Simultaneous Detection of Beta and Gamma Human Herpesviruses by Multiplex qPCR Reveals Simple Infection and Coinfection Episodes Increasing Risk for Graft Rejection in Solid Organ Transplantation


Por: Sanchez-Ponce, Yessica, Varela-Fascinetto, Gustavo, Carlos Romo-Vazquez, Jose, Lopez-Martinez, Briceida, Luis Sanchez-Huerta, Jose, Parra-Ortega, Israel, Fuentes-Panana, Ezequiel M., Morales-Sanchez, Abigail

Publicada: 1 dic 2018
Resumen:
Herpesviruses are common components of the human microbiome that become clinically relevant when a competent immunosurveillance is compromised, such as in transplantation. Members of the beta and gamma subfamilies are associated with a wide diversity of pathologies, including end-organ disease and cancer. In this study, we developed a multiplex qPCR technique with high specificity, sensitivity, efficiency and predictability that allowed the simultaneous detection and quantification of beta and gamma human herpesviruses. The technique was tested in a cohort of 34 kidney- or liver-transplanted pediatric patients followed up for up to 12 months post-transplant. Viral load was determined in 495 leukocyte-plasma paired samples collected bi-weekly or monthly. Human herpesvirus (HHV) 7 was the herpesvirus most frequently found in positive samples (39%), followed by Epstein-Barr virus (EBV) (20%). Also, EBV and HHV7 were present in the majority of coinfection episodes (62%). The share of positive samples exclusively detected either in leukocytes or plasma was 85%, suggesting that these herpesviruses tended to take a latent or lytic path in an exclusive manner. Infection by human cytomegalovirus (HCMV) and HHV6, as well as coinfection by EBV/HHV7 and EBV/HHV6/HHV7, were associated with graft rejection (RR = 40.33 (p = 0.0013), 5.60 (p = 0.03), 5.60 (p = 0.03) and 17.64 (p = 0.0003), respectively). The routine monitoring of beta and gamma herpesviruses should be mandatory in transplant centers to implement preventive strategies.

Filiaciones:
Sanchez-Ponce, Yessica:
 Childrens Hosp Mexico Federico Gomez, Res Unit Virol & Canc, Mexico City 06720, DF, Mexico

 Univ Nacl Autonoma Mexico, Postgrad Program Biol Sci, Mexico City 04510, DF, Mexico

Varela-Fascinetto, Gustavo:
 Childrens Hosp Mexico Federico Gomez, Dept Transplantat, Mexico City 06720, DF, Mexico

Carlos Romo-Vazquez, Jose:
 Childrens Hosp Mexico Federico Gomez, Dept Nephrol, Mexico City 06720, DF, Mexico

Lopez-Martinez, Briceida:
 Childrens Hosp Mexico Federico Gomez, Subdirect Diagnost Auxiliary Serv, Mexico City 06720, DF, Mexico

Luis Sanchez-Huerta, Jose:
 Childrens Hosp Mexico Federico Gomez, Dept Clin Lab, Mexico City 06720, DF, Mexico

Parra-Ortega, Israel:
 Childrens Hosp Mexico Federico Gomez, Dept Clin Lab, Mexico City 06720, DF, Mexico

Fuentes-Panana, Ezequiel M.:
 Childrens Hosp Mexico Federico Gomez, Res Unit Virol & Canc, Mexico City 06720, DF, Mexico

Morales-Sanchez, Abigail:
 Childrens Hosp Mexico Federico Gomez, Res Unit Virol & Canc, Mexico City 06720, DF, Mexico
ISSN: 19994915
Editorial
MDPI AG, POSTFACH, CH-4005 BASEL, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 10 Número: 12
Páginas:
WOS Id: 000455313100069
ID de PubMed: 30572622

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