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Evaluation of selected South African ethnomedicinal plants as mosquito repellents against the Anopheles arabiensis mosquito in a rodent model

  • 1Email author,
  • 2,
  • ^,
  • 3,
  • 4,
  • 4,
  • 2 and
  • 1
^Deceased
Malaria Journal20109:301

https://doi.org/10.1186/1475-2875-9-301

  • Received: 6 May 2010
  • Accepted: 28 October 2010
  • Published:

Abstract

Background

This study was initiated to establish whether any South African ethnomedicinal plants (indigenous or exotic), that have been reported to be used traditionally to repel or kill mosquitoes, exhibit effective mosquito repellent properties.

Methods

Extracts of a selection of South African taxa were tested for repellency properties in an applicable mosquito feeding-probing assay using unfed female Anopheles arabiensis.

Results

Although a water extract of the roots of Chenopodium opulifolium was found to be 97% as effective as DEET after 2 mins, time lag studies revealed a substantial reduction in efficacy (to 30%) within two hours.

Conclusions

None of the plant extracts investigated exhibited residual repellencies >60% after three hours.

Keywords

  • Malaria
  • Deet
  • Repellent Activity
  • Anopheles Arabiensis
  • Repellency Effect

Background

Despite ongoing efforts to control the disease, malaria still remains a serious public health problem in about 90 countries worldwide. On a global scale, malaria causes 300-500 million cases and results in 1.5-3 million deaths annually. Of these, approximately 80% of cases occur on the African continent. In the Southern Africa Development Community (SADC) mortality ranges from 0 to 128 per 100,000 population [1].

This large-scale threat to human health is transmitted by anopheline mosquitoes. These vectors feed between dusk and dawn, mostly inside houses whilst residents are asleep. However, due to behaviour modification by both vector and host, mosquitoes increasingly feed outdoors, so avoiding the insecticides sprayed on inner walls of houses in the course of vector control programmes [2].

In order to provide protection to target individuals who are outdoors during the period of active feeding, repellents are used. Repellents are applied to exposed skin, especially the arms and legs, to protect individuals against mosquitoes seeking a blood meal. The most successful active ingredient of several skin-applied mosquito repellent products is N,N-diethyl-meta-toluamide (DEET) [3]. Although presently highly effective, there have been some concerns of DEET's adverse side effects when used in high concentrations [4]. In southern Africa, limited work has been conducted on the search for natural repellent products. Although the value of numerous synthetic compounds have been investigated for repellency against Anopheles gambiae [5], there have been very few studies investigating the use of plant-derived chemicals as repellents of vectors of malaria.

Apart from employing antiplasmodials [6] and insecticidal interventions, communities in Africa have historically employed traditional methods to ward off bothersome mosquitoes, even if the association between malaria and this vector has not been made. Different methods include burning of cow dung or certain plants, or the placement of specific plant parts in and around the sleeping area. Plants have long been recognized as having insect repellent properties. In endemic malaria areas, plants have been crushed or used whole to provide protection against mosquitoes [7], or burned to this effect [8].

As part of a national programme to identify new products from medicinal plants to combat malaria, this study was initiated to establish whether any indigenous or naturalized South African ethnomedicinal plants that have been reportedly used traditionally to repel or kill mosquitoes exhibit effective mosquito repellent properties. Accordingly, extracts of a selection of a number of such taxa were tested for their mosquito repellency properties in a suitable bioassay, which assesses the potency of the test substance when applied topically to the skin.

Methods

Selection and collection of plant material

A survey of relevant literature on ethnomedicinal plants used in East and Southern Africa revealed that a number of taxa have been reported to be used as mosquito repellents, or to repel or kill other invertebrates. However, given the limited quality of documented data available, it was decided to not make a distinction between insect repellents and insecticides (both larva- and adulticides), but to rather consider a pool of plants with anti-insecticidal activity. This decision was in part based on earlier observations [9] that some plants possessing repellent properties are also insecticidal. The converse could be true. In order to select the most relevant taxa, all were ranked following the application of weighted criteria, principally ethnobotanical and chemotaxonomic (including such elements as popularity in ethnomedicinal trade, reports on insecticidal and/or mosquitocidal application, reports on insect and/or mosquito repellent application, and the known presence and diversity of repellent/insecticidal constituents in the family to which it belongs). Higher weighting was provided to plants indigenous to the Flora of southern Africa region. A similar semi-quantitative selection method has previously been applied to identify and rank anti-plasmodial plant candidates from South Africa [6].

