Affiliations 

  • 1 Institut de Génétique Moléculaire de Montpellier (IGMM), UMR5535 CNRS, 1919 route de Mende, 34293 Montpellier cedex 5, Université de Montpellier, Place Eugène Bataillon, 34095 Montpellier cedex 5, France. e-jeziorski@chu-montpellier.fr
  • 2 Laboratoire de virologie, Centre Hospitalier Régional Universitaire de Montpellier, 80 avenue A. Fliche, 34295 Montpellier cedex 5, France. v-foulongne@chu-montpellier.fr
  • 3 Hôpital Arnaud de Villeneuve, Service de Pédiatrie générale, infectiologie et immunologie clinique, Centre Hospitalier Régional Universitaire de Montpellier, 371, avenue du Doyen Gaston Giraud, 34295 Montpellier cedex 5, France. c-ludwig@chu-montpellier.fr
  • 4 Service de Chirurgie Orthopédique, Centre Hospitalier Régional Universitaire de Montpellier, 371 avenue du Doyen Gaston Giraud, 34295 Montpellier cedex 5, France. d-louahemm_sabah@chu-montpellier.fr
  • 5 Hôpital Arnaud de Villeneuve, Service de Pédiatrie générale, infectiologie et immunologie clinique, Centre Hospitalier Régional Universitaire de Montpellier, 371, avenue du Doyen Gaston Giraud, 34295 Montpellier cedex 5, France. m-rodiere@chu-montpellier.fr
  • 6 Institut de Génétique Moléculaire de Montpellier (IGMM), UMR5535 CNRS, 1919 route de Mende, 34293 Montpellier cedex 5, Université de Montpellier, Place Eugène Bataillon, 34095 Montpellier cedex 5, France. marc.sitbon@igmm.cnrs.fr
  • 7 Institut de Génétique Moléculaire de Montpellier (IGMM), UMR5535 CNRS, 1919 route de Mende, 34293 Montpellier cedex 5, Université de Montpellier, Place Eugène Bataillon, 34095 Montpellier cedex 5, France. valerie.courgnaud@igmm.cnrs.fr
Viruses, 2016 Mar;8(3):86.
PMID: 27102168 DOI: 10.3390/v8030086

Abstract

Mammalian retroviruses cause a variety of diseases in their hosts, including hematological and immunodeficiency disorders. Both human T-cell leukemia (HTLV) and human immunodeficiency (HIV) viruses originated from several independent zoonotic transmissions, indicating that cross-species transmissions from animal to humans may still occur. Thus, as the risk for retroviral transmissions from animals to humans increase, we investigated whether mammalian retroviruses are involved in selected pediatric idiopathic diseases whose symptoms evoke retroviral infections. Blood samples, sera, and synovial fluids, or bone marrow cells were collected from pediatric patients under 18 years of age with different autoimmune idiopathic diseases. Overall, we screened clinical samples from 110 children using sensitive nested and semi-nested PCR strategies targeting env genes, and a C-type retrovirus reverse transcriptase (RT) activity kit. All clinical samples were free of retroviral signatures, indicating the unlikelihood of an etiological role of the retroviruses we assessed in the pediatric diseases we tested.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.