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Trypanosoma cruzi infection: do distinct populations cause intestinal motility alteration?

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Abstract

Chagas disease, caused by Trypanosoma cruzi, is an important public health problem in Latin America. Disturbances in gastrointestinal motility are observed in 15–20% of patients at the chronic phase. We previously observed a decrease in intestinal motility in mice infected with Y strain from T. cruzi. Thus, we decided to test if infection with other T. cruzi strains also caused the intestinal disturbance. Male adult Swiss mice were infected intraperitoneally with CL–Brener clone (CL-B), Brazil strain (Br), or Dm28 clone (Dm) of T. cruzi. All infected mice presented a low cumulative mortality (CL-B, 17%; Br, 8%; Dm, 25%) at 35 days post infection (dpi) and their typical parasitemia curves. Br and Dm groups exhibited a maximal reduction of intestinal motility at 35 dpi (176.8 ± 51.3 and 198.3 ± 52.6 min, respectively), when compared with non-infected mice (90.2 ± 19.5 min). However, CL mice presented the peak of delayed intestinal transit at 12 dpi (191.0 ± 33.3 min), when compared with non-infected mice (105.6 ± 26.4 min), very close to the 15 dpi for the intense alteration (310.2 ± 67.4 min) observed with the Y strain. We clearly demonstrate a reduction in intestinal motility in mice infected with different groups of T. cruzi during the acute phase of the infection. Since Br, Dm, and CL strains presented low mortality rates in adult Swiss mice, a prospective study concerning the chronic intestinal alteration is encouraged, particularly for studies of alternative therapies.

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References

  • Adad SJ, Cançado CG, Etchebehere RM, Teixeira VP, Gomes UA, Chapadeiro E, Lopes ER (2001) Neuron count reevaluation in the myenteric plexus of chagasic megacolon after morphometric neuron analysis. Virchows Arch 438:254–258

    Article  CAS  PubMed  Google Scholar 

  • Arantes RME, Marche HHF, Bahia MT, Cunha FQ, Rossi MA, Silva JS (2004) Interferon-γ-induced nitric oxide causes intrinsic intestinal denervation in Trypanosoma cruzi-infected mice. Am J Pathol 164:1361–1368

    CAS  PubMed  Google Scholar 

  • Brener Z (1962) Therapeutic activity and criterion of cure on mice experimentally infected with Trypanosoma cruzi. Rev Inst Med Trop São Paulo 4:389–396

    CAS  PubMed  Google Scholar 

  • Caetano LC, Santello FH, Filipin MDV, Brazão V, Caetano LN, Toldo MPA, Caldeira JC, Prado C Jr (2009) Trypanosoma cruzi: dehydroepiandrosterone (DHEA) and immune response during the chronic phase of the experimental Chagas’ disease. Vet Parasitol 163:27–32

    Article  CAS  PubMed  Google Scholar 

  • Camargos ES, Franco DJ, Garcia CMMG, Dutra AP, Teixeira AL Jr, Chiari E, Machado CRS (2000) Infection with different Trypanosoma cruzi populations in rats: myocarditis, cardiac sympathetic denervation, and involvement of digestive organs. Am J Trop Med Hyg 42:604–612

    Google Scholar 

  • Contreras VT, Araújo-Jorge TC, Bonaldo MC, Thomaz N, Barbosa HS, Meirelles MNSL, Goldenberg S (1988) Biological aspects of the Dm28c clone of Trypanosoma cruzi after metacyclogenesis in chemically defined media. Mem Inst Oswaldo Cruz 83:123–133

    Article  CAS  PubMed  Google Scholar 

  • Culbertson HOJ, Kessler WR (1942) Age resistance of mice to Trypanosoma cruzi. J Parasitol 28:155–158

    Article  Google Scholar 

  • De Souza AP, Sieberg R, Li H, Cahill HR, Zhao D, Araújo-Jorge TC, Tanowitz HB, Jelicks LA (2010) The role of selenium in intestinal motility and morphology in a murine model of Typanosoma cruzi infection. Parasitol Res 106:1293–1298

    Google Scholar 

  • Develoux M, Lescure FX, Le Loup G, Pialoux G (2009) Chagas disease. Rev Méd Interne 30:686–695

    Article  CAS  PubMed  Google Scholar 

  • Fernandes O, Campbell DA (2000) Trypanosoma cruzi: cepas de eleição. In: Araújo-Jorge TC, Castro SL (eds) Doença de Chagas: manual para experimentação animal, 1st edn. Editora Fiocruz, Rio de Janeiro, pp 178–181

    Google Scholar 

  • Fernandes O, Souto RP, Castro JA, Pereira JB, Fernandes NC, Junqueira AC, Naiff RD, Barrett TV, Degrave W, Zingales B, Campbell DA, Coura JR (1998) Brazilian isolates of Trypanosoma cruzi from humans and triatomines classified into two lineages using mini-exon and ribosomal RNA sequences. Am J Trop Med Hyg 58:807–811

    CAS  PubMed  Google Scholar 

  • Freitas JM, Augusto-Pinto L, Pimenta JR, Bastos-Rodrigues L, Gonçalves VF, Teixeira SM, Chiari E, Junqueira AC, Fernandes O, Macedo AM, Machado CR, Pena SD (2006) Ancestral genomes, sex, and the population structure of Trypanosoma cruzi. PLoS Pathog 2(3):e24