From the ranked list selected plants were collected throughout South Africa. Different plant parts, namely, leaves, root, stem, fruit, flowers, seeds, twigs and bark, and combinations of the above were sourced to generate extracts. In some instances, extracts were made of the whole plant. The plant organ(s) selected for extract preparation was based largely on availability at the time of collection.

The identity of plant material was determined at the National Herbarium of South Africa (PRE) where voucher specimens have been lodged.

Extract preparation

Plant samples were separated into different components and dried in an oven at 30-60°C. The drying time and temperature varied depending on the nature of the plant part. Dried plant material was ground to a coarse powder using a hammer mill and stored at ambient temperature prior to extraction. For each extraction procedure, 100-500 g of powdered plant material was sequentially extracted, with cold dichloromethane (DCM), DCM/methanol (MeOH) (1:1), MeOH and purified water. Organic extracts were concentrated by rotary vacuum evaporation below 45°C and then further dried in vacuo at ambient temperature for 24 h. The aqueous extracts were concentrated by freeze-drying. All dried extracts were stored at -20°C.

Animal preparation

Repellent activity was assessed by topical application of the test substance to the ventral surface of test rodents, and subsequent exposure of the treated area to unfed female mosquitoes. The number of bites relative to the untreated negative control was recorded, and the repellency percentage determined. The standard WHO guidelines were adapted for use in this trial [10].

The rodent, Mastomys coucha was used for the screening of the extracts. Ethical approval for the use of live animals in this study was obtained from the Ethics Committee of the South African Medical Research Council. Animals were put into groups of four, and each plant extract was tested on two animals, whilst the remaining two animals were used as negative and positive controls respectively. Carriers for the extracts, either acetone or distilled water, were used as the untreated negative control whereas concentrated, laboratory grade DEET was used as the positive control. Crude plant samples were dissolved in either acetone or distilled water depending on their initial extraction procedure thus forming a 10 mg/ml solution. DCM and DCM/MeOH extracts were reconstituted in acetone whereas aqueous extracts were made up in distilled water.

Adult rodents were weighed individually, and injected intraperitoneally with a 1 ml solution of sodium pentobarbital (60 mg/l) per 0.225 kg of body weight. Once anaesthetized, rodents were shaved on the ventral surface and 1 ml of plant extract solution applied to the abdomens of each of two rodents. The percentage repellency was taken as the mean of the number of bites relative to the untreated negative control.

Probing activity assay

Paper cups (500 ml) were modified by replacing the base of the cup with mosquito netting held in place with a rubber band and covering the mouth of the cup with transparent plastic film. Thirty unfed 4-day old Anopheles arabiensis females were introduced into the cup and held in contact with the treated ventral surface of each anaesthetized rodent. Mosquito activity was observed through the transparent plastic film. At the end of a two-minute exposure period the number of mosquitoes probing (attempting to feed on the anaesthetized mouse, through the netting) was recorded. For those extracts with protection >80% after 2 mins, the repellency effect was determined hourly for up to three hours post application. The rodent was then returned to the animal facility and allowed to recover from the anaesthetic.

Results and discussion

A total of 115 plant extracts, derived from 24 taxa representing 14 plant families, were evaluated for their repellency properties, (Table 1). Results have been presented alphabetically by family, genus and species, and thereafter in descending order of repellency effect after the two-minute exposure period.
Table 1

Two minute mosquito repellency screening results for extracts of South African ethnomedicinal plants.

Family

Plant species

Voucher number

Plant Part

Extraction

Repellency (%)

Apiaceae

Apiaceae

EN00994

Whole plant

DCM/MeOH (1:1)

55

 

Alepidea amatymbica Eckl. & Zeyh.

    
   

Whole plant

Water

23

Asphodelaceae

Aloe greatheadii Schönland var. davyana (Schönland) Glen & D.S. Hardy

EN00021

Leaves

DCM

55

  

EN00021

Leaves

DCM/MeOH (1:1)

55

  

EN00021

Stem

DCM

53

  

EN00021

Leaves

Water

43

  

EN00021

Leaves

DCM

36

  

EN00021

Stems

DCM/MeOH (1:1)

33

  

EN00021

Stems

MeOH

31

  

EN00021

Stems

Water

27

 

Aloe ferox Mill.

