Clinical Relevance and Environmental Prevalence of Mycobacterium fortuitum Group Members. Comment on Mugetti et al. Gene Sequencing and Phylogenetic Analysis: Powerful Tools for an Improved Diagnosis of Fish Mycobacteriosis Caused by Mycobacterium fortuitum Group Members. Microorganisms 2021, 9, 797
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
NU20-09-00114
Czech Health Research Council
PubMed
34835470
PubMed Central
PMC8622867
DOI
10.3390/microorganisms9112345
PII: microorganisms9112345
Knihovny.cz E-zdroje
- Klíčová slova
- environmental prevalence, fish directed for consumption, non-tuberculous mycobacteria, potentially pathogenic mycobacteria, saprophytic environmental mycobacteria,
- Publikační typ
- časopisecké články MeSH
Mycobacterium fortuitum group (MFG) members are able to cause clinical mycobacteriosis in fish and other animals including humans. M. alvei, M. arceuilense, M. brisbanense, M. conceptionense, M. fortuitum, M. peregrinum, M. porcinum, M. senegalense, M. septicum, and M. setense were isolated from fish with mycobacteriosis. In other animals only three MFG species have been isolated: M. arceuilense from camels' milk, M. farcinogenes from cutaneous infections often described as "farcy", and M. fortuitum from different domestic and wild mammals' species. Out of 17, only 3 MFG species (M. arceuilense, M. lutetiense and M. montmartrense) have never been reported in humans. A total of eight MFG members (M. alvei, M. brisbanense, M. conceptionense, M. fortuitum subsp. acetamidolyticum, M. houstonense, M. peregrinum, M. porcinum, and M. septicum) have been isolated from both pulmonary and extrathoracic locations. In extrathoracic tissues five MFG species (M. boenickei, M. farcinogenes, M. neworleansense, M. senegalense, and M. setense) have been diagnosed and only one MFG member (M. fortuitum subsp. acetamidolyticum) has been isolated from pulmonary infection.
Microorganisms. 9:797. PubMed
Zobrazit více v PubMed
Mugetti D., Tomasoni M., Pastorino P., Esposito G., Menconi V., Dondo A., Prearo M. Gene sequencing and phylogenetic analysis: Powerful tools for an improved diagnosis of fish mycobacteriosis caused by Mycobacterium fortuitum group members. Microorganisms. 2021;9:797. doi: 10.3390/microorganisms9040797. PubMed DOI PMC
LPSN: List of Prokaryotic Names with Standing in Nomenclature. [(accessed on 6 October 2021)]. Available online: https://lpsn.dsmz.de/
Varghese B., Al-Hajoj S. A global update on rare non-tuberculous mycobacteria in humans: Epidemiology and emergence. Int. J. Tuberc. Lung Dis. 2020;24:214–223. doi: 10.5588/ijtld.19.0194. PubMed DOI
Konjek J., Souded S., Guerardel Y., Trivelli X., Bernut A., Kremer L., Welte B., Joyeux M., Dubrou S., Euzeby J.P., et al. Mycobacterium lutetiense sp. nov., Mycobacterium montmartrense sp. nov. and Mycobacterium arcueilense sp. nov., members of a novel group of non-pigmented rapidly growing mycobacteria recovered from a water distribution system. Int. J. Syst. Evol. Microbiol. 2016;66:3694–3702. doi: 10.1099/ijsem.0.001253. PubMed DOI
Asaava L.L.A., Githui W.A., Mwangi M., Mwangi E., Juma E., Moraa R., Halakhe A., Gicheru M.M. Isolation, identification and associated risk factors of non-tuberculous mycobacteria infection in humans and dromedary camels in Samburu County, Kenya. Zoonoses Public Health. 2020;67:713–731. doi: 10.1111/zph.12754. PubMed DOI
Wee W.Y., Tan T.K., Jakubovics N.S., Choo S.W. Whole-Genome sequencing and comparative analysis of Mycobacterium brisbanense reveals a possible soil origin and capability in fertiliser synthesis. PLoS ONE. 2016;11:e0152682. doi: 10.1371/journal.pone.0152682. PubMed DOI PMC
Lorencova A., Klanicova B., Makovcova J., Slana I., Vojkovska H., Babak V., Pavlik I., Slany M. Nontuberculous mycobacteria in freshwater fish and fish products intended for human consumption. Foodborne Pathog. Dis. 2013;10:573–576. doi: 10.1089/fpd.2012.1419. PubMed DOI
