Mass incursion of fishes with polymicrobial skin lesions, fin erosions and scale loss was recorded in the red spot emperor

Lethrinus lentjan (Lacepede 1802) along the Kanyakumari coast, south India during August 2009. An estimated 2.5 t of fish,

mostly the red spot emperors were found to migrate in live condition to the shore areas in a stressful state. Microbiological

analyses of tissue from sampled fishes revealed three distinct types of bacterial colonies forming 5.2 x 105 CFU g-1 of the

infected tissues. The predominant bacterial colonies were characterized as Aeromonas sp. (70.0%) followed by Flavobacterium

sp. (20%) and Vibrio sp. (10%). The Aeromonas isolate was highly susceptible to norfloxacin while the Flavobacterium and

Vibrio isolates were susceptible to chloramphenicol. The Aeromonas and Vibrio isolates exhibited protease and amylase

enzyme activities in vitro, suggesting their possible role in the progression of skin lesions and scale loss. The possibilities of

ambient unknown stressors weakening the fish and subsequent infections by these bacterial isolates are discussed

Aishwarya, M S

Kingsly, H Jose

Lipton, A P

Sarika, A R

Udayakumar, A

CMFRI Digital Repository

129Polymicrobial skin lesions in the red spot emperor, Lethrinus lentjan(Lacepede 1802) during mass incursion towards shore alongKanyakumari coast, south IndiaA. P. LIPTON, H.  JOSE KINGSLY, A. UDAYAKUMAR,M. S. AISHWARYA AND A. R. SARIKAVizhinjam Research Centre of  Central Marine Fisheries Research Institute, VizhinjamThiruvananthapuram -  695 521, Kerala, Indiae-mail: liptova@yahoo.comABSTRACTMass incursion of fishes with polymicrobial skin lesions, fin erosions and scale loss was recorded in the red spot emperorLethrinus lentjan (Lacepede 1802) along the Kanyakumari coast, south India during August 2009. An estimated 2.5 t of fish,mostly the red spot emperors were found to migrate in live condition to the shore areas in a stressful state. Microbiologicalanalyses of tissue from sampled fishes revealed three distinct types of  bacterial colonies forming 5.2 x 105 CFU g-1 of theinfected tissues. The predominant bacterial colonies were characterized as Aeromonas sp. (70.0%) followed by Flavobacteriumsp. (20%) and Vibrio sp. (10%). The Aeromonas isolate was highly susceptible to norfloxacin while the Flavobacterium andVibrio isolates were susceptible to chloramphenicol. The Aeromonas and Vibrio isolates exhibited protease and amylaseenzyme activities  in vitro, suggesting their possible role in the progression of skin lesions and scale loss. The possibilities ofambient unknown stressors weakening the fish and subsequent infections by these bacterial   isolates are discussed.Keywords: Aeromonas, Flavobacterium, Polymicrobial skin lesion, Red spot emperor, VibrioInstances of mass mortality of fish and washing ashoreof large numbers of fishes are reported during algal bloom(Subramanian and Purushothaman, 1985), drasticenvironmental changes (Pinheiro et al., 2010) includingseasonal upwelling events of anoxic or hypoxic waterconditions (Martill et al., 2008).  The crowded conditionspredispose fishes to bacterial infections as in the case oftypical aeromonad infections (Hiney and Oliver, 1999). Thesurface of marine fishes is populated by a wide variety ofbacterial genera like Vibrio spp., Pseudomonas spp.,Photobacterium spp., Alcaligenes faecalis, Acinetobactercalcoaceticus and Flexibacter spp. (Austin, 1983). Vibrioscause characteristic haemorrhagic septicaemia, externallesions and discharge of blood leading to mortality(Thompson et al., 2004). Vibrio anguillarum waspredominantly reported from coastal environments, causingsepticemia and death in both wild and cultured fishthroughout the world (Larsen et al., 1991).  