Veterinary World, EISSN: 2231-0916
Available at www.veterinaryworld.org/Vol.12/November-2019/6.pdf
RESEARCH ARTICLE
Open Access
Study on vector mosquito of zoonotic Brugia malayi in Musi Rawas,
South Sumatera, Indonesia
Budi Mulyaningsih1, Sitti Rahmah Umniyati1, Suwarno Hadisusanto2 and Erwin Edyansyah3
1. Department of Parsitology, Faculty of Medicine Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta,
Indonesia; 2. Department of Tropical Biology, Faculty of Biology, Universitas Gadjah Mada, Yogyakarta, Indonesia;
3. Postgraduate Program of Medicine, Faculty of Medicine Public Health and Nursing, Universitas Gadjah Mada,
Yogyakarta, Indonesia.
Corresponding author: Budi Mulyaningsih, e-mail: budi.mulyaningsih@ugm.ac.id
Co-authors: SRU: sitti-rahmah@ugm.ac.id, SH: suwarnohs@ugm.ac.id, EE: erwin.edyansyah@mail.ugm.ac.id
Received: 31-05-2019, Accepted: 27-09-2019, Published online: 07-11-2019
doi: www.doi.org/ 10.14202/vetworld.2019.1729-1734 How to cite this article: Mulyaningsih B, Umniyati SR, Hadisusanto S,
Edyansyah E (2019) Study on vector mosquito of zoonotic Brugia malayi in Musi Rawas, South Sumatera, Indonesia,
Veterinary World, 12(11): 1729-1734.
Abstract
Background and Aim: Studies to determine abundance, distribution, species composition, and mosquito interactions are
very important in understanding the risk of disease transmission to implement appropriate mosquito management in endemic
areas. Lymphatic filarial worms are one of the parasites that are contracted and/or transmitted by mosquitoes when sucking
the blood of infected humans or animals and then biting others. This research was conducted to study the abundance, species
composition, mosquito biting cycles, density and periodicity of mosquitoes caught in Lubuk Pauh Village, Bulang Tengah
Suku Ulu, Musi Rawas, South Sumatera, Indonesia, which is an endemic area of zoonotic Brugia malayi.
Materials and Methods: The mosquito collection was done in July 2018 using the human landing collection method for
11 h from 18.00 pm to 5.00 am Western Indonesian Time. The catching of mosquitoes was done both indoors and outdoors,
and mosquitoes were identified under a dissecting microscope using an identification key to confirm their species. Detection
of B. malayi larvae in mosquitoes was confirmed by dissection and polymerase chain reaction methods.
Results: The caught mosquitoes consisted of four species: Armigeres subalbatus, Culex quinquefasciatus, Culex vishnui,
and Mansonia uniformis. Based on the Shannon–Wiener index, Lubuk Pauh Village has low mosquito species diversity
(0.210). Ar. subalbatus was the dominant mosquito in Lubuk Pauh Village with dominance number 95.08, and it had the
most frequent activity in each of periods of indoor and outdoor collection, with the highest density (man-hour density) at
18.00-19.00 (51.750). B. malayi infective stage larvae were not found in all mosquito species caught.
Conclusion: Existence of Ar. subalbatus, Cx. quinquefasciatus, and Ma. uniformis in Lubuk Pauh Village which is an
endemic area of B. malayi shows that the area is at risk of lymphatic filariasis transmission.
Keywords: Armigeres subalbatus, Brugia malayi, lymphatic filariasis, Musi Rawas, South Sumatera.
Introduction
Lymphatic
filariasis,
commonly
called
elephantiasis, is one of the neglected tropical diseases. At present, 856 million people in 52 countries are living in areas that require preventive chemotherapy to stop the spread of this infection [1].
Epidemiologically, Indonesia is in an area that is
at high risk of contracting filariasis [2]. In South
Sumatera Province, lymphatic filariasis is present
in almost all districts. Musi Rawas Regency is one
of the endemic areas of filariasis and in 2014-2016,
29 chronic sufferers were reported in three villages
[3]. Lymphatic filarial worms are one of the parasites
that are contracted and/or transmitted by mosquitoes when sucking the blood of infected humans or
Copyright: Mulyaningsih, et al. Open Access. This article is
distributed under the terms of the Creative Commons Attribution
4.0 International License (http://creativecommons.org/licenses/
by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit
to the original author(s) and the source, provide a link to the
Creative Commons license, and indicate if changes were made.
The Creative Commons Public Domain Dedication waiver (http://
creativecommons.org/publicdomain/zero/1.0/) applies to the data
made available in this article, unless otherwise stated.
