Skip to main content
Log in

Fate and tissue distribution of Mycobacterium fortuitum through immersion challenge as a model of natural infection in Osphronemus goramy

  • Published:
Aquaculture International Aims and scope Submit manuscript

Abstract

Mycobacteriosis has been recognized as an infectious disease caused by Mycobacterium fortuitum in aquaculture. In Indonesia, mycobacteriosis outbreak has been detected in West Java, Central Java, and East Java. However, no studies have yet described the pathogenesis of mycobacteriosis in gourami. Therefore, this study was designed to detect the portal of entry and tissue distribution of M. fortuitum in gourami through immersion challenge. The immersion route was selected for the infection method as it is capable of describing the occurrence of natural disease as an infection model. This study was conducted in two steps. First, the fish was immersed in M. fortuitum concentrations of 104–108 CFU mL−1 to determine the lethal dose of 50 (LD50). Second, the fish was immersed in LD50 to examine the portal of entry and tissue distribution of M. fortuitum in gourami and to determine the nonspecific immune response of fish after infection. Results showed that the LD50 of M. fortuitum through immersion challenge in gourami was 107 CFU mL−1. The portal of entry of M. fortuitum was the skin and gills, after which it spread through blood circulation to internal organs such as the liver and kidney. Finally, it was observed that the bacteria were released through the intestine. These findings indicate the M. fortuitum infection outbreak in fish was chronic and systemic and distributed in tissues. The infected fish responded to the infection by increasing the total leukocyte count and phagocytic activity after challenge with M. fortuitum.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

Data availability

All authors agree to publish in aquaculture international.

Code availability

Not applicable.

References

  • [SNI] Standar Nasional Indonesia (2000) Produksi benih ikan gurami (Osphronemus gourami) kelas benih sebar. Badan Standarisasi Nasional, Jakarta (ID)

    Google Scholar 

  • Anderson DP, Siwicki AK (1993) Basic haematology and serology for fish health programs. Paper Presented in Second Symposium on Diseases in Asia Aquaculture “Aquatic Animal Health and the Environmental”. Phuket Thailand 25-29th October 1993

  • Barrow GI, Feltham (eds) (1993) Cowan and Steel’s manual for the identification of medical acteria. Cambridge University Press, Cambridge

    Google Scholar 

  • Biller-Takahashi JD, Takahashi LS, Saita MV, Gimbo RY, Urbinati EC (2013) Leukocytes respiratory burst activity as indicator of innate immunity of pacu Piaractus mesopotamicus. Braz J Biol 73(2):425–429

    Article  CAS  Google Scholar 

  • Blaxhall PC, Daisley KW (1973) Reutine haemotologycal methods for use with fish blood. J Fish Biol 5:577–581

    Google Scholar 

  • Broussard GW, Don GE (2007) Mycobacterium marinum produces long-term chronic infections in Medaka: a new animal model for studying human tuberculosis. Comp Biochem Physiol C Toxicol Pharmacol 145(1):45–54

    Article  CAS  Google Scholar 

  • Bruno DW, Griffiths J, Mitchell CG, Wood BP, Fletcher ZJ, Drobniewski FA, Hastings TS (1998) Pathology attributed to Mycobacterium chelonae infection among farmed and laboratoryinfected Atlantic salmon Salmo salar. Dis Aquat Org 33:101–109

    Article  CAS  Google Scholar 

  • Chin YK, Ina-Salwany MY, M Z-S, Amal MNA, Mohamad A, Lee JY, Annas S, Al-saari N (2020) Effect of skin abrasion in immersion challenge with Vibrio harveyi in Asian seabass Lates Calcarifer fingerlings. Dis Aquat Org 137:167–173

    Article  CAS  Google Scholar 

  • Defoirdt (2014) Virulence mechanisms of bacterial aquaculture pathogens and antivirulence therapy for aquaculture. Rev Aquac 6:100–114

    Article  Google Scholar 

  • Gauthier DT, Martha WR (2009) Mycobacteriosis in fishes: a review. Vet J 180:33–47

    Article  Google Scholar 

  • Gauthier DT, Rhodes MW, Vogelbein WK, Kator OCA (2003) Experimental mycobcateriosis in striped bass (Morone saxatilis). Dis Aquat Org 54:105–117

    Article  CAS  Google Scholar 

  • Genten F, Terwinghe E, Danguy A (2009) Atlas of fish histology. Science Publishers, New Hampshire

    Book  Google Scholar 

  • Harriff MJ, Bermudez LE, Kent ML (2007) Experimental exposure of zebrafish, Danio rerio (Hamilton), to Mycobacterium marinum and Mycobacterium peregrinumreveals the gastrointestinal tract as the primary route of infection:a potential model for environmental mycobacterial infection. J Fish Dis 30:567–600

    Article  Google Scholar 

  • Hashish E, Merwad A, Elgaml S, Amer A, Kamal H, Elsadek A, Marei A, Sitohy M (2018) Mycobacterium marinum infection in fish and man: epidemiologi, pathophysiology and management: A review. Vet Q 38(1):35–46

    Article  Google Scholar 

  • He RZ, Li ZC, Li SY, Li AX (2021) Development of an immersion challenge model for Streptococcus agalactiae in Nile Tilapia (Oreochromis niloticus). Aquaculture 531:735877

