Bioactivity Evaluation of Different Mango Cultivars Leaves Ethanolic Extract on
3rd - Early 4th Instar Aedes aegpyti Larvae
Hasinaah S. Candelario
[email protected]
MIMAROPA Regional Science High School-Senior High School
Pag-asa, Bansud, Oriental Mindoro, MIMAROPA Region, Philippines, 5210
Abstract: Aedes aegypti is a main vector of diseases which causes morbidity. In
response to this, various low cost and easy to prepare plant-based larvicides have been
developed. In this study, the ethanolic extract of Indian Mango (Mangifera indica),
Carabao Mango (Mangifera rostrata), Pico Mango (Mangifera sylvatica), Paho Mango
(Mangifera altissima), and Apple Mango (Mangifera laurina) leaves were evaluated for
its bioactivity on 3rd – early 4th instar Aedes aegypti larvae. Sundried and grinded
mango cultivars leaves were macerated in ethanol and purified using water bath. The
ethanolic extracts were serially diluted into five different concentrations: 10,000 ppm,
15,000 ppm, 20,000ppm, 25,000ppm and 30,000ppm with separate treatment containing
50 ml crude extract. The mortality of the larvae was recorded and evaluated for its actual
morphology before and after exposure to the extracts. One-way ANOVA results showed
significant difference among the five treatments in terms of the mortality rate wherein
treatment 6 (crude extract), obtained the highest mean average of mortality rate and
treatment 7 (negative control) the lowest. This means that the extract is dose dependent
with lethal concentration to kill 50% and 90% of the larvae at 23,988.33ppm and
86,963.689ppm for M. indica, 20,090.93ppm and 50,118.72ppm for M. rostrata,
22,908.68ppm and 68,706.84ppm for M. sylvatica, 20,417.38ppm and 68,391.165ppm
for M. altissima, and 19,998.62 and 42,657.95ppm for M. laurina respectively. In
addition, there is no significant difference among the different mango cultivars when it
comes to effectivity. This means that any of the five mango cultivars can be used for its
bioactivity against Aedes aegypti larvae. The morphology of Aedes aegypti larvae
showed that there is serious aberration on the mid-gut and swelling after experimentation.
Moreover, coloration of the larvae is also observed. Therefore, the ethanolic extracts of
the five mango cultivars are potential bio-larvicide which could be utilized to control
Aedes aegypti which is the primary vector of the dengue virus.
KEYWORDS: Plant-based larvicide, Mangifera indica, Mangifera rostrata, Mangifera
sylvatica, Mangifera altissima, Mangifera laurina, Aedes aegypti
1
Introduction
The Philippines being a tropical country is subjected to various climates. During wet
climates, mosquitoes often see this instinctively as the beginning of mating season.
Akban and Nwaueze (2015) explained that with abundance of moist and water,
mosquitoes copulate and lay eggs due to careless waste disposal, irrigation and poor
drainage which proliferates the living conditions of the parasites. Interest in the control
of Aedes aegypti lies in the fact that they act as vectors of arboviruses such as dengue,
yellow fever and chikungunya. Meanwhile, as of July, 2019, the Department of Health
reported a total of 146,062 dengue cases; thus, the declaration of national dengue
epidemic. Aedes aegypti females has a habit of collecting blood with their stingrays
especially when they lay eggs. As such, they spread diseases to their victims. One of the
solutions to eradicate this problem in mosquito is to start mortality in its larval stage.
Over the years, synthetic insecticides were introduced but although these are effective,
the insect tends to develop resistance to such products (Jirakanjanakit et al., 2007). Aside
from being costly, the use of these repellents also generates problems such as
environmental pollution and has toxic side effect to humans (Sarwar, Ahmad & Toufiq,
2009). This imposes a need for other alternative methods which are efficient, economic
and environmentally safe. Currently, plant based bio-insecticides are intensively studied
worldwide, especially in tropical countries with a high diversity of plants. Particular
attention has been paid to the study on many plant extracts for determining their
larvicidal potential against Aedes aegypti.
2
Mango, from the family Anacardiaceae, is a common domestic plant in the
Philippines. The tree often reach 15 to 18 m in height. The leaves in general are dark
green above and pale below, alternate, with no stipules, simple, leathery and varies in
shape. The roots are unbranched long taproots with a dense mass of superficial feeder
roots. The flowers are tiny, and yellowish or reddish. Native to Southern Asia, mango
has been cultivated, praised and even revered for its many uses. Mango contains
mangiferin (Ramirez et al, 2016); a unique phenolic compound known only to mango.
