Age-dependance of pteridines in the malaria vector, Anopheles stephensi

Determining the accurate age of malaria vectors is crucial to measure the risk of malaria transmission. A group of fluorescent chemicals derived from a pyrimidine-pyrazine ring structure known as pteridines from the head, thorax and whole body of adult female Anopheles stephensi were identified and...

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Main Authors: Edalat Hamideh, Akhoundi Mohammad, Basseri Hamidreza
Format: Article
Language:English
Published: De Gruyter 2017-12-01
Series:Pteridines
Subjects:
Online Access:https://doi.org/10.1515/pterid-2017-0009
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spelling doaj-dc114d75dc94463dbda6319e08c87f492021-09-05T13:59:57ZengDe GruyterPteridines0933-48072195-47202017-12-01283-415716110.1515/pterid-2017-0009Age-dependance of pteridines in the malaria vector, Anopheles stephensiEdalat Hamideh0Akhoundi Mohammad1Basseri Hamidreza2Department of Medical Entomology and Vector Control, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Medical Entomology and Vector Control, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Medical Entomology and Vector Control, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDetermining the accurate age of malaria vectors is crucial to measure the risk of malaria transmission. A group of fluorescent chemicals derived from a pyrimidine-pyrazine ring structure known as pteridines from the head, thorax and whole body of adult female Anopheles stephensi were identified and evaluated as a tool for chronological and physiological age determination of malaria vectors. The female mosquitoes were collected from an insectary colony at an interval of every 5 days, up to 30 days, and the pteridines of head, thorax and whole body were detected fluorometrically by high-pressure liquid chromatography (HPLC) using excitation and emission wavelengths of 365 and 455 nm, respectively. In addition, alteration of the pteridines compounds was compared between blood and sugar fed mosquito groups. Although four pteridines including pterin-6-carboxylic acid, biopterin, xanthopterin and isoxanthopterin were detected, some of them were absent in the head or thorax of mosquitoes. Levels of all four pteridines were similarly decreased in a linear manner throughout 30 days. No significant difference in alteration of pteridine compounds was observed between the two groups of blood or sugar fed mosquitoes. This result indicates that diet has a little effect on pteridines alteration. Age determination based on pteridines, as an age-grading technique, could be used for field collected mosquitoes, which have either sugar or blood meal. In addition, analyzing total pteridine fluorescence from only whole body could be a convenient method to estimate the age.https://doi.org/10.1515/pterid-2017-0009age determinationanopheles stephensimalariapteridinesouthern iran
collection DOAJ
language English
format Article
sources DOAJ
author Edalat Hamideh
Akhoundi Mohammad
Basseri Hamidreza
spellingShingle Edalat Hamideh
Akhoundi Mohammad
Basseri Hamidreza
Age-dependance of pteridines in the malaria vector, Anopheles stephensi
Pteridines
age determination
anopheles stephensi
malaria
pteridine
southern iran
author_facet Edalat Hamideh
Akhoundi Mohammad
Basseri Hamidreza
author_sort Edalat Hamideh
title Age-dependance of pteridines in the malaria vector, Anopheles stephensi
title_short Age-dependance of pteridines in the malaria vector, Anopheles stephensi
title_full Age-dependance of pteridines in the malaria vector, Anopheles stephensi
title_fullStr Age-dependance of pteridines in the malaria vector, Anopheles stephensi
title_full_unstemmed Age-dependance of pteridines in the malaria vector, Anopheles stephensi
title_sort age-dependance of pteridines in the malaria vector, anopheles stephensi
publisher De Gruyter
series Pteridines
issn 0933-4807
2195-4720
publishDate 2017-12-01
description Determining the accurate age of malaria vectors is crucial to measure the risk of malaria transmission. A group of fluorescent chemicals derived from a pyrimidine-pyrazine ring structure known as pteridines from the head, thorax and whole body of adult female Anopheles stephensi were identified and evaluated as a tool for chronological and physiological age determination of malaria vectors. The female mosquitoes were collected from an insectary colony at an interval of every 5 days, up to 30 days, and the pteridines of head, thorax and whole body were detected fluorometrically by high-pressure liquid chromatography (HPLC) using excitation and emission wavelengths of 365 and 455 nm, respectively. In addition, alteration of the pteridines compounds was compared between blood and sugar fed mosquito groups. Although four pteridines including pterin-6-carboxylic acid, biopterin, xanthopterin and isoxanthopterin were detected, some of them were absent in the head or thorax of mosquitoes. Levels of all four pteridines were similarly decreased in a linear manner throughout 30 days. No significant difference in alteration of pteridine compounds was observed between the two groups of blood or sugar fed mosquitoes. This result indicates that diet has a little effect on pteridines alteration. Age determination based on pteridines, as an age-grading technique, could be used for field collected mosquitoes, which have either sugar or blood meal. In addition, analyzing total pteridine fluorescence from only whole body could be a convenient method to estimate the age.
topic age determination
anopheles stephensi
malaria
pteridine
southern iran
url https://doi.org/10.1515/pterid-2017-0009
work_keys_str_mv AT edalathamideh agedependanceofpteridinesinthemalariavectoranophelesstephensi
AT akhoundimohammad agedependanceofpteridinesinthemalariavectoranophelesstephensi
AT basserihamidreza agedependanceofpteridinesinthemalariavectoranophelesstephensi
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