Comprehensive profiling of antibody responses to the human anellome using programmable phage display

Cell Rep. 2022 Dec 20;41(12):111754. doi: 10.1016/j.celrep.2022.111754.

Abstract

Anelloviruses represent a major constituent of the commensal human virome; however, little is known about their immunobiology. Here, we present "AnelloScan," a T7 phage library representing the open reading frame 1 (ORF1), ORF2, ORF3, and torque teno virus (TTV)-derived apoptosis-inducing protein (TAIP) sequences of more than 800 human anelloviruses and profile the antibody reactivities of serum samples from a cross-sectional cohort of 156 subjects by using phage-immunoprecipitation sequencing (PhIP-Seq). A majority of anellovirus peptides are not reactive in any of the subjects tested (n = ∼28,000; ∼85% of the library). Antibody-reactive peptides are largely restricted to the C-terminal region of the capsid protein ORF1. Moreover, using a longitudinal cohort of matched blood-transfusion donors and recipients, we find that most transmitted anelloviruses do not elicit a detectable antibody reactivity in the recipient and that the remainder elicit delayed responses appearing ∼100-150 days after transfusion.

Keywords: AnelloScan; CP: Microbiology; PhIP-seq; TTV; VirScan; anelloviridae; anellovirus; antibodies; torque teno virus; transfusion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anelloviridae*
  • Antibody Formation
  • Capsid Proteins / metabolism
  • Cross-Sectional Studies
  • Humans
  • Torque teno virus* / metabolism

Substances

  • Capsid Proteins