Although there are many various uses of mango, the leaves specifically have shown
different properties and activities such as antimicrobial (Bharti, 2013),
anti-hyperglycaemic (Aderibigbe, Emudianughe & Lawal, 1999) and anticancer
(Helen, Aswathy, Deepthi, Mol, Joseph & Sre, 2013). Furthermore, mango is one of
the most common and most cultivated fruits in the country of the Philippines. There
are diverse mango cultivars available such as Indian Mango (Mangifera indica),
Carabao Mango (Mangifera rostrata), Pico Mango (Mangifera sylvatica), Paho
Mango (Mangifera altissima), and Apple Mango (Mangifera laurina). Thus, in this
study, ethanolic extracts of different mango cultivars leaves were evaluated for its
efficacy as potential natural larvicide. Specifically, this work aims to determine the
mortality rate of the 3rd-early 4th Instar Aedes aegypti larvae after exposing to the
prepared treatments of M. indica, M. sylvatica, M. altissima, M. rostrata, M. laurina;
examine the morphology of the used Aedes aegypti larvae before and after treatment
exposures; and qualitatively determine the phytochemicals present in M. indica
ethanolic extract.
3
This work promotes a simpler and cheaper natural larvicide which could help locals
to address problems on rapid increase of Aedes aegypti. In addition, the study will
contribute greatly to the community concerning to the need of immediate disposal of
mosquitoes in their early stage. Thus, the implementation of the practice simulated in the
study may prevent excessive growth of the mosquitoes’ population.
Methodology
Collection and Preparation of the Plant Sample
The leaves of mango cultivars (M. indica, M. sylvatica, M. altissima, M. rostrata, M.
laurina) were collected in Gloria, Oriental Mindoro. Harvested leaves were sun-dried for
three days. Using an electric blender, the dried plant samples were powdered and 500g
sample of mango leaves were placed into a container.
The leaf samples of mango cultivars were brought to the National Institute of
Biology at University of the Philippines - Diliman for proper identification and
authentication.
Figure 1. Collecting, sun-drying and powdering of different mango cultivar leaves.
4
Ethanol Plant Extraction
Five hundred (500) g of dried of mango cultivar leaves were placed in a container
containing 1000mL of 95% ethanol. It was left soaked for 72 hours. The soaked sample
were poured into clean cheesecloth that was prepared and squeezed into another
container through a filter paper and a funnel.
Subsequent to the process, the extract were purified through the process of water
bath for 1 hour. The extracts were placed into clean amber bottles and placed in the
refrigerator before laboratory use.
Figure 2. Maceration and water bath of the mango cultivars ethanolic extract
Phytochemical Analysis
The ethanol plant extract of the mango cultivars were subjected to qualitative
phytochemical screening to detect biological constituents (Daffodil, Lincy, & Mohan,
2014), as summarized in Table 1. Presence or absence of phytochemicals in the extracts
were determined by color reactions of the compounds with specific reagents/dyes.
5
Table 1. Qualitative phytochemical screening procedures
Phytochemical Test Reagent and Positive Result
Chemicals Used
Alkaloid Mayer’s Test Hydrochloric acid, White precipitate
Mayer’s reagent
Saponin Foam Test Water Copious lather
formation
Tannin Lead Acetate Test Lead acetate White precipitate
Phenol Ferric Chloride Test Ferric chloride Blush green or red
color
Flavonoid Shindo’s Test Magnesium Red or red orange
turnings, color
Hydrochloric acid
Quinone Sulfuric Acid test Sulfuric acid Yellow precipitate
Figure 3. Phytochemical analysis of M. indica, M. rostrata, M. sylvatica, M. altissima, and M. laurina
Mosquito Acculturation
Larvicidal traps were used to collect A. aegypti eggs from open and closed habitats
and reared in a cup lined with filter paper strips and one third filled with tap water at the
Learning Resource Center of MIMAROPA Regional Science High School. A
homogenous population of late third to early fourth instars (5 days old and 4–5 mm in
length) were obtained five to seven days later.
