Open Access

Reduced susceptibility to selected synthetic pyrethroids in urban malaria vector Anopheles stephensi: a case study in Mangalore city, South India

  • Satyanarayan Tiwari1,
  • Susanta K Ghosh1Email author,
  • Vijay P Ojha1,
  • Aditya P Dash2, 3 and
  • Kamaraju Raghavendra2
Malaria Journal20109:179

Received: 29 March 2010

Accepted: 23 June 2010

Published: 23 June 2010



Synthetic pyrethroids are potent insecticides most commonly used in the vector control programme. These are applied for indoor residual sprays, space sprays and in impregnated bed nets. Resistance reduces the efficacy of insecticides. Thus, the susceptibility status of the target vector(s) is monitored routinely to select the effective ones. A study was undertaken in a malaria endemic coastal city Mangalore, Karnataka, South India, against the known malaria vector Anopheles stephensi.


The susceptibility status was assessed at diagnostic doses of DDT (4%), malathion (5%), deltamethrin (0.05%), cyfluthrin (0.15%), alphacypermethrin (0.10%), lambdacyhalothrin (0.05%) and permethrin (0.75%) using the standard WHO tube test method during October/November 2006.


Anopheles stephensi was resistant to malathion by 54.9%, but tolerant to deltamethrin by 86.1%, cyfluthrin 95.5% and alphacypermethrin 90.6%, whereas it was susceptible to DDT by 98.1%, lambdacyhalothrin 98.6% and permethrin 100.0%, respectively. The KDT50 and KDT95 values for these insecticides also showed the similar responses.


Susceptibility of An. stephensi to DDT is an important finding as this has never been used in Mangalore city, whereas its rural counterpart Anopheles culicifacies is widely resistant to this insecticide. The study explores the selection and rotation of the appropriate insecticide molecule even within the same group for effective vector management.


In recent years, there are many options and strategies to combat diseases transmitted by insect vectors. Insecticides still remain the mainstay of vector control programmes [1]. Synthetic pyrethroids are extensively being used for indoor residual sprays, space sprays and in impregnated bed nets. These are highly effective, if optimally applied, but resistance to these chemicals reduces their impact [2]. Tube and cone bioassays on sprayed surfaces and substrates to monitor the susceptibility status of the target vector(s) are effective tools to assess the efficacy of insecticides. The present work was carried out in Mangalore city, where malaria has been a serious public health problem for more than one and half decades [3]. The vector control strategies adopted to curtail malaria transmission in urban settings are anti-larval operations, whereas indoor residual spraying (IRS) is not recommended. However, personal protection measure with insecticide-treated nets (ITNs), especially with synthetic pyrethroids, has been advocated [4].

Recently under the World Bank-aided Enhanced Malaria Control Programme (EMCP), ITNs have been advocated to control malaria in rural areas. To assess the operational feasibility of ITNs in malaria control in urban areas, a study on long-lasting insecticide-treated nets (LLINs) with alphacypermethrin was carried out in the city from October 2006 to August 2007. Baseline data on susceptibility status of Anopheles stephensi to different insecticides were collected prior to the LLIN trial to explore an appropriate insecticide molecule.


Study area

Mangalore city (12°55' LN 74°47'LE, average elevation of 22 m asl) is situated on the Western coast of Arabian Sea in Karnataka, South India. It has 494,629 inhabitants living in an area of 132.45 km2. The climate is tropical with dry season (January-May), monsoon (June-August) and post-monsoon (September-December). Average temperature ranges between 16 and 35°C, average relative humidity around 85%, and 4400 mm of average annual rainfall. It is a port city with many activities that attract labour migrants (8-12% of urban population) engaged in construction related works. The recorded literacy rate is 83%. The city has 60 municipal wards, and the health services are provided by five municipal corporation hospitals and two government hospitals, besides five local medical colleges. In this city, the annual parasite incidence (API; cases per 1,000 population annually) varies from 1.2 to 3.1, and contributes nearly 15-20% of the total malaria cases with few deaths annually in Karnataka, and nearly 0.2-0.8% in India [3]. Anopheles stephensi is the main malaria vector that preferably breeds in wells, over head tanks, cement tanks, fountains and also in masonry tanks, curing waters in construction sites [5]. Active transmission is recorded during the post-monsoon months, and recently this insect vector has been incriminated in this city [5]. The vector control strategies adopted to curtail malaria transmission are anti-larval operations using chemical larvicides mainly temephos and fenthion (both organophosphorus compounds), indoor pyrethrum spray, outdoor fogging with malathion and synthetic pyrethroids especially deltamethrin and cyfluthrin. Larvivorous fish in wells, fountains, water storage cement tanks, masonry water tanks at construction sites, are additionally applied.

