Received date: August 01, 2015; Accepted date: August 18, 2015; Published date: August 24, 2015
Citation: Vyas N, Dua KK, Prakash S (2015) Larvicidal Activity of Metabolites of Metarhizium anisopliae against Aedes and Culex Mosquitoes. Entomol Ornithol Herpetol 4:162. doi: 10.4172/2161-0983.1000162
Copyright: © 2015 Vyas N, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Visit for more related articles at Entomology, Ornithology & Herpetology: Current Research
The objective of this study was to determine the larvicidal effects of entomopathogenic fungus Metarhizim anisopliae against degue, chikunguniya and filariasis disease vectors. The fungus was cultivated in the complete broth media and the extracelluar metabolites were filtered by using Whatman no.1 filter paper. Further, the filterd metabolites were conducted for its larvicidal efficacy against all instars of Ae. egypti and Cx. quenquefacistus, at five different significant concentrations (2.35, 2.65, 2.83, 2.95 and 3.05ppm). Larvae of Cx. quenquefacistus were found more susceptible than larvae of Ae. aegypti. The hightest LC99 value (663.74ppm) was resulted in the first instar of Cx. quinquefasciatus while the lowest LC99 value (309.02ppm) was found in third instar of Ae. aegypti. The findings of this preliminary study gives overview idea about the different larvicidal properties of the metabolites of M. anisopliea. Additionally it will help us to find specific larvicidal compound for mosquito borne disease control applications
Entomopathogenic fungi; Metarhizium anisopliae; Aedes aegypti; Culex quinquefasciatus
Culex and Aedes are major vectors of zoonotic diseases in tropics. It causes morbidity of millions of persons resulting in loss of mandays causing economic loss . Culex quinquefasciatus, a vectore of lymphetic filariasis, is widely distributed. On the other hand, Aedes aegypti is a vector of dengue, chikunguniya, yellow fever and that carries the arbovirus responsible for these diseases is also widely distributed in the troical and subtropical zones. In Indian scenario, almost the entire country is endemic to the mosquito borne diseasses due to favorable ecological conditions. To prevent mosquito-borne diseases and improve public health, it is necessary to control them. Mosquito in the larval stages are attractive target for pesticides because mosquitoes breed in water, and thus it is easy to deal with them in this habitat.
Numerous chemical larvicides are known to have toxic effects beyond their target pests including toxic effects to animals and human. The opportunity to substitute safer, more selective and biodegradable biocontrol agent can provide important ecological benefits. The use of microbial larvicides could decrease our dependence on chemical insecticides. The entomopathogenic fungus life cycle is associated with the synthesis and secretion of different active metabolites, including extracellular enzymes and low molecular weight compounds (toxins). These toxic byproducts mainly help the organisms to withstand and protect themselves from invading pathogens [2,3]. In general fungi produce a wide range of secondary metabolites with diverse biological activites like antibiotics, cytotoxic substances, insecticides compound that promote or inhibit growth, attractor, repellent etc .
Entomopathogenic fungal metabolites could be an alternative source for mosquito larvicides because they constitute a potential source of bioactive compounds and generally free from harmful effects. Moreover, use of these microbial larvicides in mosquito control instead of synthetic insecticides could reduce the cost and environmental pollution. The aim of present investigation is to assess the comparative efficacy of extracellular metabolites of Metarhizium anisopliae against all four larval stages of Ae. aegypti and Cx. quinquefasciatus in the laboratory.
The fungal strain of M. anisopliae (MTCC-892) was procured from the Institute of Microbial Technology, Chandigarh, India. Fungal colonies were cultured in 250 ml conical flask containing 100ml of complete broth media (0.001g FeSo4, 0.5g KCL, 1.5g KH2PO4, 0.5g MgSo47 H2O, 6g NaNO3, 0.001g ZnSO4, 1.5g Hydrolyzed Casein, 0.5g Yeast Extract, 10g Glucose, 2g Peptone and 1000ml Deionized water) fungi were incubated under static condition 25 ± 2°C for 15 ± 2 days with constant aeration in BOD.
Maintenance of mosquito larvae in the laboratory
The colonies of Ae. aegypti and Cx. quinquefasciatus were maintained in the laboratory at a temperature of 25 ± 2°C, relative humidity was 75 ± 2% and photoperiod of 14:10 (L/D).
Filtration of extracellular metabolites
Cell free culture filtrates were obtained by filtering the broth through successive Whatman No.1 filter paper after incubation. Fungal metabolites present in the filtrate were used to examine the larvicidal activities.
Mosquito larvae of Ae. aegypti and Cx. quinquefasciatus were separated and placed in separate containers (60cm × 40cm × 20cm), containing microbe free Deionized water. After that, different test concentrations of metabolites in 100ml water were prepared in 250ml beakers. Bioassays were conducted separately for each instar of mosquitoes at five selected log concentrations. Log concentrations for M. anisopliae were 2.35, 2.65, 2.83, 2.95 and 3.05ppm. To test the larvicidal activity, 20 larvae of each stage were separately exposed to 100ml of test concentrations. Similarly, the control was run to test the natural mortality, except concentrations of culture medium used instead of the fungal filtrates .
Mortality and survival were recorded after 24, 48 and 72h of the exposure. During experimental time, no food was offered to the larvae. The experiments were replicated thrice to validate results. All test containers were tightly covered with pierced aluminium foil and placed at room temperature without sunlight.
Data management and statistical analysis
The efficacy study of filtrate metabolites of M. anisopliae were assessed against larvae of Ae. aegypti and Cx. quinquefasciatus. Experimental test that demonstrated more than 20% control mortality were discarded and repeated when control mortality ranging between 5-20% was observed, and was corrected by Abbott’s formula [6,7]. The concentrations produce 50%, 90% and 99% mortality in larvae (LC50, LC90 and LC99 respectively) were calculated with their fiducial limits at 95% confidence level. The relation between probit equation and probit regression lines were drawn for each of the larval stages (Figures 1 and 2).
