SUSCEPTIBILITY STUDIES OF FARMED PACIFIC WHITE SHRIMP, Penaeus vannamei TO NON-AHPND STRAIN OF Vibrio parahaemolyticus


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Authors

  • Ananda Raja R Senior Scientist, ICAR Central Institute of Brackish water Aquaculture
  • Sridhar R Professor and Head, Central University Laboratory, Tamil Nadu Veterinary and Animal Sciences University
  • Balachandran C Former Vice-Chancellor, Tamil Nadu Veterinary and Animal Sciences University
  • Palanisammi A Dean, Veterinary College and research Institute, Tirunelveli, Tamil Nadu Veterinary and Animal Sciences University
  • Ramesh S Professor and Head, Depertment of Veterinary Pharmacology and Toxicology, MVC, Tamil Nadu Veterinary and Animal Sciences University
  • Nagarajan K Assistant Professor, department of Veterinary Pathology, MVC, Tamil Nadu Veterinary and Animal Sciences University

Keywords:

Acute hepatopancreatic necrosis disease (AHPND), early mortality syndrome (EMS), immunohistochemistry, polyclonal antibodies, Penaeus vannamei, Vibrio parahaemolyticus

Abstract

Isolation and identification of bacteria from haemolymph, stomach and hepatopancreas (HP) were carried out from 37 farms in Tamil Nadu, India to find out the prevalence of Vibrio parahaemolyticus (Vp) infections with special reference to acute hepatopancreatic necrosis disease (AHPND). Bacterial identifications were done based on the morphological, physiological and biochemical characteristics. Vp isolates were identified by polymerase chain reaction (PCR) targeting Vp specific toxR and tlh genes, human pathogenic tdh and trh genes, and AHPND causing AP1, AP2, AP3 (pirAvp) and AP4 (pirAvp and pirBvp) genes. Histopathological and immunohistochemical (IHC) techniques were employed to identify the pathology due to Vp in HP tissues. Based on the morphological, physiological, biochemical and molecular characterization, 74 isolates were identified as Vp (35.14%), V. harveyi (21.62%), V. anguillarum (16.22%), V. campbellii (10.81%), V. mimicus (8.11%), V. alginolyticus (5.41%), and V. aeruginosa (2.7%). All isolates were negative for tdh, trh, AP1, AP2, AP3 and AP4 genes. Histopathology and IHC revealed that the HP was the prime organ affected in Vp infection. It further proved that the IHC could be used as an important tool to identify the establishment of infection in hepatopancreatic tissues.

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References

Abraham, T.J., Sasmal, D., Dash, G., Nagesh, T.S., Das, S.K. Mukhopadhayay, S.K. and Ganguly, S. (2013). Epizootology and pathology of bacterial infections in cultured shrimp Penaeus monodon Fabricius 1798 in West Bengal, India. Indian Journal of Fisheries, 60: 167- 171.

Alsina, M. and Blanch, A.R. (1994). A set of keys for biochemical identification of environmental Vibrio species. Journal of Applied Microbiology, 76: 79–85.

Banerjee, S.K., Kearney, A.K., Nadon, C.A., Peterson, C.L., Tyler, K., Bakouche, L., Clark, C.G., Hoang, L., Gilmour, M.W. and Farber, J.M. (2014). Phenotypic and genotypic characterization of Canadian clinical isolates of Vibrio parahaemolyticus collected from 2000 to 2009. Journal of Clinical Microbiology, 52: 1081–1088.

Baumann, P. and Schubert, R.H.W. (1984). Family II. Vibrionaceae. Veron 1965, 5345. In: Bergey’s Manual of Systematic Bacteriology, Vol 1 (ed. by N.R. Krieg and J.G. Holt), pp. 516–550. Baltimore, MD.

Bej, A.K., Patterson, D.P., Brasher, C.W., Vickery, M.C.L., Jones, D.D. and Kaysner, C.A. (1999). Detection of total and hemolysin-producing Vibrio parahaemolyticus in shellfish using multiplex PCR amplification of tl, tdh and trh. Journal of Microbiological Methods, 36: 215–225.

