IMPACT OF ECTO AND BLOOD-SUCKING PARASITES INFECTION ON THE CHEMICAL COMPOSITION OF MUSCLES IN WILD Mugil cephalus AND Scomber scombrus FROM SYRIAN COASTS (EASTERN MEDITERRANEAN)

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Published: 2022-12-09

Page: 1209-1220


SHADE GNEDE *

Animal Production Department, Faculty of Agriculture, Tishreen University, P.O.Box-2233, Latakia, Syria and General Establishment of Fisheries and Aquatic Livings, P.O.Box-121, Latakia, Syria. 

AMAL DAYOUB

Tishreen University, Higher Institute for Environmental Research, Latakia, Syria.

MOHAMAD HASSAN

Animal Production Department, Faculty of Agriculture, Tishreen University, P.O.Box-2233, Latakia, Syria and MARBEC, Université Montpellier, Ifremer, IRD, CNRS, 34200 Sète, France.

*Author to whom correspondence should be addressed.


Abstract

The present study aimed at isolating ectoparasite species and blood-sucking parasite- affecting wild Mugil cephalus and Scomber scombrus, and evaluating the impact of infection on the chemical composition of their muscles. A total of 238 individuals of M. cephalus and 224 of S. scombrus were captured from Syrian marine waters (Eastern Mediterranean) through two years, from April 2020 to April 2022. Fish samples were examined for infection, and parasites were isolated according to the wet smears method and identified at species level. Chemical composition: proteins, fats, moisture and ash contents of muscle of two species studied were determined. Variations of these different components in the infected and non-infected samples, and according to months or season, age and sex were assessed. Results showed the infection of M. cephalus by Ligophorus mediterraneus, Ergenstrema sp. (Monogenea) and Caligus pageti (Copepoda), whereas, only one ectoparasite species: Kuhnia scombri (Monogenea) was identified from S. scombrus. This is actually the first record of Ergenstrema sp; C. pageti and K. scombri in the two species studied in Syrian marine waters. This is also the first record of Ergenstrema sp. in wild M. cephalus in the world. No significant differences in the content of moisture, protein and ash were observed between the infected and non-infected fish. Nevertheless, fat content has showed a significant (P-value <0.05) decrease in the samples infected by the blood-sucking parasites- (i.e. C. pageti and K. scombri) in both species studied. In addition, significant differences of the chemical composition according to season and age were also found, but not between females and males.

Keywords: Ectoparasites, blood-sucking parasites, chemical composition, fish muscles, Mugil cephalus, Scomber scombrus, Syrian marine waters, Eastern Mediterranean


How to Cite

GNEDE, S., DAYOUB, A., & HASSAN, M. (2022). IMPACT OF ECTO AND BLOOD-SUCKING PARASITES INFECTION ON THE CHEMICAL COMPOSITION OF MUSCLES IN WILD Mugil cephalus AND Scomber scombrus FROM SYRIAN COASTS (EASTERN MEDITERRANEAN). Asian Journal of Advances in Research, 5(1), 1209–1220. Retrieved from https://mbimph.com/index.php/AJOAIR/article/view/3245

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References

Pal J, Shukla BN, Maurya AK, Verma HO, Pandey G, Amitha A. A review on role of fish in human nutrition with special emphasis to essential fatty acid. Int J Fish Aquat Stud. 2018;6(2):427-430.

Gokoglu N, Yerlikaya P. Chemical composition of fish. Seafood chilling, refrigeration and freezing: Science and technology. John Wiley & Sons. 2015;5-37.

Ravichandran S., Kumaravel K, Florence EP. Nutritive composition of some edible fin fishes. Int J Zool Res. 2011;7(3):241.

Begum ., Minar MH. Comparative study about body composition of different SIS, shell fish and ilish; commonly available in Bangladesh. Trends Fish Res. 2012;1(1):38-42.

Rani PSCHPD, Kumar VP, Rao RK, Shameem U. Seasonal variation of proximate composition of tuna fishes from Visakhapatnam fishing harbor, east coast of India. Int J Fish Aquat Stud. 2016;4(6):308-313.