Veterinary World, EISSN: 2231-0916
animals and then biting others. The ability of vector
mosquitoes to swallow filarial worms and to support
their development after being in their bodies is an
important determinant of transmission of filariasis.
The amount of microfilaria that is sucked and that
develop into infective stage larvae (L3) is not constant and depends on many factors that influence their
maturity. Lymphatic filariasis is transmitted by many
species of mosquitoes in four principal genera—
Anopheles, Culex, Aedes and Mansonia, the distribution, ecology, biology and transmission potential
of which vary greatly. As transmission efficiency differs considerably by vector species, it is important to
understand the entomological aspects of transmission
of lymphatic filariasis. Mansonia spp is the main vector of zoonosis malayan filariasis [4]. Lymphatic filariasis is caused by three filarial worm species, namely,
Wuchereria bancrofti, Brugia malayi, and Brugia
timori. All of these species are found in Indonesia,
but more than 70% of filariasis cases in Indonesia are
caused by B. malayi. Malayan filariasis is one of the
zoonotic diseases that can be transmitted from animals to humans. This disease has reservoir hosts and
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mosquito vectors. Humans are considered the main
definitive host of filariasis, but there are several types
of animals that can act as sources of filariasis transmission. Of all the filarial worm species that infect
humans in Indonesia, only B. malayi nocturnal subperiodic type, and non-periodic type are found in animals, namely, monkey (Macaca fascicularis), lutong
or black monkey (Presbytis cristatus), and cats (Felis
catus). The presence of animals that become filariasis
reservoir host will be one of the problems in efforts
to eliminate filariasis in Indonesia [5]. Research in
Narathiwat Province, Southern Thailand, from the
results of 2515 cats, 401 cats were positive for microfilaria B. malayi [6] and in East Kalimantan from the
results of microfilariae examination in 645 cats found
14 cats positive for microfilaria B. malayi [7].
At present, there are 23 species of mosquitoes from the genera Anopheles, Culex, Mansonia,
and Armigeres that can act as filariasis vectors in
Indonesia [2]. The study aimed to determine density,
abundance, distribution, and species composition,
and host and mosquito interactions are very important in understanding the risk of disease transmission
to apply appropriate mosquito management. Thus,
understanding the factors that modulate vectors and
host distribution, density, and abundance, as well as
vector mosquito biting behavior, are important steps
in characterizing the risk of transmission and consequences of vector-borne diseases.
Materials and Methods
Ethical approval
This research was conducted in July 2018 and has
been approved by the Medical and Health Research
Ethics Commission of the Faculty of Medicine, Public
Health, and Nursing Universitas Gadjah Mada, with
numbers KE/FK/0389/EC/2018. The design of this
study was cross-sectional with a spot survey design.
Study sites
The study was conducted at four hamlets (Hamlet
I, II, III, and IV) in Lubuk Pauh Village, Bulang
Tengah Suku (BTS) Ulu Sub-district, Musi Rawas
District, South Sumatera Province, Indonesia. Musi
Rawas district is one of the endemic areas of Malayan
filariasis in South Sumatera.
Mosquito sampling
A mosquito sampling was done using human
landing collection (HLC) in two houses in every hamlet in Lubuk Pauh Village for 11 h from 18.00 pm to
05.00 am Western Indonesian Time (WIT). Catching
mosquitoes were done both indoors and outdoors
by a team of four trained volunteers per house, with
two volunteers sitting in the house, and two volunteers sitting outside the house. To determine mosquito
biting cycles, HLC was conducted hourly for 40 min
for the two groups (indoors and outdoors), each with
two persons, for two consecutive nights. Mosquitoes
caught were put in paper cups covered with net and
Veterinary World, EISSN: 2231-0916
then sorted and identified morphologically using the
identification keys with a dissecting microscope.
Detection of microfilaria/larva B. malayi in mosquitoes
Each species of mosquito caught, which was
considered to be able to act as a vector of B. malayi
was examined by dissection and molecularly with
polymerase chain reaction (PCR) methods to determine whether there were microfilariae or B. malayi
larvae by pooling method (10-25 mosquitoes). In
this method, a group of mosquitoes was put on the
object-glass, some drops of physiological saline
solution were added, and the mosquitoes were
pressed with another object-glass, until the body
of the mosquitoes separated into several parts.
Mosquitoes were then moved into a Petri dish which
has been filled with physiological saline solution to
soak the body parts of the mosquitoes. The immersion of the mosquitoes was left for 5-10 min, and
the Petri dish was observed under the dissecting
microscope.
