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In vitro Biofilm Formation in an 8-well Chamber Slide
Published on: January 20, 2011
Biofilm formation by field isolates and reference strains of Haemophilus parasuis
Hui Jin1, Rui Zhou, Mingsong Kang
1Division of Animal Infectious Disease, State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Abstract:
The ability to form biofilms for a total of 80 field isolates and 15 reference strains of Haemophilus parasuis, the etiological agent of Glasser's disease, was tested by glass tube and polystyrene microtiter plate assays. A total 43% of field isolates, including strains representing 13 serovars (except serovars 3 and 8) and non-typable strains, exhibited the ability to form biofilms at different levels via polystyrene microtiter plate assays. Among the reference strains representing 15 serovars, only serovars 2, 9, 12, 13 and 15 could not form biofilms on the polystyrene surface. A total of 85% of the strains forming biofilms at air-liquid interfaces in glass tubes also formed biofilms on polystyrene surfaces. Generally, non-virulent serovars showed a higher degree of biofilm formation than virulent serovars. The biofilm formation phenotype of most strains was maintained when cultures were passaged on agar and in broth. H. parasuis from the nasal cavities of pigs experimentally infected with biofilm-positive bacteria maintained the biofilm formation phenotype, whereas bacteria recovered from the lung and brain lost the ability to form biofilms. The biofilm-negative strains did not recover the ability to form biofilms via experimental infection. Our data indicate that most serovars of H. parasuis could form biofilms in vitro, and the biofilm formation phenotype is associated with the recovery site of the strains and is maintained when bacteria are passaged in vitro and in the upper respiratory tract.
Insights
Most Haemophilus parasuis strains, the cause of Glasser's disease, can form biofilms. Biofilm formation varies by serovar and is maintained in the upper respiratory tract but lost in deeper tissues.
Area of Science:
- Veterinary Microbiology
- Bacterial Pathogenesis
- Biofilm Formation
Background:
- Haemophilus parasuis is the primary cause of Glasser's disease in swine.
- Biofilm formation is a critical virulence factor for many bacterial pathogens.
- Understanding biofilm capacity in H. parasuis is crucial for disease control.
Purpose of the Study:
- To investigate the biofilm-forming ability of Haemophilus parasuis field isolates and reference strains.
- To determine the association between biofilm formation, serovar, virulence, and recovery site.
- To assess the stability of the biofilm phenotype during in vitro and in vivo passage.
Main Methods:
- Biofilm formation was assessed using glass tube and polystyrene microtiter plate assays.
- Field isolates and reference strains representing various serovars were tested.
- Phenotypic stability was evaluated after in vitro passaging and experimental infection in pigs.
Main Results:
- 43% of field isolates and several reference strains demonstrated biofilm formation.
- Non-virulent serovars generally exhibited higher biofilm formation than virulent ones.
- Biofilm phenotype was maintained in vitro and in nasal cavities but lost in lungs and brain.
Conclusions:
- Most H. parasuis serovars possess the in vitro capacity for biofilm formation.
- Biofilm formation is linked to the site of bacterial recovery and is influenced by host environment.
- The findings provide insights into H. parasuis persistence and pathogenesis.
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