2019
DOI: 10.1099/ijsem.0.003087
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Aestuariivirga litoralis gen. nov., sp. nov., a proteobacterium isolated from a water sample, and proposal of Aestuariivirgaceae fam. nov.

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Cited by 14 publications
(11 citation statements)
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“…We reinforce that 2.17 represents genomes with lower percentages of contamination. To complete these analyses, we also add 18 genomes [11,12,16,[18][19][20][21][22][23] deposited in public sequence repositories (Table 1), which were not explored deeply in the context of this investigation. Also according to MIMAG standards [14], these genomes were assigned with high-quality or medium-quality drafts (Table 1).…”
Section: Resultsmentioning
confidence: 99%
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“…We reinforce that 2.17 represents genomes with lower percentages of contamination. To complete these analyses, we also add 18 genomes [11,12,16,[18][19][20][21][22][23] deposited in public sequence repositories (Table 1), which were not explored deeply in the context of this investigation. Also according to MIMAG standards [14], these genomes were assigned with high-quality or medium-quality drafts (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…New taxa have been affiliated to the order Rhizobiales, which include the Aestuariivirgaceae (Rhizobiales) family proposed by [16] during the description and wholegenome-sequence of the Aestuariivirga litoralis species. This group was first described as part of an investigation to understand estuarine sediments' microbiome, highlighting significant phenotypic and genomic characterization findings.…”
Section: Introductionmentioning
confidence: 99%
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“…Water samples were collected from Pearl River Estuary (113 °39′36′′E, 22 °43′42′′N) at Guangzhou, in southern China. Isolation and purification of strain SYSU M00256-3 T were executed based on the method described by Li et al [5]. The strain was maintained on Marine Agar (MA) 2216E, and also preserved as cell suspensions in 20 % (v/v) glycerol at –80 °C.…”
Section: Full-textmentioning
confidence: 99%
“…Genomic DNA extraction and PCR amplification of the 16S rRNA gene from strain SYSU M00256-3 T were performed as described by Li et al [18]. Amplification of the 16S rRNA gene, purification, cloning, sequencing and assembly of the sequences were done as described by Li et al [5]. The assembled almost-complete 16S rRNA gene sequence was submitted to the EzBioCloud server database [19].…”
Section: Full-textmentioning
confidence: 99%