Abstract

Schistosomiasis is a neglected tropical disease of a significant public health impact. The water rat Nectomys squamipes is one of the most important non-human hosts in the schistosomiasis mansoni transmission in Brazil, being considered a wild reservoir. Cellular mechanisms that contribute to the physiological adaptation of this rodent to the Schistosoma mansoni parasite are poorly understood. Here we identified, for the first time, that a hepatic steatosis, a condition characterized by excessive lipid accumulation with formation of lipid droplets (LDs) within hepatocytes, occurs in response to the natural S. mansoni infection of N. squamipes, captured in an endemic region. Significant increases of LD area in the hepatic tissue and LD numbers/hepatocyte, detected by quantitative histopathological and ultrastructural analyses, were paralleled by increased serum profile (total cholesterol and triglycerides) in infected compared to uninfected animals. Raman spectroscopy showed high content of polyunsaturated fatty acids (PUFAs) in the liver of both groups. MALDI-TOFF mass spectroscopy revealed an amplified pool of omega-6 PUFA arachidonic acid in the liver of infected animals. Assessment of liver functional activity by the levels of hepatic transaminases (ALT and AST) did not detect any alteration during the natural infection. In summary, this work demonstrates that the natural infection of the wild reservoir N. squamipes with S. mansoni elicits hepatic steatosis in the absence of liver functional harm and that accumulation of lipids, markedly PUFAs, coexists with low occurrence of inflammatory granulomatous processes, suggesting that lipid stores may be acting as a protective mechanism for dealing with the infection.

Highlights

  • Schistosomiasis is an important neglected tropical disease caused by parasitic worms of the genus Schistosoma, with a significant socioeconomic impact [1]

  • This work demonstrates that the natural infection of the wild reservoir N. squamipes with S. mansoni elicits hepatic steatosis in the absence of liver functional harm and that accumulation of lipids, markedly polyunsaturated fatty acids (PUFAs), coexists with low occurrence of inflammatory granulomatous processes, suggesting that lipid stores may be acting as a protective mechanism for dealing with the infection

  • During the infection with S. mansoni, eggs become trapped in the liver and elicit a granulomatous inflammation characterized by accumulation of immune cells such as eosinophils, lymphocytes and macrophages intermixed with collagen fibers around the eggs [3]

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Summary

Introduction

Schistosomiasis is an important neglected tropical disease caused by parasitic worms of the genus Schistosoma, with a significant socioeconomic impact [1]. The only species of Schistosoma that occurs in the Americas is S. mansoni [1]. Human infection with this parasite causes marked chronic morbidity with development of a granulomatous reaction and severe tissue inflammation, in particular within the liver and intestines, which can lead to life-threatening hepatosplenomegaly (reviewed in [3]). The transmission of Schistosomiasis mansoni occurs largely in Brazil, affecting million people with its advanced clinical forms. As part of the World Health Organization’s strategic plan for the period of 2010–2020, Brazil is one of the endemic countries that require intensification of preventive chemotherapy and implementation of complementary public-health measures with the aim of interrupting schistosomiasis transmission [1]

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