Among thepseudomonads, P. anguilliseptica is an important pathogenof saltwater fish (Austin and Austin, 1999). Aeromonas sp.,affects a variety of non-salmonid fish (Bricknell et al.,1999). These are ubiquitous and opportunistic ones thattake advantage of stressed fishes. However, mass migratorybehavior towards coast with polymicrobial skin lesions israre and reported sparingly. Microbiological analyses ofIndian J. Fish., 58(3) : 129-133, 2011fishes exhibiting polymicrobial lesions were carried outfrom  affected fish, Lethrinus lentjan (Lacepede 1802) andthe salient findings are presented in this paper.Areas of observation and sample collectionOn 28-8-2009, stressful movement of numerous fishestowards the coast and washing ashore of them in livecondition along a stretch of coast in Kanayakumari (TamilNadu) extending from Rajakkamangalam thurai toManakudi was noticed. Investigations were conducted bya team from the Vizhinjam Research Centre of the CentralMarine Fisheries Research Institute. The areas ofobservations along the Kanyakumari coast are indicated inthe map (Fig. 1). The areas included:Manakudi (thurai) - N: 8o  05’ 39"; E: 77o 38’ 53"Pallam thurai - N: 8o  05’ 93"; E: 77o 25’ 84"Chothavilai - N: 8o  05’ 60"; E: 77o 25’ 84"Sangu thurai - N: 8o  05’ 98"; E: 77o 25’ 54"Periakadu - N: 8o  05’ 98"; E: 77o 25’ 54"Rajakkamangalam thurai - N: 8o  06’ 90"; E: 77o 22’ 35"Although the instances of washing ashore of fishes inlive conditions were confirmed upon visiting the coastalsites, 10 numbers of just dead fish could be recovered fromNote130the sea shore. Enquiries revealed that all the fishes thoughweak, were in live  condition when they emerged towardsthe shore. These were immediately  hand picked by thenearby residents, fisher folk and fish vendors and were sentto nearby markets for sale. .All the ten fishes  collected from Manakudi area(N: 8o 05’ 39"; E: 77o 38’ 53") and were identified as redspot emperor, Lethrinus lentjan (Lacepede 1802). The fishesexhibited skin erosions and scale loss along the bodysurfaces on lateral and ventral sides (Fig. 2).  An estimated2.5 t of fish, mostly red spot emperor in live and stressfulcondition  emerged from the sea towards the shore areawith similar symptoms.From the affected fishes, microbiological sampleswere collected as per the standard procedures (Austin andAustin, 1999). The tissue samples from the lesions wereaseptically excised, after surface sterilization, weighed,ground in sterilized mortar with pestle, serial dilutions weremade and then plated on Zobell Marine Agar. The plateswere incubated at room temperature (30.5±2.5 oC). After18 h of incubation, the countable colonies noted in10-3dilution were taken into account and from this, the totalbacterial load was estimated as Colony Forming Units(CFU) per g of tissue. Three distinct types of bacterialcolonies were observed. The isolates were characterized togenus level by standard methods (Austin and Austin, 1999)using selective media such as Aeromonas agar,Pseudomonas agar and Thiosulphate Citrate Bilesalt(TCBS) agar. The sensitivity of the isolates towardscommon antibiotics was evaluated by the standard discdiffusion assay (Bauer et al ., 1966).The mean bacterial load recorded  was  5.2 x 105 CFU g-1of tissue in the infected area. Three types of isolates werenoted with distinct morphological, cultural and biochemicalcharacteristics. The results of different characterization testsare summarized in Table 1.All the isolates retrieved from L. lentjan were Gramnegative rods. The isolate 1 exhibited spreading and moistnature in the Zobell Marine Agar (ZMA) plates. The sameFig. 2. Red spot emperor, Lethrinus lentjan with scale erosionsand sloughing of scales along the body surfaceA. P. Lipton  et al.Fig. 1. Location map of Kanyakumari coast indicating the migration of fish in the sampling area (arrows)131isolate formed a pinkish purple colour in the eosin methyleneblue (EMB) agar. Profuse growth of greenish colonies, thetypical characteristic feature of Aeromonas species inAeromonas isolation medium (Hi Media) was noted. Theisolate was Indole and Arginine dihydrolase positive.Considering these characteristic features, the isolate wasidentified and grouped under Aeromonas sp. ThisAeromonas  isolate from L. lentjan formed 70.0% of thetotal bacterial load from the infected tissues. The bacterialisolate produced exocellular protease and amylase. The leastpredominant bacteria, the isolate 2 forming about 10.0%exhibited greenish yellow colony formation, characteristicof Vibrio species in the TCBS agar. The isolate wassusceptible to the vibriostatic agents. Considering thesecharacteristics, the isolate 2 was grouped as Vibrio species.The Vibrio strain produced protease in its active growthphase. The isolate 3 identified as Flavobacterium sp., formedirregular and translucent mild yellow colonies in ZMATable 1. Characteristics of the three distinct types of bacterial isolates