Sharanga Santhirasegaram
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Sharanga Santhirasegaram has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Kokila Sivabalakrishnan
Department of Zoology, University of Jaffna, Jaffna, Sri Lanka
3 shared publications - Sinnathamby Noble Surendran
Department of Zoology, University of Jaffna, Jaffna, Sri Lanka
3 shared publications - Tibutius Jayadas
Department of Zoology, Faculty of Science, University of Jaffna, Jaffna, Sri Lanka
3 shared publications - Annathurai Tharsan
University of Jaffna
2 shared publications - Ranjan Ramasamy
ID-FISH Technology, 556 Gibraltar Drive, Milpitas, CA 95035, USA
2 shared publications - Vaikunthavasan Thiruchenthooran
Department of Food Chemistry and Biocatalysis, Wrocław University of Environmental and Life Sciences, Wrocław, Poland
2 shared publications
Latest Publications
- Open Access
- 1 September 2020
- Published by Sri Lanka Journals Online in Journal of the National Science Foundation of Sri Lanka
- Vol. 48 (3) , 327-331
First record of the presence of Aedes (Phagomyia) cogilli (Edwards, 1922) in Sri Lanka
- 1 September 2020
- Published by Sri Lanka Journals Online in Journal of the National Science Foundation of Sri Lanka
- Vol. 48 (3) , 327-331
Open AccessFirst record of the presence of Aedes (Phagomyia) cogilli (Edwards, 1922) in Sri Lanka
- Open Access
- 30 March 2020
- Published by Springer Nature in Parasites & Vectors
- Vol. 13 (1) , 1-9
Anopheline bionomics, insecticide resistance and transnational dispersion in the context of controlling a possible recurrence of malaria transmission in Jaffna city in northern Sri Lanka
Background: Malaria was eliminated from Sri Lanka in 2013. However, the influx of infected travelers and the presence of potent anopheline vectors can re-initiate transmission in Jaffna city, which is separated by a narrow strait from the malaria-endemic Indian state of Tamil Nadu.Methods: Anopheline larvae were collected from different habitats in Jaffna city and the susceptibility of emergent adults to DDT, malathion and deltamethrin investigated.Results: Anopheline larvae were found in wells, surface-exposed drains, ponds, water puddles and water storage tanks, with many containing polluted, alkaline and brackish water.Anopheles culicifacies,An. subpictus,An. stephensiandAn. varunawere identified in the collections. Adults of the four anopheline species were resistant to DDT.Anopheles subpictusandAn. stephensiwere resistant whileAn. culicifaciesandAn. varunawere possibly resistant to deltamethrin.Anopheles stephensiwas resistant,An. subpictuspossibly resistant whileAn. varunaandAn. culicifacieswere susceptible to malathion. DNA sequencing showed a L1014F (TTA to TTC) mutation in the IIS6 transmembrane segment of the voltage-gated sodium channel protein in deltamethrin-resistantAn. subpictus—a mutation previously observed in India but not Sri Lanka.Conclusion: Anopheles subpictusin Jaffna, likeAn. stephensi, may have recently originated in coastal Tamil Nadu. Besides infected overseas travelers, wind- and boat-borne carriage ofPlasmodium-infected anophelines across the Palk Strait can potentially reintroduce malaria transmission to Jaffna city. Adaptation to diverse larval habitats and resistance to common insecticides in anophelines are identified as potential problems for vector control should this happen.