The procedure for the detection of microfilariae or larvae of B. malayi in mosquitoes by pooling
method of 10-25 mosquitoes using PCR method was
carried out through several activities as following:
DNA isolation, running PCR, and electrophoresis.
Female mosquitoes were collected based on species.
Each pool then homogenized with a pestle in a tube
microcentrifuge containing 180 µl phosphate buffer saline (pH 7.2). DNA was further extracted from
each tube using Genomic DNA mini Kit GeneaidTM
Cat No. GB100. Lot No.JM02202, according to
company protocol. Amplification of PCR is carried
out with thermocycler using HhaI forward primers
(5 ‘GCGCATAAATTCATCAGC-3’) and reverse
HhaII (5’GCGCAAAACTTAATTACAAAAGC-3’).
The PCR mixtures contained 15 μl of Mix PCR
(GoTaq® Green Master Mix. 2×), 11 μl of ddH2O
(nuclease-free water lot. 0000123190 Promega), 2 μl
of R and F primers (20 μM), and 2 μl of the DNA
template in a total volume of 30 μl. The temperature
was programmed under the following conditions: One
cycle of initial denaturation at 94°C for 5 min, followed by 40 cycles of 94°C for 1 min (denaturation),
56°C for 1 min (annealing), and 72°C for 1 min
(extension); and a final extension step at 72°C for
10 min. Following the PCR 20 μl of each PCR product
was electrophoresed on a 2% agarose gel, stained with
ethidium bromide, and observed under UV. Mosquito
samples were found positive for the filarial parasite
(B. malayi), if exhibited amplification of 322 bp DNA
fragment [8].
Statistical analysis
The diversity of mosquito species was analyzed
by Shannon–Wiener diversity index [9]. Other entomological indexes were calculated, such as relative
abundance, species frequency, the dominant number, periodicity of mosquito, and species mosquito
density [10].
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abundance, species frequency, and dominant species
of mosquito species caught in Lubuk Pauh Village
with HLC method are shown in Table-2.
Results
Species diversity-dominance,
frequency of mosquitoes
relative
abundance
During the collection period with the HLC for 11 h
(18.00-05.00 WIT) in Lubuk Pauh, at coordinates S 3°
13’ 17.3’’; as many as, 630 mosquitoes were obtained
consisting of four mosquito species. Based on the
Shannon–Wiener index, Lubuk Pauh Village has low
mosquito species diversity (0.210). Diversity of species
was expressed by H index (H1), which included the low
category if the number is <1, medium category if the
number is more than 1, and <3 and high category if the
number is more than 3 [11]. Species diversity of mosquitoes caught in Lubuk Pauh Village, as shown in Table-1.
Based on the composition of the species of mosquito caught, Armigeres subalbatus was the dominant mosquito species (599). This study also showed
that the number of mosquitoes collected outdoors
(411) was higher than those caught indoors (219).
Mosquitoes collection were done for two consecutive
nights and there were 22 collecting hours. The relative
Density and periodicity of Ar. subalbatus
Ar. subalbatus was the dominant mosquito in
Lubuk Pauh Village, and it had the most frequent
activity in each of the periods, both indoor and outdoor collection. Density (man-hour density) of
Ar. subalbatus is presented in Table-3. Table-3 shows
that Ar. subalbatus is active all night both indoors and
outdoors, with the highest density (man-hour density)
at 18.00-19.00 WIT, which is equal to 51.750.
Behavior of Ar. subalbatus in Lubuk Pauh village
Table-1: Species diversity of mosquitoes caught in Lubuk
Pauh village by human landing collection method.
All mosquito species have their own distribution, behavior pattern, and characteristics of its habitat, which are different from others. The daily behavior pattern of mosquito activities will occur at day or
night time depending on the species. From the results
of this study, it can be seen that the Ar. subalbatus is
active all night from 18:00 to 05:00 WIT. The highest
activity of Ar. subalbatus that was collected on human
bait was between 18:00 and 19:00 WIT both indoors
and outdoors (Figure-1).
Mosquito species
B. malayi larvae detection in mosquitoes
Human landing
collection
Total
Indoors
Outdoors
206
11
1
1
219
393
18
411
Armigeres subalbatus
Culex quinquefasciatus
Culex vishnui
Mansonia uniformis
Number of mosquitoes
Dissection of Ar. subalbatus, Culex quinquefasciatus, Culex vishnui, and Mansonia uniformis that
were caught in Lubuk Pauh did not find filariasis
larvae. Similarly, the molecular examination using
the PCR methods also showed negative results. This
result means that filarial larvae were not found in all
mosquito species caught.
