Literature DB >> 9257450

Recovery of Schistosoma japonicum from experimentally infected pigs by perfusion of liver and mesenteric veins.

H O Bøgh1, A L Willingham, M V Johansen, L Eriksen, N O Christensen.   

Abstract

An optimized procedure for perfusion of pigs infected with Schistosoma japonicum was developed. The technique involves insertion of a perfusion influx tube into the thoracic descending aorta, clamping vessels to parts of the body which did not need to be perfused (the kidneys, hind legs, etc.) and placing a collection tube directly into the portal vein. In addition, the clamping technique allows for separate perfusion of the liver and intestinal veins. The perfusion medium was a sodium citrate buffer (40 degrees C) to which the vasodilator sodium nitroprusside was added. Furthermore, an experiment was conducted to investigate if the perfusion efficiency, measured by total worm recovery, could be increased if praziquantel was administered prior to perfusion. Twelve pigs were each infected with 1000 S. japonicum cercariae and their schistosomes were collected 11 weeks later by separate perfusion of the liver and intestinal veins. Six of these pigs were treated orally with praziquantel one hour before perfusion. In general, the vessels of the livers and intestines of all pigs were well perfused, judging by the resulting pale colour of the tissues. Worms from praziquantel treated pigs were collected within 5 min of perfusion as opposed to approximately 20 min in the non-treated pigs. More worms were collected from the livers of the praziquantel treated pigs, indicating a hepatic shift of schistosomes from the intestinal mesenteries. However, comparable numbers of worms were retained in the mesenteric veins following perfusion in the 2 groups, indicating that manual recovery of schistosomes from the intestinal mesenteries is necessary in addition to perfusion for obtaining the total worm counts. Another experiment was conducted to determine if the intensity and/or duration of infection had an effect on the number of worms collected by the perfusion technique. Seventy-two pigs were allocated into 3 groups of 24 pigs each, which were infected with either 100, 500 or 2000 cercariae per pig. The 3 groups were further divided into 4 subgroups of 6 pigs each which were perfused with our selective technique at 4, 11, 17 or 24 weeks post infection, respectively. All of the pigs received an oral praziquantel treatment prior to perfusion. The results indicated that increasing intensities and/or duration of infection resulted in trapping of schistosomes in intravascular inflammatory reactions which made it more difficult to collect the adult schistosomes by perfusion.

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Year:  1997        PMID: 9257450      PMCID: PMC8057037     

Source DB:  PubMed          Journal:  Acta Vet Scand        ISSN: 0044-605X            Impact factor:   1.695


  14 in total

1.  The pig as a unique host model for Schistosoma japonicum infection.

Authors:  A L Willingham; M Hurst
Journal:  Parasitol Today       Date:  1996-04

2.  The fecundity of Schistosoma mansoni in chronic nonhuman primate infections and after transplantation into naive hosts.

Authors:  R T Damian; C A Rawlings; S C Bosshardt
Journal:  J Parasitol       Date:  1986-10       Impact factor: 1.276

3.  An improved perfusion technique for recovering adult schistosomes from laboratory animals.

Authors:  R H Duvall; W B DeWitt
Journal:  Am J Trop Med Hyg       Date:  1967-07       Impact factor: 2.345

4.  The infection of laboratory hosts with cercariae of Schistosoma mansoni and the recovery of the adult worms.

Authors:  S R Smithers; R J Terry
Journal:  Parasitology       Date:  1965-11       Impact factor: 3.234

5.  Observations on cattle schistosomiasis in the Sudan, a study in comparative medicine. IV. Preliminary observations on the mechanism of naturally acquired resistance.

Authors:  H O Bushara; M F Hussein; M A Majid; B E Musa; M G Taylor
Journal:  Am J Trop Med Hyg       Date:  1983-09       Impact factor: 2.345

6.  Clinical and pathologic features of experimental Schistosoma japonicum infection in pigs.

Authors:  C V Yason; M N Novilla
Journal:  Vet Parasitol       Date:  1984-12       Impact factor: 2.738

7.  A rapid method for the infection of laboratory mice with Schistosoma japonicum.

Authors:  N A Moloney; G Webbe
Journal:  Trans R Soc Trop Med Hyg       Date:  1982       Impact factor: 2.184

8.  Praziquantel, a new board-spectrum antischistosomal agent.

Authors:  R Gönnert; P Andrews
Journal:  Z Parasitenkd       Date:  1977-07-21

9.  Experimental infection of Danish Landrace/Yorkshire crossbred pigs with Schistosoma japonicum from the People's Republic of China.

Authors:  A L Willingham; M V Johansen; B J Vennervald; N O Christensen; P Nansen
Journal:  Acta Vet Scand       Date:  1994       Impact factor: 1.695

10.  Effects of praziquantel on experimental Schistosoma bovis infection in goats.

Authors:  M V Johansen; J Monrad; N O Christensen
Journal:  Vet Parasitol       Date:  1996-03       Impact factor: 2.738

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  2 in total

1.  Immune events associated with high level protection against Schistosoma japonicum infection in pigs immunized with UV-attenuated cercariae.

Authors:  Fang Tian; Dandan Lin; Jingjiao Wu; Yanan Gao; Donghui Zhang; Minjun Ji; Guanling Wu
Journal:  PLoS One       Date:  2010-10-15       Impact factor: 3.240

2.  Multiple vaccinations with UV- attenuated cercariae in pig enhance protective immunity against Schistosoma japonicum infection as compared to single vaccination.

Authors:  Dandan Lin; Fang Tian; Haiwei Wu; Yanan Gao; Jingjiao Wu; Donghui Zhang; Minjun Ji; Donald P McManus; Patrick Driguez; Guanling Wu
Journal:  Parasit Vectors       Date:  2011-06-10       Impact factor: 3.876

  2 in total

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