Huss HH. Fresh fish--quality and quality changes: A training manual prepared for the FAO/DANIDA Training Programme on Fish Technology and Quality Control (No. 29). Food & Agriculture Org; 1988.

Huss HH, Jeppesen VF, Johansen C, Gram L. Biopreservation of fish products—a review of recent approaches and results. J Aquat Food Prod Technol. 1995;4(2):5-26.

Available:http://dx.doi.org/10.1300/J030v04n02_02

Silva JL, Chamul RS. Composition of marine and freshwater finfish and shellfish species. Marine and freshwater products handbook. Technomic Publishing, Lancaster 2000;31-45.

Islam MN, Joadder MAR. Seasonal variation of the proximate composition of freshwater Gobi, Glossogobius giuris (Hamilton) from the River Padma. Pak J Biol Sci. 2005;8(4):532-536.

Yousaf M, Salam A, Naeem M. Body composition of freshwater Wallago attu in relation to body size, condition factor and sex from southern Punjab, Pakistan. Afr J Biotechnol. 2011;10(20):4265-4268.

Naeem M, Ishtiaq A. Proximate composition of Mystus bleekeri in relation to body size and condition factor from Nala Daik, Sialkot, Pakistan. Afr J Biotechnol. 2011;10(52):10765-10773.

Daniel IE. Proximate composition of three commercial fishes commonly consumed in Akwa Ibom state, Nigeria. Int. J. Multidiscip. Acad Res. 2015;3(1).

Boran G, Karaçam H. Seasonal changes in proximate composition of some fish species from the Black Sea. Turkish J Fish Aquat Sci. 2011;11(1).

Begum M, Bhowmik S, Juliana FM, Hossain MS. Nutritional profile of hilsa fish Tenualosa ilisha (Hamilton, 1822) in six selected regions of Bangladesh. J Nutr Food Sci. 2016;6(2):567-570.

DOI: 10.4172/2155-9600.1000567

Karki S, Chowdhury S, Nath, S, Murmu P, Dora KC. Seasonal changes in proximate composition and textural attributes of farm raised chocolate mahseer (Neolissochilus hexagonolepis). J Entomol Zool Stud. 2019; 7(4):696-701.

Ben Smida MA, Marzouk B, El Cafsi M. The composition of fatty acids in the tissues of Tunisian swordfish (Xiphias gladius). Food Chem. 2009;115:522-528.

Wallace PD. Seasonal variation in fat content of mackerel (Scomber scombrus L.) caught in the western English Channel. Fisheries Research Technical Report No. 91. Ministry of Agriculture, Fisheries and Food, Directorate of Fisheries Research; 1991.

EL-Oudiani EO, Darej C, Moujahed N. Fatty acids and amino acids contents in Scomber scombrus fillets from the South East of Tunisia. Afr J Biotechnol. 2016;15(24):1246-1252.

Romotowska PE, Karlsdóttir MG, Gudjónsdóttir M, Kristinsson HG, Arason S. Seasonal and geographical variation in chemical composition and lipid stability of Atlantic mackerel (Scomber scombrus) caught in Icelandic waters. J Food Compost Anal. 2016;49:9-18.

Available:http://dx.doi.org/10.1016/j.jfca.2016.03.005

Garrido S, Rui R, Ben-Hamadou R, Cunha ME, Chícharo MA, Carl D, Lingen V. Spatio-temporal variability in fatty acid trophic biomarkers in stomach contents and muscle of Iberian sardine (Sardina pilchardus) and its relation¬ship with spawning. Mar Biol. 2008;154:1053–1065.

Available:https://doi. org/10.1007/s00227-008-0999-7

EFSA Panel on Biological Hazards (BIOHAZ). Scientific opinion on risk assessment of parasites in fishery products. EFSA J. 2010; 8(4): 1543.

