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MUTATIONS IN 1700 BP FRAGMENT OF RPOB GENE OF MULTI-DRUG RESISTANT MYCOBACTERIUM TUBERCULOSIS ISOLATE Yowani, Chandra; Sukardika, I K.; Mantik-Astawa, I N.; Junitha, I K.
INDONESIAN JOURNAL OF BIOMEDICAL SCIENCES Vol 6 No 2 (2012): Indonesian Journal of Biomedical Sciences
Publisher : Udayana University

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Abstract

This research aimed to amplify a 1700 bp fragment of rpoB gene of multidrug resistance M. tuberculosis (MDR-TB) isolate and determine types of mutation beyond the core region (hot-spot region). DNA sequencing studies indicate that more than 95% of rifampin-resistant M. tuberculosis strains have mutations within the 81-bp hot-spot region (codons 507 to 533) of the RNA polymerase ?-subunit (rpoB). Since almost 90 % of rifampicin resistant isolate are also resistant to isoniazid, mutation in rpoB gene become important as a surrogate marker for MDR-TB. MDR- TB isolates used for this research, namely isolate 885, was collected by Regional Health Laboratory of Surabaya. PCR was used to amplify the gene, on described steps : a cycle of preheating at 95°C for 15 minutes, amplifying in 45 cycles ( 1 minute at 94°C, 1 minute at 58°C, 1 minute 72°C) and post extension for 5 minutes at 72°C. The mutations were detected by sequencing and alignment using MEGA4. The result of this research showed that there were new mutations downstream of the core region of rpoB. Sequence analysis showed some mutations such as S594A, S626V, T629A. In conclusion, it is reported for the first time, new mutations at downstream region of the core region of rpoB.
SEAWEED EXTRACTS IMPROVE LIPID PROFILE OF WISTAR RAT Marhaeni Julyasih, K. Sri; Suata, K.; Wirawan, I.G.P; Mantik Astawa, I. N.
INDONESIAN JOURNAL OF BIOMEDICAL SCIENCES Vol. 5, No. 2 Mei 2011
Publisher : Udayana University

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Abstract

Hypercholesterolemia or hyperlipidemia has been established as an important risk factor of cardiovascular disease. Patients with hypercholesterolemia usually require a prolonged treatment; and the newer and more potent generation of antilipid agents are costly.In Bali there are several types of seaweed that are generally consumed by the local people and known by the local names of Bulung Boni (Caulerpa spp.) and Bulung Sangu (Gracilaria spp.). Preliminary studies on the effect of Bulung Boni and Bulung Sangu extracts appeared to improve lipid profile, but the available data are still very limited both in extent and depth, and further investigations were considered relevant and needed.This experimental study used completely blind randomized design, using a total of 24 Wistar rats divided into six sample groups of equal size, all fed with a diet high in cholesterol content. The six sample groups were respectively designated as negative control group, positive control group, and four treated sample groups, respectively fed orally with a dose of 20 mg and 60 mg extracts of Bulung Boni per 100g of body weight per day, and 20 mg and 60 mg extracts of Bulung Sangu per 100g body weight per day. Each treatment was repeated four times.Our study showed that rats fed with high-cholesterol diet and treated with oral Bulung Boni or Bulung Sangu extract at a dose of 20 mg and 60 mg/100 g bw/ day were associated with statistically significantly increased plasma HDL levels (p < 0.05), and statistically significant decreased plasma LDL and total cholesterol levels (p < 0.05) as compared with those of rats fed with high cholesterol diet without treatment with Bulung Boni or Bulung Sangu extracts.From our data it could be implied that Bulung Boni and Bulung Sangu extracts improve lipid profile in the Wiatar rat by significantly increasing plasma HDL level, and lowering LDL and total cholesterol levels.
CD4 COUNT FROM CRYOPRESERVATION OF BUFFY COAT AND PBMC Rasmaya Niruri; Inna Narayani; Wayan Tunas Artama; Mantik Astawa; Ahmad Hamim Sadewa
International Journal of Biosciences and Biotechnology Vol 2 No 2 (2015)
Publisher : Central Laboratory for Genetic Resource and Molecular Biology, Faculty of Agriculture, Udayana University in cooperation with Asia-Oceania Bioscience and Biotechnology Consortium (AOBBC)