Bell, T.A. and Lightner, D.V. (1988). A handbook of normal penaeid shrimp histology. World Aquaculture Society, Baton Rouge, LA, USA, 114pp.

Dangtip, S., Sirikharin, R., Sanguanrut, P., Thitamadee, S., Sriunyaluucksana, K., Taengchaiyaphum, S., Mavichak, R., Proespraiwong, P. and Flegel, T.W. (2015). AP4 method for two-tube nested PCR detection of AHPND isolates of Vibrio parahaemolyticus. Aquaculture Reports, 2: 158-162.

DePaola, A., Nordstrom, J.L., Bowers, J.C., Wells, J.G. and Cook, D.W. (2003). Seasonal abundance of total and pathogenic Vibrio parahaemolyticus. Applied and Environmental Microbiology, 69: 1521–1526.

FAO. (2013). Report of the FAO/MARD Technical Workshop on Early Mortality Syndrome (EMS) or Acute Hepatopancreatic Necrosis Syndrome (AHPNS) of Cultured Shrimp (under TCP/VIE/3304). 54 p. Hanoi, Viet Nam, FAO Fisheries and Aquaculture Report No. 1053, Rome.

Flegel, T.W. and Lo, C.F. (2014). Free release of primers for specific detection of bacterial isolates that cause acute hepatopancreatic necrosis disease (AHPND). Published by the Network of Aquaculture Centres in Asia and the Pacific, Bangkok, Thailand. http://www. enaca.org/modules/library/publication. publication_id=1128. Accessed 14 Feb 2015.

Franceschini-Vicentini, I.B., Ribeiro, K., Papa, L.P., Junior, J.M., Vicentini, C.A. and Valenti, P.M.C.M. (2009). Histoarchitectural features of the hepatopancreas of the Amazon river prawn Macrobrachium amazonicum. International Journal of Morphology, 27: 121-128.

George, M.R. (2002). Characterization of Vibrio spp. from farm reared shrimps and coastal waters. Ph. D. Thesis, Department of Aquaculture, Fisheries College and Research Institute, Tamil Nadu Veterinary and Animal Sciences University, Thoothukudi, India.

Greenfield, E.A. (1988). Antibodies: A laboratory manual. p. 825. Cold Spring Harbour Laboratory. NY.

Jayaprakash, N.S. (2005). Antibody based diagnostics for detection of vibrios and their biological control using antagonistic bacteria in Macrobrachium rosenbergii larval rearing system. p. 115. Ph. D. Thesis, School of environmental studies, Cochin University of Science and Technology, Cochin, Kerala, India.

Jayasree, L., Janakiram, P. and Madhavi, R. (2000). Characteristics, pathogenicity and antibiotic sensitivity of bacterial isolates from white spot diseased shrimp. Asian Fisheries Society, 13: 327-334.

Jayasree, L., Janakiram, P., Geetha, G.K., Sivaprasad, B. and Veerendra Kumar, M. (2012). Loose shell syndrome (LSS) of cultured Penaeus monodon –microbiological and histopathological investigations. Indian Journal of Fisheries, 59: 117-123.

Kim, Y.B., Okuda, J., Matsumoto, C., Takahashi, N., Hashimoto, S. and Nishibuchi, M. (1999). Identification of Vibrio parahaemolyticus strains at the species level by PCR targeted to the toxR gene. Journal of Clinical Microbiology, 37: 1173–1177.

Kita-Tsukamoto, K., Oyaizu, H., Nanba, K. and Shimidu, U. (1993). Phylogenetic relationships of marine bacteria, mainly members of the family Vibrionaceae, determined on the basis of 16S rRNA sequences. International Journal of Systematic Bacteriology, 43: 8–19.

Kumar, B.K., Deekshit, V.K., Raj, J.R.M., Rai, P., Shivanagowda, B.M., Karunasagar, I. and Karunasagar, I. (2014). Diversity of Vibrio parahaemolyticus associated with disease outbreak among cultured Litopenaeus vannamei (Pacific white shrimp) in India. Aquaculture, 433: 247–251.

Kunanopparata, A., Chaivisuthangkuraa, P., Senapinb, S., Longyanta, S., Rukpratanpornd, S., Flegel, T.W. and Sithigorngul, P. (2011). Detection of infectious myonecrosis virus using monoclonal antibody specific to N and C fragments of the capsid protein expressed heterologously. Journal of Virological Methods, 171: 141–148.