Iwanowicz DD. Overview on the effects of parasites on fish health. In Proceedings of the Third Bilateral Conference between Russia and the United States. Bridging America and Russia with Shared Perspectives on Aquatic Animal Health. 2011;176-184.

Bush AO, Fernández JC, Esch GW, Seed JR. Parasitism: The diversity and ecology of animal parasites. Cambridge University Press. 2001;580.

Alifudin M, Priyono A, Nurfatimah A. Parasites inventory on ornamental fish transported in Soekarno-Hatta airport Cengkareng, Jakarta. J Akuak Indon. 2002;1(3):123-127.

Available:http://dx.doi.org/10.19027/jai.1.123-128

Fehri-Bedoui R, Smida MAB, Mejri H. Impact of a blood-sucking parasite on the chemical composition of fatty acids in the white muscle of garfish (Belone belone, Belonidae) from Tunisian coasts (Central Mediterranean). Afr J Biotechnol. 2013;12(44):6335-6339.

Nash CE, Shehadeh ZH. Review of breeding and propagation techniques for grey mullet Mugil cephalus L. ICLARM Studies and Reviews. International center for Living Aquatic Resources Management, Manila, Philippine. 1980 ;387.

Crosetti D. Current state of capture fisheries and culture of Mugilidae. In Crosetti D, Blaber SJM eds, Biology, Ecology and Culture of Grey Mullets (Mugilidae). CRC Press, Boca Raton, FL. 2016;398–450.

Andiewati S. Taxonomic study on crustacean parasites of the flathead grey mullet (Mugil cephalus) and red seabream (Pagrus major) in Hiroshima Bay, Japan. In IOP Conference Series: Earth and Environmental Science. 2019; 253(1):012019. IOP Publishing.

Available:http://dx.doi.org/10.1088/1755-1315/253/1/012010

FAO. Species Catalogue. Scombrids of the world. An annotated and illustrated catalogue of Tunas, Mackerels, Bonitos and related species known to date. Collette BB, Nauen CE. FAO Fish Synop. 1983;125(2):137.

Jansen T, Post S, Kristiansen T, Oskarsson GJ, Boje J, MacKenzie BR, Broberg M, Siegstad H. Ocean warming expands habitat of a rich natural resource and benefits a national economy. Ecol Appl. 2016;26:2021-2032.

Available:http://dx.doi.org/10.1002/eap.1384

Rubio-Rodríguez N, Beltrán S, Jaime I, Sara M, Sanz MT, Carballido JR. Production of omega-3 polyunsaturated fatty acid concentrates: A review. Innov Food Sci Emerg Technol. 2010;11(1):1-12.

Das HP. Seasonal variations in the chemical composition and caloric content of Mugil cephalus Linnaeus from the Goa waters. Mahasagar. 1978;11(3-4):177-184.

Nikolsky GV. The ecology of fishes. Academic Press. London, 1963;352.

Lucky Z. Methods for the diagnosis of Fish diseases. Amerind publishing Co., PVT, LTD, New Delhi, Bombay, Calcutta and New York; 1977.

Pritchard MH, Kruse GO. The collection and preservation of animal parasites. University of Nebraska. Lincoln. 1982;141.

Sprostonn G. The genus Kuhnia n.g. (Trematoda: Monogenea). An examination of the value of some specific characters, including factors of relative growth. Parasitology. 1945; 36:176-190.

Available:http://dx.doi.org/10.1017/S0031182000012154

Bykhovskaya-Pavlovskaya IE, Gussev AV, Dubinina MN, Izyurnova NA, Smirnova TS. Key to parasites of freshwater fishes of the USSR, II, Moskova, Leningrad, (Translation by Birrow A, and Cale ZS, 1964). Palestine Programme for Scientific, Translation, Jerusalem. 1962 ;919.

Lambert A, Sanfilippo D. Position systematique et biologie d' Ergenstrema mugilis Paperna, 1964 (Monogenea, Monopisthocotylea) parasite de Liza (Liza) ramada (Risso, 1826) (Teleosteen, Mugilidae). Bulletin du Museum national d'histoire naturelle, no. 472, Zoologie. 1977;329:823-831.

