- Extended genome report
- Open Access
Complete genome sequence of the Robinia pseudoacacia L. symbiont Mesorhizobium amorphae CCNWGS0123
Standards in Genomic Sciencesvolume 13, Article number: 18 (2018)
Mesorhizobium amorphae CCNWGS0123 was isolated in 2006, from effective nodules of Robinia pseudoacacia L. grown in lead-zinc mine tailing site, in Gansu Province, China. M. amorphae CCNWGS0123 is an aerobic, Gram-negative, non-spore-forming rod strain. This paper characterized M. amorphae CCNWGS0123 and presents its complete genome sequence information and genome annotation. The 7,374,589 bp long genome which encodes 7136 protein-coding genes and 63 RNA coding genes, contains one chromosome and four plasmids. Moreover, a chromosome with no gaps was assembled.
Soil microorganism - rhizobia (root nodule bacteria) could establish a symbiotic relationship with Leguminosae plants, forming a special organ - root nodule, the bacteroid in the root nodules converts atmospheric N2 into ammonium [1, 2]. The ammonium could help the host plants in surviving in N-limited environmental conditions ; in turn, host plants could provide the rhizobia with carbon and energy source for their growth and functions . Establishment of this symbiosis requires successful infection in legume roots, and such infection is a multifaceted developmental process driven by the bacteria, but is ultimately under the control of the host . This mutualistic association is highly specific such that each rhizobial species/strain interacts only with a specific group of legumes, and vice versa ,this phenomenon is termed as symbiosis specificity. Rhizobium leguminosarum bv. trifolii WSM1325 could nodulate a diverse range of annual Trifolium (clover) species . Robinia pseudoacacia L. are nodulated by Mesorhizobium and Sinorhizobium species which shared similar nodulation genes .
Mesorhizobium amorphae CCNWGS0123 was isolated from the root nodules of R. pseudoacacia L. grown in lead-zinc mine tailing site in Gansu Province, China . The strain could promote the survival of its host plant in copper-, zinc- and chromium-contaminated environments . The heavy metal tolerance and resistance mechanism of this strain has been investigated in previously studies [9, 11, 12].
In Chen’s study, they found that M. amorphae CCNWGS0123 nodulate with R. pseudoacacia L. . The M. amorphae CCNWGS0123-R. pseudoacacia L. symbiosis system was selected to establish a rhizobium-legume symbiosis signal network. In order to provide some basis for the signal network establishment, the complete genome sequence and annotation of M. amorphae CCNWGS0123 genome were reported in this study.
Classification and features
M. amorphae CCNWGS0123 was isolated in 2006, from root nodules collected from R. pseudoacacia L. growing in lead-zinc mine tailing site in Gansu Province, China. M. amorphae CCNWGS0123 is a motile, non-spore forming, non-encapsulated, Gram-negative bacteria in the order Rhizobiales of the class Alphaproteobacteria . The rod-shaped bacterium is 0.41–0.65 μm wide and 0.47–1.68 μm long (Fig. 1a). M. amorphae CCNWGS0123 is nearly morphologically similar to M. amorphae ACCC 19665T (Fig. 1b). Colonies on solid media are circular, and translucent with a diameter of 1 mm growing for 7 days at 28 °C, the generation times range from 6 h to 13 h in YM broth as described by Wang in 1999 .
M. amorphae CCNWGS0123 genome contains two (100% identical) copies of 16S rRNA gene. The phylogenetic neighborhood of M. amorphae strain CCNWGS0123 in a 16S rRNA gene sequence-based tree is shown in Fig. 2. Phylogenetic analyses were performed using MEGA version 6 . The evolutionary history was inferred using the Maximum Likelihood method based on the Tamura-Nei model ; the percentage of replicate trees to which the associated taxa were clustered in the bootstrap test (500 replicates) are shown next to the branches . M. amorphae CCNWGS0123 is phylogenetically closely related to the type strain- M. amorphae ACCC 19665T, with a 16S rRNA gene sequence identity of 99.93% (1471/1472 bp).
The minimum information about the genome sequence (MIGS) is provided in Table 1.
