• google scholor
  • Views: 2707

  • PDF Downloads: 290

Total Heterotrophic Bacterial Load in the Gut of Detritus Fishes: A Case Study of Pichavaram Mangrove Environment, Southeast Coast, India

V. Thangamani1*and N. Rajendran1

DOI:http://dx.doi.org/10.12944/CWE.11.3.12

Total heterotrophic bacterial (THB) load of detritus fin and shell fishes collected from mangrove environment were investigated. The collected fish and prawn samples were subjected to the microbiological study. The THB load was higher in milk fish (Chanos chanos) (2.24 x 105CFU/g) followed by Indian white prawn (Fenneropenaeus indicus) (3.16 x 105CFU/g) than theLiza parsia(1.90 x 105CFU/g) andPenaeus monodon(1.88 x 105CFU/g). A total of 355 bacterial strains were isolated and identified, in which 64, 57, 51, 47, 44, 42, 21, 29, 355 strains were belongs toPseudomonasspp.,气单胞菌属spp., Bacillusspp., Enterobacterspp., Vibriospp., Flavobacteriumspp., Alcaligenesspp. andAcinetobacterspp.,Pseudomonasspp. and气单胞菌属spp., respectively. The present work showed that theBacillusspp。,更高的鱼和虾在肠道山姆ples studied. This work suggests that these bacteria can be effectively used as supplement in fish/prawn feed for commercial aquaculture or as probiotic to enhance the colonization in fish/prawn gut.


Heterotrophic; Investigated; Microbiological; Flavobacterium spp

Copy the following to cite this article:

Thangamani V, Rajendran N. Total Heterotrophic Bacterial Load in the Gut of Detritus Fishes: A Case Study of Pichavaram Mangrove Environment, Southeast Coast, India. Curr World Environ 2016;11(3). DOI:http://dx.doi.org/10.12944/CWE.11.3.12

Copy the following to cite this URL:

Thangamani V, Rajendran N. Total Heterotrophic Bacterial Load in the Gut of Detritus Fishes: A Case Study of Pichavaram Mangrove Environment, Southeast Coast, India. Curr World Environ 2016;11(3). Available from://www.a-i-l-s-a.com/?p=16450


Download article (pdf)
Citation Manager
Publish History


Article Publishing History

Received: 2016-01-12
Accepted: 2016-10-18

Introduction

The microorganism enters in to the digestive system of fish through food and environment and certainly not all bacteria in food which gain entry in the digestive tract of fishes establish themselves there.1They play an important role in the formation of microbes in the digestive tract of fishes.2The digestive tract of fish is rich in nutrient that provides favorable conditions for the growth of majority of bacteria that involved in the digestive process, growth and disease of the host.3The composition of intestinal microflora of animals can be altered by age, nutritional condition, developmental stages and stress. These changes can tempt disease or beneficial effect on the host animals.4Hence, it may be possible to assess the susceptibility of fish to disease by observing the composition of gut microflora. Some bacteria able to tolerate the low pH in gastric juices resist the action of bile acids, lysozyme secreted in intestines, immune responses and adheres to the mucus or enteric wall surface could persist for a relatively long time and eventually make intestinal micro flora specific to each host animal.5It is clear that bacterial species presents in the gut can influence the health and growth of the host.

The colonization of the microorganisms in the digestive system is influenced by a number of host and non-host related factors in marine and other aquatic animals. On the other hand, bacteria producing antibacterial substances were isolated from marine fish intestines5,6,7thereby suggesting that these bacteria may inhibit the establishment of invading bacteria in the fish intestine. In general, due to the bacterial degradation fishes spoil quickly and unfit for consumption. Among the bacteria,Pseudomonassp. may contribute to spoilage by the production of histamines in fish tissue.8The importance of intestinal bacteria has been established in birds and mammals. However, there is limited information is available on the bacterial load in the gut of detritus fishes. Hence, the present study was undertaken to investigate the THB load in the detritus fishes of mangrove environment.