Oda G., Winters M.A., Pacheco S.M., Sikka M.K., Bleasdale S.C., Dunn B., Boswell E., Winters B., Bumsted A., Frisch J., et al. Clusters of nontuberculous mycobacteria linked to water sources at three Veterans Affairs Medical Centers. Infect. Control Hosp. Epidemiol. 2020;41:320–330. doi: 10.1017/ice.2019.342. PubMed DOI
Jing H., Tan W., Deng Y., Gao D., Li L., Lu Z., Graviss E.A., Ma X. Diagnostic delay of pulmonary nontuberculous mycobacterial infection in China. Multidiscip. Respir. Med. 2014;9:48. doi: 10.1186/2049-6958-9-48. PubMed DOI PMC
Chamoiseau G. Etiology of farcy in African bovines: Nomenclature of the causal organisms Mycobacterium farcinogenes Chamoiseau and Mycobacterium senegalense (Chamoiseau) comb. nov. Int. J. Syst. Bacteriol. 1979;29:407–410. doi: 10.1099/00207713-29-4-407. DOI
Ridell M., Goodfellow M., Abdulle M.A. Identification of Actinomycetes isolated from cases of bovine farcy in the Sudan. Zent. Bakteriol. Mikrobiol. Hyg. A. 1985;259:43–50. doi: 10.1016/S0176-6724(85)80006-7. PubMed DOI
Bercovier H., Vincent V. Mycobacterial infections in domestic and wild animals due to Mycobacterium marinum, M. fortuitum, M. chelonae, M. porcinum, M. farcinogenes, M. smegmatis, M. scrofulaceum, M. xenopi, M. kansasii, M. simiae and M. genavense. Rev. Sci. Tech. 2001;20:265–290. doi: 10.20506/rst.20.1.1269. PubMed DOI
Tsukamura M., Yano I., Imaeda T. Mycobacterium fortuitum subspecies acetamidolyticum, a new subspecies of Mycobacterium fortuitum. Microbiol. Immunol. 1986;30:97–110. doi: 10.1111/j.1348-0421.1986.tb00925.x. PubMed DOI
Staneck J.L., Frame P.T., Altemeier W.A., Miller E.H. Infection of bone by Mycobacterium fortuitum masquerading as Nocardia asteroides. Am. J. Clin. Pathol. 1981;76:216–222. doi: 10.1093/ajcp/76.2.216. PubMed DOI
Jaubert J., Mougari F., Picot S., Boukerrou M., Barau G., Ali Ahmed S.A., Raskine L., Camuset G., Michault A., Simac C., et al. A case of postoperative breast infection by Mycobacterium fortuitum associated with the hospital water supply. Am. J. Infect. Control. 2015;43:406–408. doi: 10.1016/j.ajic.2014.12.023. PubMed DOI
Matsumoto T., Otsuka K., Tomii K. Mycobacterium fortuitum thoracic empyema: A case report and review of the literature. J. Infect. Chemother. 2015;21:747–750. doi: 10.1016/j.jiac.2015.05.012. PubMed DOI
Rathor N., Khillan V., Panda D. Catheter associated mycobacteremia: Opening new fronts in infection control. Indian J. Crit. Care Med. 2015;19:350–352. PubMed PMC
Peterson K.J. Mycobacterium fortuitum as a cause of bovine mastitis: Tuberculin sensitivity following experimental infections. J. Am. Vet. Med. Assoc. 1965;147:1600–1607. PubMed
Koehne G., Maddux R., Britt J. Rapidly growing mycobacteria associated with bovine mastitis. Am. J. Vet. Res. 1981;42:1238–1239. PubMed
Machackova M., Matlova L., Lamka J., Smolik J., Melicharek I., Hanzlikova M., Docekal J., Cvetnic Z., Nagy G., Lipiec M., et al. Wild boar (Sus scrofa) as a possible vector of mycobacterial infections: Review of literature and critical analysis of data from Central Europe between 1983 to 2001. Vet. Med.-Czech. 2003;48:51–65. doi: 10.17221/5750-VETMED. DOI
Couto S.S., Artacho C.A. Mycobacterium fortuitum pneumonia in a cat and the role of lipid in the pathogenesis of atypical mycobacterial infections. Vet. Pathol. 2007;44:543–546. doi: 10.1354/vp.44-4-543. PubMed DOI
Leissinger M.K., Garber J.B., Fowlkes N., Grooters A.M., Royal A.B., Gaunt S.D. Mycobacterium fortuitum lipoid pneumonia in a dog. Vet. Pathol. 2015;52:356–359. doi: 10.1177/0300985814531497. PubMed DOI
Delghandi M.R., El-Matbouli M., Menanteau-Ledouble S. Mycobacteriosis and infections with non-tuberculous mycobacteria in aquatic organisms: A review. Microorganisms. 2020;8:1368. doi: 10.3390/microorganisms8091368. PubMed DOI PMC
Pavlik I., Falkinham J., Kazda J. Environments providing favourable conditions for the multiplication and transmission of mycobacteria. In: Kazda J., Pavlik I., Falkinham J., Hruska K., editors. The Ecology of Mycobacteria: Impact on Animal’s and Human’s Health. 1st ed. Springer; Dordrecht, The Netherlands: Heidelberg, Germany: London, UK: New York, NY, USA: 2009. pp. 89–198. Chapter 5.