For a detailed biochemical characterization of M. amorphae CCNWGS0123, the strain was cultivated for 5 days in 30 ml of Tryptone-Yeast (TY) liquid medium at 28 °C under 200 rpm, and then harvested by centrifugation at 4000 rpm for 5 min. The harvested cells were washed three times by inoculation buffer, resuspended, and diluted in inoculation buffer to reach an optical density of OD600nm = 0.5. The suspension was used for inoculation of Biolog GN2, and GENIII plates (Biolog Inc., USA), and then the plates were incubated for several days at 28 °C. Microtiter plate reader (Bio-Rad, USA) was used for data analysis.
Analyses of the GN2 plates revealed that M. amorphae CCNWGS0123 could utilize the following substrates: β-Methyl-D-glucoside, D-galacturonic acid γ- lactone, D-xylose/aldopentose, D-galacturonic acid, I-erythritol, 2-hydroxybenzoic acid, 4-hydroxybenzoic acid, α- cyclodextrin, itaconic acid and D-malic acid. In GENIII plates, the following substrates were utilized: D-maltose, D-trehalose, D-cellobiose, gentiobiose, sucrose, D-turanose, D-raffinose, α-D-lactose, D-melibiose, β-methyl-D-glucoside, D-salicin, N-acetyl-D-glucosamine, N-acetyl-β-D-mannosamine, N-acetyl-D-galactosamine, α-D-glucose, D-mannose, D-fructose, D-galactose, D-fucose, L-fucose, L-rhamnose, D-sorbitol, D-mannitol, D-arabitol, myo-inositol, lycerol, glycyl-L-proline, L-alanine, L-arginine, L-glutamic acid, L-histidine, quinic acid, L-serine, methyl pyruvate, L-lactic acid, D-malic acid and γ-amino-butryric acid.
Compared with the previously described M. amorphae type strain- ACCC 19665T, M. amorphae CCNWGS0123 could not utilize L- phenylalanine, γ- hydroxybutyrate, L-threonine, glycogen, D- glucose histidine, Α-D-lactose, inosine, L-aspartic acid, mucic acid, L-malic acid, bromo-succinic acid in GN2 and GENIII plates.
Resilience to abiotic factors and antibiotic resistance
M. amorphae CCNWGS0123 could grow on Biolog GenIII plates at an optical density similar to that in positive control at pH 5, pH 6, 1% NaCl, and 1% sodium lactate, and to a lower optical density in lincomycin and nalidixic Acid. This strain could not grow at 4% NaCl or 8% NaCl. Moreover, the growth was inhibited by fusidic acid, D-serine, troleandomycin, rifamycin SV, minocycline, guanidine HCl, Niaproof 4, vancomycin, tetrazolium violet, tetrazolium blue, lithium chloride, potassium tellurite, aztreonam, sodium butyrate and sodium bromate.
As shown in Additional file 1: Table S1, according to nodulation test, M. amorphae CCNWGS0123 is an effective microsymbiont only for woody legumes (R. pseudoacacia L. and A. fruticose). But the strain could not nodulate with other genera of legume plants, such as Medicago sativa .
Genome sequencing information
Genome project history
Because of its ability of heavy metal resistance and establishing symbiosis with R. pseudoacacia L., M. amorphae CCNWGS0123 was selected for sequencing. Its draft genome sequence was obtained in 2012 using 454 pyrophosphate sequencing technology . To close the gap and correct some mistakes in annotation, the complete genome sequence of M. amorphae CCNWGS0123 was obtained in 2015 by using Single Molecule Real-Time (SMRT) technology. Sequencing was performed at Beijing Novogene Bioinformatics Technology Co., Ltd. The final genome assembly of M. amorphae CCNWGS0123 is of high quality and completed on five scaffolds (one chromosome and four plasmids) with a sequencing coverage of approximately 134.86 fold. The complete genome sequence of M. amorphae CCNWGS0123 was deposited in GenBank (accession numbers CP015318 - CP015322). The project information was summarized in Table 2.
Growth conditions and genomic DNA preparation
M. amorphae CCNWGS0123 was cultured in TY extract medium and allowed to grow from a single colony at 28 °C in flask agitated under 200 rpm as described previously . Cells were harvested by centrifugation at 5000 rpm, and total DNA was prepared using a TaKaRa MiniBest Bacterial Genomic DNA Extraction Kit Ver. 3.0 (Dalian, China). Thermo Scientific NanoDrop 2000 was used to quantify the DNA in order to ensure that the quality is suitable for sequencing analyses.