retrieved from the skin lesions of Lethrinus lentjanCharacterization tests Isolate- 1* Isolate- 2* Isolate- 3*Colony morphology on Zobell marine agar Low, spreading and Beige, shiny moist Dirty white andmoist colonies appearing, low crenate mild yellow irregularcolonies coloniesGram staining Gram negative short rods Gram negative, Gram negative spiral rodscomma shaped rodsBiochemical testsIndole test + + -VP test - - -Citrate utilization test - + -Catalase test + + +Arginine dihydrolase + - +Ornithine decarboxylase test - - -Growth in selective mediaMannitol salt agar (MSA) No growth No growth Yellow colouredPinkish purple colonies coloniesEosin methylene blue (EMB) agar No growth No growth Pinkish purple coloniesXylose lysine deoxycholate agar (XLD) Lactose fermenting (LF) No growth Pink coloniescoloniesMac Conkey agar No growth No growth No growthThiosuphate citrate bile salt sucrose agar (TCBS) Profuse growth Greenish yellow colonies No growthAeromonas isolation medium No growth No growth No growthPseudomonas isolation agar No growth No growth No growthde Mann Rogosa Sharpe (MRS) agar No growth No growthProtease production + + -Gelatinase - - -Amylase + - -Percentage of occurrence 70% 10% 20%+ = positive; - = Negative*Identity of the isolates:Isolate -1: Aeromonas (70%); Isolate -2: Vibrio (10%); Isolate -3: Flavobacterium (20%)Polymicrobial skin lesions in Lethrinus lentjanplates. The isolate was catalase positive and citrate negative.Yellow and pink coloration of colonies of the isolate werenoted in mannitol salt agar and in xylose lysine deoxycholateagar respectively. The isolate, however, has not producedany exocellular enzymes such as protease, amylase andgelatinase.The Aeromonas isolate was highly susceptible tocephotaxime (30 mm dia), norfoxacin (32 mm dia),co-trimoxazole (26 mm dia) followed by nalidixic acid(25 mm dia). Flavobacterium sp., was comparatively moresusceptible to chloramphenicol (27 mm), furazolidone(25 mm) and norfloxacin (25 mm) while the Vibrio isolatewas susceptible to cephotaxime (32 mm), chloramphenicol(32 mm), co-trimoxazole (32 mm), cephalexin (25 mm)and tetracycline (23 mm). The results of antibioticsusceptibility pattern of the three isolates are presented inTable 2.132Table 2. Antibiotic susceptibility pattern of the bacterial isolatesfrom L. lentjan [diameter of zone of inhibition (mm)]Antibiotic Aeromonas sp. Vibrio sp. Flavobacterium sp.Ampicillin Nil Nil NilCephalexin Nil 25 20Cephotaxime 30 32 12Chloramphenicol 18 32 27Co-Trimoxazole 26 32 NilErythromycin 15 16 20Furazolidone 16 Nil 25Gentamycin 23 Nil 12Nalidixic acid 25 12 23Nitrofurantoin 13 14 18Norfloxacin 32 11 25Oxytetracycline 12 20 14Tetracycline 21 23 NilVancomycin Nil 15 NilNil: Not susceptible (resistant)Instances of mass mortality of marine fish have beennoticed to occur all over the world mainly in the coastalwaters as occurrences in deep water areas go unnoticed.A few of these are reported as scientific publications(Pinheiro et al., 2010). In India, Durve and Alagarswami(1964) while reporting the incidence of fish mortality inAthankarai estuary near Mandapam inferred that abnormalenvironmental factors including rise in salinity levels couldhave caused such mass mortality of fishes. Blooms ofplankton population, largely dinoflagellates have beenimplicated as reasons for wide spread mortality of manyspecies of fishes. Mortality of fishes and invertebratesassociated with a bloom of Hemidiscus hardmannianus(Bacillariophyceae) present at a density of 9 to 49 x103 l-1in Parankipettai (South India) was reported by Subramanianand Purushothaman (1985). High concentration ofdinoflagellates causing red water and fish mortality werecorrelated along the Cape Town (Grindley et al., 1964). Inall these instances, the possibility of intake of biotoxinsthrough preferential diet items could have triggered thesusceptibility pattern of the fishes. The biological toxinscould be ingested by fish either through direct consumptionof macroalgae such as Caulerpa sp. or indirect consumptionof toxic epiphytic dinoflagellates by the reef fishesbelonging to Pomacentridae, Acanthuridae and Lutjanidaeas indicated by Landsberg (1995). Considering the lessmortality of fishes and other invertebrates, the biotoxins asa trigger for mass migration could not be rated high thoughit cannot be fully ruled