Materials and Methods

Pichavaram mangrove forest is located (11o27’N; 79o47’E) in the south east coast of India nearly 250 Km away from Chennai city and 15km away from the Chidambaram town on the eastern side. It is one of the typical mangrove forests in India with a high productivity of 8 tonnes of organic detritus ha/year. It consists of 52 small and large islets with a spread of 1100 ha. Of the total area, 50% covered by forests, 40% covered by water and remaining 10% by sand and mud flats. The biotope is influenced by mixing of neritic water from Bay of Bengal, brackishwater from Coleroon and Vellar estuaries and freshwater from Khan Sahib canal. Thirteen species of mangrove species and 76 mangrove associate species are present. The most dominant mangrove plant species of the study area includesRhizophoraandAvicennia.

Detritus fishes,Liza parsia(Golden mullet),Chanos chanos(Milk fish) and shrimps (Indian white prawn -Fenneropenaeus indicusand Tiger prawn -Penaeus monodon) were collected during December 2014 from the Pichavaram mangrove waters, in a sterile polythene bags and kept in an ice box at 4ºC. The collected samples were brought to the laboratory immediately for gut micro-floral analysis.

In order to analysis the gut micro floral populations the fish samples were subjected to the surface sterilization by immersion for 30 seconds in 70% ethanol. The ventral surface of the fish cut open with sterile scissors and then 1g of gut content was taken aseptically. The content was homogenized with tissue homogenizer (WW-44468-19, Argos Technologies, China) by adding 1 ml of 50% sterile sea water and transferred to 9 ml sterile blank solution. In order to enumerate of total heterotrophic bacterial load from gut of fish and prawn samples. The homogenate samples of fish and prawn was serially diluted up to 10-5and 0.1 ml of each dilution was spread (‘L’-rod method) onto petri dishes containing Zobell Marine Agar 2216 medium (Himedia) which consisted (g/l) of Peptic Digest of Animal Tissue (5), Yeast extract (1), Ferric citrate (0.1), Sodium chloride (19.45), Magnesium chloride (8.8), Sodium sulphate (3.24), Calcium chloride (1.8), Potassium chloride (0.55), Sodium bicarbonate (0.16), Potassium bromide (0.08), Stroncium chloride (0.034), Boric acid (0.022), Sodium silicate (0.004), Sodium fluorate (0.0024), Ammonium nitrate (0.0016), Disodium phosphate (0.008), Agar (15), pH (7.6 ± 0.2) and distilled water.

The inoculated plates were incubated (Thermo Scientific Incubator UE-3880000) at 37°C for 24 h, after which the colonies developed on the plate were counted and expressed as CFU/g of fish gut (Colony Forming Units). The plates were examined and counted for the number of colonies per Petri dishes. The microbial load in the given sample was calculated using the following formula and it is expressed as Colony Forming Unit (CFU) per gram of the homogenate sample.

formula1

Similarly, the shrimps gut was opened after removing the carapace and the enumeration of THB was carried out as per the procedure adopted for fish samples. Three replicates were maintained for each sample. After three to four days of incubation the bacterial colonies developed on the plates were counted, isolated, purified and preserved in the nutrient agar slants for further analysis. The purified strains were identified up to genus level based on the scheme described by Bergey’s.9Based on the Gram staining and the morphological characteristics of colonyviz.,structure, surface, elevation, color, opacity, shape, size, edge and the bacterial colonies were divided into different types and the number of colonies of each recognizable type was counted. Then the pure cultures were obtained through the repeated streaking of the few representatives of each bacterial type.

Results

Detritus fishes were studied for their total heterotrophic bacterial load. The results for fin-fishes are given in figure 1. The total heterotrophic bacterial count was high in Milk fish (Chanos chanos) 2.24 x 105CFU/g followed by Golden mullet (Lisa parsia) 1.90 x 105CFU/g (Fig.1). The gut bacterial density of shrimps is depicted in figure 2. The heterotrophic bacterial count was higher in Indian white shrimp (Fenneropenaeus indicus) 3.16 x 105CFU/g than the Tiger prawn (Penaeus monodon) 1.88 x 105CFU/g (Fig.2).

