Tải bản đầy đủ (.pdf) (5 trang)

Effect of body size and sub optimal water qual

Bạn đang xem bản rút gọn của tài liệu. Xem và tải ngay bản đầy đủ của tài liệu tại đây (490.43 KB, 5 trang )

link.springer.com

Effect of body size and sub-optimal water
quality on some hemato-immunological
parameters of spotted babylon snail
Babylonia areolata
AuthorsAuthors and affiliations
11-14 phút






Jareeporn Ruangsri
Jumreonsri Thawonsuwan
Sunee Wanlem
Boonsirm Withyachumnarnkul



Jareeporn Ruangsri
o 1
Email authorView author's OrcID profile





Jumreonsri Thawonsuwan
o 2


Sunee Wanlem
o 3
Boonsirm Withyachumnarnkul
o 4

1. 1.Department of Fishery and Coastal Resources, Faculty of Science and Industrial
TechnologyPrince of Songkla UniversityMuangThailand
2. 2.Songkhla Aquatic Animal Health Research CenterSongkhlaThailand
3. 3.Faculty of Veterinary SciencePrince of Songkla UniversitySongkhlaThailand
4. 4.Aqua Academy Farm138 Tha ChanaThailand
Original Article Aquaculture
First Online: 05 March 2018

Abstract


Cellular and humoral effectors are imperative for the innate defense mechanisms of
invertebrates, including the spotted babylon snail Babylonia areolata, a marine gastropod
belonging to the family Buccinidae. In this study, we have investigated the influence of body
size [5–8 g (small), 10–12 g (medium) and 15–17 g (large)], and culture waters of varied quality
[natural seawater, low salinity, low alkalinity, high total ammonia nitrogen (TAN) and artificial
seawater] on some hemato-immunological parameters [total hemocytic counts (THC),
hemolymphatic glucose, total protein concentration, phenoloxidase (PO), agglutinating and
lysozyme activity] of the snail. Growth performance measures and survival of test snails were
also evaluated after rearing them in culture water of varied quality. Body size did not influence
most parameters assessed, except that the lysozyme and PO activities of medium and large-size
snails were higher than those of the small-size snails. Sub-optimal culture water quality affected
hemato-immunological factors, growth and/or survival of the spotted babylon snail. Seawater
with low salinity, low alkalinity and a high TAN level caused decreased THC, hemolymphatic
glucose, and PO activity; increased lysozyme activity; and clearly retarded growth of the snail.

The snails held in artificial seawater could not survive after 4 weeks, suggesting the lack of
certain essential factors necessary for their survival.

Keywords
Growth performance Innate defense Culture water Artificial seawater Marine gastropod
This is a preview of subscription content, log in to check access.

Notes
Acknowledgements
This research was financially supported by Prince of Songkla University, Surat Thani Campus,
Thailand. Nirut Sukasem and his staff at Rajabhut Phuket University are gratefully
acknowledged for their help in conducting the experiments with sub-optimal water quality
conditions. We thank Associate Prof. Dr. Seppo Karrila for checking the English language.

References
1. Adema CM, Van der Knaap WPW, Siminia T (1991) Molluscan haemocyte-mediated
cytotoxicity: the role of reactive oxygen intermediates. Rev Aquat Sci 5:201–223Google
Scholar
2. Altena COVR, Gittenberger E (1981) The genus Babylonia (Prosobranchia, Buccinidae).
Zool Verh 188:1–57Google Scholar
3. Atkinson M (1998) Elemental composition of commercial sea salts. J Aquaricult Aquat
Sci 8:39Google Scholar
4. Bashevkin SM, Pechenik JA (2015) The interactive influence of temperature and salinity
on larval and juvenile growth in the gastropod Crepidula fornicata L. J Exp Mar Biol
Ecol 470:78–91CrossRefGoogle Scholar


5. Boyd C, Thunjai T, Boonyaratpalin M (2002) Dissolved salts in waters for inland, lowsalinity shrimp culture. GAA 5:40–45Google Scholar
6. Cawthorne DF, Beard T, Davenport J, Wickins JF (1983) Responses of juvenile Penaeus
monodon Fabricius to natural and artificial sea waters of low salinity. Aquaculture