Insecticide susceptibility tests

Susceptibility of insecticides by tube test method was carried out according to the standard WHO procedure during October/November 2006 [68] with WHO-supplied insecticide-impregnated papers as per diagnostic doses, DDT (4%), malathion (5%), deltamethrin (0.05%), cyfluthrin (0.15%), alphacypermethrin (0.10%), lambdacyhalothrin (0.05%) and permethrin (0.75%). Immature stages of anopheles mosquitoes collected from three sites, Nanthoor, Bejai and Balmatta in the city (Figure 1), brought live to the laboratory, reared to adults. Emerged An. stephensi females were fed on mice blood and full-fed mosquitoes were exposed to the insecticide-impregnated papers for 1 h. Experiments were conducted with a minimum of three replicates with matched controls for each insecticide in a room maintaining temperature at 27 ± 2°C and 80% relative humidity. The knockdown effect of each insecticide was recorded every 10 minutes over the 1-h exposure period. Exposed mosquitoes were then transferred to a recovery tube and provided with 10% glucose solution. Final mortality was recorded after 24 h of holding time in experimental and control tubes. Mortality in control between 5 and 20% was corrected with Abbott's formula [9] and expressed as corrected percent mortality.
Figure 1

Map showing the study sites in Mangalore City, Karnataka, South India.

Data analysis

Data were analysed using VassarStats software [10]. Fifty and 95% knockdown times (KDT50 and KDT95) were estimated by means of a log-time probit model using the Ldp lineR software [11, 12].


The result of bioassays is summarized in Table 1. As per the WHO criteria, mortality < 80% is considered to be resistant, 80-98% as tolerant (evaluation required) and > 98% as susceptible [6]. Accordingly, An. stephensi in Mangalore city was resistant to malathion, having 54.9% (95% CI: 46.74-72.42) mortality, but susceptible to DDT, lambdacyhalothrin and permethrin showing mortalities of 98.1% (95% CI: 92.95-103.19), 98.6% (95% CI: 94.10-103.05) and 100% respectively. Mortalities recorded to deltamethrin, cyfluthrin and alphacypermethrin were 86.1% (95% CI: 76.38-103.93), 95.5% (95% CI: 79.00-110.94) and 90.6% (95% CI: 85.34-95.90), respectively, indicating tolerance.
Table 1

Susceptibility status of An. stephensi (October/November, 2006) to standard doses of insecticides (7 such) following WHO methods* (1975) in Mangalore city, Karnataka, South India

Diagnostic insecticide dose on impregnated papers#

Mosquitoes exposed (n)

Dead mosquitoes after 24 h of exposure (n)

Mortality after 24 h of exposure (%)

Corrected mortality (%)§

KDT50 (CL)

KDT95 (CL)






Expt (95% CI)

Cont (95% CI)


DDT 4%





98.3 (92.99-103.65)

11.65 (6.33-16.89)

98.1 (92.95-103.19)

19.24 (18.87-21.48)

55.67 (47.78-68.50)

Malathion 5%





45.36 (13.98-76.74)

14.06 (10.93-17.19)

54.9 (46.74-72.42)



Deltamethrin 0.05%





86.62 (69.78-103.46)

9.62 (6.24-3.00)

86.1 (76.38-103.93)

37.33 (35.02-39.88)

72.73 (64.96-85.11)

Cyfluthrin 0.15%





95.57 (78.5-109.64)

13.93 (9.35-18.51)

95.5 (79.00-110.94)

31.74 (29.50-33.96

69.74 (62.03-81.56)

Alpha-cypermethrin 10%





91.2 (86.27-96.13)

6.03 (4.52-7.54)

90.6 (85.34-95.90)

30.33 (27.69-33.12)

83.26 (70.79-104.26)

Lambda-cyhalothrin 0.05%





98.75 (94.78-102.72)

8.33 (1.17-15.49)

98.6 (94.10-103.05)

19.20 (17.34-20.97)

50.42 (44.99-58.17)

Permethrin 0.75%





100.0 (100.0-100.0)

5.3 (4.04-6.59)

100.0 (100.0-100.0)

16.83 (14.87-18.67)

47.93 (41.35-58.52)

* Mortality recorded < 80% considered resistant, 80-98% tolerant (evaluation required), while > 98% as sensitive.