Fig.1 Total heterotrophic bacterial load in the gut of fishes


Figure 1: Total heterotrophic bacterial load in the gut of fishes
Click here to View figure

Fig. 2. Total heterotrophic bacterial load in the gut of shrimps


Figure 2: Total heterotrophic bacterial load in the gut of shrimps
Click here to View figure

A total of 355 bacterial strains were isolated from the fin-fishes and shell-fishes based on various tests performed and are categorized into eight genera. They areVibrio(44),Bacillus(51),Pseudomonas(64),Flavobacterium(42),气单胞菌属(57),Enterobacter(47),Alcaligenes(21) andAcinetobacter(29) (Table 1).

Table 1: Bacterial strains isolated from fin- fishes and shell-fishes collected from mangrove waters

Bacterial Genus

Chanos chanos

Liza parsia

Fenneropenaeus indicus

Penaeus monodon

Pseudomonas

9

20

16

19 (64)

气单胞菌属

11

14

17

15 (57)

Bacillus

9

12

13

17 (51)

Enterobacter

11

14

12

10 (47)

Vibrio

10

12

13

9 (44)

Flavobacterium

8

11

10

13 (42)

Alcaligenes

2

6

8

5 (21)

Acinetobacter

5

8

10

6 (29)

Total

73

113

127

115 (355)


Discussion

The numbers and types of bacteria associated with healthy fish are quite natural and interesting. However, the information on the gut micro-flora is generally patchy. In the present study, detritus fishes and shrimps collected from the mangrove waters were analyzed for their total heterotrophic bacteria. In general fishes have close association with environment through which the bacteria are ingested along the food and water.

The bacterial load in the gut of tilapia was high and the reasons may be that the high ambient temperature in pond water was close to optimum for many mesophilic bacteria in natural systems.10The presence of a high bacterial load in gill and intestine of fish might be due to high metabolic activity of fish associated with increased feeding rates at higher temperature.11They also reported that pond water and sediment bacteria influenced the bacterial composition of gills and intestine of tilapia. The bacterial load in the alimentary canal of a fish depends on the quantum and type of food recently ingested.12Sakataet al.,13,14reported that the lower counts obtained are more likely to represent a realistic estimate of the size of aerobic bacterial population attached to, or in intimate association with, the gut epithelium. InMugilcephalus, maximum luminous bacterial population density was observed in the hindgut and minimum was found in the foregut. InTachysurus arius, maximum luminous bacterial population density was recorded in the hindgut and minimum was found in the midgut.15The intestinal microflora of Salmonids fishes and Tilapia changes with the development.16,17MacDonaldet al.18suggested that the decline in bacterial numbers from juvenile to adult fish is an undescribed phenomenon, possibly reflecting subtle differences in the age of the surface with increasing age of the animal.

Several factors, such as bacterial host specificity, food type and water resource may explain these differences.19Bacteria in the surrounding environment and feeding habit may have influence on the composition of the gastrointestinal microbiota of fish. The most common bacteria in the gut of marine fishes wereAcinetobacter,VibrioandPseudomonas.20,21,22TheVibriowas considered as one of the predominant bacteria.22,23,24,25However, the number of isolates varied significantly among the species. The gram negative bacteria气单胞菌属hydrophila,气单胞菌属veroniiwere the most frequently isolated in the gastro intestinal regions.26Intestinal bacterial flora of tilapiaOreochromis mossambicusand optimization of alkaline protease byVirgibacillus pantothenticuswas carried out recently.27Ringoet al.,28isolatedPsychrobacterfrom the gut of marine fish, such as Arctic charr (Salvelinus alpinus) and Atlantic cod (Gadus morhua),29but its role in the gut of fish is not known. There is no marked difference in the bacterial load in different size groups of tilapia.30

In the present study the bacterial strainPseudomonassp. was predominant followed by the气单胞菌属sp. in the gut of all the fishes studied. The THB load was found to be high in milk fish (Fig.1) followed by Indian white prawn and minimum in tiger prawn (Fig.2). The present findings also confirmed the findings of Sivasubramanianet al.30that thePseudomonasspecies is predominant in the gut of tilapia fish.Bacillushas been successfully isolated from the gut of several marine fish and applied as probiotics.31,32,33ManyBacillusstrains isolated from marine fish could inhibit potential pathogens.31,33The present work suggest that these bacterial strains can effectively used as supplement in formulated fish/prawn feed or in the form of bacterial biofilm to enhance colonization in the gut. It may also be helpful in developing the probiotic for the commercial aquaculture.