32:165–174CrossRefGoogle Scholar
7. Chaitanawisuti N, Kritsanapuntu S, Santhaweesuk W (2009) Growth, production and
economic considerations for commercial production of marketable sizes of spotted
babylon Babylonia areolata, using a pilot abandoned marine shrimp hatchery and
recirculating culture system. IJRA 10:43–62CrossRefGoogle Scholar
8. Chaitanawisuti N, Kritsanapun S, Santhaweesuk W (2011a) Growth, food efficiency, and
biochemical composition of juvenile spotted babylon Babylonia areolata Link fed on
conventional trash fish and a formulated moist diet. Aquac Int 19:865–
872CrossRefGoogle Scholar
9. Chaitanawisuti N, Kritsanapuntu A, Santaweesuk W (2011b) Comparisons between two
production–scale methods for the intensive culture of juveniles spotted babylon
Babylonia areolata, to marketable sizes. Int J Fish Aquac 3:79–88Google Scholar
10. Chang YP, Liu CH, Wu CC, Chiang CM, Lian JL, Hsieh SL (2012) Dietary
administration of zingerone to enhance growth, non-specific immune response, and
resistance to Vibrio alginolyticus in Pacific white shrimp Litopenaeus vannamei
juveniles. Fish Shellfish Immunol 32:284–290CrossRefPubMedGoogle Scholar
11. Cheng W, Hsiao IS, Chen JC (2004a) Effect of ammonia on the immune response of
Taiwan abalone Haliotis diversicolor supertexta and its susceptibility to Vibrio
parahaemolyticus. Fish Shellfish Immunol 17:193–202CrossRefPubMedGoogle Scholar
12. Cheng WT, Hsiao IS, Chen JC (2004b) Effect of nitrite on immune response of Taiwan
abalone Haliotis diversicolor supertexta and its susceptibility to Vibrio
parahaemolyticus. Dis Aquat Org 60:157–164CrossRefPubMedGoogle Scholar
13. Cheng WT, Juang FM, Chen JC (2004c) The immune response of Taiwan abalone
Haliotis diversicolor supertexta and its susceptibility to Vibrio parahaemolyticus at
different salinity levels. Fish Shellfish Immunol 16:295–306CrossRefPubMedGoogle
Scholar
14. Clark MS, Husmann G, Thorne MAS, Burns G, Truebano M, Peck LS, Abele D, Philipp
EER (2013) Hypoxia impacts large adults first: consequences in a warming world. Glob
Change Biol 19:2251–2263CrossRefGoogle Scholar
15. Davis DA, Saoud IP, McGraw WJ, Rouse DB (2002) Considerations for Litopenaeus

vannamei reared in inland low salinity waters. In: Cruz-Suarez LE et al. (eds) Avances en
Nutrición Acuícola. VI. Memorias del VI Simposium Internacional de Nutricion
Acuicola. 3 al 6 de Septiembre del 2002, Cancun, Quintana Roo, Mexico, pp 73–
90Google Scholar
16. Demers NE, Bayne CJ (1997) The immediate effects of stress on hormones and plasma
lysozyme in rainbow trout. Dev Comp Immunol 21:363–373CrossRefPubMedGoogle
Scholar
17. Di GL, Zhang ZX, Ke CH, Guo JR, Xue M, Ni JB, Wang DX (2011) Morphological
characterization of the haemocytes of the ivory snail Babylonia areolata Neogastropoda
Buccinidae. J Mar Biol Assoc UK 91:1489–1497CrossRefGoogle Scholar


18. Di G, Zhang Z, Ke C (2013) Phagocytosis and respiratory burst activity of haemocytes
from the ivory snail Babylonia areolata. Fish Shellfish Immunol 35:366–
374CrossRefPubMedGoogle Scholar
19. Galloway TS, Depledge MH (2001) Immunotoxicity in invertebrates: measurement and
ecotoxicological relevance. Ecotoxicology 10:5–23CrossRefPubMedGoogle Scholar
20. Guo Y, He H (2014) Identification and characterization of a goose-type lysozyme from
sewage snail Physa acuta. Fish Shellfish Immunol 39:321–325CrossRefPubMedGoogle
Scholar
21. Hooper C, Day R, Slocombe R, Handlinger J, Benkendorff K (2007) Stress and immune
responses in abalone: limitations in current knowledge and investigative methods based
on other models. Fish Shellfish Immunol 22:363–379CrossRefPubMedGoogle Scholar
22. Hossain MS, Hussain MZ, Chowdhury SR (2006) An analysis of economic and
environmental issues associated with sea salt production in Bangladesh and Thailand
coast. Int J Ecol Environ Sci 32:159–172Google Scholar
23. Huchette S, Koh CS, Day R (2003) Growth of juvenile blacklip abalone Haliotis rubra in
aquaculture tanks: effects of density and ammonia. Aquaculture 219:457–
470CrossRefGoogle Scholar
24. Husmann G, Abele D, Rosenstiel P, Clark MS, Kraemer L, Philipp EER (2014) Agedependent expression of stress and antimicrobial genes in the hemocytes and siphon