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Abstract

This study aimed to determine CD4 count from cryopreservation of Buffy coat (BC) and PeripheralBlood Mononuclear Cell (PBMC) with and without ficoll. Fifteen EDTA Blood sample (2 ml for eachtube) were drawn from one adult healthy subject. The samples were categorized into five group beforemeasuring the CD4 level (which were fresh whole blood [Group(G)-I], BC without ficoll [fresh <GII>and frozen <G-III>] , and PBMC resulted from BC and ficoll isolation [fresh <G-IV> andfrozen <G-V>]. Each group was replicated three times. Blood storage before preparation was less thanfour hours. Two months cryopreservation using liquid nitrogen (in 40% FBS, 10% DMSO, and RPMI)was conducted. The mean value of CD4 count (cell /mu1) were 522 (G-I), 1410 (G-II), 906 (G-III), 807(G-IV), and 733 (G-V). CD4 count, after 2 month preservation in liquid nitrogen, of the BC sample (G-III) was higher (906 cell /mu1) than PBMC (G-IV) sample (733 cell /mu1).
EFFECT OF RESTING TIME ON PERIPHERAL BLOOD MONONUCLEAR CELL YIELDS Inna Narayani; Rasmaya Niruri; Nyoman Mantik Astawa
International Journal of Biosciences and Biotechnology Vol 3 No 2 (2016)
Publisher : Central Laboratory for Genetic Resource and Molecular Biology, Faculty of Agriculture, Udayana University in cooperation with Asia-Oceania Bioscience and Biotechnology Consortium (AOBBC)

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Abstract

Cryopreservation of PBMC (peripheral blood mononuclear cells) was done to preserve and analyze the number of PBMC derived from blood samples which come in at different time. The batch analysis wasperformed at the same time in order to reduce variations in results. The analysis on the cells numbers carried out after 1, 3, 6, 12, and 24 hours. Heparinized whole blood was collected from healthy subject by venipuncture, and stored at room temperature. Blood is processed by centrifugation in Ficoll density gradient following the established method of Balai Besar Veteriner Denpasar. Buffy coat layer was collected and washed twice with HBSS (Hank's balanced salt solution) and was counted in Turk’s solution. The cells were then dissolved in 1 ml of cold freezing medium containing 10% DMSO and 50% FBS (fetal bovine serum) and stored overnight at -80°C before storage in liquid nitrogen vessel for few weeks. The samples rapidly thawed in a water bath at 37°C and washed twice with PBS (phosphate buffered saline). The cells were stored in 4°C PBS and counted in Turk’s solution after 1, 3, 6, 12, and 24 hours. The results obtained were varied with a declining trend.
Effect of Maternal Antibodies on Histopathogenesis of Newcastle Disease Virus in Broiler Chickens I Made Galih Diparayoga; Nyoman Mantik Astawa; Anak Agung Ayu Mirah Adi
Veterinary Science and Medicine Journal Vol 4 No 1 (2016)
Publisher : Udayana University

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Abstract

The aims of this research were to overview the effect of maternal antibodies on the histopathological changes and viral antigen distribution of the broiler chickens challenged with ND APMV-1 virus. A total of 100 chicken were allotted into 3 treatment groups consisting of group I (titer antibodies< 23 HI Unit), group II (titer antibodies 23 – 24 HI Unit) and group III (titer antibodies> 24 HI Unit). All group I, II and III were inoculated with ND virus isolates of type viscerotropic velogenic at the dose of 1000 TCID50. The histopathological changes observed in nervous system were endotheliosis and perivascular cuffing. Immunohistochemistry staining showed that NDV infected cells were found in most organs both in inflammatory cells and in epithelial cell of many organs mainly in nervous, respiratory and digestive systems. Neurological symptoms and neural lesions were highest in group II (titer antibodies 23 – 24 HI Unit)
PEMBINAAN KELOMPOK TANI DENGAN PENYULUHAN PENINGKATAN KESEHATAN TERNAK SAPI DAN PEMANFAATAN LIMBAH TERNAK MENJADI KOMPOS G.A.Y. Kencana; I.G.N.K. Mahardika Mahardika; I.N.M. Astawa; I.B.K. Suardana; I.N. Suartha; I.A.P. Apsari; A.A.S. Kendran; S.K. Widyastuti; G.A.M.K. Dewi; I.P. Sudiarta
Buletin Udayana Mengabdi Vol 20 No 1 (2021): Buletin Udayana Mengabdi
Publisher : Lembaga Penelitian dan Pengabdian kepada Masyarakat

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1385.678 KB) | DOI: 10.24843/BUM.2021.v20.i01.p13