6
Figure 4. Larvicidal traps used to culture eggs of Aedes aegypti
Preparation of Different Concentrations of Extract
Table 2. Different Concentrations Mango Cultivars Leaves Ethanolic Extract
Treatment Volume taken from 10% Volume of water
stock solution (ml)
T1 (10,000 ppm) 5 45
T2 (15,000 ppm) 7.5 42.5
T3 (20,000 ppm) 10 40
T4 (25,000 ppm) 12.5 37.5
T5 (30,000 ppm) 15 35
T6 (Crude Extract) 50 ml crude extract
T7 (Negative Control) Distilled water
Different concentrations of Mangifera rostrata (Carabao Mango), Mangifera
sylvatica (Pico Mango), Mangifera altissima (Paho Mango), and Mangifera laurina
(Apple Mango) ethanolic extracts were prepared.
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Treatment Application
Batches of ten (10) third or fourth instar larvae were transferred by means of
droppers to small disposable test cups or vessels containing 50 ml of the different
treatments, crude extract and distilled water as negative control. Each cup was labeled
and then covered by a mosquito net. Small, unhealthy or damaged were removed and
replaced. After 48-hour exposure, larval mortality is recorded. Dead larvae are those that
cannot be induced to move when they are probed with a needle in the siphon or the
cervical region. The experiment was performed in five replicates.
Morphology Analysis
The morphology of the 3rd and early 4th instar larvae were observed before and
after the application of the plant extract using a HD-digital microscope. Swelling,
aberrations in the midgut and rear part of the larvae samples after death were also
observed.
Statistical Analysis
Data from all replicates were pooled for analysis. The lethal concentrations to kill
50% (LC50) and 90% (LC90) of larval population were calculated using linear
regression probit analysis.
One-Way Analysis of Variance (ANOVA) was used to determine the significant
difference in the number of dead mosquito larvae among the treatments. Meanwhile,
8
Two-Way Analysis of Variance (ANOVA) was used to determine the significant
difference among the effects of Mangifera rostrata (Carabao Mango), Mangifera
sylvatica (Pico Mango), Mangifera altissima (Paho Mango), and Mangifera laurina
(Apple Mango) ethanolic extracts.
Proper Disposal Procedures
After the experimentation, the treatments were thrown on one spot in which it was
poured with hot water. This method is according to the procedures given in using the
larvicide trap and following the Guidelines for Laboratory and Field Testing of Mosquito
Larvicides by World Health Organization. Chemical disposals were done according to
the proper clean up cited in the Safety Data Sheet. They were disposed on inert solids or
containerized before disposal.
Risk and Safety
According to the Safety Data Sheet of the Federal Register on rules and regulations
(2013), the use of chemicals demands personal precautions and emergency procedures in
case of accidental release measures. The use of protective equipment such as safety
glasses, gloves and protective clothing are basic standards. For safe handling, washing
possible exposed areas of the skin before the process and ventilation is required.
9
Results and Discussion
Phytochemical Screening of the Different Mango Cultivars
Table 3. Phytochemical Analysis of Mangifera indica Leaves Ethanolic Extract
Phyto- Test Result Result Result Result Result
chemical Mangifera Mangifera Mangifera Mangifera Mangifera
indica rostrata sylvatica altissima laurina
(Pico (Paho (Apple
(Indian (Carabao Mango) Mango) Mango)
Mango) Mango)
Alkaloid Mayer’s
Test
+ + + - +
Saponin Foam
+ + + + +
Test
Tannin Lead
+ + + + +
Acetate
Test
Phenol Ferric
+ + + + +
Chloride
Test
Flavonoid Shindo’s
+ + + + +
Test
Quinone Sulfuric
Acid Test
+ + + - +
Note: (+) present; (-) absent
The result of the phytochemical screening revealed the following metabolites as
present in the ethanolic extract of M. indica, M. rostrata, M. sylvatica, M. altissima and
M. laurina (Table 3).
All phytoconstituents have large roles in subjecting mortality to the Ae. Aegypti
larvae. Dietary phenolics such as flavonoids and phenolic compounds are used as
10
defense compounds and they have antioxidant properties that are used as protecting
agents against free radical-mediated disease processes. Alkaloids have antibacterial and
antifungal properties that ensure endurance against microorganisms, insects, etc. and
antimalarial activity (quinine). Saponin is antimicrobial, inhibits mold, and its
hypocholesterolaemic and anticarcinogenic properties have significantly affected the
growth, feed intake and reproduction in animals. Other than that, it is also an antioxidant,
it impairs the digestion of protein and the uptake of vitamins and minerals in the gut that
causes hypoglycaemia, and acts as antifungal and antiviral. Terpenoids have
anticarcinogenic, antimalarial activity, antibacterial and antifungal properties that inhibit
micro-organisms and reduce the risk of fungal infection. Tannins are astrigents and have
anti-inflammatory, antiseptic, antioxidant and haemostatic properties (Saxena, Nema,
Singh and Gupta, 2013).