EN00538

Fruit

DCM

68

  

BP00469

Whole plant

DCM/MeOH (1:1)

58

  

EN00538

Roots

DCM

56

  

EN00538

Stem

DCM/MeOH (1:1)

52

  

EN00538

Roots

DCM/MeOH (1:1)

50

  

EN00538

Leaves

DCM/MeOH (1:1)

40

  

EN00538

Leaves

DCM

33

  

EN00538

Stems

DCM

33

  

EN00538

Roots

Water

31

  

EN00538

Stems

Water

31

  

BP00469

Whole plant

Water

30

  

EN00538

Fruit

Water

26

  

EN00538

Leaves

Water

26

  

EN00538

Fruit

DCM/MeOH (1:1)

21

Asteraceae

*Bidens pilosa L.

EN00001

Leaves

DCM/MeOH (1:1)

43

  

EN00001

Leaves

DCM

40

  

EN00001

Leaves

Water

31

  

EN00001

Leaves

MeOH

30

 

*Chromolaena odorata (L.) R.M.King & H.Rob.

EN00052

Leaves

MeOH

80

  

EN00052

Leaves

DCM

76

  

EN00052

Whole plant

MeOH

68

  

EN00052

Leaves

DCM/MeOH (1:1)

67

  

EN00052

Whole plant

DCM

61

  

EN00052

Whole plant

DCM/MeOH (1:1)

57

  

EN00052

Flowers

MeOH

50

  

EN00052

Leaves

Water

46

  

EN00052

Whole plant

Water

31

  

EN00052

Flowers

Water

25

  

EN00052

Flowers

DCM

18

  

EN00052

Flowers

DCM/MeOH (1:1)

15

 

*Eclipta prostrata (L.) L.

DS00616

Whole plant

Water

67

  

DS00616

Whole plant

DCM/MeOH (1:1)

20

 

Litogyne gariepina (DC.) Anderb.

EN00213

Roots

DCM

83

  

EN00213

Roots

Water

30

  

EN00213

Roots

DCM/MeOH (1:1)

28

Buddlejaceae

Nuxia floribunda Benth.

BP00669

Leaves

DCM/MeOH (1:1)

85

   

Leaves

Water

28

Chenopodiacae

*Chenopodium ambrosioides L.

BP00545

Leaves

DCM/MeOH (1:1)

87

  

BP00545

Twigs

DCM/MeOH (1:1)

31

  

BP00545

Leaves

DCM/MeOH (1:1)

25

 

*Chenopodium opulifolium Schrad. ex W.D.J.Koch & Ziz

DS00390

Roots

Water

97

  

DS00390

Stems

Water

67

  

DS00390

Roots

DCM/MeOH (1:1)

33

  

DS00390

Leaves

DCM/MeOH (1:1)

33

  

DS00390

Stems

DCM/MeOH (1:1)

30

  

DS00390

Leaves

Water

20

Euphorbiaceae

Croton pseudopulchellus Pax

HV00052

Leaves

DCM/MeOH (1:1)

33

  

HV00052

Leaves

Water

25

 

Spirostachys africana Sond.

EN00346

Stems

DCM/MeOH (1:1)

48

  

EN00346

Stems

Water

33

  

EN00346

Stems

DCM

28

  

BP00230

Leaves and twigs

DCM/MeOH (1:1)

18

Fabaceae

Dichrostachys cinerea (L.) Wright & Arn. subsp. africana Brenan & Brummitt

EN00101

Leaves

MeOH

67

  

EN00101

Stems

DCM/MeOH (1:1)

65

  

EN00101

Stems

DCM

50

  

EN00101

Leaves

Water

46

  

EN00101

Stems

Water

33

  

EN00101

Leaves

DCM/MeOH (1:1)

33

  

EN00101

Leaves

DCM

28

 

Mundulea sericea (Willd.) A.Chev.

BP00043

Leaves

DCM/MeOH (1:1)

76

  

BP00043

Leaves

DCM

72

  

BP00043

Leaves

MeOH

48

  

BP00043

Leaves

Water

26

 

Philenoptera violacea (Klotzsch) Schrire (syn.

