COULD THE ACUTE STRONGYLOIDES VENEZUELENSIS INFECTION CAUSE NON-REVERSIBLE HOST MORPHOLOGICAL CHANGES?

Autores

  • Anna Júlia Fernandes Figueiredo Universidade Federal de Mato Grosso (UFMT)
  • Flávia da Silva Resende Universidade Federal de Mato Grosso (UFMT)
  • Vitor Luís Tenório Mati Universidade Federal de Lavras (UFLA)
  • Luana Anjos-Ramos Universidade Federal de Mato Grosso (UFMT)

DOI:

https://doi.org/10.25110/arqsaude.v27i8.2023-001

Palavras-chave:

Strongyloidiasis, Morphometry, Host-Parasite Relationship, Strongyloides spp

Resumo

Although research has investigated the host-parasite relationship in Strongyloides venezuelensis infection in the scope of its immunological implications, the morphological consequences of this response for the host organism are yet to be explored. Our objective was to perform an organ morphometric analysis in Wistar rats infected with the intestinal parasite Strongyloides venezuelensis compared with infected rats treated with ivermectin. Twenty-six animals composed three groups: control (non-infected), infected (infected with 2,000 Strongyloides venezuelensis larvae), and infected treated (infected with 2,000 Strongyloides venezuelensis larvae and treated with ivermectin). All rodents were killed 21 days after infection and morphometric analysis of different organs was performed. The results showed significantly higher body and fecal weight in the infected-treated group. The weight of the small intestine increased considerably in the infected group and decreased in the infected-treated group. Pancreas, right kidney, and heart volume increased in the infected group compared with the control group. Despite treatment, the volumes of the stomach, brain, and left kidney increased in both the infected groups compared with the control group indicating the possibility of non-reversible host morphological adaptations. S. venezuelensis infection can augment both, volume and weight of organs – not necessarily related to the Strongyloides expulsion process – even if the acute infection had been in remission. A potential explanation for these host adaptations, including the occurrence of organ plasticity, are briefly discussed. The following steps encompass a histological analysis to verify the occurrence of hypertrophy/hyperplasia and observe if such morphological alterations remain after infection.

Referências

AHMAD, Arine Fadzlun; HADIP, Faizah; NGUI, Romano; LIM, Yvonne A. L.; MAHMUD, Rohela. Serological and molecular detection of Strongyloides stercoralis infection among an Orang Asli community in Malaysia. Parasitology Research, [S. l.], v. 112, n. 8, p. 2811–2816, 2013. DOI: 10.1007/s00436-013-3450-z.

AMPANOZI, Garyfalia; KRINKE, Eileen; LABERKE, Patrick; SCHWEITZER, Wolf; THALI, Michael J.; EBERT, Lars C. Comparing fist size to heart size is not a viable technique to assess cardiomegaly. Cardiovascular Pathology, [S. l.], v. 36, p. 1–5, 2018. DOI: 10.1016/j.carpath.2018.04.009. Disponível em: https://doi.org/10.1016/j.carpath.2018.04.009.

ANJOS-RAMOS, L.; GAMA, L. A.; MATI, V. L. T.; CORÁ, L. A.; FUJIWARA, R. T.; AMERICO, M. F. Evaluation of gastrointestinal transit after infection with different loads of Strongyloides venezuelensis in rats. Acta Tropica, [S. l.], v. 156, p. 43–47, 2016. a. DOI: 10.1016/j.actatropica.2015.12.010. Disponível em: http://dx.doi.org/10.1016/j.actatropica.2015.12.010.

ANJOS-RAMOS, L.; GAMA, L. A.; MATI, V. L. T.; CORÁ, L. A.; FUJIWARA, R. T.; AMERICO, M. F. Evaluation of gastrointestinal transit after infection with different loads of Strongyloides venezuelensis in rats. Acta Tropica, [S. l.], v. 156, 2016. b. DOI: 10.1016/j.actatropica.2015.12.010.

BEKNAZAROVA, Meruyert; WHILEY, Harriet; ROSS, Kirstin. Strongyloidiasis: A disease of socioeconomic disadvantage. International Journal of Environmental Research and Public Health, [S. l.], v. 13, n. 5, 2016. DOI: 10.3390/ijerph13050517.

BELINELO, V. J.; GOUVÊIA, M. I.; COELHO, M. P.; ZAMPROGNO, A. C.; FIANCO, B. A.; OLIVEIRA, L. G. A. Enteroparasitas em hortaliças comercializadas na cidade de São Mateus, ES, Brasil. Arquivos de Ciência da Saúde Unipar, Umuarama, [S. l.], v. 13, n. 1, p. 33–36, 2009.