Schinsky M.F., Morey R.E., Steigerwalt A.G., Douglas M.P., Wilson R.W., Floyd M.M., Butler W.R., Daneshvar M.I., Brown-Elliott B.A., Wallace R.J., Jr., et al. Taxonomic variation in the Mycobacterium fortuitum third biovariant complex: Description of Mycobacterium boenickei sp. nov., Mycobacterium houstonense sp. nov., Mycobacterium neworleansense sp. nov. and Mycobacterium brisbanense sp. nov. and recognition of Mycobacterium porcinum from human clinical isolates. Int. J. Syst. Evol. Microbiol. 2004;54:1653–1667. PubMed
Kim S.Y., Moon S.M., Jhun B.W., Kwon O.J., Huh H.J., Lee N.Y., Lee S.H., Shin S.J., Kasperbauer S.H., Huitt G.A., et al. Species distribution and macrolide susceptibility of Mycobacterium fortuitum complex clinical isolates. Antimicrob. Agents Chemother. 2019;63:e02331-18. doi: 10.1128/AAC.02331-18. PubMed DOI PMC
Lazo-Vasquez A.F., Gonzales-Zamora J.A. Mycobacterium peregrinum pacemaker pocket infection: A case report and review of the literature. Case Rep. Infect. Dis. 2020;2020:8831026. doi: 10.1155/2020/8831026. PubMed DOI PMC
Gcebe N., Michel A.L., Hlokwe T.M. Non-tuberculous Mycobacterium species causing mycobacteriosis in farmed aquatic animals of South Africa. BMC Microbiol. 2018;18:32. doi: 10.1186/s12866-018-1177-9. PubMed DOI PMC
Kusar D., Zajc U., Jencic V., Ocepek M., Higgins J., Zolnir-Dovc M., Pate M. Mycobacteria in aquarium fish: Results of a 3-year survey indicate caution required in handling pet-shop fish. J. Fish Dis. 2017;40:773–784. doi: 10.1111/jfd.12558. PubMed DOI
Davarpanah M., Azadi D., Shojaei H. Prevalence and molecular characterization of non-tuberculous mycobacteria in hospital soil and dust of a developing country, Iran. Microbiology (Reading) 2019;165:1306–1314. doi: 10.1099/mic.0.000857. PubMed DOI
Kazda J., Pavlik I., Falkinham J., Hruska K. The Ecology of Mycobacteria: Impact on Animal’s and Human’s Health. 1st ed. Springer; Dordrecht, The Netherlands: Heidelberg, Germany: London, UK: New York, NY, USA: 2009. 520p
Matlova L., Kaevska M., Moravkova M., Beran V., Shitaye J.E., Pavlik I. Mycobacteria in peat used as a supplement for pigs: Failure of different decontamination methods to eliminate the risk. Vet. Med.-Czech. 2012;57:212–217. doi: 10.17221/5924-VETMED. DOI
Skoric M., Mrlik V., Svobodova J., Beran V., Slany M., Fictum P., Pokorny J., Pavlik I. Infection in a Komodo dragon (Varanus komodoensis) caused by Mycobacterium intracellulare: A case report. Vet. Med.-Czech. 2012;57:163–168. doi: 10.17221/5857-VETMED. DOI
Moravkova M., Lamka J., Kriz P., Pavlik I. The presence of Mycobacterium avium subsp. avium in common pheasants (Phasianus colchicus) living in captivity and in other birds, vertebrates, non-vertebrates and the environment. Vet. Med.-Czech. 2011;56:333–343.
Slany M., Makovcova J., Jezek P., Bodnarova M., Pavlik I. Relative prevalence of Mycobacterium marinum in fish collected from aquaria and natural freshwaters in central Europe. J. Fish Dis. 2014;37:527–533. doi: 10.1111/jfd.12135. PubMed DOI
Slany M., Jezek P., Fiserova V., Bodnarova M., Stork J., Havelkova M., Kalat F., Pavlik I. Mycobacterium marinum infections in humans and tracing of its possible environmental sources. Can. J. Microbiol. 2012;58:1–6. doi: 10.1139/w11-104. PubMed DOI
Modra H., Bartos M., Hribova P., Ulmann V., Hubelova D., Konecny O., Gersl M., Kudelka J., Voros D., Pavlik I. Detection of mycobacteria in the environment of the Moravian Karst (Bull Rock Cave and the relevant water catchment area): The impact of water sediment, earthworm castings and bat guano. Vet. Med.-Czech. 2017;62:153–168. doi: 10.17221/126/2016-VETMED. DOI
Dual Infection of an Open Fracture Caused by Mycobacterium setense and Clostridium celerecrescens
Nontuberculous Mycobacteria: Ecology and Impact on Animal and Human Health