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Updated: Jun 1, 2025

Identification of Rare Bacterial Pathogens by 16S rRNA Gene Sequencing and MALDI-TOF MS
Published on: July 11, 2016
Scrofimicrobium appendicitidis sp. nov., isolated from a patient with ruptured appendicitis
Hiu-Yin Lao1, Annette Y P Wong2, Timothy Ting-Leung Ng1
1Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong Special Administrative Region, Hong Kong, PR China.
Abstract:
A clinical isolate, R131, was isolated from the peritoneal swab of a patient who suffered from ruptured appendicitis with abscess and gangrene in Hong Kong in 2018. Cells are facultatively anaerobic, non-motile, Gram-positive coccobacilli. Colonies were small, grey, semi-translucent, low convex and alpha-haemolytic. The bacterium grew on blood agar but not on Brain Heart Infusion (BHI) and Mueller-Hinton agars. It was negative for catalase, oxidase, indole and aesculin hydrolysis. The initial identification attempts via matrix-assisted laser desorption ionization-time of flight mass spectrometry and 16S rRNA gene sequencing yielded inconclusive results. The 16S rRNA gene analysis showed that R131 shared >99% nucleotide identity with certain uncultured Actinomycetales bacteria. In this retrospective investigation, a complete genome of R131 was constructed, disclosing a DNA G+C content of 64%. Phylogenetic analysis showed that the bacterium was mostly related to Scrofimicrobium canadense WB03_NA08, which was first described in 2020. However, its 16S rRNA gene shared only 94.15% nucleotide identity with that of S. canadense WB03_NA08. Notably, the orthoANI between R131 and S. canadense WB03_NA08 was 67.81%. A pan-genome analysis encompassing R131 and 4 Scrofimicrobium genomes showed 986 core gene clusters shared with the Scrofimicrobium species, along with 601 cloud genes. The average nucleotide identity comparisons within the pan-genome analysis ranged from 59.78 to 62.51% between R131 and the other Scrofimicrobium species. Correspondingly, the dDDH values ranged from 19.20 to 22.30%, while the POCP values spanned from 57.48 to 60.94%. Therefore, a novel species, Scrofimicrobium appendicitidis sp. nov., is proposed. The type strain is R131T (=JCM 36615T=LMG 33627T).
Insights
A novel bacterial species, Scrofimicrobium appendicitidis, was identified from a clinical isolate (R131) causing appendicitis. Genomic and phylogenetic analyses confirmed its distinctness from known Scrofimicrobium species.
Area of Science:
- Microbiology
- Genomics
- Bacterial Taxonomy
Background:
- A clinical isolate, R131, was obtained from a patient with ruptured appendicitis, abscess, and gangrene in Hong Kong.
- Initial identification using MALDI-TOF MS and 16S rRNA gene sequencing was inconclusive, suggesting a potential novel bacterium.
Purpose of the Study:
- To fully characterize the clinical isolate R131 through whole-genome sequencing and comprehensive phylogenetic analysis.
- To determine the taxonomic status of isolate R131 and propose a new species if warranted.
Main Methods:
- Isolation and phenotypic characterization of the bacterial strain R131.
- Whole-genome sequencing and assembly of the R131 genome.
- Phylogenetic analysis using 16S rRNA gene sequences and whole-genome data (orthoANI, pan-genome analysis, dDDH, POCP).
Main Results:
- Isolate R131, a Gram-positive coccobacillus, exhibited specific growth characteristics and biochemical test results.
- Genome sequencing revealed a DNA G+C content of 64%.
- Phylogenetic analyses indicated that R131 is related to the genus Scrofimicrobium but distinct, with low average nucleotide identity (67.81%) and dDDH values (19.20–22.30%) compared to S. canadense.
Conclusions:
- The genomic and phylogenetic data strongly support the classification of R131 as a novel species within the genus Scrofimicrobium.
- The proposed novel species is named Scrofimicrobium appendicitidis sp. nov., with R131 as the type strain.
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