Average Mortality Rate of Aedes Aegypti
Table 4. Average Mortality Rate of Aedes aegypti Applied with Different Treatments
of Mangifera indica (Indian Mango)
R1 R2 R3 R4 R5 Mean
T1 (10,000ppm) 4 1 5 3 1 2.8
T2 (15,000ppm) 3 1 4 2 4 2.8
T3 (20,000ppm) 1 3 7 4 2 3.4
T4 (25,000ppm) 2 4 7 7 9 5.8
T5 (30,000ppm) 2 4 8 8 9 6.2
T6 (Crude extract) 10 10 10 10 10 10
T7 Negative Control 5 2 1 0 1 1.8
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Among the treatments of Mangifera indica, treatment six has the highest mortality
rate with mean of 10. This means that treatment six, or the crude extract of M. indica, has
the highest possibility of larval death, followed by treatment 5 with 30,000ppm,
treatment 4 with 25,000ppm, treatment 3 with 20,000ppm, treatment 2 with 15,000ppm
and treatment 1 with 10,000ppm concentrations respectively. The lowest mortality rate is
exhibited by treatment 7 with mean of 1.8, being the negative control treatment using
distilled water. The mortality of Ae. aegypti is directly proportional with the
concentrations of the ethanolic extract.
In the study of Yousaf and Zuharah (2015), M. indica extract is proven to have
strong larvicidal activity among the plants from the Anacardiaceae family tested, having
the the second lowest lethal concentration values. In addition to that, Mohammed and
Chadee cited that the toxic properties and efficacy of M. indica varies by the solvent
used or selected.
Table 5. Average Mortality Rate of Aedes aegypti Applied with Different Treatments of
Mangifera rostrata (Carabao Mango)
R1 R2 R3 R4 R5 Mean
T1 (10,000ppm) 2 2 3 1 2 2
T2 (15,000ppm) 3 3 4 2 4 3.2
T3 (20,000ppm) 2 3 5 6 4 4
T4 (25,000ppm) 5 5 5 6 8 5.8
T5 (30,000ppm) 7 8 8 9 8 8
T6 (Crude extract) 10 10 10 10 10 10
T7 Negative 2 1 0 2 1 1.2
12
Among the treatments of Mangifera rostrata, treatment six has the highest mortality
rate with mean of 10. This means that treatment six, or the crude extract of M. rostrata,
has the highest possibility of larval death, followed by treatment 5 with 300,00ppm,
treatment 4 with 25,000ppm, treatment 3 with 20,000ppm, treatment 2 with 15,000ppm
and treatment 1 with 10,000ppm concentrations respectively. The lowest mortality rate is
exhibited by treatment 7 with mean of 1.2, being the negative control treatment using
distilled water. The mortality of Ae. aegypti is directly proportional with the
concentrations of the ethanolic extract.
Table 6. Average Mortality Rate of Aedes aegypti Applied with Different Treatments
of Mangifera sylvatica (Pico Mango)
R1 R2 R3 R4 R5 Mean
T1 (10,000ppm) 2 3 2 1 2 2
T2 (15,000ppm) 2 2 3 4 4 3
T3 (20,000ppm) 5 2 3 3 4 3.4
T4 (25,000ppm) 4 4 8 6 3 5
T5 (30,000ppm) 8 6 8 8 6 7.2
T6 (Crude extract) 10 9 10 10 9 9.6
T7 Negative Control 4 1 2 2 1 2
Among the treatments of Mangifera sylvatica, treatment six has the highest
mortality rate with mean of 9.6. This means that treatment six, or the crude extract of M.
sylvatica, has the highest possibility of larval death, followed by treatment 5 with
30,000ppm, treatment 4 with 25,000ppm, treatment 3 with 20,000ppm, treatment 2 with
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15,000ppm and treatment 1 with 10,000ppm concentrations respectively. The lowest
mortality rate is exhibited by treatment 7 with mean of 2, being the negative control
treatment using distilled water. The mortality of Ae. aegypti is directly proportional with
the concentrations of the ethanolic extract.