#Supplied by WHO.

§Corrected mortality was calculated following Abott's formula (1925).

Confidence limit could not be calculated due to large g values.

Exp: Experimental; Cont: Control; CI: Confidence interval; CL: Confidence limit

The knockdown effect determined over a 1-h period indicated that, KDT50 and KDT95 for malathion was the highest among the seven insecticides tested. These values were also higher for deltamethrin, cyfluthrin and alphacypermethrin than DDT, lambdacyhalothrin and permethrin (Table 1).


Resistance to both DDT and malathion in An. stephensi was reported earlier from the rural area of Harayana [13], from urban areas of Goa [14], and Delhi [15]. In Bikaner district of Rajasthan, it was reported resistant to DDT and tolerant to both malathion and permethrin [16]. The present study showed that An. stephensi is susceptible to DDT and permethrin, whereas it is resistant to malathion. The KDT50 and KDT95 values were also maximum for malathion and minimum for permethrin, suggesting that the knockdown resistance mechanism could be operating in the mosquito population, as has been demonstrated in lab in An. stephensi with deltamethrin [17].

In Mangalore city, the possible reason for the development of resistance in An. stephensi to malathion and low mortalities in deltamethrin and cyfluthrin could be attributed to selective pressure from fogging, IRS including anti-larval operations with these molecules for more than a decade. Tolerance in alphacypermethrin could be the consequence of cross-resistance among synthetic pyrethroid molecules exhibiting similar resistance mechanism [17, 18].


Susceptibility of An. stephensi to DDT is an important finding, whereas its rural counterpart Anopheles culicifacies is widely resistant to this insecticide [18]. The reason could be that this molecule has never been used in Mangalore city [3], thus maintaining a status of susceptibility in the area in absence of selection pressure.

In the ITN programme, only synthetic pyrethroids are being used for impregnation of nets. A recent report indicated the evolution of resistance in An. gambiae to pyrethroids in Africa [2], and the reduced susceptibility of An. stephensi to deltamethrin, cyfluthrin and alphacypermethrin in Mangalore city is a matter of concern. In view of the current scenario, emphasis could be given on other methods of vector control, preferably biocontrol with larvivorous fish and different formulations of biolarvicides especially Bacillus thuringiensis var. israelensis under the integrated vector management programme [19, 20]. In Mangalore city, open dug wells are present in the courtyard almost in every house and these serve as major foci (ecological niche) for An. stephensi. The construction activities begin in the vicinity of such wells leads to profuse breeding of An. stephensi in the curing waters, masonry tanks and other water collection created during the activities. Immigrant labourers from malaria endemic areas act as reservoirs add to the problem immensely who reside near to these sites. The current application of fogging should be discontinued as these are not recommended for routine vector control programme [4]. Thus the malaria control operation in the city should focus alternatively on anti-larval strategies [4]. Fortnightly application of biolarvicides in the curing waters in the construction areas and introduction of larvivorous fish particularly Poecilia[19, 20] in all the breeding habitats especially in wells would be the best option for anti-larval measures. Integrated vector management strategies specific to this urban setting need to be optimally used for its appropriate implementation.



To the staff of National Institute of Malaria Research (NIMR), Bangalore Centre for their technical assistance. To Dr. P.K. Kar, NIMR, Bangalore centre for reviewing and to Dr. Chaitali Ghosh, S.R. Nova Pvt. Ltd., Bangalore for editing the manuscript.