Abstract

Pengabdian Masyarakat berjudul: "Pembinaan Kelompok Tani Niti Sari Desa Baturiti, Kecamatan Baturiti” merupakan salah satu Hibah Program Udayana Untuk Masyarakat (PUMA). Tujuan pengabdian ini untuk memberikan pembinaan kepada Kelompok Tani Niti Sari tentang cara meningkatkan kesehatan sapi dan memanfaatkan limbah pertanian menjadi kompos organik plus. Metode yang digunakan untuk mencapai tujuan tersebut diawali dengan memberikan penyuluhan kepada anggota Kelompok Tani Niti sari, selanjutnya didukung dengan praktek langsung di lapangan. Penyuluhan yang diberikan meliputi: Penyuluhan kesehatan sapi, penyuluhan kesehatan reproduksi sapi, penyuluhan teknologi tepat guna pertanian dengan memanfaatkan limbah pertanian menggunakan jamur Trichoderma untuk dibuat kompos plus. Kompos plus Trichoderma yang dihasilkan dalam pembinaan ini diharapkan dapat mengatasi permasalahan penyakit tanaman kubis milik petani Niti Sari. Penyuluhan sudah dilaksanakan tanggal 05 Juli 2019 diawali pertemuan dengan Kepala Desa Baturiti, dengan Kelompok Tani Niti Sari dan dilanjutkan dengan pembinaan Kelompok Tani. Kegiatan penyuluhan dibuka oleh Camat Baturiti, Ketua LPPM Unud, Tripika Kecamatan Baturiti, Kepala Desa beserta aparat Desa, Kelompok Tani Niti Sari dan Kelompok Tani se Desa Baturiti dan Banjar Tamantanda. Dengan demikian diharapkan Kelompok Tani Niti Sari dan Kelompok Tani disekitarnya mampu menyerap alih teknologi yang diajarkan oleh Tim Pengabdi dari Universitas Udayana.
SOSIALISASI PENYAKIT ZOONOSIS ESCHERICHIA COLI O157:H7 SERTA PELAYANAN KESEHATAN SAPI DI DUSUN LAMPU DESA CATUR KINTAMANI BANGLI I W. Suardana; I.B.N. Swacita; I.N. Suartha; I G.N. Sudisma; M.D. Rudyanto; I.G.M. Krisna Erawan; I.N. Suarsana; I.W. Batan; P.A. Sisyawati Putriningsih; T. Sari Nindia; A.L.T. Rompis; I.N. Mantik Astawa; K. Karang Agustina; I.H. Utama; I.G.A. Suartini; I.M. Sukada; I.K. Suada; A.A.A. Mirah Adi
Buletin Udayana Mengabdi Vol 16 No 2 (2017)
Publisher : Lembaga Penelitian dan Pengabdian kepada Masyarakat

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Abstract

Ternak sapi yang menderita diare berpeluang besar untuk ditemukan adanya agen zoonosis E. coli O157:H7 mengingat sapi sebagai reservoir utama dari agen tersebut.Transmisi penularan strain bakteri ini ke manusia umumnya terjadi melalui konsumsi daging yang kurang dimasak, produk susu yang tidak dipasteurisasi, air yang terkontaminasi feses. Dusun Lampu sebagai salah satu Dusun di Desa Catur merupakan salah satu daerah potensial untuk pengembangan ternak khususnya sapi sehingga menjadikan program pelayanan kesehatan di wilayah tersebut sangat potensial untuk dilakukan. Hasil kegiatan pengabdian masyarakat berupa sosialisasi penyakit zoonosis E. coli O157:H7 serta pelayanan kesehatan ternak sapi di Dusun ini, memperlihatkan respon positif yang dicirikan dengan cukup banyaknya jumlah ternak yang memperoleh pelayanan yaitu sejumlah 65 ekor sapi dari 35 petani ternak. Jenis pelayanan yang dilakukan meliputi tindakan spraying atau pemberian butox terhadap semua ternak sapi yaitu 65 ekor (100%), disusul dengan pemberian vitamin pada 52 ekor (80%), pemberian obat cacing sebanyak 39 ekor (60%), serta pemberian delladryl pada 1 ekor sapi (1,5%). Hasil ini mengindikasikan bahwa program pengabdian yang dilakukan cukup efektif dapat menyentuh kebutuhan dasar petani ternak, sehingga benar-benar dapat dirasakan manfaatnya.
Identifikasi Sel-sel Target Virus Penyakit Jembrana dengan Teknik Imunositokimia Ganda I Ketut Berata; I Nyoman Mantik Astawa
Biota : Jurnal Ilmiah Ilmu-Ilmu Hayati Vol 16, No 2 (2011): June 2011
Publisher : Universitas Atma Jaya Yogyakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24002/biota.v16i2.105

