In Vivo Anti-Vibrio Evaluation of Sponge-Associated Bacteria on the Survival Rate of Litopenaeus vannamei Infected with Pathogenic Vibrio Species

Main Article Content

Jepri Agung Priyanto
Galuh Adhiyaksa Ashari
Munti Yuhana
Aris Tri Wahyudi

Abstract

Sponge-associated bacteria are considered a rich source of bioactive compounds particularly to reduce the risk of Vibrio harveyi and Vibrio parahaemolyticus infection. The present study aimed to analyse the effectiveness of 19 isolates to control Vibrio infection in vivo. All 19 isolates displayed a non-pathogenic characteristic on shrimps (cell density of 106 cells/mL) as analysed using the pathogenicity test. The mortality caused by both Vibrio spp. on 50% of the shrimp population (LC50 value) had a cell density of 105 cells/mL as determined using the proportion interval method. On the basis of the challenge test, all isolates improved the survival rate of infected shrimps in diverse effectivities up to 89%, which was nearly 30% higher than the infected control. Two isolates coded as D6.9, and P5.20 reduced shrimp mortality after infection with Vibrio spp. 16S rRNA-based identification showed these isolates were closely similar to different genera of Bacillus and Staphylococcus. The extract derived from the most prospective isolate, D6.9, was dominated by 1-hydroxy-6-(3-isopropenyl-cycloprop-1-enyl)-6-methyl-heptan-2-one, hexadecanoic acid, 4-epicyclomusalenone [(24S)-24-methyl-28-norcycloart-25-en-3-one], and 2,4-dimethyl acetoacetanilide. This observation suggested these isolates characterised by in vivo anti-Vibrio activity need to be further developed as biocontrol candidates.

Article Details

How to Cite
In Vivo Anti-Vibrio Evaluation of Sponge-Associated Bacteria on the Survival Rate of Litopenaeus vannamei Infected with Pathogenic Vibrio Species. (2023). Tropical Life Sciences Research, 34(2), 299–311. https://doi.org/10.21315/tlsr2023.34.2.15
Section
Original Article

References

Azemin A, Klappa P and Omar M S S. (2015). Bacteriocin isolated from Halomonas sp.: A bacterial ding protein? The Malaysian Journal of Analytical Sciences 19(4): 831– 840.

Bibi F, Yasir M, Al-Sofyani A, Naseer M I and Azhar E I. (2020). Antimicrobial activity of bacteria from marine sponge Suberea mollis and bioactive metabolites of Vibrio sp. EA348. Saudi Journal of Biological Sciences 27(4): 1139–1147. https://doi. org/10.1016/j.sjbs.2020.02.002

Food and Agriculture Organization (FAO). (2016). The state of world fisheries and aquaculture 2016: Contributing to food security and nutrition for all. https://www. fao.org/3/i5555e/i5555e.pdf (Accessed on 21 July 2022).

Gao X, Liu Y, Miao L, Li E, Hou T and Liu Z. (2017). Mechanism of anti-Vibrio activity of marine probiotic strain Bacillus pumilus H2, and characterization of the active substance. AMB Express 7(23): 1–10. https://doi.org/10.1186/s13568-017-0323-3

Gunalan B, Soundarapandian P, Anand T, Kotiya A S and Nina T S. (2014). Disease occurrence in Litopenaeus vannamei shrimp culture systems in different geographical regions of India. International Journal of Aquaculture 4(4): 24–28. https://doi.org/10.5376/ija.2014.04.0004

Hamza F, Kumar A R and Zinjarde S. (2018). Coculture induced improved production of biosurfactant by Staphylococcus lentus SZ2: Role in protecting Artemia salina against Vibrio harveyi. Enzyme and Microbial Technology 114: 33–39. https://doi. org/10.1016/j.enzmictec.2018.03.008