    Article  CAS  Google Scholar 

  • Hongslo T, Jansson E (2009) Health survey of aquarium fish in Swedish pet-shops. Bull Eur Assoc Fish Pathol 29(5):163–174

    Google Scholar 

  • Hrubec TC, Smith SA (2000) Hematology of fish. In: Feldman BV, Zinkl JG, Jain NC (eds) Schalm’s veterinary hematology. Lippincott Williams and Wilkins, Philadelphia, pp 1120–1125

    Google Scholar 

  • Lopez V, Risalde MA, Contreras M, Mateos-Hernandez L, Vicente J, Gortazar C, de la Fuente J (2018) Heat-inactivated Mycobacterium bovis protects zebrafish against mycobacteriosis. J Fish Dis 1−14

  • Madigan MT, Martinko JM, Parker J (2003) Brock biology of microorganisms tenth edition. Upper Saddle River, Hoboken

  • Novotny L, Halouzka R, Matlova L, Vavra O, Bartosova L, Slany M, Pavlik I (2010) Morphology and distribution of granulomatous inflammation in freshwater ornamental fish infected with mycobacteria. J Fish Dis 33:947–955

    Article  CAS  Google Scholar 

  • Pusat Data, Statistik, dan Informasi (Sidatik) Kementerian Kelautan dan Perikanan (KKP) (2018) Satu data produksi kelautan dan perikanan Tahun 2017

  • Reed MJ, Muench M (1938) A simple method for estimating fifty percent endpoints. Am J Hyg 27:493–497

    Google Scholar 

  • Ringo E, Myklebust R, Mayhew TM, Olsen RE (2007) Bacterial translocation pathogenesis in the digestive tract of larvae and fry. Aquaculuture 268:251–264

    Article  Google Scholar 

  • Satheeshkumar P, Ananthan G, Kumar DS, Jagadeesan L (2011) Haematology and biochemical parameters of different feeding behavior of teleost fishes from Vellar estuary, India. Comp Clin Pathol 21(6):1–5

    Google Scholar 

  • Shan Y, Fang C, Cheng C, Wang Y, Peng J, Fang W (2015) Immersion infection of germ-free zebrafish with Listeria monocytogenes induces transient expression of innate immune response genes. Front Microbiol 6(373):1–11

    CAS  Google Scholar 

  • Sukenda, Wakabayashi H (2001) Adherence and infectivity of green fluorescent protein-labeled Pseudomonas plecoglossicida to ayu (Plecoglossus altivelis). Fish Pathol 36:161–167

    Article  CAS  Google Scholar 

  • Supriyadi H, Taufik P, Taukhid (2003) Karakterisasi patogen, inang spesifik, dan sebaran mycobacteriosis. J Pen Perik Indonesia 9(2):39–45

    Google Scholar 

  • Talaat AM, Reimschuessel R, Trucksis M (1997) Identification of mycobacterium infected fish to the species level using polymerase chain reaction and restriction enzyme analysis. Vet Microbiol 58:229–237

    Article  CAS  Google Scholar 

  • Talaat AM, Trucksis M, Kane AS, Reimschuessel R (1999) Pathogenicity of Mycobacterium fortuitum and Mycobacterium smegmatis to goldfish, Carassius auratus. Vet Microbiol 66:151–164

    Article  CAS  Google Scholar 

  • Uribe C, Folch H, Enriquez R, Moran G (2011) Innate and adaptive immunity in teleost fish: a review. Vet Med 56(10):486–503

Download references

Acknowledgements

The authors are very grateful to Research Institute for Freshwater Aquaculture and Fisheries Extension, Bogor, Indonesia, as the M. fortuitum bacteria provider. We would like to thank the laboratory staff of aquatic organism health in the IPB University for facility support and Mr. Dendi Hidayatullah and Mr. Hasan Nasrullah for their advice and the technical support.

Funding

This research was partially supported by PTUPT Research Grant No: 1/E/KP.PTNBH/2020 and 1/AMD/E1/KP.PTNBH/2020 from Ministry of Research, Technology and Higher Education, Indonesia.

Author information

Authors and Affiliations

Authors

Contributions

Maulina Agriandini performed the experiment, analyzed the data, and wrote the first version of the manuscript. Sukenda designed the study and wrote the first version of manuscript. Widanarni designed the study, reviewed the first version of the manuscript, and approved for publication. Angela Mariana Lusiastuti designed the study, reviewed the first version of the manuscript, and approved for publication.

Corresponding author

Correspondence to Sukenda Sukenda.

Ethics declarations

Ethics approval

All experiments in this study associated with fish complied with animal welfare and were conducted according to protocol number 181-2020, approved by the Ethics Committee on Animal Use of the IPB University, April 2020.

Consent to participate

All authors consented to participate in all aspects of this study and publication.

Conflict of interest

The authors declare no competing interests.

Additional information

Handling Editor: Brian Austin

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Agriandini, M., Sukenda, S., Widanarni, W. et al. Fate and tissue distribution of Mycobacterium fortuitum through immersion challenge as a model of natural infection in Osphronemus goramy. Aquacult Int 29, 1979–1989 (2021). https://doi.org/10.1007/s10499-021-00729-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10499-021-00729-y

Keywords

Navigation