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Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 98, No. 2, March, 2003, pp. 223-226 Oviposition Response of the Mosquito, Culex quinquefasciatus to the Secondary Metabolite(s) of the Fungus, Trichoderma viride I Geetha, KP Paily, V Padmanaban, K Balaraman+
Vector
Control Research Centre (Indian Council of Medical Research), Indira Nagar, Pondicherry
605 006, India WHO - World Health Organization 1963. Technical Report Series, No. 265. Received
24 June 2002 Code Number: oc03059
Secondary metabolites produced by Trichoderma viride, a deuteromycetes fungus, under submerged culture condition were formulated and evaluated for oviposition attractancy against gravid females of Culex quinquefasciatus mosquito. At a concentration of 10 µg ml-1 the formulation showed remarkable attractancy with an oviposition active index (OAI) of +0.52. When the oviposition attractancy of the formulation was compared with a known oviposition attractant, p-cresol, both at 10 µg ml-1, the former was found to be more attractive to result in 70% egg laying than the later with 30% egg laying. Thin layer chromatography fractions of the secondary metabolites showed that a fraction with Rf value of 0.88 was highly active as oviposition attractant with an OAI of +0.65. Further work on identification of the active principle(s) of the microbial formulation might lead to an oviposition attractant useful in mosquito vector management.
Key words: Trichoderma viride - secondary metabolites - mosquito oviposition attractancy - Culex quinquefasciatus Mosquitoes are known to locate their specific hosts and oviposition sites by sensing chemical signals, besides various physical stimuli, that are detected by sensory receptors on the antennae (Davis & Bowen 1994). By using oviposition attractants, vector mosquitoes could be attracted to chosen sites for laying eggs. Various chemicals serve as oviposition attractants for mosquitoes even when present in relatively small quantities (Beehler & Mulla 1993). Oviposition attractants are known to be produced by microorganisms also (Hazard et al. 1967, Rockett 1987, Hasselschwert & Rockett 1988, Beehler et al. 1994). Among deuteromycetes fungi, Trichoderma species are known to produce aromatic/volatile secondary meta-bolite(s) (Kikuchi et al. 1974, Keszler et al. 2000, Sarhy-Bagnon et al. 2000, Kalyani et al. 2000). In the present study secondary metabolite(s) produced by the fungus Trichoderma viride was evaluated for oviposition attractancy against gravid females of Culex quinquefasciatus and the results are presented in this paper. MATERIALS AND METHODS A natural strain of T. viride (F24), obtained from the culture collection of Vector Control Research Centre (VCRC) was subcultured on Sabouraud Dextrose Agar (SDA) (glucose 40 g; peptone 10 g; agar 20 g; distilled water 1000 ml; pH 4.5-5.0) slants and incubated for 5 days to attain sporulation. Then a loopful of spores were inoculated to 50 ml Sabouraud Dextrose Broth (SDB) (glucose 40 g; peptone 10 g; agar 20 g; distilled water 1000 ml; pH 4.5-5.0) in a 250 ml conical flask and incubated on a rotary shaker (New Brunswuck Scientific Co., New Jersey, USA) at 110 rpm and at 30°C for 3 days. From the seed culture, 2% of the inoculum was transferred to 200 ml of SDB and incubated for 15 days at the above mentioned conditions. The culture was filtered through Whatman no.1 filter paper, the mycelial mass was discarded, and the culture filtrate was lyophilized. The residue was dissolved in 50% ethanol at a ratio of 500 mg of residue in 10 ml of ethanol. This formulation was code named as VCRC F24 and used for oviposition attractancy tests. Determination of optimum concentration of VCRC F24 and p-cresol for oviposition attractancy test - Three-day-old Cx. quinquefasciatus Say female mosquitoes, an indigenous strain obtained from a laboratory colony maintained at VCRC, were fed on fowl blood and maintained for two days on raisins at 28 ± 2oC and 70-80% RH. Gravid female mosquitoes were used for the determination of oviposition attractancy using standard procedure (WHO 1963). Different concentrations (5 µg ml-1, 10 µg ml-1 and 15 µg ml-1) of VCRC F24 and a known oviposition attractant, p-cresol (a volatile