Hossain M I, Kamal M M, Mannan M A, Bhuyain M A B and Hossain M I. (2013). Effects of probiotics on growth and survival of shrimps (Paneus monodon) in coastal pond at Khulna, Bangladesh. Journal of Science Research 5(2): 363–370. https://doi. org/10.3329/jsr.v5i2.11815

Jamal M T, Abdulrahman I A, Harbi M A and Chithambaran S. (2019). Probiotics as alternative control measures in shrimp aquaculture: A review. Journal of Applied Biology & Biotechnology 7(3): 69–77. https://doi.org/10.7324/JABB.2019.70313

Jayashree P, Shridhar N B, Vijaykumar M, Suhasini K, Jayakumar and Satyanarayana M L. (2012). Toxicological studies of Ficus Virens in wistar albino rat. International Research Journal of Pharmacy 3(12): 84-87.

Joshi J, Srisala J, Truong V H, Chen I, Nuangsaeng B, Suthienkul O, Lo C F, Flegel T W, Sritunyalucksana K and Thitamadee S. (2014). Variation in Vibrio parahaemolyticus isolates from a single Thai shrimp farm experiencing an outbreak of acute hepatopancreatic necrosis disease (AHPND). Aquaculture 428-429: 297–302. https://doi.org/10.1016/j.aquaculture.2014.03.030

Kandasamy S, Baggu C, Javagal M R, Lingamallu J R, Yenamandra V and Aradhya S M. (2014). Antioxidant properties of isolated compounds from banana rhizome. Journal of Food Science 79(5): H988–H1001. https://doi.org/10.1111/1750- 3841.12414

Kim B S, Jang S Y, Bang Y J, Hwang J, Koo Y, Jang K K, Lim D, Kim M H and Choi S H. (2018). Qstatin, a selective inhibitor of quorum sensing in Vibrio species. mBio 9(1): e02262-17. https://doi.org/10.1128/mBio.02262-17

Krishnan K R, James F and Mohan A. (2016). Isolation and characterization of n-hexadecanoic acid from Canthium parviflorum leaves. Journal of Chemistry and Pharmaceutical Research 8(8): 614–617.

Lee L H, Mutalib N S A, Law J W F, Wong S H and Letchumanan V. (2018). Discovery on antibiotic resistance patterns of Vibrio parahaemolyticus in Selangor reveals carbapenemase producing Vibrio parahaemolyticus in marine and freshwater fish. Frontiers in Microbiology 9(2513): 1–13. https://doi.org/10.3389/fmicb.2018.02513

Leiva S, Alvarado P, Huang Y, Wang J and Garrido I. (2015). Diversity of pigmented Gram-positive bacteria associated with marine macroalgae from Antarctica. FEMS Microbiology Letters 362(24): 1–6. https://doi.org/10.1093/femsle/fnv206

Matobole R M, Zyl L J V, Parker-Nance S, Davies-Coleman M T and Trindade. (2017). Antibacterial activities of bacteria isolated from the marine sponges Isodictya compressa and Higginsia bidentifera collected from Algoa Bay, South Africa. Marine Drugs 15(47): 1–19. https://doi.org/10.3390/md15020047

Marchesi J R, Sato T, Weightman A J, Martin T A, Fry J C, Iom S J and Wade W G. (1998). Design and evaluation of useful bacterium-specific PCR primers that amplify genes coding for bacterial 16S rRNA. Applied and Environmental Microbiology 64(2): 795–799. https://doi.org/10.1128/AEM.64.2.795-799.1998

Muthukrishnan S, Defoirdt T, Ina-Salwany M Y, Yusoff F M, Shariff M, Ismail S I and Natrah I. (2019). Acute hepatopancreatic necrosis disease (AHPND) in Penaeus vannamei (Boone, 1931) isolated from Malaysian shrimp ponds. Aquaculture. 511(15): 1–8. https://doi.org/10.1016/j.aquaculture.2019.734227

