2021
DOI: 10.1101/2021.11.05.467470
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ANI, Mash and Dashing equally differentiate between Klebsiella species

Abstract: Species of the genus Klebsiella are among the most important multidrug resistant human pathogens, though they have been isolated from a variety of environments. Given the need for quickly and accurately classifying newly sequenced Klebsiella genomes, we compared 982 Klebsiella genomes using different species-delimiting measures: Average Nucleotide Identity (ANI), which is becoming a standard for species delimitation, as well as Mash, Dashing, and DNA compositional signatures, which can be run in a fraction of … Show more

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Cited by 1 publication
(2 citation statements)
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“…The most abundant genes were related to carbohydrate transport and metabolism (Table S2). The 999 genomes of strains of members of the genus Bacteroides, registered in GenBank, were compared with that of strain CBA7301 T using the FastANI calculator in Genome Taxonomy Database (GTDB) [15]. The strains that showed average nucleotide identity (ANI) values of more than 90 % with CBA7301 T were as follows: Bacteroides acidifaciens (GCF_903181435.1) (91.5 %), uncultured Bacteroides sp.…”
Section: Genome Featuresmentioning
confidence: 99%
See 1 more Smart Citation
“…The most abundant genes were related to carbohydrate transport and metabolism (Table S2). The 999 genomes of strains of members of the genus Bacteroides, registered in GenBank, were compared with that of strain CBA7301 T using the FastANI calculator in Genome Taxonomy Database (GTDB) [15]. The strains that showed average nucleotide identity (ANI) values of more than 90 % with CBA7301 T were as follows: Bacteroides acidifaciens (GCF_903181435.1) (91.5 %), uncultured Bacteroides sp.…”
Section: Genome Featuresmentioning
confidence: 99%
“…The cells of CBA7301 T were Gram-stain-negative. Growth at different temperatures (10,15,20,25,30,35,40, 45 and 50 °C), pH levels (5.0, 6.0, 7.0, 8.0, 9.0 and 10.0) and NaCl concentrations (0, 0.5, 1.0, 2.0, 3.0, 4.0 and 5.0 %) on tryptic soy broth medium was determined in triplicate. pH of the culture media was adjusted using Na 2 HPO 4 /NaH 2 PO 4 (pH 5.0-7.0), Tris-HCl (pH 8.0-9.0) and Na 2 CO 3 /NaHCO 3 (pH 10.0) buffers.…”
Section: Physiology and Chemotaxonomymentioning
confidence: 99%