Effects of inflammatory stimuli on the development of Mycoplasma bovis pneumonia in experimentally challenged calves

IF 2.4 2区 农林科学 Q3 MICROBIOLOGY Veterinary microbiology Pub Date : 2024-07-30 DOI:10.1016/j.vetmic.2024.110203
Ksenia Vulikh , DeLenn Burrows , Jose Perez-Casal , Saeid Tabatabaei , Jeff L. Caswell
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Abstract

Many cattle infected with Mycoplasma bovis remain healthy while others develop severe chronic respiratory disease. We hypothesized that inflammatory stimuli such as co-pathogens worsen disease outcomes in M. bovis-infected calves. Calves (n=24) were intrabronchially inoculated with M. bovis and either killed bacterial lysate, transient M. haemolytica infection, or saline. Caseonecrotic lesions developed in 7/7 animals given M. haemolytica and M. bovis compared to 2/8 given M. bovis with no inflammatory stimulus, and 6/9 animals given bacterial lysate and M. bovis (P=0.01). Animals receiving M. haemolytica and M. bovis had more caseonecrotic foci in lungs than those receiving M. bovis with no inflammatory stimulus (median = 21 vs 0; P = 0.01), with an intermediate response (median = 5) in animals given bacterial lysate. In addition to caseonecrotic foci, infected animals developed neutrophilic bronchiolitis that appeared to develop into caseonecrotic foci, peribronchiolar lymphocytic cuffs that were not associated with the other lesions, and 4 animals with bronchiolitis obliterans. The data showed that transient lung inflammation at the time of M. bovis infection provoked the development of caseonecrotic bronchopneumonia, and the severity of inflammation influenced the number of caseonecrotic foci that developed. In contrast, caseonecrotic lesions were few or absent in M. bovis-infected calves without a concurrent inflammatory stimulus. These studies provide insight into how caseonecrotic lesions develop within the lung of M. bovis-infected calves. This and other studies suggest that controlling co-pathogens and harmful inflammatory responses in animals infected with M. bovis could potentially minimize development of M. bovis caseonecrotic bronchopneumonia.

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炎症刺激对实验性牛犊支原体肺炎发病的影响
许多感染了牛支原体的牛仍然健康,而其他牛则会患上严重的慢性呼吸道疾病。我们推测,炎症刺激(如共病原体)会加重牛支原体感染犊牛的病情。犊牛(n=24)经支气管内接种牛海绵状芽孢杆菌和杀死的细菌裂解液、一过性溶血霉菌感染或生理盐水。7/7的动物接种了溶血霉菌和牛海绵状芽孢杆菌,2/8的动物接种了牛海绵状芽孢杆菌但没有炎症刺激,6/9的动物接种了细菌裂解物和牛海绵状芽孢杆菌(P=0.01)。接受溶血霉菌和牛海绵状芽孢杆菌治疗的动物比接受无炎症刺激的牛海绵状芽孢杆菌治疗的动物肺部有更多的酪质坏死灶(中位数 = 21 vs 0;P = 0.01),而接受细菌裂解液治疗的动物则有中等程度的反应(中位数 = 5)。除病变灶外,受感染的动物还出现了似乎发展成病变灶的嗜中性支气管炎、与其他病变无关的支气管周围淋巴细胞袖套,以及 4 只闭塞性支气管炎动物。数据显示,感染包虫病时短暂的肺部炎症会引发病例性支气管肺炎,炎症的严重程度会影响病例性支气管肺炎病灶的数量。与此相反,在没有并发炎症刺激的情况下,牛海绵状芽孢杆菌感染的犊牛很少出现或不出现病变。这些研究有助于深入了解牛海绵状芽孢杆菌感染的犊牛肺部是如何发生病变的。这项研究和其他研究表明,控制牛海绵状芽孢杆菌感染动物的共病原体和有害炎症反应有可能最大限度地减少牛海绵状芽孢杆菌致病性支气管肺炎的发生。
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来源期刊
Veterinary microbiology
Veterinary microbiology 农林科学-兽医学
CiteScore
5.90
自引率
6.10%
发文量
221
审稿时长
52 days
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.
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