Table 7. Average Mortality Rate of Aedes aegypti Applied with Different Treatments
of Mangifera altissima (Paho Mango)
R1 R2 R3 R4 R5 Mean
T1 (10,000ppm) 4 3 2 2 3 2.8
T2 (15,000ppm) 5 2 3 4 3 3.4
T3 (20,000ppm) 4 2 4 4 5 3.8
T4 (25,000ppm) 6 5 7 5 8 6.2
T5 (30,000ppm) 7 8 7 6 8 7.2
T6 (Crude extract) 10 10 10 10 10 10
T7 Negative 5 2 1 0 2 2
Among the treatments of Mangifera altissima, treatment six has the highest
mortality rate with mean of 10. This means that treatment six, or the crude extract of M.
altissima, has the highest possibility of larval death, followed by treatment 5 with
30,000ppm, treatment 4 with 25,000ppm, treatment 3 with 20,000ppm, treatment 2 with
15,000ppm and treatment 1 with 10,000ppm concentrations respectively. The lowest
mortality rate is exhibited by treatment 7 with mean of 2, being the negative control
treatment using distilled water. The mortality of Ae. aegypti is directly proportional with
the concentrations of the ethanolic extract.
14
Table 8. Average Mortality Rate of Aedes aegypti Applied with Different Treatments
of Mangifera laurina (Apple Mango)
R1 R2 R3 R4 R5 Mean
T1 (10,000ppm) 1 0 1 3 2 1.4
T2 (15,000ppm) 3 3 2 2 4 2.8
T3 (20,000ppm) 3 6 4 5 6 4.8
T4 (25,000ppm) 6 5 6 5 7 5.8
T5 (30,000ppm) 8 7 8 9 9 8.2
T6 (Crude extract) 9 10 10 10 9 9.6
T7 Negative 0 2 1 1 0 0.8
Among the treatments of Mangifera laurina, treatment six has the highest mortality
rate with mean of 10. This means that treatment six, or the crude extract of M. laurina,
has the highest possibility of larval death, followed by treatment 5 with 30,000ppm,
treatment 4 with 25,000ppm, treatment 3 with 20,000ppm, treatment 2 with 15,000ppm
and treatment 1 with 10,000ppm concentrations respectively. The lowest mortality rate is
exhibited by treatment 7 with mean of 0.8, being the negative control treatment using
distilled water. The mortality of Ae. aegypti is directly proportional with the
concentrations of the ethanolic extract.
15
Difference on Mortality Rate of Aedes aegypti
Table 9. Difference on Mortality Rate of Aedes aegypti Applied with Different
Treatments of Mangifera indica (Indian Mango)
Source of
Variation SS df MS F P-value F crit
Between Groups 244.3429 6 40.72381 9.255411 1.282E-05 2.445259
Within Groups 123.2 28 4.4
For the results of mortality as shown in the table, there is significant difference
among the five mortality treatments on the mortality rate of the mosquito larvae at p
1.282E-05 < 0.05 level. These results suggest that high concentrations of the Mangifera
indica really have an effect on the mortality effect on the larvae of Ae. aegypti.
Table 10. Difference on Mortality Rate of Aedes aegypti Applied with Different
Treatments of Mangifera rostrata (Carabao Mango)
Source of
Variation SS df MS F P-value F crit
Between Groups 311.1429 6 51.85714 55 3.31E-14 2.445259
Within Groups 26.4 28 0.942857
For the results of mortality as shown in the table, there is significant difference
among the five mortality treatments on the mortality rate of the mosquito larvae at p
3.31E-14 < 0.05 level. These results suggest that high concentrations of the Mangifera
rostrata really have an effect on the mortality effect on the larvae of Ae. aegypti.
16
Table 11. Difference on Mortality Rate of Aedes aegypti Applied with Different
Treatments of Mangifera sylvatica (Pico Mango)
Source of
Variation SS df MS F P-value F crit
Between Groups 247.2 6 41.2 29.42857 7.3942E-11 2.445259
Within Groups 39.2 28 1.4
For the results of mortality as shown in the table, there is significant difference
among the five mortality treatments on the mortality rate of the mosquito larvae at p
7.3942E-11 < 0.05 level. These results suggest that high concentrations of the Mangifera
sylvatica really have an effect on the mortality effect on the larvae of Ae. aegypti.