    Article  PubMed  Google Scholar 

  • Geraldino RS, Ferreira AJ, Lima MA, Cabrine-Santos M, Lages-Silva E, Ramirez LE (2006) Interstitial cells of Cajal in patients with chagasic megacolon originating from a region of old endemicity. Pathophysiology 13:71–74

    Article  CAS  PubMed  Google Scholar 

  • Huang H, Chan J, Wittner M, Jelicks LA, Morris SA, Factor SM, Weiss LM, Braunstein VL, Bacchi CJ, Yarlett N, Chandra M, Shirani J, Tanowitz HB (1999) Expression of cardiac cytokines and inducible form of nitric oxide synthase (NOS2) in Trypanosoma cruzi-infected mice. J Mol Cell Cardiol 31:75–88

    Article  CAS  PubMed  Google Scholar 

  • Huang H, Petkova SB, Cohen AW, Bouzahzah B, Chan J, Zhou JN, Factor SM, Weiss LM, Krishnamachary M, Mukherjee S, Wittner M, Kitsis RN, Pestell RG, Lisanti MP, Albanese C, Tanowitz HB (2003) Activation of transcription factors AP-1 and NF-kappa B in murine Chagasic myocarditis. Infect Immun 71:2859–2867

    Article  CAS  PubMed  Google Scholar 

  • Koberle F (1968) Chagas’ disease and Chagas’ syndromes: the pathology of American trypanosomiasis. Adv Parasitol 6:63–116

    Article  CAS  PubMed  Google Scholar 

  • Lopes MF, Cunha JM, Bezerra FL, Gonzalez MS, Gomes JE, Silva JR Lapa e, Garcia ES, Dos Reis GA (1995) Trypanosoma cruzi: both chemically induced and triatomine-derived metacyclic trypomastigotes cause the same immunological disturbances in the infected mammalian host. Exp Parasitol 80:194–204

    Article  CAS  PubMed  Google Scholar 

  • Marona HRN, Lucchesi MBB (2004) Protocol to refine intestinal motility test in mice. Lab Anim 38:257–260

    Article  CAS  PubMed  Google Scholar 

  • Moncayo A, Silveira AC (2009) Current epidemiological trends for Chagas disease in Latin America and future challenges in epidemiology, surveillance and health policy. Mem Inst Oswaldo Cruz 104(Suppl 1):17–30

    PubMed  Google Scholar 

  • Nakayama H, Ferreira ME, Ariasi AR, Bilbao NV, Torres S, Schinini A, Fournet A (2001) Experimental treatment of chronic Trypanosoma cruzi infection in mice with 2-NPropylquinoline. Phytother Res 15:630–632

    Article  CAS  PubMed  Google Scholar 

  • Ny L, Li H, Mukherjee S, Persson K, Holmqvist B, Zhao D, Shtutin V, Huang H, Weiss LM, Machado FS, Factor SM, Chan J, Tanowitz HB, Jelicks LA (2008) A magnetic resonance imaging study of intestinal dilation in Trypanosoma cruzi-infected mice deficient in nitric oxide synthase. Am J Trop Med Hyg 79:760–767

    CAS  PubMed  Google Scholar 

  • Oliveira GM, Medeiros MM, da Silva BW, Santana R, Araújo-Jorge TC, Souza AP (2008) Applicability of the use of charcoal for the evaluation of intestinal motility in a murine model of Trypanosoma cruzi infection. Parasitol Res 102:747–750

    Article  PubMed  Google Scholar 

  • Petkova SB, Tanowitz HB, Magazine HI, Factor SM, Chan J, Pestell RG, Bouzahzah B, Douglas SA, Shtutin V, Morris SA, Tsang E, Weiss LM, Christ GJ, Wittner M, Huang H (2000) Myocardial expression of endothelin-1 in murine Trypanosoma cruzi infection. Cardiovasc Pathol 9:257–265

    Article  CAS  PubMed  Google Scholar 

  • Rezende JM, Luquetti A (1994) Chagasic megavisceras. In Chagas’ disease and the nervous system. PAHO Sci Publ 547:149–171

    Google Scholar 

  • Silveira AB, Freitas MA, de Oliveira EC, Neto SG, Luquetti AO, Furness JB, Correa-Oliveira R, Reis D (2009) Glial fibrillary acidic protein and S-100 colocalization in the enteroglial cells in dilated and nondilated portions of colon from chagasic patients. Hum Pathol 40:244–251

    Article  PubMed  Google Scholar 

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Acknowledgments

We are grateful to Marcos and Marcelo Meuser for their excellent technical assistance. We are also grateful to Dr Linda A. Jelicks for reviewing this manuscript. This work was supported by CNPq (Comissão Nacional de Desenvolvimento Científico e Tecnológico)/Decit and Instituto Oswaldo Cruz-Fiocruz. This study was performed in accordance with the guidelines established by the FIOCRUZ Committee of Ethics in Animal Use, license number (0099/01) for the research, resolution 6.899/09.

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Correspondence to Andréa Pereira de Souza.

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de Melo Medeiros, M., Araújo-Jorge, T.C., Batista, W.S. et al. Trypanosoma cruzi infection: do distinct populations cause intestinal motility alteration?. Parasitol Res 107, 239–242 (2010). https://doi.org/10.1007/s00436-010-1871-5

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