MM00019

Stems

DCM

55

 

Lonchocarpus capassa Rolfe)

    
  

MM00019

Leaves

DCM/MeOH (1:1)

31

  

MM00019

Stems

Water

30

  

MM00019

Leaves

DCM/MeOH (1:1)

30

  

MM00019

Seeds

Water

28

  

MM00019

Roots

DCM/MeOH (1:1)

28

  

MM00019

Leaves

Water

27

  

MM00019

Bark

DCM/MeOH

26

  

MM00019

Roots

Water

21

  

MM00019

Bark

Water

20

Lamiaceae

Leucas martinicensis (Jacq.) R.Br.

EN00183

Leaves

DCM

86

  

EN00183

Leaves

DCM/MeOH (1:1)

52

  

EN00183

Leaves

Water

26

 

Mentha longifolia (L.) Huds.

EN00296

Whole plant

DCM/MeOH (1:1)

56

  

EN00296

Whole plant

DCM

55

  

EN00296

Whole plant

Water

18

 

Plectranthus laxiflorus Benth.

EN00195

Leaves

Water

55

  

EN00195

Leaves

DCM

53

  

EN00195

Leaves

DCM/MeOH (1:1)

38

Malvaceae

Sida cordifolia L.

FP00185

Whole plant

DCM/MeOH (1:1)

87

  

FP00185

Whole plant

Water

40

Meliaceae

*Melia azedarach L.

DS00379

Leaves

DCM/MeOH (1:1)

60

  

DS00379

Leaves

Water

33

Pedaliaceae

Ceratotheca triloba (Bernh.) Hook.f.

BP00646

Leaves

DCM/MeOH (1:1)

50

  

BP00646

Twigs

DCM/MeOH (1:1)

40

  

BP00646

Twigs

Water

31

  

BP00646

Leaves

Water

30

  

BP00646

Fruit

Water

26

Rutaceae

Clausena anisata (Willd.) Hook.f. ex Benth.

DS00090

Leaves

DCM/MeOH (1:1)

56

  

DS00090

Stems

DCM/MeOH (1:1)

31

  

DS00090

Stems

Water

31

  

DS00090

Leaves

Water

16

Solanaceae

*Datura stramonium L.

EN00769

Leaves

DCM/MeOH (1:1)

81

  

EN00769

Fruit

DCM/MeOH (1:1)

40

  

EN00769

Leaves

Water

30

  

EN00769

Fruit

Water

23

Vitaceae

Cissus cornifolia (Baker) Planch.

MM00008

Stems

DCM/MeOH (1:1)

45

  

MM00008

Roots

DCM/MeOH (1:1)

34

  

MM00008

Leaves and flowers

DCM/MeOH (1:1)

31

  

MM00008

Roots

Water

30

  

MM00008

Stems

Water

25

  

MM00008

Leaves and flowers

Water

25

* exotic to South Africa

Stringent criteria were used to assess the biological activity, in order to determine their potential as plant-derived repellents. Since these were crude plant extracts, a mosquito repellency effect of 80% was considered significant for further investigation. Seven samples from seven taxa showed ≥80% repellency, whereas the remaining 109 samples gave between 15 and 76% efficacy relative to the negative control. However, a repellent is only effective if it has a long-lasting effect. Since DEET is known to have an eight hour effect, for the purposes of these investigations, substantial repellency (>80%) after three hours was taken to be an indication of high activity worth of further investigation. To ensure that the highly active extracts maintained a constant repellent effect over a period of three hours, five of the seven samples indicating repellency ranging from 83 to 97% were subjected to a time lag trial (Table 2). This further evaluation was deemed an important requirement in considering their further industrial development, as market competitors of DEET should necessarily exhibit repellency over an extended period.
Table 2

Time lag repellency tests using a selection of active extracts from initial two minute trials

Family

Plant species

Plant part

Extraction

Repellency%

    

(minutes post application)

    

60

120

180

Asteraceae

Litogyne gariepina

Roots

DCM

75

52

57

Buddlejaceae

Nuxia floribunda

Leaves

DCM/MeOH(1:1)

43

42

35

Chenopodiaceae

Chenopodium opulifolium

Roots

Water

97

17

30

Lamiaceae

Leucas martinicensis

Leaves

DCM

60

57

49

Malvaceae

Sida cordifolia

Whole Plant

DCM/MeOH(1:1)

40

23

10

Negative control

  

Distilled water

10

20

20

Negative control

  

Acetone

17

20

33

Positive control

  

DEET

100

100

100

From the time lag studies, it was found that post-application, the most active extracts rapidly lost activity. Compared to the positive control, DEET, these extracts were not long-lasting.

