iTRAQ-based proteomic analysis of Deinococcus radiodurans in response to 12 C 6+ heavy ion irradiation

• Published in: BMC microbiology 2022-11, Vol.22 (1), p.264
• Main Authors: Gao, Yuan, Li, Naikang, Zhou, Yanxia, Zhang, Zhenpeng, Zhang, Yao, Fan, Pengcheng, Zhou, Hangfan, Zhang, Tao, Chang, Lei, Gao, Huiying, Li, Yanchang, Kang, Xianjiang, Xie, Qiong, Lyu, Zhitang, Xu, Ping
• Format: Article
• Language: English
• Subjects: Antioxidants - metabolism; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Deinococcus - genetics; Deinococcus - metabolism; Deinococcus - radiation effects; Escherichia coli - genetics; Heavy Ions; Proteome - metabolism; Proteomics
• ISSN: 1471-2180
• DOI: 10.1186/s12866-022-02676-x

Deinococcus radiodurans (D. radiodurans) is best known for its extreme resistance to diverse environmental stress factors, including ionizing radiation (IR), ultraviolet (UV) irradiation, oxidative stress, and high temperatures. Robust DNA repair system and antioxidant system have been demonstrated to contribute to extreme resistance in D. radiodurans. However, practically all studies on the mechanism underlying D. radiodurans's extraordinary resistance relied on the treated strain during the post-treatment recovery lag phase to identify the key elements involved. The direct gene or protein changes of D. radiodurans after stress have not yet been characterized. In this study, we performed a proteomics profiling on D. radiodurans right after the heavy ion irradiation treatment, to discover the altered proteins that were quickly responsive to IR in D. radiodurans. Our study found that D. radiodurans shown exceptional resistance to C heavy ion irradiation, in contrast to Escherichia coli (E.coli) strains. By using iTRAQ (Isobaric Tags for Relative and Absolute Quantitation)-based quantitative mass spectrometry analysis, the kinetics of proteome changes induced by various dosages of C heavy ion irradiation were mapped. The results revealed that 452 proteins were differentially expressed under heavy ion irradiation, with the majority of proteins being upregulated, indicating the upregulation of functional categories of translation, TCA cycle (Tricarboxylic Acid cycle), and antioxidation regulation under heavy ion irradiation. This study shows how D. radiodurans reacts to exposure to C heavy ion irradiation in terms of its overall protein expression profile. Most importantly, comparing the proteome profiling of D. radiodurans directly after heavy ion irradiation with research on the post-irradiation recovery phase would potentially provide a better understanding of mechanisms underlying the extreme radioresistance in D. radiodurans.