Metagenomic analysis of potential pathogens from blood donors in Guangzhou, China

Transfus Med. 2020 Feb;30(1):61-69. doi: 10.1111/tme.12657. Epub 2019 Dec 17.

Abstract

Objectives: This study aimed to identify the emerging/reemerging pathogens in blood donation samples.

Background: A metagenomic analysis has previously been used to look for pathogens but in this study, the relationship with aminotransferase (ALT) is described.

Methods/materials: Excluding samples reactive to hepatitis B virus, hepatitis C virus, human immunodeficiency syndrome virus or syphilis and plasma samples were stratified into three groups of ALT levels (IU/L): A ≤ 50, B 51 to 69 and C ≥ 70, respectively. Each group was mixed in a pool of 100 samples, from which DNA and cDNA libraries were established for next generation sequencing and analysis. Pathogens of interest were identified by immunoassays, nested-polymerase chain reaction, phylogenetic analysis and pathogen detection in follow-up donors.

Results: Several new or reemerging transfusion-transmitted pathogens were identified; Streptococcus suis, Babesia species and Toxoplasma gondii were found in the three ALT groups, Epstein-Barr virus (EBV) only in group C. Ten S. suis nucleic acid positive samples were detected, all closely phylogenetically related to reference strains. A donor in group A carried both S. suis genome and specific IgM in follow-up samples. This strain was identified as nontoxic S. suis. Five samples contained a short fragment of Babesia species SpeI-AvaI gene, while T. gondii was identified in 20 samples as a short fragment of 18S rDNA gene. In group C, two samples contained EBV genome.

Conclusions: Blood donations that contained S. suis, Babesia species and T. gondii sequences might represent potential transfusion risks. EBV, a potential cause of elevated ALT, was detected. Metagenomic analysis might be a useful technology for monitoring blood safety.

Keywords: ALT; blood donor; blood safety; metagenomics; pathogens.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Babesia / genetics*
  • Blood Donors*
  • Blood-Borne Pathogens*
  • Donor Selection
  • Female
  • Humans
  • Male
  • Metagenome*
  • Metagenomics*
  • Middle Aged
  • Streptococcus suis / genetics*
  • Toxoplasma / genetics*
  • Viruses / genetics*