AI Article Synopsis

  • A new gram-negative microaerophilic bacterial strain, PAGU2000, was isolated from a patient with fever in Japan and identified using a detailed taxonomic analysis.
  • Genetic analysis revealed that PAGU2000 is closely related to Helicobacter valdiviensis, sharing 97.5% of the 16S rRNA gene sequence, but with a lower-than-expected nucleotide identity for species classification.
  • The study proposes that PAGU2000 is a novel species within the Helicobacter genus, named Helicobacter higonensis, and provides insights into its unique characteristics and biochemical traits.

Article Abstract

We have previously isolated a gram-negative microaerophilic strain, PAGU2000 from a patient presenting with a fever in Kumamoto Prefecture, Japan. The present study aimed to comprehensively analyze the taxonomy of the isolated strain using a polyphasic approach. The 16S rRNA gene sequence analysis indicated that the strain was a member of enterohepatic Helicobacter. The strain PAGU2000 shared a 97.5% 16S rRNA gene nucleotide identity with Helicobacter valdiviensis, and this taxonomic position was confirmed by phylogenetic analysis of the GyrA amino acid sequences. The proposed strain PAGU2000 has a 1.482 Mbp chromosome with a DNA G + C content of 31.3 mol% and encodes 1520 predicted coding sequences. The average nucleotide identity between the strain PAGU2000 and type strain of H. valdiviensis was 70.3%, which was lower than the recommended threshold of 95% for species delineation. The strain PAGU2000 was a motile, non-spore-forming, and spiral-shaped bacterium, exhibiting catalase and oxidase activities but not urease and nitrate reduction. This study demonstrates that the isolate represents a novel species within enterohepatic Helicobacter, for which the name Helicobacter higonensis is proposed (type strain: PAGU2000 = GTC 16811 = LMG 33095). In this study, we describe the phenotypic and morphological features of this strain and propose an emended description of some biochemical traits of H. valdiviensis.

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Source
http://dx.doi.org/10.1111/1348-0421.13127DOI Listing

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