# Virulence and resistance gene analysis of Rothia nasimurium by whole gene sequencing

**Authors:** Ziyue Lu, Sun He, Ali Adnan, Wenyu Fan, Jinliang Sheng, Yanming Sun, Yanbing Zhang, Gang Wang

PMC · DOI: 10.1038/s41598-025-95405-z · 2025-03-27

## TL;DR

This study analyzed a drug-resistant Rothia nasimurium strain from sick sheep in China, identifying its virulence and resistance genes and pathogenic effects.

## Contribution

The study provides new insights into the virulence and antibiotic resistance mechanisms of a pathogenic Rothia nasimurium strain.

## Key findings

- The strain Y1 showed resistance to 9 antibiotics and sensitivity only to amikacin and vancomycin.
- Draft genome sequencing revealed 112 virulence-related genes, including those for adhesion, hemolysin, and iron uptake.
- Animal tests confirmed that Y1 causes lung damage, coat loss, and skin inflammation.

## Abstract

A batch of sheep in a sheep farm in Xinjiang, China, died suddenly; a bacterial strain was isolated from the abdominal fluid of the sick and dead sheep, and identified as Rothia nasimurium by 16S sequencing, and the strain Y1 was subjected to drug sensitivity test with Draft gene sequencing. The results of the drug sensitivity test revealed the strain’s resistance to 9 antibiotics, with sensitivity exhibited solely towards amikacin and vancomycin. Phylogenetic tree analysis confirmed that it was related to Rothia nasimurium strain E1706032 and Rothia sp.SD9660Na. The draft genome sequencing results showed that the total length of the gene was 2,387,685 bp, and the GC content was 59.35%. VFDB database analysis identified 112 annotated genes in Y1, including those related to bacterial adhesion, regulation, nutrient metabolism factors, hemolysin, immunomodulation, and iron uptake proteins. CARD database analysis showed that Y1 was resistant to a variety of antibiotics such as glycopeptides, tetracyclines, aminoglycosides and polypeptides. Animal pathogenicity tests have shown that Y1 can cause lung damage, coat loss and skin inflammation. This study revealed a series of virulence and drug resistance genes and pathogenicity of Y1. The results of this study have important reference value for prevention and treatment of Rothia infection in the future.

## Linked entities

- **Proteins:** LOC106077773 (uncharacterized LOC106077773)
- **Chemicals:** amikacin (PubChem CID 37768), vancomycin (PubChem CID 14969), glycopeptides (PubChem CID 56928060)
- **Species:** Rothia nasimurium (taxon 85336), Rothia sp. SD9660Na (taxon 3047030), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** lung damage (MESH:D008171), coat loss (MESH:D058456), skin inflammation (MESH:D007249), Rothia infection (MESH:D007239)
- **Chemicals:** aminoglycosides (MESH:D000617), glycopeptides (MESH:D006020), amikacin (MESH:D000583), vancomycin (MESH:D014640), SD9660Na (-), tetracyclines (MESH:D013754), iron (MESH:D007501)
- **Species:** Ovis aries (domestic sheep, species) [taxon 9940], Rothia nasimurium (species) [taxon 85336], Rothia sp. (in: high G+C Gram-positive bacteria) (species) [taxon 1885016]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11950441/full.md

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Source: https://tomesphere.com/paper/PMC11950441