Genome sequencing and assembly
The genome of M. amorphae CCNWGS0123 was sequenced using SMRT technology at the Beijing Novogene Bioinformatics Technology Co., Ltd. A 10 kb library was constructed; SMRT Analysis 2.3.0 was used to filter the low-quality reads; and then the filtered reads were assembled to generate scaffold without gaps. The total genome sequence was 7,343,952 bp long, consisting of one chromosome and four plasmids, and with an average coverage of 134.86 fold. The overview of the genome information is shown in Table 3.
Gene prediction was performed by using GeneMarkS (http://topaz.gatech.edu/) with integrated model that combine the GeneMarkS generated (native) and Heuristic model parameters . A whole genome Blast search  (E-value is less than 1e-5; minimal alignment length percentage is larger than 40%) was performed against six databases, namely, Kyoto Encyclopedia of Genes and Genomes [21,22,23], Clusters of Orthologous Groups [24, 25], Non-Redundant Protein Database databases (NR), SwissProt  and Gene Ontology  and TrEMBL . Transfer RNA (tRNA) genes were predicted using tRNAscan-SE ; rRNA genes were predicted using rRNAmmer , and small RNA (sRNA) were predicted by BLAST against Rfam  database. PHAST  was used for prophage prediction (http://phast.wishartlab.com/) and CRISPR Finder  was used for CRISPR identification.
M. amorphae CCNWGS0123 genome was consisted of one 6,268,270 bp circular chromosome, one 948,568 bp circular symbiotic plasmid (pM0123d), and three non-circular plasmids (pM0123a-c), whose length ranged from 7607 bp to 102,093 bp (Table 3, Fig. 3). As shown in Table 3, the genome had an average G + C content of 62.87%. The number of predicted genes is 7136. The chromosome contained 53 tRNAs, 4 sRNAs, two copies of 5S, 16S, and 23S rRNA genes. A total of 4758 (66.68%) protein-coding genes were annotated by COG database. The COG assignment of the functional genes is summarized in Table 4. The genome contained highest number of functional genes participating in amino acid transport and metabolism (765), followed by general function prediction only (734). The gene assignments in the six databases are summarized in Table 5. Ten incomplete prophases were identified in chromosome, and two intact prophases were identified in pM0123d. Only four CRISPRs were identified throughout the genome.
Extended insights from the genome sequence
Genomic comparison between M. amorphae CCNWGS0123 and other Mesorhizobium species
The genome of M. amorphae CCNWGS0123 was compared with those of four Mesorhizobium strains, including M. huakuii 7653R, M. loti MAFF303099, M. ciceri WSM1271 and M. opportunistum WSM2075. The general features of the five Mesorhizobium genomes were summarized in Table 6. Totally, 6918 orthologous groups of genes were identified in the five Mesorhizobium strains. Among these groups, 1024 groups were conserved among the five genomes, and these orthologous groups were termed as the core genome of the five Mesorhizobium genomes (Fig. 4). Additionally, 2159 orthologous groups were present in four of the five genomes; 1912 orthologous groups were found in three genomes; and the remaining 1833 orthologous groups are present in two genomes. M. amorphae CCNWGS0123 had 1147 strain specific genes, occupied 16.07% of the total coding genes.
A total of 3700 genes could find their corresponding genes in the KEGG database; these genes participate in 132 KEGG metabolism pathways (Additional file 2: Table S2), including amino acid metabolism, carbohydrate metabolism, and nucleotide metabolism pathways. A specific metabolism pathway, namely, Nitrogen metabolism was observed in M. amorphae CCNWGS0123 (Fig. 5), 48 genes participate in nitrogen biosynthesis and degradation (Additional file 3: Table S3). Three genes, nifK, nifD and nifH participate in biosynthesis of the key enzyme- nitrogenase.
Nitrogen fixation genes
Nitrogen fixation related genes homologous to N2 fixation genes in Klebsiella pneumoniae [33, 34] are referred to as nif genes; the other genes which are also essential in symbiotic N2 fixation but sharing no homology to K. pneumoniae are called fix genes . A total of 29 nif/fix genes were found in M. amorphae CCNWGS0123 genome (Additional file 4: Table S4), and most of these genes display a relatively high similarity with those of other Mesorhizobium species based on amino acid sequences, except for NifV (< 35%).