BEN SHELDON. Book Reviews Host Parasite Evolution : General. [S. l.], v. 14, n. 2, p. 1998, 1998.

BETHONY, Jeff; BROOKER, Simon; ALBONICO, Marco; GEIGER, Stefan M.; LOUKAS, Alex; DIEMERT, David; HOTEZ, Peter J. Soil-transmitted helminth infections : ascariasis , trichuriasis , and hookworm. The Lancet, [S. l.], v. 367, p. 1521–1532, 2006.

BETTS, A.; GRAY, C.; ZELEK, M.; MACLEAN, R. C.; KING, K. C. High parasite diversity accelerates host adaptation and diversification. Science, [S. l.], v. 360, n. 6391, p. 907–911, 2018. DOI: 10.1126/science.aam9974.

BOGAN, THE LATE J. A.; MCKELLAR, Q. A. The pharmacodynamics of ivermectin in sheep and cattle. Journal of Veterinary Pharmacology and Therapeutics, [S. l.], v. 11, n. 3, p. 260–268, 1988. DOI: 10.1111/j.1365-2885.1988.tb00151.x.

BRELOER, MINKA; ABRAHAM, DAVID. Strongyloides infection in rodents: immune response and immune regulation. Parasitology, [S. l.], v. 144, n. 03, p. 295–315, 2017. DOI: 10.1017/S0031182016000111. Disponível em: https://www.cambridge.org/core/product/identifier/S0031182016000111/type/journal_article.

BUCK, J. C.; WEINSTEIN, S. B.; YOUNG, H. S. Ecological and Evolutionary Consequences of Parasite Avoidance. Trends in Ecology and Evolution, [S. l.], v. 33, n. 8, p. 619–632, 2018. DOI: 10.1016/j.tree.2018.05.001. Disponível em: https://doi.org/10.1016/j.tree.2018.05.001.

CABRAL, Anna Caryna; IÑIGUEZ, Alena Mayo; MORENO, Taiza; BÓIA, Marcio Neves; CARVALHO-COSTA, Filipe Anibal. Clinical conditions associated with intestinal strongyloidiasis in Rio de Janeiro, Brazil. Revista da Sociedade Brasileira de Medicina Tropical, [S. l.], v. 48, n. 3, p. 321–325, 2015. DOI: 10.1590/0037-8682-0019-2015.

CANGA, Aránzazu González; PRIETO, Ana M. Sahagú.; DIEZ LIÉBANA, M. José; MARTÍNEZ, Nélida Fernández; SIERRA VEGA, Matilde; GARCÍA VIEITEZ, Juan J. The pharmacokinetics and interactions of ivermectin in humans - A mini-review. AAPS Journal, [S. l.], v. 10, n. 1, p. 42–46, 2008. DOI: 10.1208/s12248-007-9000-9.

DREW, Georgia C.; STEVENS, Emily J.; KING, Kayla C. Microbial evolution and transitions along the parasite–mutualist continuum. Nature Reviews Microbiology, [S. l.], v. 19, n. 10, p. 623–638, 2021. DOI: 10.1038/s41579-021-00550-7. Disponível em: http://dx.doi.org/10.1038/s41579-021-00550-7.

GIUNCHETTI, Rodolfo Cordeiro; MARTINS-FILHO, Olindo Assis; CARNEIRO, Cláudia Martins; MAYRINK, Wilson; MARQUES, Marcos José; TAFURI, Washington Luiz; CORRÊA-OLIVEIRA, Rodrigo; REIS, Alexandre Barbosa. Histopathology, parasite density and cell phenotypes of the popliteal lymph node in canine visceral leishmaniasis. Veterinary Immunology and Immunopathology, [S. l.], v. 121, n. 1–2, p. 23–33, 2008. DOI: 10.1016/j.vetimm.2007.07.009.

GUZZO, Cynthia A.; FURTEK, Christine I.; PORRAS, Arturo G.; CHEN, Cong; TIPPING, Robert; CLINESCHMIDT, Coleen M.; SCIBERRAS, David G.; HSIEH, John Y. K.; LASSETER, Kenneth C. Safety, tolerability, and pharmacokinetics of escalating high doses of ivermectin in healthy adult subjects. Journal of Clinical Pharmacology, [S. l.], v. 42, n. 10, p. 1122–1133, 2002. DOI: 10.1177/009127002401382731.

HERNÁNDEZ-CHAVARÍA, Francisco; AVENDAÑO, Leticia. A Simple Modification of the Baermann Method for Diagnosis of Strongyloidiasis. Memorias do Instituto Oswaldo Cruz, [S. l.], v. 96, n. 6, p. 805–807, 2001. DOI: 10.1590/S0074-02762001000600011.