out.Another possibility is the alterations in ambientenvironment brought about by upwelling events duringmonsoon. Off Kanyakumari coast, upwelling is effectedby the south-west monsoon winds (Smitha et al., 2008).With the onset of the south-west monsoon in May, weak tomoderate upwelling occurs off the Kanyakumari coast andspreads northwards along the coast as the monsoonadvances, reaching up to Goa coast during peak monsoonseason (July to August). Maheswaran et al. (2000) reportedstrong signals of upwelling observed off Kanyakumari andthe concomitant reduction in sea surface temperature nearthe coast by 1.7 oC off Kanyakumari. Oceanographicchanges due to monsoon along the coast have been alsopublished by Rao et al, (1992).In the present instance, predominantly L. lentjan wasaffected and the phenomenon of migration towards theshore areas was noted only on one day and was not repeated.Sloughing or withering of scales were noticed in affectedfishes. It has been reported earlier that scale loss could beattributed to the stress and resulting dieresis in salmonidfishes (Smith, 1993). Thus, the incursion of L. lentjan withpolymicrobial lesions on body surface could be attributedto the ambient stressful conditions as well as secondaryinvasion by opportunistic pathogenic microbes. Similartrend of multiple pathogens infecting tropical reef fishesalong the Florida coast was reported by Landsberg (1995).According to the author, no primary pathogen could bedetected from the reef fishes affected by the infections. Itis possible that unknown stressors might have weakenedthe fish, which could have subsequently become susceptibleto a number of microbial pathogens including secondaryor opportunistic bacteria. The necrosis and erosions in finand skin could have been caused by the exocellular enzymeactivities of the bacteria lodged on the skin of the weakenedfish. In the in vitro tests, protease activity was noted inAeromonas and Vibrio isolates. The Aeromonas spp. havebeen  isolated from naturally infected fish in brackish waterfishes such as mullets and sea breams (Manal I. El-Barbary,2010). Vibrio damsela causing skin ulcer in damsel fishwas reported by Lov et al. (1981). Vibrios producingexocellular enzymes are known to degrade hardy bodysurface areas of fish such as the sea horse, Hippocampuskuda (Thampiraj et al., 2010).In the natural marine environment, whenever chronicstressors or disease affect the marine fish population, themoribund fish or recently dead fish will be quickly removedfrom the affected area by predation, wind or prevailingwater currents. Detection of such outbreaks is rare unlessthey occur closer to the shore areas as in the present reportedincidence.AcknowledgementsThe authors are thankful and grateful to Dr. G. SydaRao, Director, CMFRI for the facilities and encouragement.A. P. Lipton  et al.133ReferencesAustin, B. 1983. Bacterial microflora associated with a coastalmarine fish rearing unit. J. Mar. Biol. Ass. (UK)., 63:583-592.Austin, B. and Austin, D. A. 1999. Bacterial fish pathogens.In: Diseases of farmed and wild fish, Vol. 2, Springer-PraxisPublishing, Ltd., London, p. 265-307.Bauer, A. W., Kirby, W. M. M., Sherris, J. 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Res., 24 (SI 3): 95-102.Subramanian, A. and Purushothaman, A. 1985. Mass mortalityof fish and invertebrates with a bloom of Hemidiscushardmannianus (Bacillariphyceae) in Parankipettai(Southren India). Limnol. Oceanogr., 39 (4): 910-911.Thampiraj, S., Lipton, A. P. and Chauhan, G. S. 2010.Characterization and infectivity evaluation of Vibrio harveyicausing white patch disease among captive reared seahorses,Hippocampus kuda. Indian J. Mar. Sci., 39 (1): 151-156.Thompson, L. F., Iida, T. and Swings, J. 2004. Biodiversity ofVibrios. Microbiol.  Molecular Biol. Rev., 68: 403-431.Date of Receipt : 09.11.2010Date of Acceptance : 08.08.2011Polymicrobial skin lesions in Lethrinus lentjan

Polymicrobial skin lesions in the red spot emperor, Lethrinus lentjan

(Lacepede 1802) during mass incursion towards shore along

Kanyakumari coast, south India

http://eprints.cmfri.org.in/8763/1/11122-23281-1-SM.pdf

Polymicrobial skin lesions in the red spot emperor, Lethrinus lentjan (Lacepede 1802) during mass incursion towards shore along Kanyakumari coast, south India

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