Palomo S, González I, de la Cruz M, Martín J, Tormo J R, Anderson M, Hill R T, Vicente F, Reyes F and Genilloud O. (2013). Sponge-derived Kocuria and Micrococcus spp. as sources of the new thiazolyl peptide antibiotic kocurin. Marine Drugs 11(4): 1071–1086. https://doi.org/10.3390/md11041071

Phelan R W, Barret M, Cotter P D, O’Connor P M, Chen R, Morrissey J P, Dobson A D W, O’Gara F and Barbosa T M. (2013). Subtilomycin: A new lantibiotic from Bacillus subtilis strain MMA7 isolated from the marine sponge Haliclona simulans. Marine Drugs 11(6): 1878–1898. https://doi.org/10.3390/md11061878

Prastya M E, Astuti R I, Batubara I, Takagi H and Wahyudi A T. (2020). Natural extract and its fractions isolated from the marine bacterium Pseudoalteromonas flavipulchra STILL-33 have antioxidant and antiaging activities in Schizosaccharomyces pombe. FEMS Yeast Research 20(3): 1–14. https://doi.org/10.1093/femsyr/ foaa014

Priya N P, Firdous A P, Jeevana R and Aravindakshan K K. (2015). Cytotoxic and antitumour studies of acetoacetanilide N(4)-methyl(phenyl)thiosemicarbazone and its transition metal complexes. Indian Journal of Pharmaceutical Sciences 77(6): 655–660. https://doi.org/10.4103/0250-474x.174981

Priyanto J A, Purwaningtyas W E, Ferantika D, Tohir D, Astuti R I and Wahyudi A T. (2022). Natural extracts derived from marine sponge-associated bacteria with diverse nonribosomal peptide synthetase genes have anticancer activities. Journal of Applied Pharmaceutical Science 12(4): 54–63. https://doi.org/10.7324/ JAPS.2021.110908

Reed L J and Muench H. (1938). A simple method of estimating fifty per cent endpoints. The American Journal of Hygiene 27(3): 493–497. https://doi.org/10.1093/ oxfordjournals.aje.a118408

Rini A F, Yuhana M and Wahyudi A T. (2017). Potency of sponge-associated bacteria producing bioactive compounds as biological control of vibriosis on shrimps. Jurnal Akuakultur Indonesia 16(1): 41–50. https://doi.org/10.19027/jai.16.1.41-50

Riyanti, Balansa W, Liu Y, Sharma A, Mihajlovic S, Hartwig C, Leis B, Rieuwpassa F J, Ijong F, Wägele H, König G M and Schäberle T F. (2020). Selection of sponge associated bacteria with high potential for the production of antibacterial compounds. Scientific Reports 10: 1–14. https://doi.org/10.1038/s41598-020-76256-2

Srinivas D, Venkatrayalu C H and Laxamappa B. (2016). Identifying diseases affecting farmed Litopenaeus vannamei in different areas of Nellore district in Andhra Pradesh, India. International Journal of Fisheries and Aquatic Studies 4(2): 447– 451.

Wahyudi A T, Priyanto J A, Maharsiwi W and Astuti R I. (2018). Screening and characterization of sponge-associated bacteria producing bioactive compounds anti-Vibrio sp. American Journal of Biochemistry and Biotechnology 14(3): 221–229. https://doi. org/10.3844/ajbbsp.2018.221.229

Wahyudi A T, Priyanto J A, Wulandari D R and Astuti R I. (2019). In vitro antibacterial activities of marine sponge-associated bacteria against pathogenic Vibrio spp. causes vibriosis in shrimps. International Journal of Pharmacy and Pharmaceutical Sciences. 11(11): 33–37. https://doi.org/10.22159/ijpps.2019v11i11.34814

Wijayanto D, Nursanto D B, Kurohman F and Nugroho R A. (2017). Profit maximization of white leg shrimp (Litopenaeus vannamei) intensive culture in Situbondo Regency, Indonesia. AACL Bioflux 10(6): 1436–1444.