaneous reactions revealed extensive cross-reactivity between both parasites, although the establishment of conventional limits for considering a reaction positive allowed the specific diagnosis of acute or chronic trichinellosis with different fractions. Delayed-type reactions were specific with all fractions except one, and different fractions reacted during either the acute or the chronic phase of trichinellosis. HA detected anti- Trichinella antibodies in all the rabbits 9 to 10 days postinfection, in all trichinellosis patients, and in none of the healthy people. Correlation between HA and bentonite agglutination titers and other considerations suggest that HA with the selected fraction detects early antibodies. HA inhibition tests with A. suum extract suggest lack of HA cross-reactivity between the A. suum - and T. spiralis -selected fractions. The use of different fractions in diverse tests for clinical or epidemiological studies is suggested.

scholarly journals Nucleotidase Cascades Are Catalyzed by Secreted Proteins of the Parasitic Nematode Trichinella spiralis

2002 ◽  
Vol 70 (9) ◽  
pp. 4917-4924 ◽  
Author(s):  
Kleoniki Gounaris
Keyword(s):  
Molecular Mass ◽  
Adenosine Deaminase ◽  
Parasitic Nematode ◽  
Trichinella Spiralis ◽  
Purinergic Signaling ◽  
Physiological Role ◽  
Apparent Molecular Mass ◽  
Extracellular Nucleotides ◽  
Secreted Proteins ◽  
Mediated Effects

ABSTRACT Extracellular nucleotides are signaling molecules whose receptor-mediated effects are involved in a variety of physiological responses in mammalian tissues. An overwhelming body of data indicate that inflammatory and other immune responses can be modulated by the availability and local concentrations of nucleotides via nucleotide receptor signaling, but this is only just beginning to be investigated in the context of infectious disease. Evidence is provided here that the parasitic nematode Trichinella spiralis can catalyze the conversion and thus modulate both the availability and concentration of extracellular nucleotides by means of the following secreted exoenzymes: apyrase, 5′-nucleotidase, and adenosine deaminase. These enzymes were characterized in terms of substrate specificity, kinetic behavior, pH, divalent cation preferences, and response to a series of compounds. The secreted 5′-nucleotidase was identified as a protein with an apparent molecular mass of 67 kDa after N-terminal amino acid sequencing of the purified protein. The presence of adenosine deaminase was confirmed in the secreted products by Western blotting with an antibody against a mammalian enzyme, as a protein with an apparent molecular mass of 38 kDa. These secreted proteins constitute an enzymatic cascade which catalyzes the degradation of extracellular nucleotides, with a potential physiological role in the regulation of purinergic signaling.

Characterization of TsDAF-21/HSP90 protein from the parasitic nematode Trichinella spiralis

2014 ◽  
Vol 113 (6) ◽  
pp. 2209-2217 ◽  
Author(s):  
Yurong Yang ◽  
Weiwen Qin ◽  
Hengtong Qiu ◽  
Yan Liu
Keyword(s):  
Parasitic Nematode ◽  
Trichinella Spiralis ◽  
Hsp90 Protein

Immunological regulation of colonic ion transport

1989 ◽  
Vol 256 (2) ◽  
pp. G396-G403 ◽  
Author(s):  
D. A. Russell ◽  
G. A. Castro
Keyword(s):  
Guinea Pigs ◽  
Trichinella Spiralis ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Antigenic Stimulation ◽  
Synthesis Inhibitor ◽  
Combined Use ◽  
Maximum Elevation ◽  
Prostaglandin Synthesis Inhibitor ◽  
Stimulation Of

Challenge of distal colonic epithelium from Trichinella spiralis-infected guinea pigs with parasite-derived antigen elevated short-circuit current (Isc) for approximately 60 min. The maximum elevation (delta Isc) was approximately 250 microA/cm2 at 5 min after the addition of trichinella antigen. The antigen-induced alterations in Isc were of greater magnitude and duration than those evoked in jejunum. Colonic electrical resistance was transiently reduced after exposure to antigen. There was no significant effect of antigen on electrical parameters of colon from nonimmunized (uninfected) guinea pigs. The antihistamine pyrilamine (10(-5) M) and the prostaglandin synthesis inhibitor indomethacin (10(-6) M) reduced the colonic Isc response to antigen by 40% when used in combination but had insignificant effects when used singly. In contrast, the jejunal Isc response to antigen was totally eliminated by the combined use of those inhibitors. Antigenic stimulation of sensitized colon released histamine and prostaglandin E2 (PGE2). However, the histamine released was only about one-tenth that stimulated by antigen in the jejunum, and PGE2 released was only one-tenth of that stimulated by bradykinin in the colon. PGE2 was not released after antigenic stimulation of jejunum. The antigen-induced colonic delta Isc was reduced approximately 50% by either furosemide or tetrodotoxin. Although histamine- and indomethacin-sensitive factors contribute greatly to the mediation of the antigen-induced delta Isc in jejunum, these autacoids contribute to a lesser extent to the antigen-induced delta Isc in guinea pig colon.

scholarly journals A SOLUBLE ANTIGEN OF LYMPHOCYTIC CHORIOMENINGITIS

1940 ◽  
Vol 71 (1) ◽  
pp. 43-53 ◽  
Author(s):  
J. E. Smadel ◽  
M. J. Wall ◽  
R. D. Baird
Keyword(s):  
Guinea Pigs ◽  
Complement Fixation ◽  
Lymphocytic Choriomeningitis ◽  
Immune Serum ◽  
Splenic Tissue ◽  
The Other ◽  
Soluble Antigen ◽  
Precipitin Reaction ◽  
Other Hand ◽  
Protein Nature

