Chintha K. Premachandre , Pin Shie Quah , Bang Manh Tran , Elizabeth Vincan , Georgia Deliyannis , Chinn Yi Wong , Andrés Diaz-Méndez , David C. Jackson , Patrick C. Reading , Glenn F. Browning , Paola K. Vaz , Nadeeka K. Wawegama
{"title":"用于研究牛支原体呼吸道感染的牛气管器官组织。","authors":"Chintha K. Premachandre , Pin Shie Quah , Bang Manh Tran , Elizabeth Vincan , Georgia Deliyannis , Chinn Yi Wong , Andrés Diaz-Méndez , David C. Jackson , Patrick C. Reading , Glenn F. Browning , Paola K. Vaz , Nadeeka K. Wawegama","doi":"10.1016/j.vetmic.2024.110340","DOIUrl":null,"url":null,"abstract":"<div><div><em>In vitro</em> three-dimensional organoid models simulate key aspects of the structure and function of <em>in vivo</em> organs and have been used to study physiology, host-pathogen interactions, pathogenesis and pharmacodynamics. Although most organoid studies have been developed using human or mouse tissues, recent advancements have enabled the establishment of intestinal and respiratory tract organoids from domestic animal samples. <em>Mycoplasma bovis</em> causes chronic respiratory tract infections in cattle with significant health and economic consequences. The pathogenesis and virulence factors of <em>M. bovis</em> have been studied in several <em>in vitro</em> infection models, but the use of organoids has not been examined previously. In this study, we assessed the feasibility of using a matrix-embedded bovine tracheal organoid system to study respiratory infections with <em>M. bovis</em>. Bovine tracheal organoids were inoculated with <em>M. bovis</em> strain MbovMil and incubated for 72 hours to investigate the ability of <em>M. bovis</em> to proliferate, attach and invade the organoids. <em>M. bovis</em> was able to infect the organoids, resulting in a mean 260-fold increase in the titre of viable <em>M. bovis</em> by 72 hours post-inoculation. Examination of the infected organoids using transmission electron microscopy revealed the presence of mycoplasmas within the organoid cells and membrane bound clusters of <em>M. bovis</em> inside the intercellular junctions. Our findings indicate that bovine tracheal organoids can be used as a model system for studying respiratory tract infections caused by <em>M. bovis</em>.</div></div>","PeriodicalId":23551,"journal":{"name":"Veterinary microbiology","volume":"300 ","pages":"Article 110340"},"PeriodicalIF":2.4000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bovine tracheal organoids for studying Mycoplasma bovis respiratory infections\",\"authors\":\"Chintha K. Premachandre , Pin Shie Quah , Bang Manh Tran , Elizabeth Vincan , Georgia Deliyannis , Chinn Yi Wong , Andrés Diaz-Méndez , David C. Jackson , Patrick C. Reading , Glenn F. Browning , Paola K. Vaz , Nadeeka K. Wawegama\",\"doi\":\"10.1016/j.vetmic.2024.110340\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>In vitro</em> three-dimensional organoid models simulate key aspects of the structure and function of <em>in vivo</em> organs and have been used to study physiology, host-pathogen interactions, pathogenesis and pharmacodynamics. Although most organoid studies have been developed using human or mouse tissues, recent advancements have enabled the establishment of intestinal and respiratory tract organoids from domestic animal samples. <em>Mycoplasma bovis</em> causes chronic respiratory tract infections in cattle with significant health and economic consequences. The pathogenesis and virulence factors of <em>M. bovis</em> have been studied in several <em>in vitro</em> infection models, but the use of organoids has not been examined previously. In this study, we assessed the feasibility of using a matrix-embedded bovine tracheal organoid system to study respiratory infections with <em>M. bovis</em>. Bovine tracheal organoids were inoculated with <em>M. bovis</em> strain MbovMil and incubated for 72 hours to investigate the ability of <em>M. bovis</em> to proliferate, attach and invade the organoids. <em>M. bovis</em> was able to infect the organoids, resulting in a mean 260-fold increase in the titre of viable <em>M. bovis</em> by 72 hours post-inoculation. Examination of the infected organoids using transmission electron microscopy revealed the presence of mycoplasmas within the organoid cells and membrane bound clusters of <em>M. bovis</em> inside the intercellular junctions. Our findings indicate that bovine tracheal organoids can be used as a model system for studying respiratory tract infections caused by <em>M. bovis</em>.</div></div>\",\"PeriodicalId\":23551,\"journal\":{\"name\":\"Veterinary microbiology\",\"volume\":\"300 \",\"pages\":\"Article 110340\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary microbiology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0378113524003626\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary microbiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378113524003626","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Bovine tracheal organoids for studying Mycoplasma bovis respiratory infections
In vitro three-dimensional organoid models simulate key aspects of the structure and function of in vivo organs and have been used to study physiology, host-pathogen interactions, pathogenesis and pharmacodynamics. Although most organoid studies have been developed using human or mouse tissues, recent advancements have enabled the establishment of intestinal and respiratory tract organoids from domestic animal samples. Mycoplasma bovis causes chronic respiratory tract infections in cattle with significant health and economic consequences. The pathogenesis and virulence factors of M. bovis have been studied in several in vitro infection models, but the use of organoids has not been examined previously. In this study, we assessed the feasibility of using a matrix-embedded bovine tracheal organoid system to study respiratory infections with M. bovis. Bovine tracheal organoids were inoculated with M. bovis strain MbovMil and incubated for 72 hours to investigate the ability of M. bovis to proliferate, attach and invade the organoids. M. bovis was able to infect the organoids, resulting in a mean 260-fold increase in the titre of viable M. bovis by 72 hours post-inoculation. Examination of the infected organoids using transmission electron microscopy revealed the presence of mycoplasmas within the organoid cells and membrane bound clusters of M. bovis inside the intercellular junctions. Our findings indicate that bovine tracheal organoids can be used as a model system for studying respiratory tract infections caused by M. bovis.
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.