TY - JOUR
T1 - Expanding magnetic organelle biogenesis in the domain Bacteria
AU - Lin, Wei
AU - Zhang, Wensi
AU - Paterson, Greig A.
AU - Zhu, Qiyun
AU - Zhao, Xiang
AU - Knight, Rob
AU - Bazylinski, Dennis A.
AU - Roberts, Andrew P.
AU - Pan, Yongxin
N1 - Funding Information:
We thank Xianyu Huang from the State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (Wuhan), and Zhiqi Zhang from Shennongjia National Park Administration for their contributions to the collection of acidic peatland soil samples. We thank Li Liu, Jia Liu, Runjia Ji, Yan Chen, Yuan Fang, Jingqi Sun, Fuxian Wang, and Courtney L. Wagner for the assistance with fieldwork. We thank Patrick De Deckker for suggesting field sampling sites and David Gordon and Samantha Burn for granting access to laboratory and materials at the Australian National University that enabled MTB extraction after our Australian fieldwork.
Funding Information:
This work was supported by the Strategic Priority Research Program of Chinese Academy of Sciences (XDA17010501), the National Natural Science Foundation of China (NSFC) Grants 41621004 and 41822704, the Youth Innovation Promotion Association of the Chinese Academy of Sciences, the Natural Environment Research Council Independent Research Fellowship NE/P017266/1, and the Australian Research Council Grant DP140104544. Acknowledgments
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Background: The discovery of membrane-enclosed, metabolically functional organelles in Bacteria has transformed our understanding of the subcellular complexity of prokaryotic cells. Biomineralization of magnetic nanoparticles within magnetosomes by magnetotactic bacteria (MTB) is a fascinating example of prokaryotic organelles. Magnetosomes, as nano-sized magnetic sensors in MTB, facilitate cell navigation along the local geomagnetic field, a behaviour referred to as magnetotaxis or microbial magnetoreception. Recent discovery of novel MTB outside the traditionally recognized taxonomic lineages suggests that MTB diversity across the domain Bacteria are considerably underestimated, which limits understanding of the taxonomic distribution and evolutionary origin of magnetosome organelle biogenesis. Results: Here, we perform the most comprehensive metagenomic analysis available of MTB communities and reconstruct metagenome-assembled MTB genomes from diverse ecosystems. Discovery of MTB in acidic peatland soils suggests widespread MTB occurrence in waterlogged soils in addition to subaqueous sediments and water bodies. A total of 168 MTB draft genomes have been reconstructed, which represent nearly a 3-fold increase over the number currently available and more than double the known MTB species at the genome level. Phylogenomic analysis reveals that these genomes belong to 13 Bacterial phyla, six of which were previously not known to include MTB. These findings indicate a much wider taxonomic distribution of magnetosome organelle biogenesis across the domain Bacteria than previously thought. Comparative genome analysis reveals a vast diversity of magnetosome gene clusters involved in magnetosomal biogenesis in terms of gene content and synteny residing in distinct taxonomic lineages. Phylogenetic analyses of core magnetosome proteins in this largest available and taxonomically diverse dataset support an unexpectedly early evolutionary origin of magnetosome biomineralization, likely ancestral to the origin of the domain Bacteria. Conclusions: These findings expand the taxonomic and phylogenetic diversity of MTB across the domain Bacteria and shed new light on the origin and evolution of microbial magnetoreception. Potential biogenesis of the magnetosome organelle in the close descendants of the last bacterial common ancestor has important implications for our understanding of the evolutionary history of bacterial cellular complexity and emphasizes the biological significance of the magnetosome organelle. [MediaObject not available: see fulltext.]
AB - Background: The discovery of membrane-enclosed, metabolically functional organelles in Bacteria has transformed our understanding of the subcellular complexity of prokaryotic cells. Biomineralization of magnetic nanoparticles within magnetosomes by magnetotactic bacteria (MTB) is a fascinating example of prokaryotic organelles. Magnetosomes, as nano-sized magnetic sensors in MTB, facilitate cell navigation along the local geomagnetic field, a behaviour referred to as magnetotaxis or microbial magnetoreception. Recent discovery of novel MTB outside the traditionally recognized taxonomic lineages suggests that MTB diversity across the domain Bacteria are considerably underestimated, which limits understanding of the taxonomic distribution and evolutionary origin of magnetosome organelle biogenesis. Results: Here, we perform the most comprehensive metagenomic analysis available of MTB communities and reconstruct metagenome-assembled MTB genomes from diverse ecosystems. Discovery of MTB in acidic peatland soils suggests widespread MTB occurrence in waterlogged soils in addition to subaqueous sediments and water bodies. A total of 168 MTB draft genomes have been reconstructed, which represent nearly a 3-fold increase over the number currently available and more than double the known MTB species at the genome level. Phylogenomic analysis reveals that these genomes belong to 13 Bacterial phyla, six of which were previously not known to include MTB. These findings indicate a much wider taxonomic distribution of magnetosome organelle biogenesis across the domain Bacteria than previously thought. Comparative genome analysis reveals a vast diversity of magnetosome gene clusters involved in magnetosomal biogenesis in terms of gene content and synteny residing in distinct taxonomic lineages. Phylogenetic analyses of core magnetosome proteins in this largest available and taxonomically diverse dataset support an unexpectedly early evolutionary origin of magnetosome biomineralization, likely ancestral to the origin of the domain Bacteria. Conclusions: These findings expand the taxonomic and phylogenetic diversity of MTB across the domain Bacteria and shed new light on the origin and evolution of microbial magnetoreception. Potential biogenesis of the magnetosome organelle in the close descendants of the last bacterial common ancestor has important implications for our understanding of the evolutionary history of bacterial cellular complexity and emphasizes the biological significance of the magnetosome organelle. [MediaObject not available: see fulltext.]
KW - Last bacterial common ancestor
KW - Magnetosome
KW - Magnetotactic bacteria
KW - Magnetotaxis
KW - Prokaryotic organelle
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U2 - 10.1186/s40168-020-00931-9
DO - 10.1186/s40168-020-00931-9
M3 - Article
C2 - 33126926
AN - SCOPUS:85094659149
SN - 2049-2618
VL - 8
JO - Microbiome
JF - Microbiome
IS - 1
M1 - 152
ER -