tissue of the Antarctic bivalve Laternula elliptica exposed to injury and starvation. Cell
Stress Chaperones 19:15–32CrossRefPubMedGoogle Scholar
25. Hyvarinen A, Nikkila E (1962) Specific determination of blood glucose with O-toludine.
Clin Chem Acta 7:140–143CrossRefGoogle Scholar
26. Kovac N, Glavas N, Dolenec M, Smuc NR, Slejkovec Z (2013) Chemical composition of
natural sea salt from the Secovlje Salina (Gulf of Trieste, northern Adriatic). Acta Chim
Slov 60:706–714PubMedGoogle Scholar
27. Kritsanapuntu S, Chaitanawisuti N, Santhaweesuk W, Natsukari SY (2006) Effects of
water exchange regimes on growth, survival and shell normality of the hatchery reared
juvenile spotted babylon Babylonia areolata Link 1807 in a recirculating seawater
system. Aquac Int 14:587–594CrossRefGoogle Scholar
28. Kritsanapuntu S, Chaitanawisuti N, Santhaweesuk W, Natsukari Y (2008) Growth
performances for monoculture and polyculture of hatchery-reared juvenile spotted
babylon Babylonia areolata Link 1807, in large-scale earthen ponds. Aquac Res
39:1556–1561CrossRefGoogle Scholar
29. Kritsanapuntu S, Chaitanawisuti N, Natsukari Y (2009) Growth and water quality for
growing-out of juvenile spotted babylon Babylonia areolata, at different water-exchange
regimes in a large-scale operation of earthen ponds. Aquac Int 17:77–84CrossRefGoogle
Scholar
30. Kritsanapuntu S, Chaitanawisuti N, Santaweesuk W (2013) Effects of dietary partial
replacement of tuna oil by corn oil in formulated diets for growth performance and
proximate composition of juvenile spotted babylon Babylonia areolata under hatchery
conditions. J Aquac Res Dev 4:197CrossRefGoogle Scholar
31. Loker ES (2010) Gastropod immunobiology. Adv Exp Med Biol 708:17–
43CrossRefPubMedGoogle Scholar
32. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the
Folin phenol reagent. J Biol Chem 193:265–275PubMedGoogle Scholar


33. Lucas A (1996) Physical concepts of bioenergetics. In: Lucas A (ed) Bioenergetics of

aquatic animals. Taylor and Francis, FranceGoogle Scholar
34. Panichasuk P (1996) Areola babylon Babylonia areolata Link 1807. Thai Fish Gaz
49:107–117Google Scholar
35. Ruangsri J, Lokesh J, Fernandes JMO, Kiron V (2014) Transcriptional regulation of
antimicrobial peptides in mucosal tissues of Atlantic cod Gadus morhua L. in response to
different stimuli. Aquac Res 45:1893–1905CrossRefGoogle Scholar
36. Santarem M, Figueras A (1995) Basic studies on defense mechanisms of mussels. In:
Stolen JS et al (eds) Techniques in fish immunology 4. Immunology and pathology of
aquatic invertebrates, SOS, Fair HavenGoogle Scholar
37. Soderhall K, Rogener W, Soderhall I, Newton RP, Ratcliffe NA (1988) The properties
and purification of a Blaberus craniifer plasma protein which enhances the activation of
haemocyte prophenoloxidase by a β 1, 3-glucan. Insect Biochem 18:323–
330CrossRefGoogle Scholar
38. Sung HH, Chang HJ, Her CH, Chang JC, Song YL (1998) Phenoloxidase activity of
hemocytes derived from Penaeus monodon and Macrobrachium rosenbergii. J Invertebr
Pathol 71:26–33CrossRefPubMedGoogle Scholar
39. Supamattaya K, Ruangsri J, Kiriratnikom S, Suanyuk N (2002) Normal immunophysiological parameters in black tiger shrimp Penaeus monodon and the effects of
environmental stress and diseases. Fish Sci 68:983–984CrossRefGoogle Scholar
40. Vedamanikam VJ, Hayimad T (2013) Effect of mixtures of metals on the spotted babylon
snail Babylonia areolata under different temperature conditions. Toxicol Environ Chem
95:1388–1394CrossRefGoogle Scholar
41. Xue M, Ke CH, Wang DX, Wei YJ, Xu YB (2010) The combined effects of temperature
and salinity on growth and survival of hatchery-reared juvenile spotted babylon
Babylonia areolata Link 1807. J World Aquac Soc 41:116–122CrossRefGoogle Scholar

Copyright information
© Japanese Society of Fisheries Science 2018




×