- 30 March 2020
- Published by Springer Nature in Parasites & Vectors
- Vol. 13 (1) , 1-9
Open AccessAnopheline bionomics, insecticide resistance and transnational dispersion in the context of controlling a possible recurrence of malaria transmission in Jaffna city in northern Sri Lanka
Background: Malaria was eliminated from Sri Lanka in 2013. However, the influx of infected travelers and the presence of potent anopheline vectors can re-initiate transmission in Jaffna city, which is separated by a narrow strait from the malaria-endemic Indian state of Tamil Nadu.Methods: Anopheline larvae were collected from different habitats in Jaffna city and the susceptibility of emergent adults to DDT, malathion and deltamethrin investigated.Results: Anopheline larvae were found in wells, surface-exposed drains, ponds, water puddles and water storage tanks, with many containing polluted, alkaline and brackish water.Anopheles culicifacies,An. subpictus,An. stephensiandAn. varunawere identified in the collections. Adults of the four anopheline species were resistant to DDT.Anopheles subpictusandAn. stephensiwere resistant whileAn. culicifaciesandAn. varunawere possibly resistant to deltamethrin.Anopheles stephensiwas resistant,An. subpictuspossibly resistant whileAn. varunaandAn. culicifacieswere susceptible to malathion. DNA sequencing showed a L1014F (TTA to TTC) mutation in the IIS6 transmembrane segment of the voltage-gated sodium channel protein in deltamethrin-resistantAn. subpictus—a mutation previously observed in India but not Sri Lanka.Conclusion: Anopheles subpictusin Jaffna, likeAn. stephensi, may have recently originated in coastal Tamil Nadu. Besides infected overseas travelers, wind- and boat-borne carriage ofPlasmodium-infected anophelines across the Palk Strait can potentially reintroduce malaria transmission to Jaffna city. Adaptation to diverse larval habitats and resistance to common insecticides in anophelines are identified as potential problems for vector control should this happen.
- Open Access
- 8 July 2019
- Published by Springer Nature in Parasites & Vectors
- Vol. 12 (1) , 1-8
Development of the major arboviral vector Aedes aegypti in urban drain-water and associated pyrethroid insecticide resistance is a potential global health challenge
Aedes aegypti were found developing in the water in open public drains (drain-water, DW) in Jaffna city in northern Sri Lanka, a location where the arboviral diseases dengue and chikungunya are endemic. Susceptibilities to the common insecticides dichlorodiphenyltrichloroethane (DDT), malathion, propoxur, permethrin and deltamethrin and activities of the insecticide-detoxifying enzymes carboxylesterase (EST), glutathione S-transferase (GST) and monooxygenase (MO) were compared in adult Ae. aegypti developing in DW and fresh water (FW). DW Ae. aegypti were resistant to the pyrethroids deltamethrin and permethrin, while FW Ae. aegypti were susceptible to deltamethrin but possibly resistant to permethrin. Both DW and FW Ae. aegypti were resistant to DDT, malathion and propoxur. Greater pyrethroid resistance in DW Ae. aegypti was consistent with higher GST and MO activities. The results demonstrate the potential for insecticide resistance developing in Ae. aegypti adapted to DW. Urbanization in arboviral disease-endemic countries is characterized by a proliferation of open water drains and therefore the findings identify a potential new challenge to global health.
- 8 July 2019
- Published by Springer Nature in Parasites & Vectors
- Vol. 12 (1) , 1-8
Open AccessDevelopment of the major arboviral vector Aedes aegypti in urban drain-water and associated pyrethroid insecticide resistance is a potential global health challenge
Aedes aegypti were found developing in the water in open public drains (drain-water, DW) in Jaffna city in northern Sri Lanka, a location where the arboviral diseases dengue and chikungunya are endemic. Susceptibilities to the common insecticides dichlorodiphenyltrichloroethane (DDT), malathion, propoxur, permethrin and deltamethrin and activities of the insecticide-detoxifying enzymes carboxylesterase (EST), glutathione S-transferase (GST) and monooxygenase (MO) were compared in adult Ae. aegypti developing in DW and fresh water (FW). DW Ae. aegypti were resistant to the pyrethroids deltamethrin and permethrin, while FW Ae. aegypti were susceptible to deltamethrin but possibly resistant to permethrin. Both DW and FW Ae. aegypti were resistant to DDT, malathion and propoxur. Greater pyrethroid resistance in DW Ae. aegypti was consistent with higher GST and MO activities. The results demonstrate the potential for insecticide resistance developing in Ae. aegypti adapted to DW. Urbanization in arboviral disease-endemic countries is characterized by a proliferation of open water drains and therefore the findings identify a potential new challenge to global health.