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Fish Is One of The Most Consumed Seafood and It Is A Highly Perishable Food Product
Fish Is One of The Most Consumed Seafood and It Is A Highly Perishable Food Product
According to Gram and Dalgaard (2002), there are three modes of fish spoilage: Oxidation,
Enzymatic and Microbial spoilage. This essay is aimed at giving an account toward the
qualitative and quantitative microbial contamination of fish, describing the mechanism of fish
and shellfish spoilage and to further comprehend fish and shellfish diseases mostly in
Eswatini.
Freshly caught fish will be almost free from bacteria but the surface slime, gills and intestine
may contain considerable load of bacteria. When the fish is dead, these bacteria start
attacking the flesh causing spoilage and produce undesirable compounds. The nature and type
of bacteria present in a fish depends upon the water from where it is caught and methods used
for handling of the fish after its catch. The important changes brought out by the action of the
bacteria in fish are as follows (Gram & Dalgaard, 2002).
Reduction of trimethylamineoxida (TMAO) to trimethylamine (TMA)
Marine fish contains a small percentage of odourless TMAO which is reduced to an offensive
smelling TMA by the action of bacteria.
The bacterial action of amino acids present in the fish muscle leads to formation of primary
amines. Examples are formation of histamine from histidine, arginine from glutamic acid etc.
This bacterial action may cause food poisoning in extreme cases.
Breakdown in Urea
The high concentration of urea in the flesh of some fishes is degraded to ammonia by the
microorganisms. The formation of ammonia is accompanied by an offensive odour.
In a study carried by Dalgaard (1995), whereby the importance of the different groups of
microorganisms were evaluated by comparison of microbial spoilage activity determined in
model substrates and in product experiments. The yield factor for production of
trimethylamine (YTMA/CFU) and the cell concentration determined at the time of off-odour
detection were used as quantitative measurements of microbial spoilage activity. On average
cells of P. phosphoreum produced 30 times more TMA than cells of S. putrefaciens,
YTMA/CFU of the two organisms were 10(-8.0) mg-N TMA/cfu and 10(-9.5) mg-N
TMA/cfu, respectively. With these yield factors the level of TMA found in spoiled packed
cod (30 mg-N TMA/100g) corresponds to about 10(7) cfu/g of P. phosphoreum and to 10(8)-
10(9) cfu/g of S. putrefaciens. 10(7) cfu/g of P. phosphoreum were actually found in spoiled
packed cod suggesting this organism could be responsible for spoilage. High cell
concentrations of more than 10(8) cfu/g of S. putrefaciens were required for production of
detectable off-odours and is was concluded that this organism is without importance for
spoilage of packed cod.
Gram and Huss (1996), stated that, Shewanella putrefaciens and Pseudomonas spp. are the
specific spoilage bacteria of iced fresh fish regardless of the origin of the fish. Modified
atmosphere stored marine fish from temperate waters are spoiled by the carbon dioxide
resistant Photobacterium phosphoreum whereas Gram-positive bacteria are likely spoilers of
carbon dioxide packed fish from fresh or tropical waters. Fish products with high salt
contents may spoil due to growth of halophilic bacteria (salted fish) or growth of anaerobic
bacteria and yeasts (barrel salted fish). Whilst the spoilage of fresh and highly salted fish is
well understood, much less is known about spoilage of lightly preserved fish products. It is
concluded that the spoilage is probably caused by lactic acid bacteria, certain psychotrophic
Enterobacteriaceae and Photobacterium phosphoreum.
However Gram and Dalgaard (2002), also stated that the other modes of Fish and shellfish
spoilage also includes; Oxidative and Enzymatic spoilages.
Oxidative spoilage
Lipid oxidation is a major cause of deterioration and spoilage of fish that contain high oil/fat
content stored fat in their flesh. Oxidation typically involves the reaction of oxygen with the
double bonds of fatty acids. In fish, lipid oxidation can occur enzymatically or non-
enzymatically. Lipid oxidation promotes protein denaturation, modification of the protein,
electrophoretic profiles, nutritional losses, and endogenous antioxidant systems losses. Lipid
hydrolysis and oxidation cause “belly burst” in fish in which the enzymes and
microorganisms of the digestive tract cause massive gas development (Gram & Dalgaard,
2002).
Enzymatic spoilage
After capture, biological and chemical changes take place in dead fish due to the action of
various enzymes found in fish. The digestive enzymes cause extensive autolysis which results
in fish muscle softening, rupture of the belly wall, and drain out of the blood. Several
proteolytic enzymes are found in fish that contribute to degradation in fish muscle and fish
products during storage and processing. Proteolysis is responsible for the degradation of
proteins which leads to fish spoilage by microbial growth (Gopakumar,2000).
The fish spoilage is also caused by psychrotrophic, aerobic, or facultative anaerobic Gram-
negative bacteria such as Pseudomonas, Moraxella, Acinetobacter, Shewanella putrifaciens,
Vibrio, Flavobacterium, Photobacterium, and Aeromonas. Gram-positive bacteria such
as Staphylococcus spp., Micrococcus, Bacillus, Clostridium, Corynebacterium, Brochothric
thermosphacta, and Streptococcus are found in fish. (Gram & Huss, 2000). It is therefore,
important to distinguish non spoilage microflora from spoilage bacteria as many of the
bacteria present do not actually contribute to spoilage (Huss, 1995).