Acknowledgement

We are thankful to The Principal, Govt. Arts College, Chidambaram for providing necessary facilities, Dr. K. Saravanakumar for his help in shaping the manuscript and to UGC, New Delhi for financial support through MRP project [ENVI-2013-37633].

References

  1. Wang, Y.B., J.R. Li and J. Lin, 2008. Probiotics in Aquaculture: Challenges and outlook.,281:1-4.
  2. Strom, E. and J.A. Olafsen, 1990. The indigenous microflora of wild captured juvenile cod in net-pen rearing. In: Lesel R (ed.) Microbiology in Poecilotherms. Elsevier, Amsterdam, 181-185.
  3. Hansen, G. H., E. Strom and J.A. Olafsen, 1992. Effect of different holding regimes on the intestinal microflora of herring (Clupea harengus) larvae.Appl. Environ. Microbiol.,58: 461–470.
  4. Campbell, A.C. and A. Buswell, 1983. The intestinal microflora of farmed Dover sole (Solea Solea) at different stages of fish development. J. Appl. Bacteriol.,55: 215-223.
    CrossRef
  5. Olsson, J. C., A. Westerdhal, P. L. Conway and S. Kjelleberg, 1992. Intestinal colonization potential of turbot (Scophthalumus maximus) and dap (Limanda limanda)-associated bacteria with inhibitory effects againstVibrio anguillarum.Envir. micro.,58: 551-556.
  6. Aiso, K., U. Simidu, K. Hasuo, 1968. Microflora in the digestive tract of inshore fish in Japan.Gen. Microbiol.,52: 361–364.
    CrossRef
  7. Onarheim, A.M. and J. Raa, 1990. Characterization and possible biological significance of autochthonous flora in the intestinal mucosa of sea water fish. In: Lesel R (ed) Microbiology in Poecilotherms. Elsevier, Amsterdam.
  8. Austin, B, 2006. The Bacterial Microflora of Fish, Revised.The Scientific World Journal,6: 931–945.
    CrossRef
  9. Bergey’s manual of determinative bacteriology, 1984. Williams and Wilkins Co., Baltimore, 9th, MD., pp. 220-229.
  10. Rheinheimer, G., 1985. Aquatic microbiology, 3rd ed. University of Kiel, West Germany. John Wiley and Sons, Chichester, New York, Brisbane, Tornoto, p. 257.
  11. Al-Harbi, A.H. and N. Uddin, 2005. Bacterial biodiversity of tilapia (Oreochromis niloticus) cultured in brackish water in Saudi Arabia.,250: 566-572.
  12. Seki, H., 1969. Marine microorganisms associated with the food of young salmon.Microb.,17: 252-255.
  13. Sakata, T., M. Nakaji, D. Kakimoto, 1978. Microflora in the digestive tract of marine fish. I. General characterization of the isolates from yellow tail.Mem. Fac. Fish., 27: 65-71.
    CrossRef
  14. Sakata, T., J. Okabayashi, D. Kakimoto, 1980. Variation in the intestinal microflora of Tilapia reared in fresh water and seawater.Jpn.Soc. Sci. Fish.,46(3): 313-317.
  15. Ramesh, A. and V.K. Venugopalan, 1989. Role of luminous bacteria in chitin degradation in the intestine of fish.MIRCEN-J. Appl. Microbiol. Biotecnol.,5: 55-59.
  16. Yoshimizu, M., T. Kimura and M. Sakai, 1980. Microflora of the embryo and fry of salmonids.日本。社科。鱼。46: 967-975.
    CrossRef
  17. Sugita, H., Y. Ishida, Y.Deguchi and H. Kadota, 1982. Aerobic microflora attached to the wall surface in the gastro-intestine ofTilapia nilotica.Coll. Agric. Vet. Med. Nihon Univ., 3: 302-306.
  18. MacDonald, N.L., J.R. Stark and B. Austin, 1986. Bacterial microflora in the gastrointestinal tract of Dover sole (Solea Solea), with emphasis on the possible role of bacteria in the nutrition of the host.FEMS Microbiol. Lett.,35: 107–111.