Lavilla-Pitogo, C.R., Baticados, M.C.L., Cruz-Lacierda, E.R. and de la Pena, R. (1990). Occurrence of luminous bacterial disease of Penaeus monodon larvae in the Philippines. Aquaculture, 91: 1–13.

Letchumanan, V., Yin, W-F., Lee, L-H. and Chan, K-G. (2015). Prevalence and antimicrobial susceptibility of Vibrio parahaemolyticus isolated from retail shrimps in Malaysia. Frontiers in Microbiology, 6: 1-11.

Lightner D.V. (1993). Diseases of cultured penaeid shrimp. In: CRC handbook of mariculture, vol. 1. Crustacean aquaculture (ed. J. P. McVey), pp 393– 486. Boca Ratan, FL. CRC Press.

Lightner, D.V., Redman, C.R., Pantoja, B.L., Noble, L.M., Nunan and Tran, L. (2013). Documentation of an emerging disease (Early mortality syndrome) in SE Asia and Mexico. OIE reference laboratory for shrimp diseases, Department of Veterinary Science and Microbiology, School of Animal and Comparative Biomedical Sciences. Accessed 16 Feb 2016.

Liu, C.H., Cheng, W., Hsu, J.P. and Chen, J.C. (2004). Vibrio alginolyticus in the white shrimp Litopenaeus vannamei confirmed by polymerase chain reaction and 16S rDNA sequencing. Diseases of Aquatic Organisms, 61: 169–174.

Nordstrom, J.L., Vickery, M.C.L., Blackstone, G.M., Murray, S.L. and DePaola, A. (2007). Development of a multiplex real-time PCR assay with an internal amplification control for the detection of total and pathogenic Vibrio parahaemolyticus bacteria in oysters. Applied and Environmental Microbiology, 73: 5840–5847.

Piedad-Pascual, F., Coloso, R.M. and Tamse, C.T. (1983). Survival and some histological changes in Penaeus monodon Fabricius juveniles fed various carbohydrates. Aquaculture, 31: 169-180.

Raja, R. and Jithendran, K.P. (2015). Aquaculture disease diagnosis and health management. In: Advances in marine and brackishwater aquaculture. Eds: Perumal et al., Springer (India), Pvt. Ltd. pp. 247-256.

Raja, R.A., Panigrahi, A., De, D. and Sujeet Kumar. (2017c). White spot disease in Penaeus monodon associated with Vibrio mimicus in Sunderban India. Indian Journal of Fisheries, 64: 56-60.

Raja, R.A., Sridhar, R., Balachandran, C., Palanisammi, A., Ramesh, S. and Nagarajan, K. (2017a). Pathogenicity profile of Vibrio parahaemolyticus in farmed Pacific white shrimp, Penaeus vannamei. Fish and Shellfish Immunology, 67: 368-381.

Raja, R.A., Sridhar, R., Balachandran, C., Palanisammi, A., Raesh, S. and Nagarajan, K. (2017b). Prevalence of Vibrio spp. with special reference to Vibrio parahaemolyticus in farmed penaeid shrimp Penaeus vannamei (Boone, 1931) from selected districts of Tamil Nadu, India. Indian Journal of Fisheries, 64: 122-128.

Robertson, P.A.W., Calderon, J., Carrera, L., Stark, J.R., Zherdmant, M. and Austin, B. (1998). Experimental Vibrio harveyi infections in Penaeus vannamei larvae. Diseases of Aquatic Organisms, 32: 151-155.

Ruangpan, L. and Kitao, T. (1991). Vibrio bacteria isolated from black tiger shrimp, Penaeus monodon Fabricius. Journal of Fish Diseases, 14: 383–388.

Ruimy, R., Breittmayer, V., Elbaze, P., Lafay, B., Boussemart, O., Gauthier, M. and Christine, R. (1994). Phylogenetic analysis and assessment of the genera Vibrio, Photobacterium, Aeromonas, and Plesiomonas deduced from small subunit rRNA sequences. International Journal of Systematic Bacteriology, 44: 416–426.