Huss (1995) further stated that lactic acid bacteria (LAB) can predominate in fish storage
under vacuum or carbon dioxide storage. Some parasites can also be transmitted by fish,
including tapeworm (Diphyllobothrium latum), nematodes (Anisakis simplex and Capillaria
philippinensis), and trematodes (Opisthorchis and Paragonimus). Spoilage compounds are
produced by microorganisms during the storage of fresh fish. Liston (1980) stated that
proteins are degraded by the proteases into peptides and amino acids, whereas lipids are
degraded by lipases into fatty acids, glycerol and other compounds.
In an article by Hong, Regenstein and Luo (2017), stated that most fishing activities in
Eswatini are carried out in dams such Maguga dam mainly during leisure time, therefore
Eswatini imports most of its fish. The most available fish species includes Tilapia and
Catfish. Hong et al (2017) further stated that cases of fish related diseases in Eswatini may be
due to the consumption an infected fish or raw or undercooked fish. In as much as the
prevalence rate is minimal, fish disease may be bacterial, fungal and parasitic.
Novotny, Dvorska, Lorencova, Beren and Pavlik (2004), anchored Hong’s et al (2017)
finding that fish and shellfish have been identified as reservoirs for; Viral Diseases,
Helminthic Diseases, Bacterial Diseases, Parasitic Diseases, Fungal Diseases. Novotny,
Dvorska, Lorencova, Beren and Pavlik (2004), further described the following as follows;
Viral Diseases
Of the known reported virus infections of oysters, "Ovacystis" infection is the most common,
but it is probably of little economic importance. It can be detected histologically as
hypertrophy of the ovarian follicles. The effect of this virus upon reproductive. Performance
has not been evaluated. A herpes virus infection has been described by Austin Farley (1972)
in oysters. Apparently, expression of the disease was temperature dependent and was found
in oysters’ cultivated in the heated effluent of a power plant. When pathogen that produces
serious economic losses in adult shellfish in warm climates. Sirolpidium sp. is a common
infection of hatchery-reared larval shellfish.
Helminthic Diseases
Among the helminth parasites of shellfish, trematode, cestode, and nematode parasites may
be found. Larval forms of trematodes (especially Bucephalus sp.) and cestodes (especially
Tylocephalum sp.) are of economic importance as shellfish pathogens that often produce
sterility in affected shellfish. Most of the larval forms mature in fish which serve as definitive
hosts. Some are of public health significance
Bacterial Diseases
The outbreak of cholera has been related to the consumption of shellfish in Africa.
Parasitic Diseases
Protozoans Shellfish protozoan infections are very common. This is especially true of the
ciliates that are common inhabitants of shellfish tissues. They become especially active when
other pathogens such as bacterial agents are present. Hexamita sp. and the amoeboid protozoa
are pathogenic. When shellfish are maintained under adverse conditions, such as extreme
temperatures, protozoa may actively invade shellfish tissues and produce deterioration or
spoilage.
Fungal Diseases
Dalgaard, P., H.L. Madsen, N. Samieian and J. Emborg, (2006). Biogenic amine formation
and microbial spoilage in chilled garfish (Belone belone) effect of modified
atmosphere packaging and previous frozen storage. J. Applied Microbiol., 101: 80-95.
DOI: 10.1111/j.1365-2672.2006. 02905.
Gram, L., & Dalgaard, P. (2002). Fish spoilage bacteria–problems and solutions. Current
opinion in biotechnology, 13(3), 262-266.
Gram, L. and H.H. Huss, (2000). Fresh and Processed Fish and Shellfish. In: The
Microbiological Safety and Quality of Foods, Lund, B.M., A.C. BairdParker and
G.W. Gould (Eds.). Chapman and Hall, London, ISBN: 10: 0834213230, pp: 472-
506.
Gram, L. and P. Dalgaard, (2002). Fish spoilage bacteriaproblems and solutions. Current
Opinion Biotechnol., 13: 2
Gopakumar, K. (2000). Enzymes and Enzyme products as Quality Indices. Seafood Enzymes,
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products. International journal of food microbiology, 33(1), 121-137.
Gram, L., & Huss, H. H. (2000). Fresh and processed fish and shellfish. In The
microbiological safety and quality of food (pp. 472-506). Aspen Publishers.
Huss, H. H., Jeppesen, V. F., Johansen, C., & Gram, L. (1995). Biopreservation of fish
products—a review of recent approaches and results. Journal of aquatic food product
technology, 4(2), 5-26.
Huss, H.H., (1988). Fresh Fish: Quality and Quality Changes. FAO Fisheries Series No. 29,
FAO, Rome, Italy, ISBN: 92-5-102395-6, pp: 132. Huss, H.H., 1995. Quality and
quality changes in fresh fish. FAO Fisheries Technical Paper 348, FAO, Rome, Italy.
http://www.fao.org/DOCREP/V7180E/V7180E00.HTM
Novotny, L., Dvorska, L., Lorencova, A., Baranov., & Pavlik, I. (2000). Fish; A potential
source of bacterial pathogens for human being. Veterinarni medicina, 49 (9), 343-358