IRIEMENAM, Nnaemeka C.; SANYAOLU, Adekunle O.; OYIBO, Wellington A.; FAGBENRO-BEYIOKU, Adetayo F. Strongyloides stercoralis and the immune response. Parasitology International, [S. l.], v. 59, n. 1, p. 9–14, 2010. DOI: 10.1016/j.parint.2009.10.009. Disponível em: http://dx.doi.org/10.1016/j.parint.2009.10.009.

KNOPP, Stefanie et al. Diagnostic accuracy of Kato-Katz, FLOTAC, Baermann, and PCR methods for the detection of light-intensity hookworm and Strongyloides stercoralis infections in Tanzania. American Journal of Tropical Medicine and Hygiene, [S. l.], v. 90, n. 3, p. 535–545, 2014. DOI: 10.4269/ajtmh.13-0268.

MARRA, Nelson Mendes; CHIUSO-MINICUCCI, Fernanda; MACHADO, Gabriel Capella; ZORZELLA-PEZAVENTO, Sofia Fernanda Gonçalves; FRANÇA, Thaís Graziela Donegá; ISHIKAWA, Larissa Lumi Watanabe; AMARANTE, Alessandro F. T.; SARTORI, Alexandrina; AMARANTE, Mônica R. V. Migratory route of Strongyloides venezuelensis in Lewis rats: Comparison of histological analyses and PCR. Experimental Parasitology, [S. l.], v. 127, n. 2, p. 334–339, 2011. a. DOI: 10.1016/j.exppara.2010.08.006. Disponível em: http://dx.doi.org/10.1016/j.exppara.2010.08.006.

MARRA, Nelson Mendes; CHIUSO-MINICUCCI, Fernanda; MACHADO, Gabriel Capella; ZORZELLA-PEZAVENTO, Sofia Fernanda Gonçalves; FRANÇA, Thaís Graziela Donegá; ISHIKAWA, Larissa Lumi Watanabe; AMARANTE, Alessandro F. T.; SARTORI, Alexandrina; AMARANTE, Mônica R. V. Migratory route of Strongyloides venezuelensis in Lewis rats: Comparison of histological analyses and PCR. Experimental Parasitology, [S. l.], v. 127, n. 2, p. 334–339, 2011. b. DOI: 10.1016/j.exppara.2010.08.006.

MENDONÇA, Jalvita C.; GAMA, Loyane A.; HAUSCHILDT, Andrieli T.; CORÁ, Luciana A.; AMÉRICO, Madileine F. Gastrointestinal effects of ivermectin treatment in rats infected with Strongyloides venezuelensis. Acta Tropica, [S. l.], v. 194, n. March, p. 69–77, 2019. DOI: 10.1016/j.actatropica.2019.03.024. Disponível em: https://doi.org/10.1016/j.actatropica.2019.03.024.

MØLLER, Anders Pape. A review of developmental instability, parasitism and disease infection, genetics and evolution. Infection, Genetics and Evolution, [S. l.], v. 6, n. 2, p. 133–140, 2006. DOI: 10.1016/j.meegid.2005.03.005.

OKTAR, Nezih; OZER, Haluk; DEMIRTAS, Eren. Central nervous system strongyloides stercoralis. a case report. Turkish Neurosurgery, [S. l.], v. 30, n. 5, p. 776–779, 2020. DOI: 10.5137/1019-5149.jtn.22886-18.2.

OLSEN, Annette et al. Strongyloidiasis - the most neglected of the neglected tropical diseases? Transactions of the Royal Society of Tropical Medicine and Hygiene, [S. l.], v. 103, n. 10, p. 967–972, 2009. DOI: 10.1016/j.trstmh.2009.02.013.

POULIN, Robert; THOMAS, F. Phenotypic variability induced by parasites: Extent and evolutionary implications. Parasitology Today, [S. l.], v. 15, n. 1, p. 28–32, 1999. DOI: 10.1016/S0169-4758(98)01357-X.

REYES, Felix; SINGH, Navneet; ANJUMAN-KHURRAM, Nigar; LEE, Jihae; CHOW, Lillian. Strongyloides Hyperinfection Syndrome causing fatal meningitis and septicemia by Citrobacter koseri. IDCases, [S. l.], v. 10, n. August, p. 102–104, 2017. DOI: 10.1016/j.idcr.2017.09.005. Disponível em: http://dx.doi.org/10.1016/j.idcr.2017.09.005.

RIVERO, Juan C.; INOUE, Yoichi; MURAKAMI, Noboru; HORII, Yoichiro. Age- and sex-related changes in susceptibility of wistar rats to Strongyloides venezuelensis infection. Journal of Veterinary Medical Science, [S. l.], v. 64, n. 6, p. 519–521, 2002. DOI: 10.1292/jvms.64.519.

