IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR

Sarcoptes scabiei is a zoonotic skin-borne mite named scabies. The purpose of this study was to investigate the genetic characterization of Sarcoptes scabiei var.cuniculi from local rabbits as baseline data of genetic information. This research used scraping rabbits from Surabaya and Malang which th...

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Main Author: KURNIA DESIANDURA, 061414253006
Format: Theses and Dissertations NonPeerReviewed
Language:Indonesian
Indonesian
Published: 2017
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Online Access:http://repository.unair.ac.id/66736/1/TPKMV.18.17%20.%20Des.i%20-%20ABSTRAK.pdf
http://repository.unair.ac.id/66736/2/TPKMV.18.17%20.%20Des.i%20-%20SEC.pdf
http://repository.unair.ac.id/66736/
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spelling id-langga.667362017-12-31T14:57:35Z http://repository.unair.ac.id/66736/ IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR KURNIA DESIANDURA, 061414253006 SF600-1100 Veterinary medicine Sarcoptes scabiei is a zoonotic skin-borne mite named scabies. The purpose of this study was to investigate the genetic characterization of Sarcoptes scabiei var.cuniculi from local rabbits as baseline data of genetic information. This research used scraping rabbits from Surabaya and Malang which then conducted native examination, separation of mites, and DNA extract for Polymerase Chain Reaction (PCR) process. PCR is done using the researcher's primary design, forward (5'TCT TAG GGG CTG GTA TTA GTA TG 3 ') and reverse (5'-AGT TCC TCT ACC AGT TCC AC-3'). Thermocycling is performed in an automatic thermocycler (Biorad) with hot prefix at 95 °C for 5 minutes; 35 cycles 94 °C for 1 minute, 55 °C for 1 minute, and 72 °C for 1 minute; and the final addition at 72°C for 5 minutes. The PCR results were followed by homologous sequencing and analysis. As a result, S.scabiei var.cuniculifrom Surabaya and Malang rabbits can be detected with these primers whose electrophoresis result is 289bp according to the target. Both the sequencing resulted in a 99% homology rate, and varied between 93 to 98% when compared to GenBank data, China and Australia. These results indicate that between samples and data from GenBank are identical species. 2017 Thesis NonPeerReviewed text id http://repository.unair.ac.id/66736/1/TPKMV.18.17%20.%20Des.i%20-%20ABSTRAK.pdf text id http://repository.unair.ac.id/66736/2/TPKMV.18.17%20.%20Des.i%20-%20SEC.pdf KURNIA DESIANDURA, 061414253006 (2017) IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR. Thesis thesis, Universitas Airlangga. http://lib.unair.ac.id
institution Universitas Airlangga
building Universitas Airlangga Library
country Indonesia
collection UNAIR Repository
language Indonesian
Indonesian
topic SF600-1100 Veterinary medicine
spellingShingle SF600-1100 Veterinary medicine
KURNIA DESIANDURA, 061414253006
IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR
description Sarcoptes scabiei is a zoonotic skin-borne mite named scabies. The purpose of this study was to investigate the genetic characterization of Sarcoptes scabiei var.cuniculi from local rabbits as baseline data of genetic information. This research used scraping rabbits from Surabaya and Malang which then conducted native examination, separation of mites, and DNA extract for Polymerase Chain Reaction (PCR) process. PCR is done using the researcher's primary design, forward (5'TCT TAG GGG CTG GTA TTA GTA TG 3 ') and reverse (5'-AGT TCC TCT ACC AGT TCC AC-3'). Thermocycling is performed in an automatic thermocycler (Biorad) with hot prefix at 95 °C for 5 minutes; 35 cycles 94 °C for 1 minute, 55 °C for 1 minute, and 72 °C for 1 minute; and the final addition at 72°C for 5 minutes. The PCR results were followed by homologous sequencing and analysis. As a result, S.scabiei var.cuniculifrom Surabaya and Malang rabbits can be detected with these primers whose electrophoresis result is 289bp according to the target. Both the sequencing resulted in a 99% homology rate, and varied between 93 to 98% when compared to GenBank data, China and Australia. These results indicate that between samples and data from GenBank are identical species.
format Theses and Dissertations
NonPeerReviewed
author KURNIA DESIANDURA, 061414253006
author_facet KURNIA DESIANDURA, 061414253006
author_sort KURNIA DESIANDURA, 061414253006
title IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR
title_short IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR
title_full IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR
title_fullStr IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR
title_full_unstemmed IDENTIFIKASI MOLEKULER Sarcoptes scabiei var. cuniculi PENYEBAB SKABIES PADA KELINCI DI KOTA SURABAYA DAN MALANG JAWA TIMUR
title_sort identifikasi molekuler sarcoptes scabiei var. cuniculi penyebab skabies pada kelinci di kota surabaya dan malang jawa timur
publishDate 2017
url http://repository.unair.ac.id/66736/1/TPKMV.18.17%20.%20Des.i%20-%20ABSTRAK.pdf
http://repository.unair.ac.id/66736/2/TPKMV.18.17%20.%20Des.i%20-%20SEC.pdf
http://repository.unair.ac.id/66736/
http://lib.unair.ac.id
_version_ 1681149150560780288