ABSTRACT
We report the draft genome sequence of Enterobacter hormaechei strain F10K, a multidrug-resistant bacterium isolated from the feces of a captive common peafowl. The assembled genome is approximately 4.63 Mbp in size, with a guanine–cytosine (GC) content of 55.5% and an estimated completeness of 99.27%.
KEYWORDS: draft genome, E. hormaechei, multidrug resistance, virulence factors, peafowl
ANNOUNCEMENT
Enterobacter hormaechei, a gram-negative bacterium of the Enterobacter cloacae complex (ECC) (1). It is an opportunistic pathogen that affects immunocompromised hosts (2, 3). Although uncommon in animals (4), E. hormaechei has recently been identified as a multidrug-resistant ECC species causing various infections in pigs, cattle, sheep, and fox (5–9).
Freshly voided fecal samples were aseptically collected from a 2-year-old common peafowl diagnosed to show respiratory distress with open-mouth breathing and whitish diarrhea before death. The bird was housed at the Wildlife Reproduction and Conservation Field Laboratory, Gazipur Agricultural University (24.09° N, 90.41° E), Bangladesh. Samples were collected using sterile stool tubes, kept at 4°C in an icebox, and transported to the lab for processing within 24 h. Feces samples were diluted with sterile distilled water, vortexed, and preserved for further analysis. For E. hormaechei isolation, samples were enriched overnight in nutrient broth (Oxoid, UK) at 37°C under aerobic conditions, serially diluted (10⁻³), and streaked onto MacConkey agar (Oxoid). After 24 h of incubation, distinct colonies were subcultured to obtain pure isolates. The bacterium was identified as E. hormaechei based on colony morphology, Gram staining (gram-negative rods, pink colonies), and biochemical tests, including the Methyl Red-Voges-Proskauer (MR-VP) test (10, 11). Species-level identification of E. hormaechei was confirmed using the VITEK-2 system v.9.01 (12). The F10K isolate showed resistance to ampicillin, aztreonam, cefoxitin, chloramphenicol, ciprofloxacin, nalidixic acid, nitrofurantoin, oxacillin, and tetracycline, as determined by Kirby-Bauer disk diffusion following Clinical and Laboratory Standards Institute M100 (2023) guidelines (13). For DNA extraction, strain F10K was grown in nutrient broth at 37°C for 18–24 h under aerobic conditions. Genomic DNA was extracted with the QIAamp DNA Mini Kit (QIAGEN, Germany) and quantified using NanoDrop 2000 (Thermo Fisher, USA) (14, 15). Whole genome sequencing libraries were constructed from 1 ng of DNA using the Nextera DNA Flex Kit (Illumina, USA) following the manufacturer’s instructions. The process involved enzymatic fragmentation and size selection, and sequencing was performed on an Illumina MiSeq platform using a 2 × 250 bp paired-end protocol. Raw reads (n = 4,244,402) were trimmed with Trimmomatic v.0.39 (16) and assessed with FastQC v.0.12.1 (17).
Genome assembly was performed with SPAdes v.4.2.0 (18) and annotated using the National Center for Biotechnology Information Prokaryotic Genome Annotation Pipeline v.6.10 (19). Genome completeness, virulence factor genes (VFGs), antibiotic resistance genes (ARGs), metabolic pathways, and pathogenic potential were evaluated using CheckM v.1.2.3 (20), VFDB v.6.0 (21), ResFinder 4.0 (22), RAST server (23), and PathogenFinder2 v.0.5.0 (24), respectively, with default parameters for all software unless otherwise specified.
The key genomic features of E. hormaechei F10K are shown in Table 1. We identified 22 ARGs, 21 VFGs, and 372 functional subsystems. The strain was associated with 105 pathogenic families by yielding a pathogenicity score of 0.966. These findings highlight E. hormaechei F10K as a potential pathogen associated with respiratory illness and enteritis in peafowls, emphasizing its relevance for veterinary and public health research.
TABLE 1.
Genomic features of the E. hormaechei F10K isolated from the feces of a captive common peafowl with respiratory illness and enteritisa
| Genomic features | E. hormaechei strain F10K |
|---|---|
| Genome size (bp) | 4,632,952 |
| Genome coverage (×) | 112 |
| Genome completeness (%) | 99.27 |
| CheckM contamination (%) | 0.62 |
| No. of contigs | 50 |
| Contig N50 (bp) | 312,937 |
| GC content (%) | 55.5 |
| Coding sequences (CDSs) | 4,402 |
| Protein-coding genes | 4,358 |
| No. of SEED subsystems | 372 |
| No. of VFGs | 21 |
| No. of ARGs | 22 |
| PathogenFinder2 score | 0.966 |
| Genome accessions | JBOEQC000000000 |
| Sequence Read Archive accessions | SRR33697069 |
SEED, Subsystems Enabling the Effective Determination of function.
ACKNOWLEDGMENTS
This work was supported by research grants from the Ministry of Science and Technology, Government of Bangladesh (grant no. SRG-131044).
Contributor Information
Abu Nasar Md. Aminoor Rahman, Email: aminoor69@gau.edu.bd.
M. Nazmul Hoque, Email: nazmul90@gau.edu.bd.
David Rasko, University of Maryland School of Medicine, Baltimore, Maryland, USA.
DATA AVAILABILITY
The whole-genome shotgun sequencing project of Enterobacter hormaechei strain F10K has been deposited in GenBank and the National Center for Biotechnology Information Sequence Read Archive (SRA) under BioProject accession number PRJNA1267841. The SRA accession is listed in Table 1. The version described in this paper is version JBOEQC000000000.1.
ETHICS APPROVAL
The Animal Research Ethics Committee (AREC) of Gazipur Agricultural University (Gazipur, Bangladesh) reviewed and approved the experimental procedures of this study (reference number FVMAS/AREC/2023/55 [9 March 2025]).
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Data Availability Statement
The whole-genome shotgun sequencing project of Enterobacter hormaechei strain F10K has been deposited in GenBank and the National Center for Biotechnology Information Sequence Read Archive (SRA) under BioProject accession number PRJNA1267841. The SRA accession is listed in Table 1. The version described in this paper is version JBOEQC000000000.1.