Table 12. Difference on Mortality Rate of Aedes aegypti Applied with Different
Treatments of Mangifera altissima (Paho Mango)
Source of
Variation SS df MS F P-value F crit
Between Groups 245.4857 6 40.91429 31.47253 3.33E-11 2.445259
Within Groups 36.4 28 1.3
For the results of mortality as shown in the table, there is significant difference
among the five mortality treatments on the mortality rate of the mosquito larvae at p
3.33E-11 < 0.05 level. These results suggest that high concentrations of the Mangifera
altissima really have an effect on the mortality effect on the larvae of Ae. aegypti.
17
Table 13. Difference on Mortality Rate of Aedes aegypti Applied with Different
Treatments of Mangifera laurina (Apple Mango)
Source of Variation SS df MS F P-value F crit
Between Groups 335.7714 6 55.9619 64.21858 4.52E-15 2.445259
Within Groups 24.4 28 0.871429
For the results of mortality as shown in the table, there is significant difference
among the five mortality treatments on the mortality rate of the mosquito larvae at p
4.52E-15 < 0.05 level. These results suggest that high concentrations of the Mangifera
laurina really have an effect on the mortality effect on the larvae of Ae. aegypti.
Table 14. Difference Among the Mango Cultivars Ethanolic Extract
Source of
Variation SS df MS F P-value F crit
Sample 4.457142857 4 1.114285714 0.105901521 0.980308959 2.431965056
Columns 17.2 4 4.3 0.408671253 0.802193113 2.431965056
Interaction 38.05714286 16 2.378571429 0.226059015 0.99928434 1.711346961
Within 1578.285714 150 10.52190476
Total 1638 174
The result of Two-Factor ANOVA, as shown in Table 14, shows no significant
difference among the mortality rates of Ae. Aegypti applied with the five mango cultivars
ethanolic extract. This means that any of the five mango cultivars can be used against Ae.
Aegypti for its larvicidal bioactivity.
18
Probit Analysis of Lethal Concentration of Mango Cultivars Ethanolic Extract
Table 15. Lethal Concentration LC50 and LC90
Mango Cultivars LC50 (ppm) LC90 (ppm)
M. indica (Indian Mango) 23,988.33 86,963.689
M. rostrata (Carabao Mango) 20,090.93 50,118.72
M. sylvatica (Pico Mango) 22,908.68 68,706.84
M. altissima (Paho Mango) 20,417.38 68,391.165
M. laurina (Apple Mango) 19,998.62 42,657.95
Using the regression equation, values of lethal concentration at 50% and 90% were
held at 23,988.33ppm and 86,963.689ppm for M. indica. This means that the guarantee
that half of the population was killed will be at concentration value of 23,988.33ppm and
potential at 90% will be 86,963.689ppm. For M. rostrata, values of lethal concentration
at 50% and 90% were 20,090.93ppm and 50,118.72ppm. For M. sylvatica, values of
lethal concentration at 50% and 90% were 22,908.68ppm and 68,706.84ppm. For M.
altissima, values of lethal concentration at 50% and 90% were 20,417.38ppm and
68,391.165ppm. For M. laurina, values of lethal concentration at 50% and 90% were
19,998.62ppm and 42,657.95ppm. Out of the five mango cultivars, M. laurina exhibited
the lowest 50% and 90% lethal concentration needed, while M. indica the highest.
According to the OPP classification criteria for acute toxicity, oral toxicity of the
extract is deemed to be Category IV while the dermal toxicity is classified as Category
III. Both have the signal word “caution”. This means that there is no hazard statement
19
required however as caution, the product may be harmful when swallowed and harmful
if in contact with skin.
Morphology of Aedes aegypti
Figure 5. Before and After Treatment of M. indica ethanolic extract
Figure 6. Before and After Treatment of M. rostrata ethanolic extract
Figure 7. Before and After Treatment of M. sylvatica ethanolic extract
Figure 8. Before and After Treatment of M. altissima ethanolic extract
20
Figure 9. Before and After Treatment of M. laurina ethanolic extract
The figures above showed the digital microscopic photos of the larvae before and
after treatments of the mango cultivars ethanolic extracts. In Figure 5, the body was
hollow yet there the midgut is still present. There is also presence of coloration. This is
due to tannin which acts as a dye and astringent that produces the capability to preserve
tissues (Schrijvers et al., 1989) and as a result, has been used as preservatives for wood
products (Asante et al., 2017). In figure 6, the midgut of the larvae separates or rips into
two after application of the ethanolic extracts. In figure 7, swelling of the Ae. Aegypti
larvae is evident. In Figure 8, there is coloration and disintegration of the midgut. In
Figure 9, swelling of the Ae. Aegypti larvae is also evident.