All instar of the Ae. aegypti and Cx. quinquefasciatus appeared to be susceptible to the crude metabolites of M anisopliae.
LC values and chi-square analysis for Cx. quinquefasciatus larvae
The estimates of LC50, LC90 and LC99 values for M. anisopliae against Cx. quinquefasciatus have shown with their fiducial limits and probits equations (Table 1). It has shown that LC values were higher for the first instar than other instars. The probits were plotted against respective log concentrations and strait lines were drawn by eye to fit the points for each instar (Figure 1). The LC values for third instar indicate that it was most tolerant to M. anisopliae metabolites. A strong positive correlation was found between concentrations of fungal filtrate and percentage mortality of Cx. quinquefasciatus larvae (r=0.83, 0.87, 0.84 and 0.72 for all instars). The observed lethal concentrations have shown degree of susceptibility to fungal metabolites amongst the four larval larval stages of Cx. quinquefasciatus in order of instar 1st >2nd >4th>3rd.
|Instars||ProbitEquations||LC50||95٪ CL||LC90||95٪ CL||LC99||95٪ CL|
|1.2656x + 1.877
1.5328x + 0.9143
1.4304x + 1.2455
1.5699x + 0.6177
45.17 – 36.28
123.18 – 86.36
485.06 – 448.24
Table 1: Probit equations and susceptibilities of Culex quinquefasciatus against extracellular metabolites of Metarhizium anisopliae with 95٪ confidential limit (CL).
The calculated chi-square values at 3 df were 6.22, 1.64, 2.79 and 2.98 for all the instars. The calculated chi square values for Cx. quinquefasciatus were lower than critical values of chi-square at 0.05 significant levels. Therefore, the values for chi-square test were statistically not significant at 95% confidence level. It would suggest that there was no significant difference between expected and observed data. The small values of chi-square confirmed the adequate representation of probit regression lines (Figure 1) for the experimental data.
LC values and chi-square analysis for Ae. aegypti larvae
Lethal concentration of metabolites are shown in Table 2 with their fiducial limits and probit equations. The probits were plotted against respective log concentration for each instar (Figure 2). LC90 value was lower for the third instar than for the other instars. Whereas, the highest value of LC99 was recorderd in first instar . A strong corelation was found between concentrations of metabolites and percentage of larval mortality (r=0.96,0.76.0.69 and 0.90 for the all instars). Lethal concentrations have shown the degree of susceptibility to fungal metabolites among the four instar of Ae. aegypti in order of instar 1st >4th >2nd >3rd.
|Instars||Probit Equations||LC50||95 ٪ CL||LC90||95 ٪ CL||LC99||95 ٪ CL|
2.265x – 2.285
2.294x – 0.552
Table 2: Probit equations and susceptibilities of Aedes aegypti against extracellular metabolites of Metarhizium anisopliae with 9٪ confidential limit (CL).
Chi-square values at 3 df were 0.32, 10.43, 7.09 and for the values of the all instars. The values of Chi-square for 2nd and 4th instars were higher than the original value of chi-square at 0.05 significant only for 2nd and 4th instars at 95% confidential level, which suggest that there was no significant differences between expected and observed data. The small value of chi-square confirmed the adequate representation probit regression line (Figure 2).
Mosquito transmitted disease remains a major source of illness. To manage mosquito population, biological control is the use of natural enemies. Microbial larvicides are especially valuable because their toxicity to non-target animals and human is extremely low. An important benefit of microbial metabolites is that they can be used to replace, at least in part, some more hazardous chemical pest control agents. A number of entomopathogenic fungi have been used effectively to control the mosquito vectors for last few decades. However, studies on the effects of extracellular metabolites on mosquito larvae and nontarget organisms appear to be very limited in comparison to the use of spores and mycelia of the fungi .
In the present investigation extracellular secondary metabolites of M. anisopliae were found effective against the all larvae of Ae. aegypti and Cx. quinquefasciatus. In both cases the first instars were found more susteptible than third instars. However, among the two vectors Cx. quinquefasciatus was found more susceptible than Ae. aegypti. Auther has also used the same concentration of this metabolites against the An. stephensi and non target aquatic organisms in the laboratory and According to this studies, metabolites of M. anisopleai was found safe for the nontargets . Our present investigation of the efficacy can be further extended with the test of isolated molecules on mosquito larvae. In other studies, Lagenidim giganteum [8-10], Tricophytom ajjeloi , Chrysosporium tropicum  were also tested in the laboratory against mosquito larvae. Beauveria bassiana, Paecilocyces fumosoroseus, and Fusarium moniliforme produce mosquito larvicidal compound like cyclodepsipeptide, including beauvericin and the enniatin complex .
Fungal metabolites have the greatest potential in intelligently designed and carefully applied in mosquito management programes. Expanded use of microbial larvicide will depend heavily on the balance between production costs and ecological considerations. Fungal metabolites could be alternative source for mosquito larvicides because they constitute a potential source of bioactive compounds and generally free from harmful effects. Use of fungal metabolites in mosquito control instead of synthetic insecticides could reduce the cost and environmental pollution. Further studies on identification of active compounds, toxicity and field trials are needed to recommend the active fraction of microbial metabolites for development of ecofriendly stategies for the control of the mosquito vectors.
Author is grateful to the Director of the Dayalbagh Educational Institute for providing experimental facilities. The financial support was provided by Department of Science and Technology to Prof. Soam Prakash is also acknowledged.