DNA barcoding and surveillance sampling strategies for Culicoides biting midges (Diptera: Ceratopogonidae) in southern India

dc.contributor.authorHarrup, Lara E.
dc.contributor.authorLaban, Swathi
dc.contributor.authorPurse, Bethan V.
dc.contributor.authorReddy, Yarabolu Krishnamohan
dc.contributor.authorReddy, Yella Narasimha
dc.contributor.authorByregowda, Sonnahallipura Munivenkatappa
dc.contributor.authorKumar, Naveen
dc.contributor.authorPurushotham, Kondappa Muniramaiah
dc.contributor.authorKowalli, Shrikant
dc.contributor.authorPrasad, Minakshi
dc.contributor.authorPrasad, Gaya
dc.contributor.authorBettis, Alison A.
dc.contributor.authorDe Keyser, Rien
dc.contributor.authorLogan, James
dc.contributor.authorGarros, Claire
dc.contributor.authorGopurenko, David
dc.contributor.authorBellis, Glenn
dc.contributor.authorLabuschagne, Karien
dc.contributor.authorMathieu, Bruno
dc.contributor.authorCarpenter, Simon
dc.date.accessioned2016-09-19T06:14:59Z
dc.date.available2016-09-19T06:14:59Z
dc.date.issued2016-08-22
dc.descriptionAdditional file 1: Table S1. GenBank sequences used in genetic analyses of Culicoides from southern India. Table S2. Barcode Index Numbers (BINs) assigned within the Barcode of Life Database (BOLD) for specimens collected within this study.en_ZA
dc.descriptionAdditional file 2: Table S3. Uncorrected percentage sequence distances, mean with range shown in parentheses. Intraspecific distances are shown in bold along the diagonal, interspecific distances are shown in the lower triangle (NA indicates comparison not possible due to singleton specimen present; number of specimens per species (n) shown in brackets with the number of specimens originating from this study; followed by the number originating from GenBank in parentheses).en_ZA
dc.description.abstractBACKGROUND : Culicoides spp. biting midges transmit bluetongue virus (BTV), the aetiological agent of bluetongue (BT), an economically important disease of ruminants. In southern India, hyperendemic outbreaks of BT exert high cost to subsistence farmers in the region, impacting on sheep production. Effective Culicoides spp. monitoring methods coupled with accurate species identification can accelerate responses for minimising BT outbreaks. Here, we assessed the utility of sampling methods and DNA barcoding for detection and identification of Culicoides spp. in southern India, in order to provide an informed basis for future monitoring of their populations in the region. METHODS : Culicoides spp. collected from Tamil Nadu and Karnataka were used to construct a framework for future morphological identification in surveillance, based on sequence comparison of the DNA barcode region of the mitochondrial cytochrome c oxidase I (COI) gene and achieving quality standards defined by the Barcode of Life initiative. Pairwise catches of Culicoides spp. were compared in diversity and abundance between green (570 nm) and ultraviolet (UV) (390 nm) light emitting diode (LED) suction traps at a single site in Chennai, Tamil Nadu over 20 nights of sampling in November 2013. RESULTS : DNA barcode sequences of Culicoides spp. were mostly congruent both with existing DNA barcode data from other countries and with morphological identification of major vector species. However, sequence differences symptomatic of cryptic species diversity were present in some groups which require further investigation. While the diversity of species collected by the UV LED Center for Disease Control (CDC) trap did not significantly vary from that collected by the green LED CDC trap, the UV CDC significantly outperformed the green LED CDC trap with regard to the number of Culicoides individuals collected. CONCLUSIONS : Morphological identification of the majority of potential vector species of Culicoides spp. samples within southern India appears relatively robust; however, potential cryptic species diversity was present in some groups requiring further investigation. The UV LED CDC trap is recommended for surveillance of Culicoides in southern India.en_ZA
dc.description.departmentZoology and Entomologyen_ZA
dc.description.librarianam2016en_ZA
dc.description.sponsorshipThis study was funded by the Biotechnology and Biological Sciences Research Council (BBSRC), Department for International Development (DFID) and Scottish Government grant BB/H009205/1, BB/H009167/1 and BB/ H009493/1 as part of the Combating Infectious Diseases of Livestock for International Development initiative. With additional support provided by BBSRC grant BB/K021214/1; AB was also supported with funding from the London School of Hygiene and Tropical Medicine. The Indian Council of Agricultural Research supported this study through its Hisar, Chennai, Bengaluru and Hyderabad centres under the All Indian Network Programme on Bluetongue.en_ZA
dc.description.urihttp://www.parasitesandvectors.comen_ZA
dc.identifier.citationHarrup, LE, Laban, S, Purse, BV, Reddy, YK, Reddy, YN, Byregowda, SM, Kumar, N, Purushotham, KM, Kowalli, S, Prasad, M, Prasad, G, Bettis, AA, De Keyser, R, Logan, J, Garros, C, Gopurenko, D, Bellis, G, Labuschagne, K, Mathieu, B & Carpenter, S 2016, 'DNA barcoding and surveillance sampling strategies for Culicoides biting midges (Diptera: Ceratopogonidae) in southern India', Parasites & Vectors, vol. 9, art. no. 461, pp. 1-20.en_ZA
dc.identifier.issn1756-3305
dc.identifier.other10.1186/s13071-016-1722-z
dc.identifier.urihttp://hdl.handle.net/2263/56733
dc.language.isoenen_ZA
dc.publisherBioMed Centralen_ZA
dc.rights© 2016 The Author(s). Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License.en_ZA
dc.subjectCulicoidesen_ZA
dc.subjectArbovirusen_ZA
dc.subjectDNA barcodesen_ZA
dc.subjectSurveillanceen_ZA
dc.subjectBluetongue virus (BTV)en_ZA
dc.subjectcytochrome c oxidase I (COI)en_ZA
dc.subjectLight-emitting diodes (LEDs)en_ZA
dc.subjectBarcode of Life Data System (BOLD)en_ZA
dc.titleDNA barcoding and surveillance sampling strategies for Culicoides biting midges (Diptera: Ceratopogonidae) in southern Indiaen_ZA
dc.typeArticleen_ZA

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