Gussev AV. Key of freshwater fish parasites. Institute of Zoology, Academy of Science, Section II, Leningrad, USSR. 1985;425.

Sarabeev VL, Balbuena JA, Euzet L. Taxonomic status of Ligophorus mugilinus (Hargis, 1955) (Monogenea: Ancyrocephalidae), with a description of a new species of Ligophorus from Mugil cephalus (Teleostei: Mugilidae) in the Mediterranean basin. J Parasitol. 2005;91:1444–1451.

Available:http://dx.doi.org/10.1645/GE-418R.1

Dmitrieva EV, Gerasev PI, Merella P, Pugachev ON. Redescriptions of Ligophorus cephali Rubtsova, Balbuena, Sarabeev, Blasco-Costa & Euzet, 2006 and L. chabaudi Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae), with notes on the functional morphology of the copulatory organ. Syst Parasitol. 2009;73(3):175-191.

Available:http://dx.doi.org/10.1007/s11230-009-9192-8

Russell FS. A new species of Caligus from Egypt, Caligus pageti, sp. N. Ann Mag Nat Hist. 1925;15(90):611-618.

Available:http://dx.doi.org/10.1080/00222932508633257

Bush AO, Lafferty KD, Lotz JM, Shostak AW. Parasitology meets ecology on its own terms: Margolis et al. revisited. J Parasitol. 1997;84:575–583.

Available:https://doi.org/10.2307/3284227

AOAC: Association of Official Analytical Chemists. Official methods of analysis of the association of analytical chemists, 18th edn. AOAC, Maryland; 2005.

R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria;

Available:URL http://www.R-project.org/. 2016.

Johnson SC, Bravo S, Nagasawa K, Kabata Z, Hwang J, Ho J, Shih CT. A review of the impact of parasitic copepods on marine aquaculture. Zool Stud. 2004;43:229-43.

Rohde K. The ecological niches of parasites. In Rohde K ed. Marine Parasitology Wallingford, Oxon: CSIRO Melbourne and CABI. 2005; 286-293.

Llewellyn J, Green JE, Kearn GC. A check-list of monogenean (platyhelminth) parasites of Plymouth hosts. J Mar Biol Assoc UK .1984;64(4):881-887.

Available:http://dx.doi.org/10.1017/S0025315400047299

Van den Broek WLF. The effects of Lernaeocera branchialis on the Merlangius merlangus population in the Medway Estuary. J Fish Biol. 1978;13(6):709-715.

Matthews BE. An introduction to parasitology. Cambridge University Press; 1998.

Roberts L, Janovy J.. Foundations of Parasitology. 6th Ed.. USA: McGraw-Hill Companies, Inc; 2000.

El-Aiatt O. Some biological aspects of 9 fish species from the Mediterranean coast, North Sinai, Egypt, with special reference to Grey mullet, Mugil cephalus (Linnaeus, 1758). Egypt J Aquat Biol Fish. 2022;26(1):45-62.

Available:http://dx.doi.org/10.21608/ejabf.2022.214034

Love RM. The biochemical composition of fish. In Brown ME ed, The physiology of fishes. Academic Press, New York. 1957; 401-418.

Available:http://dx.doi.org/10.1016/B978-1-4832-2817-4.50016-0

Das HP. Food of the grey mullet Mugil cephalus (L.) from the Goa region. Mahasagar. 1977;10(1-2):35-43.

EL-Oudiani S, Chetoui I, Darej C, Moujahed N. Sex and seasonal variation in proximate composition and fatty acid profile of Scomber scombrus (L. 1758) fillets from the Middle East Coast of Tunisia. Grasas y aceites. 2019;70(1):e285-e285.

Available:http://dx.doi.org/10.3989/gya.0235181

Anderson WW. Larval development, growth, and spawning of striped mullet (Mugil cephalus) along the south Atlantic coast of the United States. US Government Printing Office 2; 1958.