» Articles » PMID: 23174003

Salinity-tolerant Larvae of Mosquito Vectors in the Tropical Coast of Jaffna, Sri Lanka and the Effect of Salinity on the Toxicity of Bacillus Thuringiensis to Aedes Aegypti Larvae

Overview
Journal Parasit Vectors
Publisher Biomed Central
Date 2012 Nov 24
PMID 23174003
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Dengue, chikungunya, malaria, filariasis and Japanese encephalitis are common mosquito-borne diseases endemic to Sri Lanka. Aedes aegypti and Aedes albopictus, the major vectors of dengue, were recently shown to undergo pre-imaginal development in brackish water bodies in the island. A limited survey of selected coastal localities of the Jaffna district in northern Sri Lanka was carried out to identify mosquito species undergoing pre-imaginal development in brackish and saline waters. The effect of salinity on the toxicity of Bacillus thuringiensis israelensis larvicide to Ae. aegypti larvae at salinity levels naturally tolerated by Ae. aegypti was examined.

Methods: Larvae collected at the selected sites along the Jaffna coast were identified and salinity of habitat water determined in the laboratory. The LC₅₀ and LC₉₀ of B. thuringiensis toxin, the active ingredient of a commercial formulation of the larvicide BACTIVEC®, were determined with Ae. aegypti larvae. Bioassays were also carried out at salinities varying from 0 to 18 ppt to determine the toxicity of Bacillus thuringiensis to fresh and brackish water-derived larvae of Ae. aegypti.

Results: Larvae of four Anopheles, two Aedes, one Culex and one Lutzia species were collected from brackish and saline sites with salinity in the range 2 to 68 ppt. The LC₅₀ and LC₉₀ of B. thuringiensis toxin for the second instar larvae of Ae. aegypti in fresh water were 0.006 ppm and 0.013 ppm respectively, with corresponding values for brackish water populations of 0.008 and 0.012 ppm respectively. One hundred percent survival of second instar fresh water and brackish water-derived Ae. aegypti larvae was recorded at salinity up to 10 and 12 ppt and 100% mortality at 16 and 18 ppt, yielding an LC₉₀ for salinity of 13.9 ppt and 15.4 ppt at 24 h post-treatment respectively for the two populations. Statistical analysis showed significantly reduced toxicity of B. thuringiensis to fresh and brackish water-derived Ae. aegypti larvae at high salinities.

Conclusion: A variety of mosquito vectors of human diseases undergo pre-imaginal development in brackish or saline waters in coastal areas of the Jaffna district in northern Sri Lanka. Salinity has a small but significant negative impact on the toxicity of B. thuringiensis toxin to Ae. aegypti larvae at salinity levels where Ae. aegypti larvae are found in the environment. This has implications for the use of B. thuringiensis toxin as a larvicide in brackish waters.

Citing Articles

Effect of salinity on the oviposition and growth of .

Choi J, Choi K Ecol Evol. 2024; 14(4):e11289.

PMID: 38660469 PMC: 11040096. DOI: 10.1002/ece3.11289.


Breeding Habitat Preference of the Dengue Vector Mosquitoes and from Urban, Semiurban, and Rural Areas in Kurunegala District, Sri Lanka.

Herath J, De Silva W, Weeraratne T, Karunaratne S J Trop Med. 2024; 2024:4123543.

PMID: 38318417 PMC: 10843871. DOI: 10.1155/2024/4123543.


Resistance to the larvicide temephos and altered egg and larval surfaces characterize salinity-tolerant Aedes aegypti.

Sivabalakrishnan K, Thanihaichelvan M, Tharsan A, Eswaramohan T, Ravirajan P, Hemphill A Sci Rep. 2023; 13(1):8160.

PMID: 37208485 PMC: 10198600. DOI: 10.1038/s41598-023-35128-1.


Bionomic aspects of dengue vectors Aedes aegypti and Aedes albopictus at domestic settings in urban, suburban and rural areas in Gampaha District, Western Province of Sri Lanka.

Dalpadado R, Amarasinghe D, Gunathilaka N, Ariyarathna N Parasit Vectors. 2022; 15(1):148.

PMID: 35477476 PMC: 9044863. DOI: 10.1186/s13071-022-05261-3.


An Experimental Evaluation of Toxicity Effects of Sodium Chloride on Oviposition, Hatching and Larval Development of .

Guo X, Zhou S, Wu J, Zhang X, Wang Y, Li Z Pathogens. 2022; 11(2).

PMID: 35215204 PMC: 8878149. DOI: 10.3390/pathogens11020262.


References
1.
Cavrini F, Gaibani P, Pierro A, Rossini G, Landini M, Sambri V . Chikungunya: an emerging and spreading arthropod-borne viral disease. J Infect Dev Ctries. 2009; 3(10):744-52. DOI: 10.3855/jidc.169. View

2.
Rattanarithikul R, Harbach R, Harrison B, Panthusiri P, Jones J, Coleman R . Illustrated keys to the mosquitoes of Thailand. II. Genera Culex and Lutzia. Southeast Asian J Trop Med Public Health. 2005; 36 Suppl 2:1-97. View

3.
Peiris J, Amerasinghe F, Amerasinghe P, Ratnayake C, Karunaratne S, Tsai T . Japanese encephalitis in Sri Lanka--the study of an epidemic: vector incrimination, porcine infection and human disease. Trans R Soc Trop Med Hyg. 1992; 86(3):307-13. DOI: 10.1016/0035-9203(92)90325-7. View

4.
Jude P, Dharshini S, Vinobaba M, Surendran S, Ramasamy R . Anopheles culicifacies breeding in brackish waters in Sri Lanka and implications for malaria control. Malar J. 2010; 9:106. PMC: 2864285. DOI: 10.1186/1475-2875-9-106. View

5.
Nyarango P, Gebremeskel T, Mebrahtu G, Mufunda J, Abdulmumini U, Ogbamariam A . A steep decline of malaria morbidity and mortality trends in Eritrea between 2000 and 2004: the effect of combination of control methods. Malar J. 2006; 5:33. PMC: 1501031. DOI: 10.1186/1475-2875-5-33. View