Host-Associated Phages Disperse across the Extraterrestrial Analogue Antarctica

被引:5
作者
Rahlff, Janina [1 ,5 ]
Bornemann, Till L., V [1 ]
Lopatina, Anna [2 ]
Severinov, Konstantin [3 ]
Probst, Alexander J. [1 ,4 ]
机构
[1] Univ Duisburg Essen, Dept Chem Environm Microbiol & Biotechnol, Grp Aquat Microbial Ecol, Essen, Germany
[2] Natl Res Ctr Kurchatov Inst, Inst Mol Genet, Moscow, Russia
[3] Skolkovo Inst Sci & Technol, Moscow, Russia
[4] Univ Duisburg Essen, Ctr Water & Environm Res, Essen, Germany
[5] Linnaeus Univ, Ctr Ecol & Evolut Microbial Model Syst, Dept Biol & Environm Sci, EEMiS, SE-39182 Kalmar, Sweden
关键词
viruses; extreme environments; astrovirology; metagenomics; cryosphere; Ralstonia; RALSTONIA-SOLANACEARUM; MICROBIAL CHARACTERIZATION; FILAMENTOUS BACTERIOPHAGE; COMMUNITY COMPOSITION; BACTERIAL POPULATION; VIRUSES; ALIGNMENT; GENOMES; ARCHAEA; RADIATION;
D O I
10.1128/aem.00315-22
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Extreme Antarctic conditions provide one of the closest analogues of extraterrestrial environments. Since air and snow samples, especially from polar regions, yield DNA amounts in the lower picogram range, binning of prokaryotic genomes is challenging and renders studying the dispersal of biological entities across these environments difficult. Here, we hypothesized that dispersal of host-associated bacteriophages (adsorbed, replicating, or prophages) across the Antarctic continent can be tracked via their genetic signatures, aiding our understanding of virus and host dispersal across long distances. Phage genome fragments (PGFs) reconstructed from surface snow metagenomes of three Antarctic stations were assigned to four host genomes, mainly Betaproteobacteria, including Ralstonia spp. We reconstructed the complete genome of a temperate phage with nearly complete alignment to a prophage in the reference genome of Ralstonia pickettii 12D. PGFs from different stations were related to each other at the genus level and matched similar hosts. Metagenomic read mapping and nucleotide polymorphism analysis revealed a wide dispersal of highly identical PGFs, 13 of which were detected in seawater from the Western Antarctic Peninsula at a distance of 5,338 km from the snow sampling stations. Our results suggest that host-associated phages, especially of Ralstonia sp., disperse over long distances despite the harsh conditions of the Antarctic continent. Given that 14 phages associated with two R. pickettii draft genomes isolated from space equipment were identified, we conclude that Ralstonia phages are ideal mobile genetic elements to track dispersal and contamination in ecosystems relevant for astrobiology. IMPORTANCE Host-associated phages of the bacterium Ralstonia identified in snow samples can be used to track microbial dispersal over thousands of kilometers across the Antarctic continent, which functions as an extraterrestrial analogue because of its harsh environmental conditions. Due to the presence of these bacteria carrying genome-integrated prophages on space-related equipment and the potential for dispersal of host-associated phages demonstrated here, our work has implications for planetary protection, a discipline in astrobiology interested in preventing contamination of celestial bodies with alien biomolecules or forms of life. Host-associated phages of the bacterium Ralstonia identified in snow samples can be used to track microbial dispersal over thousands of kilometers across the Antarctic continent, which functions as an extraterrestrial analogue because of its harsh environmental conditions. Due to the presence of these bacteria carrying genome-integrated prophages on space-related equipment and the potential for dispersal of host-associated phages demonstrated here, our work has implications for planetary protection, a discipline in astrobiology interested in preventing contamination of celestial bodies with alien biomolecules or forms of life.
引用
收藏
页数:15
相关论文
共 123 条
[1]   ExoMars 2016 Schiaparelli Module Trajectory and Atmospheric Profiles Reconstruction [J].
Aboudan, A. ;
Colombatti, G. ;
Bettanini, C. ;
Ferri, F. ;
Lewis, S. ;
Van Hove, B. ;
Karatekin, O. ;
Debei, S. .
SPACE SCIENCE REVIEWS, 2018, 214 (05)
[2]   Alignment-free d2* oligonucleotide frequency dissimilarity measure improves prediction of hosts from metagenomically-derived viral sequences [J].
Ahlgren, Nathan A. ;
Ren, Jie ;
Lu, Yang Young ;
Fuhrman, Jed A. ;
Sun, Fengzhu .
NUCLEIC ACIDS RESEARCH, 2017, 45 (01) :39-53
[3]   Molecular and biological characterization of φRs551, a filamentous bacteriophage isolated from a race 3 biovar 2 strain of Ralstonia solanacearum [J].
Ahmad, Abdelmonim Ali ;
Stulberg, Michael J. ;
Mershon, John Patrick ;
Mollov, Dimitre S. ;
Huang, Qi .
PLOS ONE, 2017, 12 (09)
[4]   The sea surface microlayer as a source of viral and bacterial enrichment in marine aerosols [J].
Aller, JY ;
Kuznetsova, MR ;
Jahns, CJ ;
Kemp, PF .
JOURNAL OF AEROSOL SCIENCE, 2005, 36 (5-6) :801-812
[5]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[6]  
Amato P., 2012, Microbe, V7, P119, DOI [DOI 10.1128/MICROBE.7.119.1, DOI 10.1128/MICR0BE.7.119.1]
[7]   METAVIRALSPADES: assembly of viruses from metagenomic data [J].
Antipov, Dmitry ;
Raiko, Mikhail ;
Lapidus, Alla ;
Pevzner, Pavel A. .
BIOINFORMATICS, 2020, 36 (14) :4126-4129
[8]   Microbial preference for different size classes of organic carbon: a study from Antarctic snow [J].
Antony, Runa ;
Mahalinganathan, K. ;
Krishnan, K. P. ;
Thamban, Meloth .
ENVIRONMENTAL MONITORING AND ASSESSMENT, 2012, 184 (10) :5929-5943
[9]   Host recognition and integration of filamentous phage φRSM in the phytopathogen, Ralstonia solanacearum [J].
Askora, Ahmed ;
Kawasaki, Takeru ;
Usami, Shoji ;
Fujie, Makoto ;
Yamada, Takashi .
VIROLOGY, 2009, 384 (01) :69-76
[10]   Two different evolutionary lines of filamentous phages in Ralstonia solanacearum: their effects on bacterial virulence [J].
Askora, Ahmed ;
Yamada, Takashi .
FRONTIERS IN GENETICS, 2015, 6