Authors’ Affiliations

National Institute of Malaria Research, ICMR Complex, Poojanahalli
National Institute of Malaria Research
World Health Organization South East Asia Regional Office


  1. Devine GJ, Ogusuku E: Adaptability is key when monitoring insecticide resistance. Bull World Health Organ. 2009, 87: 887-10.2471/BLT.09.073502.PubMed CentralView ArticlePubMedGoogle Scholar
  2. N'Guessan R, Corbel V, Akogbeto M, Rowland M: Reduced efficacy of insecticide-treated nets and indoor residual spraying for malaria control in pyrethroid resistance area, Benin. Emerg Infect Dis. 2007, 13: 199-206. 10.3201/eid1302.060631.PubMed CentralView ArticlePubMedGoogle Scholar
  3. National Vector Borne Disease Control Programme (NVBDCP): Annual Reports on Malaria and other Vector Borne Diseases. 2008, Directorate of Health and Family Welfare Services, Government of Karnataka, BangaloreGoogle Scholar
  4. National Vector Borne Disease Control Programme (NVBDCP): Operational Manual for Implementation of Malaria Control Programme. Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India, New Delhi. 2009, []Google Scholar
  5. Ghosh SK, Tiwari SN, Raghavendra K, Sathyanarayan TS, Dash AP: Observations on sporozoite detection in naturally infected sibling species of the Anopheles culicifacies complex and variants of Anopheles stephensi in India. J Biosci. 2008, 33: 333-336. 10.1007/s12038-008-0052-5.View ArticlePubMedGoogle Scholar
  6. WHO: Manual on practical entomology in malaria. Part II. Method and Techniques. 1975Google Scholar
  7. WHO: Mimeographed document. WHOVBC/81 805. 1981, Geneva: World Health Organization, 1-7.Google Scholar
  8. Mittal PK, Adak T, Singh OP, Raghavendra K, Subbarao SK: Reduced susceptibility to deltamethrin in Anopheles culicifacies sensu lato, in Ramamnathapuram district, Tamil Nadu -- Selection of a pyrethroid-resistant strain. Curr Sci. 2002, 82: 185-188.Google Scholar
  9. Abbott WS: A method of computing the effectiveness of insecticide. J Econ Entomol. 1925, 18: 265-267.View ArticleGoogle Scholar
  10. VassarStats statistical software website. []
  11. Log-time probit model software website. []
  12. Finney DJ: Probit Analysis. 1971, Cambridge University Press: Cambridge, UK, 3Google Scholar
  13. Subbarao SK, Sharma VP, Vasantha K, Adak T: Effect of malaria spraying on four anopheline species and the development of resistance in Anopheles stephensi in Mandora, Harayana. Indian J Malariol. 1994, 21: 109-114.Google Scholar
  14. Thavaselvam D, Kumar A, Sumodan PK: Insecticide susceptibility status of Anopheles stephensi, Culex quinquefasciatus and Aedes aegypti in Panaji, Goa. Indian J Malariol. 1986, 23: 65-67.Google Scholar
  15. Sharma VP, Sharma GK, Ansari MA, Mittal PK, Razdan RK, Batra CP: Impact of malathion thermal fogging on mosquito population in Delhi and its place in malaria control. Indian J Malariol. 1986, 23: 65-67.PubMedGoogle Scholar
  16. Bansal SK, Singh KV: Insecticide susceptibility status of some anophelines in district Bikaner, Rajasthan. Indian J Malariol. 1996, 33: 1-6.PubMedGoogle Scholar
  17. Gyathri V, Murthy PB: Reduced susceptibility to deltamethrin and kdr mutation in An. stephensi Liston, a malaria vector in India. J Am Mosq Cont Assoc. 2006, 22: 678-688. 10.2987/8756-971X(2006)22[678:RSTDAK]2.0.CO;2.View ArticleGoogle Scholar
  18. Dash AP, Adak T, Raghavendra K, Singh OP: The biology and control of malaria vectors in India. Curr Sci. 2007, 92: 1571-1578.Google Scholar
  19. Ghosh SK, Dash AP: Larvivorous fish against malaria vectors: a new outlook. Trans R Soc Trop Med Hyg. 2007, 101: 1063-1064. 10.1016/j.trstmh.2007.07.008.View ArticlePubMedGoogle Scholar
  20. Tiwari SN, Ghosh SK, Mittal PK, Dash AP: Effectiveness of a granular formulation of Bacillus thuringiensis var. israelensis (Bti) against larvae of malaria vectors in laboratory and field conditions, India. Vector-Borne Zoon Dis. 2010, 10: Published online May 2010, ahead of print, DOI: 10.1089/vbz.2009.0197.Google Scholar


© Tiwari 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 (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.