Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/37343
Title: MyD88 Signaling Is Directly Involved in the Development of Murine Placental Malaria
Authors: Barboza, Renato [UNIFESP]
Reis, Aramys Silva
Silva, Leandro Gustavo da
Hasenkamp, Lutero
Benevides Pereira, Keitty Raquel
Saraiva Camara, Niels Olsen
Costa, Fabio Trindade Maranhão [UNIFESP]
D'Imperio Lima, Maria Regina
Alvarez, Jose Maria
Boscardin, Silvia Beatriz
Epiphanio, Sabrina [UNIFESP]
Farias Marinho, Claudio Romero
Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual de Campinas (UNICAMP)
Issue Date: 1-Feb-2014
Publisher: Amer Soc Microbiology
Citation: Infection and Immunity. Washington: Amer Soc Microbiology, v. 82, n. 2, p. 830-838, 2014.
Abstract: Malaria is a widespread infectious disease caused by the parasite Plasmodium. During pregnancy, malaria infection leads to a range of complications that can affect both the mother and fetus, including stillbirth, infant mortality, and low birth weight. in this study, we utilized a mouse model of placental malaria (PM) infection to determine the importance of the protein MyD88 in the host immune response to Plasmodium during pregnancy. Initially, we demonstrated that Plasmodium berghei NK65GFP adhered to placental tissue via chondroitin sulfate A and induced PM in mice with a C57BL/6 genetic background. To evaluate the involvement of MyD88 in the pathology of PM, we performed a histopathological analysis of placentas obtained from MyD88(-/-) and wild-type (WT) mice following infection on the 19th gestational day. Our data demonstrated that the detrimental placental alterations observed in the infected mice were correlated with the expression of MyD88. Moreover, in the absence of this protein, production of interleukin 6 (IL-6) and tumor necrosis factor alpha (TNF-alpha) was significantly reduced in the infected mice. More importantly, in contrast to fetuses from infected WT mice, which exhibited a reduction in body weight, the fetuses from infected MyD88(-/-) mice did not display significant weight loss compared to their noninfected littermates. in addition, we observed a decrement of maternal care associated with malaria infection, which was attenuated in the MyD88-deficient mice. Collectively, the results of this study illustrate the pivotal importance of the MyD88 signaling pathway in the pathogenesis of placental malaria, thus presenting new possibilities for targeting MyD88 in therapeutic interventions.
URI: http://repositorio.unifesp.br/handle/11600/37343
ISSN: 0019-9567
Other Identifiers: http://dx.doi.org/10.1128/IAI.01288-13
Appears in Collections:Em verificação - Geral

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