Conclusion
Based on the results, the study showed that Indian Mango (Mangifera indica),
Carabao Mango (Mangifera rostrata), Pico Mango (Mangifera sylvatica), Paho Mango
(Mangifera altissima), and Apple Mango (Mangifera laurina) leaves ethanolic extracts
are effective against mosquito larvae. This is initially supported by the phytoconstituents
such as tannin, alkaloids, flavonoids, terpenoids and phenolic compounds present in the
extract. In addition, it was found that there is significant difference among the prepared
21
treatments of the different mango cultivars ethanolic extracts wherein treatment 6 (crude
extract) exhibited highest mortality rate for Ae. aegypti larvae. This means that the five
mango cultivars ethanolic extract is dose dependent. The results of the study also showed
no significant difference among the five mango cultivars ethanolic extracts. It means that
any of the mango cultivars aforementioned can be used for its larvicidal potential. The
morphology of Ae. aegypti shows that there is serious aberration on the mid-gut and
swelling after experimentation. This may be associated to the presence of
phytoconstituents flavonoids, terpenoids, alkaloids, phenolic compounds and saponin.
Recommendations
For plant extraction, it is best if the ratio of the sample and the solvent is 1:3. This is
to ensure reserves in case complications occur in mosquito rearing. It is also best to use
rotary evaporator to purify the extracts properly. Make sure the cap of the bottle of the
plant extraction is sealed and keep the bottle refrigerated at all times.
Acknowledgment. The researcher would like to express sincerest gratitude to Ms.
Mischelle F. Puntod for providing great supervision during the experimentation period.
References
Abdalla A. (2017), Damage caused by Castor seed oil and its Ethanolic Extract on
Anopheles arabienses larvae. Geriza State, Sudan. Faculty of Science, University of
Hail, KSA, Saudi Arabia
22
Akaban, I.O.M. & Nwabueze, E. (2015). A Survey of Mosquito Larval Habitats and
Species Distribution in Rivers State University of Science and Technology
Nkpolu Porthacourt, Nigeria. International Journal of Science and Research
(IJSR), ISN: 2319- 7064.
Almiron, G., et al. (2008). Larvicide and oviposition deterrent effects of fruit and leaf
extracts from Melia azedarach L. on Aedes aegypti (L.) (Diptera: Culicidae).
Bioresource Technology, 99 (2008): 3066–3070.
Andrew J., and Ananya B. (2013). Morphonology and Morphometry of
Aedes aegypti Adult Mosquito. India. www.sciencedomain.org
Asante, B., Haapala, B., Li, P., Liimatainen, H., Sirviö, J.H. (2017). Adsorption Of
Tannin Onto Functionalized Nanocellulose.
Bharti, R. P. (2013). Studies on Antimicrobial Activity and Phytochemical Profile of
Mangifera Indica Leaf Extract. IOSR Journal Of Environmental Science,
Toxicology And Food Technology (IOSR-JESTFT), 7(3). e-ISSN: 2319-2402, p-
ISSN: 2319-2399.
Christophers, S.R. (1960) Aedes aegypti (L.). The Yellow Fever Mosquito, its Life
History, Bionomics and Structure. Cambridge Univ. Press, London.
Derese, S., et. al. Medicinal Spices and Vegetables from Africa: Mangifera
indica L. Anacardiaceae. http://dx.doi.org/10.1016/B978-0-12-809286-6.00021-2
Doughari, J.H. (2012). Phytochemicals: Extraction Methods, Basic Structures and
Mode of Action as Potential Chemotherapeutic Agents. Phytochemicals - A
Global Perspective of Their Role in Nutrition and Health, (Ed.), InTech, DOI:
10.5772/26052.
Finney, D. J.(1952). Probit Analysis. (2nd Ed), Journal of the Institute of Actuaries.
78 (3) :388-390.
Hemingway, R.W. & Laks, P.E.(2012). Plant Polyphenols: Synthesis, Properties,
Significance. Springer Science & Business Media. 625.