pentane), was prepared in tap water. In the case of p-cresol, a stock solution of 1mg ml-1 was made in ethanol and diluted to the required levels with tap water. Tap water with equal amount of ethanol served as control for VCRC F24 and p-cresol. Two hundred ml of each of the test/control solutions held in disposable bowls (capacity, 250 ml) were placed in the floor of a mosquito cage (size, 55 x 55 x 55 cm). One hundred numbers of fully gravid female mosquitoes were released into the cage. For each test at any given time, not more than two bowls were kept in the opposite corners of the cage. The cages were kept at 28 ± 2oC and 70-80% RH. On each occasion, the experiment was set up at 16:00 h and observations for presence of egg rafts, if any, were made at 10:00 h the next day. The number of egg rafts laid in each bowl were counted and the percentage of egg rafts laid in each concentration was calculated from the total number of egg rafts laid in both test and control solutions. Each experiment was repeated four times and on each occasion the position of the disposable cups were changed. Oviposition active index (OAI) of test material - OAI of any test material was determined by placing in a cage, one bowl containing test material and another bowl containing tap water with ethanol as control. OAI of different concentrations of the VCRC F24 and p-cresol was calculated by using the formula (Kramer & Mulla 1979)
where, Nt is the number of egg rafts laid in test solution and Ns is the number of egg rafts laid in control. As suggested by Kramer and Mulla (1979), compounds with an OAI of +0.3 and above are considered as attractants, while those with - 0.3 and below are considered as repellents. Oviposition attractancy of VCRC F24 in comparison with p-cresol - The oviposition attractancy of VCRC F24 was compared with p-cresol by testing them at their optimal concentrations required for oviposition attractancy i.e., 10 µg ml-1. This experiment was conducted by keeping two disposable bowls in a cage, one with VCRC F24 and the other with p-cresol as oviposition media, at the opposite corners. The number of egg rafts laid in the oviposition bowls were counted and percentage of egg rafts laid in each bowl was calculated from the total number of egg rafts laid in both VCRC F24 and p-cresol. Attempts were made to isolate the active principle of the secondary metabolite and for this, the lyophilized culture filtrate was extracted with methanol, the solvent was evaporated and the residue was re-dissolved in methanol (200 mg in 25 ml). The dissolved residue was subjected to thin layer chromatography (TLC) analysis. Both analytical (0.25 mm layer thickness) and preparative (0.5 mm layer thickness) TLC were carried out on silica gel plates using chloroform-methanol (70:30) as solvent system and spots were visualized by exposing the plates to iodine vapours. From the preparative TLC plates, major bands (at Rf 0.92, 0.88, 0.84, 0.24 and 0.12) were scrapped out and extracted with methanol. The purity of the bands was tested on analytical TLC and the solvent was evaporated. The residue was dissolved in ethanol and tested against gravid Cx. quinquefasciatus at a concentration of 10 µg ml-1. Each fraction was tested for OAI individually along with tap water containing ethanol as control. RESULTS Optimum concentration for oviposition attractancy - In the case of VCRC F24, among the three concentrations tested, 10 µg ml-1 and 15 µg ml-1 attracted more number of gravid females for oviposition and that resulted in 75.9 and 75.9% egg rafts, respectively (Table). With respect to p-cresol, maximum oviposition was observed at 10 µg ml-1 with 73.6% egg rafts. Hence the optimum concentration for oviposition attractancy of both VCRC F24 and p-cresol was determined to be 10 µg ml-1. OAI - The data on the OAI of VCRC F24 and p-cresol are presented in the Table. At 5 µg ml-1 level VCRC F24 was attractive with an OAI of +0.4. At concentrations of 10 µg ml-1 and 15 µg ml-1 the OAI was +0.52. In the case of p-cresol, at 5 µg ml-1 level it was not attractive to gravid females as the OAI was +0.2. With increasing concentration of 10 µg ml-1 and 15 µg ml-1, the OAI was respectively +0.47 and +0.32. Oviposition attractancy of VCRC F24 in comparison with p-cresol - The data on the percentage of egg rafts laid by gravid Cx. quinquefasciatus in VCRC F24 compared to that in p-cresol is illustrated in Fig. 1. The results indicated that VCRC F24 was more attractive with 68.8% of egg rafts than p-cresol with 29.5% egg rafts. Oviposition attractancy of TLC fractions - Among the TLC fractions (Fig. 2) tested at 10 µg ml-1 level, those with Rf values 0.92, 0.88, 0.84 and 0.24 attracted gravid Cx. quinquefasciatus for oviposition. OAI of these fractions were respectively, +0.57, +0.65, +0.48 and +0.3. DISCUSSION Various volatile chemicals produced by microorganisms are known to be attractive to gravid mosquitoes to locate oviposition sites for egg laying (Rockett 1987). The bacterium, Aerobacter aerogenes, isolated from hay infusion has been reported to produce chemicals which stimulated gravid females of Aedes aegypti (L.) and Cx. quinquefasciatus Say to lay eggs (Hazard et al. 1967). Similarly, protein hydrolysate solutions with their bacterial contaminants have been found to be attractive to gravid Cx. quinquefasciatus (Beehler et al. 1994). T. viride, a deuteromycetes fungus, is widely used in agriculture as a biocontrol agent against fungal diseases of plants. Under submerged culture conditions it produces many mycotoxins like trichodermin, alamethicin, trichoviridin, trichotoxin etc. and a volatile, aromatic secondary metabolite, 6-pentyl-alpha- pyrone (Eveleigh 1985). In the present study, the metabolite(s) was found to exhibit a novel activity viz. mosquito oviposition attractancy. It was observed that, when tested at concentrations of 5 µg ml-1, 10 µg ml-1 and 15 µg ml-1, more number of gravid females were attracted to test solutions containing VCRC F24 than to the control solution. Increase in the concentration of the test solution from 5 µg ml-1 to 10 µg ml-1 was found to increase the percentage of egg rafts laid. However, further increase in concentration to 15 µg ml-1 did not increase the percentage oviposition and hence, the lowest concentration at which the highest percentage of egg rafts laid, i.e. 10 µg ml-1 , was considered as the optimum concentration required for oviposition attractancy. This was true with that of different concentrations of p-cresol also and 10 µg ml-1 was considered as optimum for comparing the effectiveness of VCRC F 24. With respect to the OAI, a concentration of 5 µg ml-1 of VCRC F24 was attractive to gravid female mosquitoes (OAI +0.3) where as p-cresol did not show oviposition attractancy at this concentration (OAI +0.2). P-cresol has been reported to be an attractant to Ae. triseriatus at a concentration of 3 µg ml-1 (Bentley et al. 1979). The higher dosage of p-cresol required during the present study might be due to the difference in the species of the mosquitoes against which it was tested. Interestingly, VCRC F24 showed higher oviposition attractancy than p-cresol. Thin layer chromatography results showed that among the four bands which were positive for oviposition attractancy, the one with Rf value of 0.88 had higher attractancy with an OAI of +0.65. Compared to the crude material (VCRC F24 formulation) the attractancy was found to be more with the fraction. The production of the oviposition attractant factor can be enhanced by optimising the media components and cultivation conditions. Oviposition attractants are important as they could be used in mosquito trapping for identification, surveillance and control. The present study shows that the microbial formulation, VCRC F24 from T. viride is attractive to gravid females of Cx. quinquefasciatus and further work on the identification of the active principle(s) and enhancement of the production or synthesis of analogues might result in a product, which could be used in integrated vector management. ACKNOWLEDGEMENTS To Dr PK Das, Director, Vector Control Research Centre for suggestions and encouragement, to Dr SL Hoti and Dr Nisha Mathew for their help in chromatography and to Mr A Ramamoorthy and Mr S Venugopalan for their technical assistance. REFERENCES
Copyright 2003 Instituto Oswaldo Cruz - Fiocruz The following images related to this document are available:Photo images[oc03059f1.jpg] [oc03059t1.jpg] [oc03059f2.jpg] |
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