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Updated: May 9, 2026

Assessing Biofilm Dispersal in Murine Wounds
Published on: August 7, 2021
Bacterial biofilm formation after nasal packing in nasal mucosa-wounded mice
Yanjun Wang1, Shan Chen, Jianjun Chen
1Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Background:
Bacterial biofilm plays an important role in recalcitrant chronic rhinosinusitis. Staphylococcus aureus is a crucial pathogen in chronic rhinosinusitis and S. aureus biofilm is related to unfavorable postoperative outcomes. Although S. aureus is known to be the most common bacteria leading to postoperative infection, whether biofilm forms on the wound surface after functional endoscopic sinus surgery and the relationship between biofilm formation and surgery are still not clear. This study was designed to observe whether S. aureus biofilm forms in mice with wounded nasal mucosa mice after bacteria inoculation.
Methods:
Three hundred twenty-four wild-type male C57BL/6 mice were recruited for the experiment. Except for the four used in the preliminary experiment, the mice were randomly divided into four groups: a wound plus packing group (group A), a wound group (group B), a packing group (group C), and a control group (group D). After treatment, groups A, B, and C were inoculated with S. aureus suspension at 1 × 10(9) CFU/mL in the right nasal cavity; sterile physiological saline was used instead of bacteria suspension for group D. Confocal laser scanning microscopy was used to detect the biofilm. A nasal lavage culture was also completed.
Results:
Biofilm formation was found in group A on the 3rd, 7th, and 15th days after inoculation with growth rates of 10, 25, and 40%, respectively. Three cases of biofilm were also detected in group B on the 15th day postinoculation. There was no biofilm observed on the nasal mucosa in group C or D. The nasal lavage culture showed that the inoculated bacteria stayed on the nasal mucosa temporarily after inoculation.
Conclusion:
Our results indicate that a nasal wound, nasal packing, and the existence of pathogenic bacteria are all essential elements for biofilm formation in healthy mice. This result indicated that biofilm formation may be avoided by shortening the duration of nasal packing and reducing the nasal wound.
Insights
Nasal wounds, packing, and Staphylococcus aureus are essential for biofilm formation in mice. Reducing nasal wound duration and packing may prevent biofilm in chronic rhinosinusitis patients.
Area of Science:
- Microbiology
- Otorhinolaryngology
- Surgical Research
Background:
- Bacterial biofilm, particularly Staphylococcus aureus, is implicated in chronic rhinosinusitis (CRS) and poor surgical outcomes.
- The formation of S. aureus biofilm on surgical wounds after functional endoscopic sinus surgery (FESS) remains unclear.
- Understanding biofilm formation is crucial for improving FESS success rates.
Purpose of the Study:
- To investigate the formation of Staphylococcus aureus biofilm on wounded nasal mucosa in a mouse model.
- To determine the conditions necessary for biofilm development post-surgery.
Main Methods:
- 324 male C57BL/6 mice were divided into four groups: wound plus packing, wound only, packing only, and control.
- Groups A, B, and C were inoculated with S. aureus; group D received saline.
- Confocal laser scanning microscopy and nasal lavage cultures were used to detect biofilm and bacterial presence.
Main Results:
- Biofilm formation was observed in 10%, 25%, and 40% of the wound plus packing group on days 3, 7, and 15, respectively.
- Three cases of biofilm were detected in the wound-only group by day 15.
- No biofilm was observed in the packing-only or control groups, suggesting wound, packing, and bacteria are necessary.
Conclusions:
- Nasal wounds, nasal packing, and the presence of pathogenic bacteria are essential for S. aureus biofilm formation in mice.
- Shortening nasal packing duration and minimizing nasal wounds may prevent biofilm formation.
- These findings offer insights into preventing postoperative infections after FESS.
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