23
Jirakanjanakit, N., Rongnoparut, P., Saengtharatip, S., Chareonviriyaphap, T., Duchon,
S., Bellec, C. & Yoksan, S. (2007). Insecticide susceptible/resistance status in Aedes
(Stegomyia) aegypti and Aedes (Stegomyia) albopictus (Diptera: Culicidae) in
Thailand during 2003-2005. Journal of Economic Entomology (in press).
Laboratory Biosafety Manual (2004), World Health Organization. Retrieved from
https://www.who.int/csr/resources/publications/biosafety/Biosafety7.pdf
Mamta S., et. Al (2013), Jornal of Pharmacology and Phytochemistry. Retrieved from
phytojournal.com
Mary Helen, P.A., Aswathy, M.R., Deepthi, K.G., Rathi Mol, R., Jaison Joseph, J.
and Jaya Sree, S. (2013). Phytochemical Analysis and Anti-cancer Activity of
Leaf Extract of Mangiferin indica (Kotutukonam Varika).
Maslbo, M. and He, Q.(2008). Major Mango Polyphenols and Their Potential
Significance to Human Health. Comprehensive Reviews in Food Science and
Food Safety, 7, 309 - 319.
Noratto, G.D. et al. (2010). Anticarcinogenic Effects of Polyphenolics from Mango
(Mangifera indica) Varieties. Journal of Agricultural and Food Chemistry, 58,
4104 – 4112. DOI:10.1021/jf903161g
Ramirez et al. (2016). Extraction of Mangiferin and Chemical Characterization and
Sensorial Analysis of Teas from Mangifera indica L. Leaves of the Ubá Variety.
Beverages.2, 33.
Rey, D., David, J.P., Besnard, G., Jullien, J.L., Lagneau, C. and Meyran, J.C.(2001),
Comparative sensitivity of larval mosquitoes to vegetable polyphenols versus
conventional insecticides. Entomologia Experimentalis et Applicata, 98:
361–367. DOI:10.1046/j.15707458.2001.00793.x
Saxena, M., Saxena, J., Nema, R., Singh, D. and Gupta, A. (2013). Phytochemistry
of Medicinal Plants. Journal of Pharmacognosy and Phytochemistry, 1(6):
168-182.
24
Schrijvers, A. H., Frederik, P.M., Stuart M.C., van der Vusse, G.J., Reneman, R.S.
(1989). Dual effect of tannic acid on the preservation and ultrastructure of
phosphatidyl choline vesicles. Mol Cell Biochem, 88(1-2):91-6.
Stuart, G. (2016). Mangifera indica. Philippine Alternative Medicine. Retrieved June
13, 2017 from http://www.stuartxchange.com/Mango.html
Yousaf, A. & Zuharah, W.F. (2015). Lethal response of the dengue vectors to the plant
extracts from family Anacardiaceae. Asian Pacific Journal of Tropical
Biomedicine, 5(10): 812-818. https://doi.org/10.1016/j.apjtb.2015.05.016
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Appendix
Flow Chart
Preparation and Extraction of Plant Sample
Collection of Mango Washing of Mango Drying of leaves Powdering of dried leaves
cultivars leaves cultivars leaves
Extract filtration Squeezing of macerated Maceration Weighing of powdered
leaves leaves
Water Bathe The extracts were poured in
a bottle
26
Phytochemical Testing
Preparation of Chemicals and Putting a small amount of Test of Saponin: Extract was
Laboratory Equipment to be extract shaken with 2 ml of water.
used
PRESENT: All cultivars
Test of Flavonoid: A few Mg Test of Phenol: A few drops Test of Alkaloids: Extract
turnings and a few drops of of ferric chloride solution was mixed with little amount
hydrochloric acid were added were added in the extract of dilute hydrochloric acid
to the extract and were boiled and Mayer’s reagent
PRESENT: All cultivars
for five minutes
PRESENT: Carabao, Piko
and Apple Mango
Test of Quinone: The extract was mixed with Test of Tannin: Lead Acetate
few drops of aqueous sodium hydroxide was added to the extract
solution 27
PRESENT: All cultivars
PRESENT: Carabao, Piko and Apple Mango
Treatment Applications (Mangifera indica)
28
Treatment Applications (Mangifera rostrata)
29
Treatment Applications (Mangifera sylvatica)
30
Treatment Applications (Mangifera altissima)
31
Treatment Applications (Mangifera laurina)
32
33