Rhizobia could establish symbiotic interactions with many legume species, and convert atmospheric N2 into ammonium. In rhizobial strains, two cluster genes, namely, nodulation and nitrogen fixation genes, play crucial roles in these processes [2, 36]. Nodulation factors (NFs), as key signals in rhizobia, are encoded by three groups of nodulation genes. The first group contained common nod genes, whose products are required in the backbone of NF structrures (nodABC); these genes are present in nearly all of rhizobia strains. The second group included the host-specific nod genes participating in species-specific modifications of the NF core (nodEF, nodG, nodH, nodPQ and nodRL). The third group included the regulatory genes (nodD, nolR and nodVW) [37, 38].
As shown in Additional file 5: Table S5, M. amorphae CCNWGS0123 genome contained 12 nodulation genes. Compared with the other four Mesorhizobium strains, M. amorphae CCNWGS0123 contained the lowest number of nodulation genes. Moreover, most of the proteins encoded by these genes displayed low sequence similarities with the corresponding proteins in other Mesorhizobium strains based on amino acid sequences, with exceptions of NodF (> 95%) and NodN (> 97%).
Genes related to heavy metal resistance
M. amorphae CCNWGS0123 was isolated from R. pseudoacacia L. nodules who grown in lead-zinc mine tailing site, the strain could help its host plant to survive in copper-, zinc-, and chromium-contaminated environments [9, 10]. The strain possesses multiple heavy metal tolerance and equilibrium ability . Compared with other Mesorhizobium strains, M. amorphae CCNWGS0123 contained more genes participating in heavy metal resistance and transport. As shown in Additional file 6: Table S6, a total of 46 genes participating in heavy mental (Ag, As, Cd, Co, Cu, Hg, Mo or Zn) resistance and transport were identified in M. amorphae CCNWGS0123 genome. Genes participating in heavy mental resistance and transport were also identified in other Mesorhizobium genomes, 32 genes were identified in M. huakuii 7653R genome, 35 genes were identified in M. loti MAFF303099 genome, 28 genes were identified in M. ciceri WSM1271 genome and 26 genes were identified in M. opportunistum WSM2075 genome.
Compared with the other four strains, M. amorphae CCNWGS0123 contained 10 specific genes involved in heavy mental As (mea0123GM001797, mea0123GM002757, mea0123GM004652 and mea0123GM006759), Cd/Zn/Co (mea0123GM001790 and mea0123GM004338), Cu (mea0123GM001765, mea0123GM006395, mea0123GM006849) and Cu/Ag (mea0123GM001789) resistance and transport and one CadZ encoding gene (mea0123GM000975). These genes may play important roles in helping survival in heavy mental-contaminated soil.
The previous study presents the complete genome sequence of M. amorphae CCNWGS0123 which was isolated from R. pseudoacacia L. grown in lead-zinc mine tailing site. A total of 46 genes involved in heavy metal tolerance were identified in the whole genome sequence. As predicted by Wang , M. amorphae strains harbor one 0.9 Mb symbiotic plasmid. M. amorphae CCNWGS0123 genome contains a circular symbiotic plasmid with 0.95 Mb. Symbiosis related genes (nodulation and nitrogen fixation genes) were found in the symbiotic plasmid (pM0123d). Compared with other Mesorhizobium stains, M. amorphae CCNWGS0123 contained different number and genetic constitution of symbiosis genes. The complete genome sequence of M. amorphae CCNWGS0123 will provide some bases in studying the heavy metal tolerance mechanism and signal regulation during symbiosis process.
Clusters of Orthologous Groups
Kyoto Encyclopedia of Genes and Genomes
Non-Redundant Protein Database databases
scanning electron microscope
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We would like to thank Gehong Wei and Minxia Chou from Northwest A&F University, China for their kindly help. This work was funded by the National key Research and Development Program (2016YFD0200308) and the National Natural Science Foundation of China (41671261).
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Table S3. Genes participating in nitrogen synthesis and degradation. (DOCX 18 kb)
Table S6. Genes involved in heavy metal resistant and homeostasis throughout the whole genome. (XLSX 13 kb)