None of the extracts satisfied the 80% repellent activity cut off point after three hours. The most active species, Chenopodium opulifolium (Chenopodiaceae) was found only 30% effective relative to the negative control after three hours post application (Table 2). However, as only crude extracts were assayed in all repellency trials it is possible that active constituents isolated from roots of C. opulifolium could show prolonged repellency.

In considering the plant families used in this study, two of the seven most active extracts belong to the Asteraceae family. Artemisia absinthium has been shown to possess tick repellent properties [9]; the authors found that this plant synthesized volatiles that exhibited insecticidal properties. Previous studies have shown that plants belonging to the Fabaceae [11, 12] are noted for their larvicidal activity. Park et al [13] found that monoterpenes from the Lamiaceae could be used to repel mosquitoes of the genus Culex, Similarly, octacosane derived from Moschosma polystachyum (Lamiaceae) was effective in repelling Culex [14].

Globally, an enormous amount of work has been completed in trying to develop mosquitocidal compounds from plants. The use of plants as larvicides or adulticides is not a novel concept. A number of the insecticides currently used for malaria control are products of plants [15]. Limited research has been completed on the search for natural repellent products Apium graveolens (Apiaceae) is capable of repelling Aedes, Anopheles and Mansonia species [16], whilst the essential oils of ginger, Zingiber officinale (Zingiberaceae) and rosemary, Rosmarinus officinalis (Lamiaceae) were found to be repellent towards Anopheles stephensi, Aedes aegypti and Culex quinquefasciatus [17]. However, whilst in these reports the percentage of mosquitoes repelled were lower than observed in most plants reported in the present study, the longevity of effect was greater. Nevertheless, these studies used vectors that are not found in southern Africa.

A study conducted in western Kenya [8] has shown limited efficacy of traditionally used mosquito repellents; plants were either burnt or used whole, resulting in a maximum repellency effect of 52% against An. gambiae.

Numerous studies have been completed where chemicals have been tested for repellency effect against An. gambiae [18, 19]. There is limited information available on the use of plant-derived chemicals as repellents of mosquitoes, especially An. gambiae.

Although all extracts demonstrated some bioactivity (15-97%), none of the extracts tested displayed repellency comparable to DEET after a prolonged period. Even though cognisance was taken of the fact that these were crude plant extracts none of them exceeded the minimum acceptable repellency level (80%) during time lag studies. Organic extracts of the plants in general showed more potent repellency relative to their corresponding aqueous extract. This indicates that the lower molecular weight compounds may be contributing to the repellency properties rather than the macromolecules generally found in aqueous based extracts. Exceptions were the three species Eclipta prostrata (Asteraceae), Chenopodium opulifolium (Chenopodiaceae) and Plectranthus laxiflorus (Lamiaceae), where water extracts were found more potent than their corresponding organic extracts. A further noticeable trend was that the extracts of leaves showed better repellency than extracts of other plant organs from the same species, indicating that volatile components such as essential oils could play a more important role, when formulated appropriately, as plant-sourced mosquito repellents. Notable exceptions to this trend were Litogyne gariepina and Chenopodium opulifolium, the root extracts of which showed >80% initial repellency.

A limitation of the current study is that volatile compounds were not specifically targeted for mosquito repellency investigation. In this regard, other studies have shown that ethyl acetate extracts of selected plants significantly reduce probing activity of Aedes aegypti [20].

Conclusions

None of the plants investigated in the current study proved to be a potential candidate for the development of commercial repellents from crude extracts due to their rapid loss of efficacy.

Declarations

Acknowledgements

We gratefully acknowledge the Department of Science and Technology of South Africa for the Innovation Fund Grant (Project 31313).

Authors’ Affiliations

(1)
South African Medical Research Council, 491 Ridge Road, Overport, Durban, 4001, South Africa
(2)
Biosciences, CSIR, P.O. Box 395, Pretoria, 0002, South Africa
(3)
Ethnobotany Unit, South African National Biodiversity Institute, University of KwaZulu-Natal, PO Box 52099, Berea Road 4007/School of Chemistry, Howard College Campus, Durban, 4041, South Africa
(4)
South African Medical Research Council, P.O. Box 19070, Tygerberg, 7505, South Africa

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Copyright

© Maharaj et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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