PLoS ONE (Jan 2016)

Comparative Analysis of Immune Repertoires between Bactrian Camel's Conventional and Heavy-Chain Antibodies.

  • Xinyang Li,
  • Xiaobo Duan,
  • Kai Yang,
  • Wei Zhang,
  • Changjiang Zhang,
  • Longfei Fu,
  • Zhe Ren,
  • Changxi Wang,
  • Jinghua Wu,
  • Ruxue Lu,
  • Yanrui Ye,
  • Mengying He,
  • Chao Nie,
  • Naibo Yang,
  • Jian Wang,
  • Huanming Yang,
  • Xiao Liu,
  • Wen Tan

DOI
https://doi.org/10.1371/journal.pone.0161801
Journal volume & issue
Vol. 11, no. 9
p. e0161801

Abstract

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Compared to classical antibodies, camel heavy chain antibodies (HCAbs) are smaller in size due to lack of the light chain and the first constant domain of the heavy chain (CH1 region). The variable regions of HCAbs (VHHs) are more soluble and stable than that of conventional antibodies (VHs). Even with such simple structure, they are still functional in antigen binding. Although HCAbs have been extensively investigated over the past two decades, most efforts have been based upon low throughput sequence analysis, and there are only limited reports trying to analyze and describe the complete immune repertoire (IR) of camel HCAbs. Here we leveraged the high-throughput data generated by Next Generation Sequencing (NGS) of the variable domains of the antibody heavy chains from three Bactrian camels to conduct in-depth comparative analyses of the immunoglobulin repertoire. These include analyses of the complementary determining region 3 (CDR3) length and distribution, mutation rate, antibody characteristic amino acids, the distribution of the cysteine (Cys) codons, and the non-classical VHHs. We found that there is higher diversity in the CDR2 than in the other sub-regions, and there is a higher mutation rate in the VHHs than in the VHs (P Arg AA substitution at the first position of framework 4 for all types of clones. We present, for the first time, a relatively complete picture of the Bactrian camel antibody immune repertoire, including conventional antibody (Ab) and HCAbs, using PCR and in silico analysis based on high-throughput NGS data.