    CrossRef
  19. Verner-Jeffreys, D.W., R.J. Shields, I.R. Bricknell and T.H. Birkbeck, 2003. Changes in the gut associated micro-flora during the development of Atlantic halibut (Hippog-lossus hippoglossus L.) larvae in three British hatcheries. , 219: 21-42.
  20. Cahill, M. M., 1990, Bacterial flora of Fishes: A review.Eco.,19, 21-41.
    CrossRef
  21. Gatesoupe, F.J., J.L.Z. Infante, C. Cahu, and P. Quazuguel, 1997. Early weaning of sea bass larvae,Dicentrarchus labrax: the effect on microbiota, with particular attention to iron supply and exo-enzymes.,158: 117-127.
  22. Munro, P.D., A. Barbour and T.H. Birkbeck, 1994. Comparison of the gut bacterial flora of start-feeding larval turbot reared under different conditions.App.Bact., 77: 560–566.
    CrossRef
  23. Olafsen, J.A., 2001. Interactions between fish larvae and bacteria in marine aquaculture.,200: 223-247.
  24. Sugita, H., and Y. Ito, 2006. Identification of intestinal bac-teria from Japanese flounder (Paralichthys olivaceus) and their ability to digest chitin.Appl. Micro.,43: 336-342.
    CrossRef
  25. Eddy, S.D., and S.H. Jones, 2002. Microbiology of summer flounderParalichthys dentatusfingerling production at a marine fish Hatchery.Aqua., 211: 9-28.
    CrossRef
  26. Molinari, L.M., D.O. Scoaris, R.B. Pedroso, N.L.R. Bittencourt, C.V. Nakamura, T. Ueda-Nakamura, B.A.A. Filho, and B.P.D. Filho, 2003. Bacterial microflora in the gastrointestinal tract of Nile tilapia,Oreochochromis niloticus, cultured in a semi-intensive system.Acta Scie. Biol. Sci.,25: 267–271.
  27. Thillaimaharani, K. A., A. R. Logesh, K. Sharmila, B. Kaja Magdoom and M. Kalaiselvam, 2012. Studies on the intestinal bacterial flora of tilapiaOreochromis mossambicusand optimization of alkaline protease byVirgibacillus pantothenticus.J.Micro. Antimicrob.,4(5): 79-87.
    CrossRef
  28. Ringo, E., S. Sperstad, R. Myklebust, T.M. Mayhew and R.E. Olsen, 2006a. The effect of dietary insulin on aerobic bacteria associated with hindgut of Arctic charr (Salvelinus alpinus).Aqua. Res.,37: 891-897.
    CrossRef
  29. Ringo, E., Sperstad, S., Myklebust, R., Refstie, S., and Krogdahl, A., 2006b, Characterisation of the microbiota as-sociated with intestine of Atlantic cod (Gadus morhua) The effect of fish meal, standard soybeanmeal and a biopro-cessed soybean meal.Aqua, 261: 829-841.
    CrossRef
  30. Sivasubramanian, K., S. Ravichandran and R. Kavitha, 2012. Isolation and Characterization of Gut Micro Biota from Some Estuarine Fishes.Sci.,2(2): 1-6.
    CrossRef
  31. Kennedy, S.B., J.W. Tucker, C.L. Neidic, G.K. Vermeer, V.R. Cooper, J.L. Jarrell and D.G. Sennett, 1998. Bacterial management strategies for stock enhancement of warm water marine fish: a case study with common snook (Centropomus undecimalis).Mar. Sci.,62: 573-588.
  32. Velmurugan, S. and S. Rajagopal, 2009. Beneficial uses of probiotics in mass scale production of marine ornamental fish.J. Micro. Res.,3: 185-190.
  33. Sugita, H., Y. Hirose, N. Matsuo and Y. Deguchi, 1998. Production of the antibacterial substance byBacillussp. strain NM 12, an intestinal bacterium of Japanese coastal fish.Aquac.,165: 269-280.
    CrossRef
Creative Commons License
This work is licensed under a创作共用署名4.0国际公司ense.