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Isolation and Identification of Bacterial Species Associated with Spoilage of Clarias gariepinus.

Ibrahim TA1*and Adetuyi O2

1Department of Food Science and Technology, Rufus Giwa Polytechnic, PMB 1019, Owo, Ondo State, Nigeria.

2Department of Fishery and Aquaculture Technology, Rufus Giwa Polytechnic, PMB 1019, Owo, Ondo state, Nigeria.

*Corresponding Author:
Ibrahim TA
Department of Food Science and Technology
Rufus Giwa Polytechnic, PMB 1019
Owo, Ondo State, Nigeria

Received date:11 July 2013Accepted date:19 September 2013

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Abstract

本研究进行隔离并标识bacteria species that are associated with fish spoilage using standard bacteriological techniques. The results of the bacteriological quality of the cat fish showed variation in the total bacterial and coliform counts to different anatomical parts (skins, gills and intestine). The highest total bacterial counts was recorded from gills (83 x 105cfu/ml) and lowest in skin (53 x 105cfu/ml) from cat fish. The total coliform counts of the cat fish ranges from 16 x 103cfu/ml, 36 x 103cfu/ml and 43 x 103cfu/ml in skin, intestine and gills respectively. A total of 288 colonies belonging to eleven genera where identified after comparing the morphological characteristics, gram staining reaction, biochemical tests and sugar utilization with those of known taxa. The identified genera were Streptococcus sp., Staphylococcus sp., Salmonella sp., Shigella sp., Pseudomonas sp., E. coli, Klebsiella sp., Enterobacter sp., Enterococcus sp., Campylobacter sp., and Proteus sp. The prevalence of these genera shows that Pseudomonas sp ( 96.95% ) was the most prevalent on all the anatomical parts followed by E. coli (14.64%) Enterococcus sp (9.74%), Klebsiella sp., (6.90%), Enterobacter sp (6.72%). The presence of these bacteria genera could pose serious health problem if consumed, it is therefore advised that proper care must be taken to prevent spoilage of the fish through major preservation techniques.

Keywords

Fish, Bacteria, Spoilage, Identification, Preservation, Anatomical

Introduction

The African catfish is farmed in concrete basins in Africa. Farming started in early 1970´s as field trials did show that African catfish is a fast growing fish which is very robust. African catfish tolerates a large variety of feedstuffs and is very resistant to changing and suboptimal water conditions [20]. It is found to be able to being farmed in high densities reaching production levels of 6-16 MT/ha on an annual basis when raised in monocultures and fed high quality fish feed. Most of the African catfish is sold alive into the market. The African catfish are harvested at an age of 6 to 8 month having a weight of 200-300g.The meat of African catfish is mildly flavoured and has a tender texture If heavy and continuous overfeeding occurs phytoplankton growth will bloom which occasionally leads to a muddy flavour of the meat [10]. Spawning in catfish is initiated artificially by hormone injection or injection of grinded pituitary glands of catfish or Tilapia into the ripe female. Spawning takes place in the night following injection where the female is placed with a male in a special net [14]. The following day both the female and the male are removed. The eggs do hatch and after 3- 4 days the larvae are developed and transferred to the nursing pond were they are grown for 3-4 weeks until they have developed to fingerlings and transferred to the growing pond. In Africa, fish are widely consumed as a remarkable some of animal protein. Fish production from rivers is influenced by a number of factors; hydrological requires, fishing pressure and environmental degradation [21]. The flesh of fish is usually infected with a wide range of microbes present in the water body. These bacteria are often found in the scales, gills, gut and alimentary tract of the fish. The bacteria present on the body of internal organs of fish indicate the extent of pollution of the water environment hence the bacteria flora of the fish depicts the bacteria flora of the water environment [16]. Fresh fish spoilage can be rapid after it is caught, the spoilage process (Rigor Mortis) will start within 12hours of their catch in the high ambient temperatures of the tropics (4). Rigor mortis is the process through which fish loses its flexibility due to stiffening of fish mussels after few hour of its death [1]. Most fish species degrade as a result of digestive enzymes and lipases, microbial spoilage from surface bacteria and oxidation [3]. During fish spoilage, there is a breakdown of various components and the formation of new compounds. Composition of the microflora on newly caught fish depends on the microbial contents of the water in which the fish live. Fish microflora includes bacterial species such as Pseudomonas, Alcaligens, Vibrio, Serratia and Micrococcus [11]. Microbial growth and metabolism is a major causes of fish spoilage which produce amines, biogenic amines such as putrescine, histramine and cadaverine, organic acids, sulphide, alcohols, aldehydes and ketones with unpleasant and unacceptable off-flavors [7,9]. This study was carried out to isolate and identify bacterial species associated with the spoilage of body of fresh fish preserved at ambient temperature.

Materials And Method

Collection of fish samples

The fishes use for this research study were bought from local market, Oja-Ikoko in Owo, Ondo State.

Isolation of bacterial species from the fish

About 2g of the fleshy part of the head part, the trunk and tail region of the spoilt fishes were cut and mixed in 10mls of sterile distilled water and mixed gently several times. 1ml of the stock solution was used in serial dilution to make a dilution up to 103. Exactly 0.5ml of the fish part samples were introduced to the surface of already prepared nutrient agar (for total bacteria count), MacConkey (for total coliform count) and EMB (for total E-coli count). The plates were incubated at 37°C for 24 hours.