ROSSETTO, Anna; BACCARANI, Umberto; LORENZIN, Dario; RISALITI, Andrea; VIALE, Pierluigi; BRESADOLA, Vittorio; ADANI, Gian Luigi. Case Report Disseminate Fungal Infection after Acute Pancreatitis in a Simultaneous Pancreas-Kidney Recipient. [S. l.], v. 2010, p. 10–12, 2010. DOI: 10.1155/2010/898245.

SATOU, Tadaaki; KOGA, Masataka; KOIKE, Kazuo; TADA, Isao; NIKAIDO, Tamotsu. Nematocidal activities of thiabendazole and ivermectin against the larvae of Strongyloides ratti and S. venezuelensis. Veterinary Parasitology, [S. l.], v. 99, n. 4, p. 311–322, 2001. DOI: 10.1016/S0304-4017(01)00472-1.

SIDDIQUI, Afzal A.; BERK, Steven L. Diagnosis of Strongyloides stercoralis infection. Clinical Infectious Diseases, [S. l.], v. 33, n. 7, p. 1040–1047, 2001. DOI: 10.1086/322707.

SIECK, Gary C. Physiology in perspective: Anatomy and physiology—structure and function in biology. Physiology, [S. l.], v. 34, n. 6, p. 379–380, 2019. DOI: 10.1152/physiol.00029.2019.

SOUSA-RIBEIRO, C.; TAVORE, L. N. C.; ANJOS-RAMOS, L. Strongyloides venezuelensis infection augments arterial blood pressure in male wistar rats. Acta Tropica, [S. l.], v. 190, 2019. DOI: 10.1016/j.actatropica.2018.12.007.

TAKAMURE, A. Migration route of Strongyloides venezuelensis in rodents. International Journal for Parasitology, [S. l.], v. 25, n. 8, p. 907–911, 1995.

THOMAS B. NUTMAN. Human infection with Strongyloides stercoralis and other related Strongyloides species. Parasitology, [S. l.], v. 144, n. 3, p. 263–273, 2017. DOI: 10.1016/j.physbeh.2017.03.040.

TRACHTENBERG, Barry H.; HARE, Joshua M. Inflammatory cardiomyopathic syndromes. Circulation Research, [S. l.], v. 121, n. 7, p. 803–818, 2017. DOI: 10.1161/CIRCRESAHA.117.310221.

TRAILOVIĆ, Saša M.; NEDELJKOVIĆ, Jelena Trailović. Central and peripheral neurotoxic effects of ivermectin in rats. Journal of Veterinary Medical Science, [S. l.], v. 73, n. 5, p. 591–599, 2011. DOI: 10.1292/jvms.10-0424.

UTKUALP, Nevin; ERCAN, Ilker. Anthropometric measurements usage in medical sciences. BioMed Research International, [S. l.], v. 2015, p. 7, 2015. DOI: 10.1155/2015/404261.

VENNERVALD, B. J.; POLMAN, K. Helminths and malignancy. Parasite Immunology, [S. l.], v. 31, n. 11, p. 686–696, 2009. DOI: 10.1111/j.1365-3024.2009.01163.x.

VINEY, Mark; KIKUCHI, Taisei. Strongyloides ratti and S. venezuelensis - Rodent models of Strongyloides infection. Parasitology, [S. l.], v. 144, n. 3, p. 285–294, 2017. DOI: 10.1017/S0031182016000020.

YASUDA, Koubun; MATSUMOTO, Makoto; NAKANISHI, Kenji. Importance of both innate immunity and acquired immunity for rapid expulsion of S. venezuelensis. Frontiers in Immunology, [S. l.], v. 5, n. MAR, p. 1–5, 2014. DOI: 10.3389/fimmu.2014.00118.

ZAHA, O; HIRATA, T, KINJO, F; SAITO, A. Strongyloidiasis-Progress in Diagnosis and Treatment. Internal Medicine, [S. l.], v. 39, n. 9, p. 695–700, 2000.

Downloads

Publicado

01-08-2023

Como Citar

Figueiredo, A. J. F., Resende, F. da S., Mati, V. L. T., & Anjos-Ramos, L. (2023). COULD THE ACUTE STRONGYLOIDES VENEZUELENSIS INFECTION CAUSE NON-REVERSIBLE HOST MORPHOLOGICAL CHANGES?. Arquivos De Ciências Da Saúde Da UNIPAR, 27(8), 4135–4152. https://doi.org/10.25110/arqsaude.v27i8.2023-001

Edição

Seção

Artigos