599
29
1
1
630
Table-2: The relative abundance, species frequency, and dominance numbers of mosquitoes caught in Lubuk Pauh
Village with the human landing collection method.
Mosquito species
Number of mosquitoes
Human landing collection
Relative abundance Species frequency Dominance numbers
(%)
Armigeres subalbatus
Culex quinquefasciatus
Culex vishnui
Mansonia uniformis
599
29
1
1
95.08
4.60
0.16
0.16
1.00
0.86
0.04
0.04
95.08
3.96
0.006
0.006
Species frequency without %, Dominance numbers without %
Table-3: The MHD of Ar. subalbatus from Lubuk Pauh village, July 2018.
Mosquito collecting time
18.00-19.00
19.00-20.00
20.00-21.00
21.00-22.00
22.00-23.00
23.00-24.00
24.00-01.00
01.00-02.00
02.00-03.00
03.00-04.00
04.00-05.00
Armigeres subalbatus density (MHD)
Indoors
Outdoors
17.250
7.500
5.625
7.125
7.500
7.125
4.875
5.625
6.000
5.625
5.250
34.500
16.500
11.625
9.000
9.000
10.500
13.875
11.250
7.875
10.875
9.000
Total of MHD
51.750
24.000
17.250
16.125
16.500
17.625
18.750
16.875
13.875
16.500
14.250
MHD=Man-hour density
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Figure-1: Periodicity of Armigeres subalbatus from Lubuk
Pauh village.
Discussion
Lubuk Pauh Village is one of the endemic areas
of Malayan filariasis in South Sumatera, Indonesia
(S 3° 13’ 17.3’’). This village is still categorized as an
underdeveloped village, located on the banks of the
Musi River with a typology of rubber plantation land
so that the majority of the population works as rubber
farmers. In this area, four species of mosquitoes were
found, which included Ar. subalbatus, Cx. quinquefasciatus, Cx. Vishnui, and Ma. uniformis, with low
mosquito species diversity (Shannon–Wiener index
0.210). This finding is probably due to the landing
collection of the mosquitoes that were only done twice
in July 2018 because it was a preliminary study to find
out the picture of mosquitoes found in endemic areas
of Malayan filariasis. At that time, in the area, it was in
the dry season and experiencing drought. Mosquitoes
are cosmopolite insects, which are widespread in the
tropic and sub-tropic regions. Seasonally, the changing of the environment also affects their activity and
impacts on their diversity, distribution, and density.
Research has shown that mosquitoes can be competent vectors, efficient distributors, and reinforcing
agents for various parasites in animal and human populations [11,12].
The most dominant mosquito caught was
Ar. subalbatus, which is commonly found close to
human dwellings, especially in suburban areas with
poor sanitation that contains polluted water such
as septic tanks. The density (man-hour density) of
Ar. subalbatus outdoors was higher than indoors. This
was allegedly due to the character of Ar. subalbatus
that is more exophilic. Ar. subalbatus is closely linked
with artificial habitats and also breeds in tree holes and
has been known to be a vector of Japanese encephalitis virus, a vector of filarial worm W. bancrofti in
India and the dog heartworm Dirofilaria immitis in
Peninsular Malaysia [13-15]. This mosquito species is
also the vector for the zoonotic Brugia pahangi infection in Malaysia, and therefore should now be categorized as a medically important mosquito species. Its
central role in the transmission of zoonotic B. pahangi must be considered important in future studies on
filarial infections [16].
Veterinary World, EISSN: 2231-0916
In this study, the dominance numbers of
Cx. quinquefasciatus, Cx. vishnui, and Ma. uniformis were very low. Cx. quinquefasciatus is a vector of the W. bancrofti urban type, and in Pekalongan
(Central Java), Indonesia, it has been confirmed
that Cx. quinquefasciatus is a W. bancrofti vector. Shriram et al. reported that Cx. quinquefasciatus is a W. bancrofti diurnal subperiodic type vector
in Nicobarase, Nicobar Island, and India [17]. Iris
et al. also reported that Cx. quinquefasciatus is a
W. bancrofti vector in Tanzania [18]. In the research
conducted by Safitri on Cx. quinquefasciatus from
Barito Kuala District, Kalimantan, B. malayi larvae
were found [19]. This finding can happen because the
environment in these places is suitable for Cx. quinquefasciatus and B. malayi worms. Research conducted by Yahya et al. shows that Cx. quinquefasciatus has more potential to be a B. malayi vector than
Ar. subalatus [20].