Characterization of bacterial isolates

After 24 hours of incubation, the bacterial populations were counted; the morphological characteristics of the isolates were examined. Pure culture of the bacteria species were obtained on bjoe bottles before been subjected to gram staining reaction and biochemical tests such as oxidase, catalase, coagulase, citrate, sugar utilization as described by Cheesebrough [6]. The dichotomous key results were compared with the standard characterized bacteria in the Berger’s Manual of Systemic Bacteriology.

Results

Table 1showed the total bacterial and coliform count of different parts of cat fish. It showed that on the skin, the total bacterial count (TBC) was 53 x 105cful/ml, and total coliform count (TCC) was 16 x 103cful/ml. The TBC was 62 x 103and TCC was 36 x 103on the interface and on the gills, TBC was 83 x 105while TCC was 43 x 103.Table 2showed the gram staining and biochemical test of 260 pure isolates of the bacterial species. It showed that only 11 general specie were obtained from the whole total count. The probable bacteria werestreptococcus sp., Staphylococcus sp., Salmonella sp., E. coli, Enterobacter sp., Enterococcus sp., Campylobacter sp., Proteus sp., Pseudomonas sp., Klebsiella sp.Table 3showed the number of occurrence and percentage occurrence of these bacterial isolates. In the different part of the cat fish, on the skin, the dominant bacterial wasStaphylococcus sp.,(16), (27.59%) followed byShigella sp.(12) (20.69%) whileSalmonella sp.was the least (04) (6.90%). On the intestine,Pseudomonas sp.was the highest (08) (19.59%) followed byE. coli(15) (16.30%) whileCampylobacter sp.was the least occurred bacterial species (07) (7.60). on the gills,Pseudomonas spandE. coliwere also the high occurring species with 23 (10.91%) and (19) (17.27%) colonies respectively.Campylobacter sp(09), (8.19%) andSalmonella sp.(06) (5.45%) were the least occurring bacteria. The bacteriological study ofbacterial sp. Associated with different anatomical parts of cat fish showed that these parts contained at least eleven genera of bacteria. The total bacterial counts and total coliform counts obtained in the study don’t concur with the results of Yagoub [19]. The occurrence of some gram negative bacteria (Salmonella sp, Shigella sp, E coli, Enterobacter sp, Enterococcus sp, Proteus sp, Pseudomonas sp, klebsiella spand gram positive bacteria (Streptococcus sp, Staphylococcus sp, Enterococcus sp) is in concurrence with Turker and Usta [17]. In this study isolation of pathogenic enterobacteriacaea such as Salmonella sp, Shigella sp and the pathogenic E. coli from the collected samples indicated public health hazards and concern. The presence ofSalmonella spin the fishes sampled was in conformity with the result obtained by Hatha and Lakshmanaperumaisamy [12]. The isolation of klebsiella sp and Proteus sp, Shigella sp from this fish indicated feacal and environment pollution and this support the findings of Yagoub and Ahmed [18] and Najiah et al., [15]. The occurrence of this pathogenic bacteria especiallyE. coliin food (fish and fish products) may influence human health by inducing diseases/infections and cause abdominal pain, acute gastroenteritis, bloody/aumucoid diarrhea nausea vomiting and fever [2].

food-and-dairy-technology-Total-bacteria

Table 1:Total bacteria and coliform count of different parts of cat fish

food-and-dairy-technology-Gran-staining-reaction

Table 2:Gran staining reaction and biochemical test of pure culture isolate of bacteria from different parts of cat fish

food-and-dairy-technology-bacterial-species

Table 3:Incidence of bacterial species on the different parts of cat fish

温度和pH值对苏限制因素rvival of bacteria in fish products, these facts are used during the process of pasteurization and heat treatment, particularly of offal [8]. In the technology of marine animal processing by cooking, the following critical aspects of marine animals are significant the duration of cooking, temperature of steam, water and other mediaracy of thermometer and other monitoring and timing devices. For unpreserved fish, spoilage is a result of gram-negative, fermentative bacteria (such as Vibrionaceae), whereas psychrotolerant gram-negative bacteria (such as Pseudomonas spp and Shewanella spp.) tend to spoil chilled fish [11]. It is therefore important to distinguish non spoilage microflora from spoilage bacteria as many of the bacteria present do not actually contribute to spoilage [21]. Bacteriological criteria for fishery products, sea shellfish and molluscs have been elaborated both on international (Codex Committee on Food Hygiene) and European levels (Competent European Institution). Microbiological criteria, including samples plans and methods of analysis, are laid down when there is a need to protect public health, microbiological criteria for fish and fishery products include quantification of the counts of E. coli, thermo-tolerant coliform, mesophilic aerobic bacteria and pathogenic V. parahaemolyticus is performed during the production. At the finished product stage, the measure monitored is the quantification of the count of S. aureus and detection of bacteria of salmonella genus as their presence indicates recontamination of a finished product (Council Directive 91/493/EEC). Enterobactereacea (E. coli, Shigella sp, Salmonella sp, Enterobacter sp, Klebsiella sp) was isolated from skin, intestine, guts of cat fish. A different species of enterobactereacea was earlier isolated from channel catfish in the united states [5,17] and cultured fish from other parts of the world [8,9]. Results of biochemical tests were similar to those reported by other investigators including [5,13].

Conclusion

From the results obtained, it could be conclude that fish spoilage organisms are mostly caused by the bacteria’s although, some of the bacterial species are associated with the water environment of the fish.These bacterial species are capable of causing infections in man.

References

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