Ling Chen , Juan Sun , Jialian Hu , Ye Tian , Pengfei Du , Qianqian Guo , Chenghuai Yang , Qianyi Zhang , Saixiang Feng , Ming Liao
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引用次数: 0
Abstract
Infectious coryza is an acute respiratory disease in chickens caused by Avibacterium paragallinarum. Lipooligosaccharides (LOSs) and capsular polysaccharides are important components of Av. paragallinarum. Herein, we identified that gene cluster L6 and two genes waaF, waaQ were associated with LOS synthesis, and two genes acbD and ccbF1 were involved in capsular synthesis. Mutant and complementary strains of these genes were generated by natural transformation. Wild-type strains produced LOS that yielded an upper and lower band. In comparison, ΔwaaQ and ΔwaaF yielded a truncated lower band and lacked the upper band, while ΔL6 did not exhibit the upper band, and the lower band was identical to that of the wild-type strain. The survival rates of wild-type strain, ΔwaaF, ΔwaaQ, and ΔL6 in chicken serum were 4.89 % ± 0.27 %, 0.0013 % ± 0.0002 %, 0.43 % ± 0.05 %, and 3.1 % ± 0.35 %, respectively. Notably, the resistances of ΔwaaF, ΔwaaQ, and ΔL6 to chicken serum were significantly lower than that of parent strain. By contrast, the survival rate of the ΔacbD strain was 55.17 % ± 0.61 %, and its resistance to chicken serum was significantly higher than that of the wild-type strain (p < 0.001). Deletion of the waaF, waaQ, L6, acbD, and ccbF1 genes resulted in enhanced formation of biofilm without altering immunogenicity in chickens. The ΔwaaF, ΔwaaQ, and ΔccbF1 strains exhibited heightened susceptibility to fowlicidin-2. Furthermore, ΔwaaF, ΔacbD, and ΔccbF1 strains shown a decrease in pathogenicity (p < 0.05). These results are valuable for advancing research on the pathogenesis of Av. paragallinarum.
期刊介绍:
Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal.
Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge.
Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.