Very few Ma. uniformis were caught in Lubuk
Pauh Village, BTS Ulu Sub-district, Musi Rawas
District, South Sumatera Province, Indonesia.
The previous study showed that Ma. uniformis in
Sedang, Suak Tapeh, Banyuasin, South Sumatera,
and also in Karanganyar Village, Banyuasin, South
Sumatera were the dominant mosquito [21,22]. The
Indonesian Ministry of Health reported that in South
Sumatera, filariasis is caused by B. malayi and the
vector is Ma. uniformis [23]. The character of Ma.
uniformis breeding places can affect the incidence
of lymphatic filariasis. The research of Sapada
et al. in Banyuasin (South Sumatera) and Zen in
East Lampung showed that environmental conditions with many aquatic plants such as swamps and
ponds can be ideal breeding places for Mansonia
spp. and are associated with the incidence of lymphatic filariasis [24,25]. Ma. uniformis is the main
vectors of zoonotic B. malayi nocturnal subperiodic type in South Sumatera Province, Indonesia,
and in Southeast Asia, however, in Africa, Ma. uniformis and Mansonia africana are the main vectors
of W. bancrofti [5,23,26]. Studies of bloodsucking
mosquito activity can be used to take preventive
measures to avoid filariasis vector mosquito bites.
Many factors can influence potential vectors to be
positive for microfilaria including the amount of
microfilariae that are sucked is sufficient or not to
develop in the body of a mosquito. The requirements for mosquitoes to become vectors include
the age of mosquitoes, contact between humans and
animals (hosts) with mosquitoes, the frequency of
bloodsucking, and the susceptibility of mosquitoes
to parasites [10]. The estimated capacity to be a
vector is influenced by environmental, behavioral,
biochemical, and cellular factors that influence
the relationship between vectors, pathogens that
will be transmitted by vectors, and hosts where the
pathogen will be transmitted. Behavior and environmental factors have a role in distinguishing the
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mosquitoes’ capacity as vectors [27]. Knowledge of
mosquito endemicity and mosquito vector density is
very important as important parameters to assess the
success of vector control programs [2].
In this study, no filariasis larvae were found in
all mosquitoes caught by dissection and PCR methods, so the infection rates could not be determined.
Thus, filariasis vectors in this area cannot be determined because the discovery of filariasis larvae in the
mosquito’s body is needed to confirm mosquitoes as
vectors. In addition, the discovery of Ar. subalbatus,
which is very dominant in Lubuk Pauh Village, can
also be considered as a filariasis vector because in
Papua Armigeres spp. have also been identified as filariasis vectors makers of human and animal-sourced
disease control [23]. The existence of certain mosquito
species, especially mosquitoes transmitting diseases
in an area can be important information to be followed
up. The results of this study can be used as supporting
data for programs in conducting vector control activities. Continuous (longitudinal) observations of certain
species as vectors need to be done routinely to provide more complete and useful information for policy
programs.
Competing Interests
Conclusion
5.
In Lubuk Pauh Village as a nocturnal subperiodic B. malayi endemic area, four mosquito species
were caught, and Ar. subalbatus was the dominant
species, and it had the most frequent activity in each
of the periods, both indoor and outdoor collection.
Other mosquitoes collected were Cx. quinquefasciatus, Cx. vishnui, and Ma. uniformis although in small
numbers. B. malayi larvae were not found in all mosquito species caught; however, the discovery of Ar.
subalbatus, Cx. quinquefasciatus, and Ma. uniformis
indicates that the area is at risk of transmission of lymphatic filariasis. Further studies need to be carried out
with several mosquito samples to illustrate the effect
of climate on the presence of mosquitoes in an area.
The authors declare that they have no competing
interests.
Publisher’s Note
Veterinary World remains neutral with regard
to jurisdictional claims in published institutional
affiliation.
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Authors’ Contributions
BM designed the study, SRU and SH conducted
the field survey, and EE collected mosquito samples.
All authors drafted, revised, read, and approved the
final manuscript.
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Acknowledgments
The authors express our gratitude to the various
parties who have assisted in the implementation of this
research, including the Head of Lubuk Pauh Village,
Volunteer Catchers of Mosquitoes and Technicians
from the Department of Parasitology, Faculty of
Medicine, Public Health, and Nursing Universitas
Gadjah Mada: Mr. Purwono, Mrs. Kuswati, and Mrs.
Rumbiwati for helping laboratory work. This study
was financially supported by the Faculty of Medicine,
Public Health, and Nursing Universitas Gadjah Mada,
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