The soluble antigen of lymphocytic choriomeningitis which is readily separable from the virus is a relatively stable substance and appears to be of a protein nature. A specific precipitin reaction can be demonstrated when immune serum is added to solutions of antigen which have been freed of certain serologically inactive substances. The complement-fixation and precipitation reactions which occur in the presence of immune serum and non-infectious extracts of splenic tissue obtained from guinea pigs moribund with lymphocytic choriomeningitis seem to be manifestations of union of the same soluble antigen and its antibody. On the other hand, the antisoluble substance antibodies and neutralizing substances appear to be different entities.

scholarly journals INFECTION OF GUINEA PIGS BY APPLICATION OF VIRUS OF LYMPHOCYTIC CHORIOMENINGITIS TO THEIR NORMAL SKINS

1940 ◽  
Vol 72 (4) ◽  
pp. 331-343 ◽  
Author(s):  
Howard J. Shaughnessy ◽  
Joseph Zichis
Keyword(s):  
Virus Infection ◽  
Guinea Pigs ◽  
Normal Skin ◽  
Clinical Signs ◽  
Lymphocytic Choriomeningitis ◽  
Cross Infection ◽  
Virus Suspension ◽  
Intact Skin

As shown in Table I, 97 guinea pigs were used in this study. Fifty-seven were exposed by placing a virus suspension on their normal skins. Of this number, 34 had screw-top capsules attached to them. Thirteen were exposed by spreading the virus suspension on their feed and cage litter. Ten were inoculated intracerebrally to establish the potency of the virus. The remaining 17 were not exposed artificially to the virus and were employed as controls to detect cross infection. Twenty-two guinea pigs, to which capsules were attached, died as a result of virus infection; 1 died of unknown causes and 11 survived without showing any clinical signs of the infection. Sixteen of the animals without the capsules died of virus infection and 7 did not become infected. The 10 guinea pigs that were inoculated intracerebrally became infected and died. None of the animals that were exposed by spreading the virus on the feed and the litter in the cages, or those used as unexposed controls, developed any clinical signs of infection with lymphocytic choriomeningitis. It is realized that minute abrasions, not visible with a hand lens, may have been present in the skins of these guinea pigs. However, any condition of this nature would be a factor encountered in any normal skin. In view of these facts, it is believed that these results indicate that the virus of lymphocytic choriomeningitis may infect guinea pigs through the normal, apparently intact, skin.

scholarly journals Immune response to stage-specific surface antigens of the parasitic nematode Trichinella spiralis.

1981 ◽  
Vol 154 (1) ◽  
pp. 210-215 ◽  
Author(s):  
M Philipp ◽  
P M Taylor ◽  
R M Parkhouse ◽  
B M Ogilvie
Keyword(s):  
Primary Infection ◽  
Time Course ◽  
Parasitic Nematode ◽  
Trichinella Spiralis ◽  
Serum Antibody ◽  
Surface Antigens ◽  
Surface Proteins ◽  
Infective Larvae ◽  
Intestinal Worms

Rats were infected with the nematode Trichinella spiralis and the primary serum antibody response to antigenic surface proteins of infective larvae, intestinal worms, and newborn larvae was studies. 1 wk after infection, the sera contained antibodies to surface antigens of both infective larvae and intestinal worms. These early sera, however, failed to react with newborn larvae surface antigens. In addition, adsorption of sera with living intestinal worms or infective larvae removed antibodies to surface antigens of the homologous stage only. Finally, the time-course of appearance of antibodies that mediate eosinophil adherence to the surface of each stage of the parasite. We concluded that in a primary infection in rats, the surface proteins of T. spiralis used in this study are antigenically stage specific. Furthermore, they could be targets for the stage-specific, antibody-dependent eosinophil-mediated destruction of this parasite, known to occur in vitro.

scholarly journals IMMUNIZATION OF GUINEA PIGS WITH A MODIFIED STRAIN OF LYMPHOCYTIC CHORIOMENINGITIS VIRUS

1937 ◽  
Vol 66 (3) ◽  
pp. 317-324 ◽  
Author(s):  
Erich Traub
Keyword(s):  
Guinea Pigs ◽  
Serial Passage ◽  
Lymphocytic Choriomeningitis ◽  
White Mouse ◽  
Lymphocytic Choriomeningitis Virus ◽  
High Virulence ◽  
Different Strains ◽  
Highly Virulent

A strain of choriomeningitis virus which was highly virulent for guinea pigs, as isolated from a naturally infected white mouse, has been markedly attenuated for guinea pigs by serial intracerebral passage through white mice. The change of virulence occurred before the 8th serial passage. The modified virus as a rule produces fever in guinea pigs but no other symptoms, and the infection is followed by a very solid immunity. Parallel passages of the same strain through guinea pigs have maintained its high virulence for this species but slightly reduced its pathogenicity for mice. These observations indicate that the differences in virulence for guinea pigs noted before (1, 2) with different strains of choriomeningitis virus obtained from infected stock mice may be due not only to differences in the susceptibility of guinea pigs but also to variations in the virulence of the virus. A marked degree of resistance was demonstrable in several guinea pigs on the 4th, 8th, and 10th day after injection with modified virus, when antivirus could not yet be detected in the serum. Circulating antivirus appears therefore to play a secondary part in their immunity, which seems to be closely associated with the tissues as in mice.

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