Full annotation of serum virome in Chinese blood donors with elevated alanine aminotransferase levels.

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  • Author(s): Li G;Li G; Zhou Z; Zhou Z; Yao L; Yao L; Xu Y; Xu Y; Wang L; Wang L; Fan X; Fan X; Fan X
  • Source:
    Transfusion [Transfusion] 2019 Oct; Vol. 59 (10), pp. 3177-3185. Date of Electronic Publication: 2019 Aug 08.
  • Publication Type:
    Clinical Trial; Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-2995 (Electronic) Linking ISSN: 00411132 NLM ISO Abbreviation: Transfusion Subsets: MEDLINE
    • Publication Information:
      Original Publication: Arlington, Va. : American Association Of Blood Banks
    • Subject Terms:
    • Abstract:
      Background: A serum alanine aminotransferase (ALT) test is currently demanded for blood donation in China. One of the major reasons to include such a test is possible etiology of known or unknown hepatotropic viruses. However, this hypothesis has never been examined convincingly.
      Study Design and Methods: The study recruited 90 Chinese blood donors that were divided into three groups based on their ALT values. Serum virome from these donors was explored using a metagenomics approach with enhanced sensitivity resolved at single sequencing reads.
      Results: Anellovirus and pegivirus C (GBV-C) were detected among these donors. None of them were found solely in donors with abnormal liver enzyme. Anellovirus was highly prevalent (93.3%) and the co-infection with multiple genera (alpha, beta, and gammatorquevirus) were more common in the donors with normal ALT values in comparison to those with elevated ALT (single/double/triple Anellovirus genera, 1/3/24 vs. 7/7/14 or 6/7/13, p = 0.009). For unmapped reads that accounted for 15 ± 14.9% of the data, similarity-based (BLASTN, BLASTP, and HMMER3) and similarity-independent (k-mer frequency) analysis identified several circular rep encoding ssDNA (CRESS-DNA) genomes. Direct PCR testing indicated these genomes were likely reagent contaminants.
      Conclusion: Viral etiology is not responsible for elevated ALT levels in Chinese blood donors. The ALT test, if not abandoned, should be adjusted for its cutoff in response to donor shortage in China.
      (© 2019 AABB.)
    • References:
      Transfusion. 2016 Sep;56(9):2248-55. (PMID: 27306718)
      PLoS Pathog. 2017 Mar 22;13(3):e1006292. (PMID: 28328962)
      BMC Bioinformatics. 2010 Apr 13;11:187. (PMID: 20388221)
      Oncogene. 2006 Jun 26;25(27):3771-7. (PMID: 16799618)
      Biochem Biophys Res Commun. 2013 Jul 5;436(3):525-9. (PMID: 23764402)
      PLoS One. 2013 Apr 17;8(4):e60595. (PMID: 23613733)
      Blood Transfus. 2016 Sep;14(5):400-7. (PMID: 27136432)
      Semin Liver Dis. 1995 Feb;15(1):110-20. (PMID: 7597441)
      Nucleic Acids Res. 2007 Jan;35(Database issue):D61-5. (PMID: 17130148)
      Transfusion. 2015 Aug;55(8):1889-99. (PMID: 25721073)
      Nucleic Acids Res. 2017 Jan 4;45(D1):D491-D498. (PMID: 27789703)
      Annu Rev Virol. 2017 Sep 29;4(1):159-180. (PMID: 28715975)
      Genomics. 2017 Mar;109(2):83-90. (PMID: 28131802)
      Hepatology. 2018 Jan;67(1):328-357. (PMID: 28714183)
      Nucleic Acids Res. 1999 Jan 15;27(2):573-80. (PMID: 9862982)
      Nat Rev Microbiol. 2017 Mar;15(3):183-192. (PMID: 28090077)
      Nucleic Acids Res. 2009 Jan;37(Database issue):D448-54. (PMID: 18845571)
      J Infect Dis. 2018 Sep 8;218(8):1185-1187. (PMID: 30007368)
      Hepatology. 2008 Apr;47(4):1363-70. (PMID: 18366115)
      Nat Genet. 2011 Oct 16;43(11):1131-8. (PMID: 22001757)
      Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):10264-9. (PMID: 23716702)
      Nature. 2017 Oct 5;550(7674):61-66. (PMID: 28953883)
      J Clin Microbiol. 2000 May;38(5):1926-30. (PMID: 10790123)
      Clin Infect Dis. 2017 Oct 16;65(9):1477-1485. (PMID: 29020199)
      Biotechniques. 2017 Jul 1;63(1):21-27. (PMID: 28701144)
      Am J Gastroenterol. 1994 Oct;89(10):1836-9. (PMID: 7942678)
      Front Microbiol. 2017 Apr 04;8:566. (PMID: 28421059)
      Microbiome. 2017 Jul 6;5(1):69. (PMID: 28683828)
      Nat Methods. 2012 Mar 04;9(4):357-9. (PMID: 22388286)
      Arch Virol. 2015 Apr;160(4):893-908. (PMID: 25680568)
      PLoS One. 2014 Aug 20;9(8):e105067. (PMID: 25140992)
      Semin Liver Dis. 2008 May;28(2):142-52. (PMID: 18452114)
      BMC Bioinformatics. 2010 Aug 18;11:431. (PMID: 20718988)
      J Comput Biol. 2012 May;19(5):455-77. (PMID: 22506599)
      Emerg Infect Dis. 2016 Oct;22(10):1839-41. (PMID: 27648613)
      Nucleic Acids Res. 2016 Jan 4;44(D1):D279-85. (PMID: 26673716)
      Clin Microbiol Infect. 2017 Oct;23(10):688-690. (PMID: 28288831)
      J Virol. 2013 Nov;87(22):11966-77. (PMID: 24027301)
      Bioinformatics. 2011 Mar 15;27(6):863-4. (PMID: 21278185)
      Transfusion. 2017 Feb;57(2):273-279. (PMID: 28194856)
      Mol Biol Evol. 2016 Jul;33(7):1870-4. (PMID: 27004904)
      Nucleic Acids Res. 1994 Nov 11;22(22):4673-80. (PMID: 7984417)
      Transfus Med Rev. 2017 Apr;31(2):89-93. (PMID: 28012709)
      N Engl J Med. 1997 Mar 13;336(11):741-6. (PMID: 9052651)
    • Grant Information:
      R21 AI117128 United States AI NIAID NIH HHS; AI117128 United States NH NIH HHS
    • Accession Number:
      EC 2.6.1.2 (Alanine Transaminase)
    • Publication Date:
      Date Created: 20190809 Date Completed: 20200609 Latest Revision: 20221207
    • Publication Date:
      20231215
    • Accession Number:
      PMC6785372
    • Accession Number:
      10.1111/trf.15476
    • Accession Number:
      31393615