Selvin, J.L. and Lipton, A.P. (2003). Vibrio alginolyticus associated with white spot disease of Penaeus monodon. Diseases of Aquatic Organisms, 57: 147-150.

Silvester, R., Alexander, D. and Ammanamveetil, M.H.A. (2015). Prevalence, antibiotic resistance, virulence and plasmid profiles of Vibrio parahaemolyticus from a tropical estuary and adjoining traditional prawn farm along the southwest coast of India. Annals of Microbiology, 65: 2141-2149.

Sithigorngul, P., Rukpratanporn, S., Longyant, S., Chaivisuthangkura, P., Sithigorngul, W. and Menasveta, P. (2002). Monoclonal antibodies specific to yellow-head virus (YHV) of Penaeus monodon. Diseases of Aquatic Organisms, 49: 71–76.

Soonthornchai, W., Rungrassamee, W., Karoonuthaisiri, N., Jarayabhand, P., Klinbunga, S., Soderhall, K. and Jiravanichpaisal, P. (2010). Expression of immune-related genes in the digestive organ of shrimp, Penaeus monodon, after an oral infection by Vibrio harveyi. Developmental and Comparative Immunology, 34: 19–28.

Soto-Rodriguez, S.A., Gomez-Gil, B., Lozano, R., del Rio-Rodriguez, R., Dieguez, A.L. and Romalde, J.L. (2012). Virulence of Vibrio harveyi responsible for the ‘‘Bright-red’’ Syndrome in the Pacific white shrimp Litopenaeus vannamei. Journal of Invertebrate Pathology, 109: 307–317.

Sudha, S., Mridula, C., Silvester, R. and Hatha, A.A.M. (2014). Prevalence and antibiotic resistance of pathogenic Vibrios in shellfishes from Cochin market. Indian Journal of Geo-Marine Sciences, 43: 815-824.

Tran, L., Nunan, L., Redman, R.M., Mohney, L., Pantoja, C.R., Fitzsimmons, K. and Lightner, D.V. (2013). Determination of the infectious nature of the agent of acute hepatopancreatic necrosis syndrome affecting penaeid shrimp. Diseases of Aquatic Organisms, 105: 45–55.

Velmurugan, S., Palanikumar, P., Velayuthani, P., Donio, M.B.S., Michael Babu, M., Lelin, C., Sudhakar, S. and Citarasu, T. (2015). Bacterial white patch disease caused by Bacillus cereus, a new emerging disease in semi-intensive culture of Litopenaeus vannamei. Aquaculture, 444: 49–54.

Venkateswaran, K., Dohmoto, N. and Harayama, S. (1998). Cloning and nucleotide sequence of the gyrB gene of Vibrio parahaemolyticus and its application in detection of this pathogen in shrimp. Applied and Environmental Microbiology, 64: 681–687.

Yang, Y.T., Chen, I.T., Lee, C.T., Chen, C.Y., Lin, S.S., Hor, L.I., Tseng, T.C., Huang, Y.T., Sritunyalucksana, K., Thitamadee, S., Wang, H.C. and Lo, C.F. (2014). Draft genome sequences of four strains of Vibrio parahaemolyticus, Three of which cause early mortality syndrome/ acute hepatopancreatic necrosis disease in Shrimp in China and Thailand. Genome Announcements, 2: e00816-14.

Zhou, J., Fang, W., Yang, X., Zhou, S., Hu, L., Li, X., Qi, X., Su, H. and Xie, L. (2012). A nonluminescent and highly virulent Vibrio harveyi strain is associated with ‘‘Bacterial white tail disease’’ of Litopenaeus vannamei shrimp. PLoS ONE, 7: e29961.

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19-11-2022

Published

29-11-2022

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How to Cite

R, A. R., R, S., C, B., A, P., & S, R. (2022). SUSCEPTIBILITY STUDIES OF FARMED PACIFIC WHITE SHRIMP, Penaeus vannamei TO NON-AHPND STRAIN OF Vibrio parahaemolyticus (N. K, Trans.). Indian Journal of Veterinary and Animal Sciences Research, 50(6), 53-68. https://epubs.icar.org.in/index.php/IJVASR/article/view/130453