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Coxsackievirus B4 Exposure Results in Variable Pattern Recognition Response in the Kidneys of Female Non-Obese Diabetic Mice Before Establishment of Diabetes.
Walter, Debra L; Benner, Sarah E; Oaks, Rosemary J; Thuma, Jean R; Malgor, Ramiro; Schwartz, Frank L; Coschigano, Karen T; McCall, Kelly D.
Afiliação
  • Walter DL; Interdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, Ohio, USA.
  • Benner SE; Department of Biological Sciences, College of Arts and Sciences, Ohio University, Athens, Ohio, USA.
  • Oaks RJ; Interdisciplinary Program in Molecular and Cellular Biology, Ohio University, Athens, Ohio, USA.
  • Thuma JR; Department of Biological Sciences, College of Arts and Sciences, Ohio University, Athens, Ohio, USA.
  • Malgor R; Program in Biological Sciences, Honors Tutorial College, Ohio University, Athens, Ohio, USA.
  • Schwartz FL; Department of Biomedical Sciences and Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA.
  • Coschigano KT; Department of Specialty Medicine, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, USA.
  • McCall KD; The Diabetes Institute, Ohio University, Athens, Ohio, USA.
Viral Immunol ; 33(7): 494-506, 2020 09.
Article em En | MEDLINE | ID: mdl-32352894
End-stage renal disease (ESRD) is described by four primary diagnoses, diabetes, hypertension, glomerulonephritis, and cystic kidney disease, all of which have viruses implicated as causative agents. Enteroviruses, such as coxsackievirus (CV), are a common genus of viruses that have been implicated in both diabetes and cystic kidney disease; however, little is known about how CVs cause kidney injury and ESRD or predispose individuals with a genetic susceptibility to type 1 diabetes (T1D) to kidney injury. This study evaluated kidney injury resulting from coxsackievirus B4 (CVB4) inoculation of non-obese diabetic (NOD) mice to glean a better understanding of how viral exposure may predispose individuals with a genetic susceptibility to T1D to kidney injury. The objectives were to assess acute and chronic kidney damage in CVB4-inoculated NOD mice without diabetes. Results indicated the presence of CVB4 RNA in the kidney for at least 14 days post-CVB4 inoculation and a coordinated pattern recognition receptor response, but the absence of an immune response or cytotoxicity. CVB4-inoculated NOD mice also had a higher propensity to develop an increase in mesangial area 17 weeks post-CVB4 inoculation. These studies identified initial gene expression changes in the kidney resulting from CVB4 exposure that may predispose to ESRD. Thus, this study provides an initial characterization of kidney injury resulting from CVB4 inoculation of mice that are genetically susceptible to developing T1D that may one day provide better therapeutic options and predictive measures for patients who are at risk for developing kidney disease from T1D.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Enterovirus Humano B / Infecções por Coxsackievirus / Diabetes Mellitus Tipo 1 / Receptores de Reconhecimento de Padrão Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Viral Immunol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Enterovirus Humano B / Infecções por Coxsackievirus / Diabetes Mellitus Tipo 1 / Receptores de Reconhecimento de Padrão Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Viral Immunol Ano de publicação: 2020 Tipo de documento: Article