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Metabolic Dysregulation in Hepacivirus Infection of Common Marmosets (Callithrix jacchus).

Publication ,  Journal Article
Manickam, C; Wachtman, L; Martinot, AJ; Giavedoni, LD; Reeves, RK
Published in: PLoS One
2017

Chronic hepatitis C has been associated with metabolic syndrome that includes insulin resistance, hepatic steatosis and obesity. These metabolic aberrations are risk factors for disease severity and treatment outcome in infected patients. Experimental infection of marmosets with GBV-B serves as a tangible, small animal model for human HCV infection, and while virology and pathology are well described, a full investigation of clinical disease and the metabolic milieu is lacking. In this study six marmosets were infected intravenously with GBV-B and changes in hematologic, serum biochemical and plasma metabolic measures were investigated over the duration of infection. Infected animals exhibited signs of lymphocytopenia, but platelet and RBC counts were generally stable or even increased. Although most animals showed a transient decline in blood glucose, infection resulted in several fold increases in plasma insulin, glucagon and glucagon-like peptide 1 (GLP-1). All infected animals experienced transient weight loss within the first 28 days of infection, but also became hypertriglyceridemic and had up to 10-fold increases in adipocytokines such as resistin and plasminogen activator inhibitor 1 (PAI-1). In liver, moderate to severe cytoplasmic changes associated with steatotic changes was observed microscopically at 168 days post infection. Collectively, these results suggest that GBV-B infection is accompanied by hematologic, biochemical and metabolic abnormalities that could lead to obesity, diabetes, thrombosis and atherosclerosis, even after virus has been cleared. Our findings mirror those found in HCV patients, suggesting that metabolic syndrome could be conserved among hepaciviruses, and both mechanistic and interventional studies for treating HCV-induced metabolic complications could be evaluated in this animal model.

Duke Scholars

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2017

Volume

12

Issue

1

Start / End Page

e0170240

Location

United States

Related Subject Headings

  • Metabolic Diseases
  • Male
  • Liver
  • Lipid Metabolism
  • Insulin
  • Hepatitis C, Chronic
  • Glucagon-Like Peptide 1
  • Glucagon
  • General Science & Technology
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Manickam, C., Wachtman, L., Martinot, A. J., Giavedoni, L. D., & Reeves, R. K. (2017). Metabolic Dysregulation in Hepacivirus Infection of Common Marmosets (Callithrix jacchus). PLoS One, 12(1), e0170240. https://doi.org/10.1371/journal.pone.0170240
Manickam, Cordelia, Lynn Wachtman, Amanda J. Martinot, Luis D. Giavedoni, and R Keith Reeves. “Metabolic Dysregulation in Hepacivirus Infection of Common Marmosets (Callithrix jacchus).PLoS One 12, no. 1 (2017): e0170240. https://doi.org/10.1371/journal.pone.0170240.
Manickam C, Wachtman L, Martinot AJ, Giavedoni LD, Reeves RK. Metabolic Dysregulation in Hepacivirus Infection of Common Marmosets (Callithrix jacchus). PLoS One. 2017;12(1):e0170240.
Manickam, Cordelia, et al. “Metabolic Dysregulation in Hepacivirus Infection of Common Marmosets (Callithrix jacchus).PLoS One, vol. 12, no. 1, 2017, p. e0170240. Pubmed, doi:10.1371/journal.pone.0170240.
Manickam C, Wachtman L, Martinot AJ, Giavedoni LD, Reeves RK. Metabolic Dysregulation in Hepacivirus Infection of Common Marmosets (Callithrix jacchus). PLoS One. 2017;12(1):e0170240.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2017

Volume

12

Issue

1

Start / End Page

e0170240

Location

United States

Related Subject Headings

  • Metabolic Diseases
  • Male
  • Liver
  • Lipid Metabolism
  • Insulin
  • Hepatitis C, Chronic
  • Glucagon-Like Peptide 1
  • Glucagon
  • General Science & Technology
  • Female