Abstract

Penelitian bertujuan untuk mengidentifikasi sel target virus Jembrana dengan teknik imunositokimia ganda. Penelitian ini menggunakan sapi Bali yang diinokulasi dengan virus Jembrana secara intramuskuler. Pada demam hari kedua setelah inokulasi virus, sapi dinekropsi. Limpa diambil secara aseptik, kemudian direndam dalam buffer formalin 10% selama 24 jam. Potongan limpa diproses untuk pembuatan sediaan histologis dengan menggunakan cryomicrotome. Preparat histologis limpa diwarnai dengan teknik imunositokimia ganda. Untuk mengidentifikasi subset limfosit digunakan antibody monoclonal anti BoCD4 + dan anti BoCD8 + , serta diamino benzidine (DAB) sebagai substrat. Pada pewarnaan ini, sel-sel terinfeksi akan tampak berwarna biru, sedangkan sel-sel marka BoCD4 + atau BoCD8 + akan tampak berwarna coklat. Untuk identifikasi sel-sel terinfeksi virus Jembrana digunakan antibodi monoklonal anti-capsid JDV (BB-Vet Denpasar) dan nitro blue tetrazolium (NBT) sebagai substrat. Hasil penelitian menunjukkan bahwa sel-sel yang terinfeksi virus Jembrana hanya bermarka BoCD4 + , dan sama sekali tidak pada sel BoCD8 + . Simpulan penelitian ini adalah sel-sel BoCD4 + merupakan sel target virus Jembrana.
Immunological Detection of Avian Influenza Virus in Infected Ducks by Monoclonal Antibodies Against AIV-H5N1 NYOMAN MANTIK ASTAWA; IDA BAGUS OKA WINAYA; LUH PUTU AGUSTINI; NINING HARTANINGSIH
Microbiology Indonesia Vol. 1 No. 3 (2007): December 2007
Publisher : Indonesian Society for microbiology

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (192.217 KB) | DOI: 10.5454/mi.1.3.5

Abstract

In order to establish a detection method for avian influenza virus (AIV) infection in ducks, monoclonal antibodies (MAbs) against the virus were produced. The virus used for the production of the monoclonal antibodies was AIV-H5N1 of Indonesian origin. Immortal mouse myeloma were fused with the lymphocytes derived from the spleen of mice immunized with the virus. The MAbs were tested for their specificity by enzyme linked immunosorbent assay (ELISA) and western blotting using formaldehyde inactivated virus and normal allantoic fluid as a negative control. Twelve MAbs which were specific against AIV were isolated and 8 of them were used for detecting of AIV antigen in duck&rsquo;s tissues. AIV antigen was detected in paraffin embedded tissues of AIV-infected ducks by immunohistochemistry using MAbs. AIV antigen was not detected in ducks, which were confirmed to be AIV negative. In the infected ducks, high intensity of AIV infection was detected in proventricle gland and small intestine. The AIV antigen with a lesser intensity was also detected in lungs, spleen, and bursa of Fabricius, but hardly detected in muscle, brain, and several other issues. This study shows a clear evidence that MAbs produced in this study are applicable for use in immunological detection of AIV in infected duck tissues.
Ekspresi sel fibroblas yang rendah pada ligamentum sakrouterina sebagai faktor risiko terjadinya prolaps uterus derajat III-IV di RSUP Sanglah Denpasar, Bali-Indonesia Yosevangelika Hutabarat; I Wayan Megadhana; Ketut Suwiyoga; Nyoman Mantik Astawa; Arthawan Arthawan
Intisari Sains Medis Vol. 11 No. 2 (2020): (Available online: 1 August 2020)
Publisher : DiscoverSys Inc.

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (283.008 KB) | DOI: 10.15562/ism.v11i2.793

Abstract

Introduction: Uterine prolapse is the fall of the uterus into the vaginal due to the failure of the pelvic floor supporting ligaments. Uterine prolapse has multifactorial risk factors, but in every case of uterine prolapse, weakness in the pelvic floor, including the sacrouterine ligament, is always found. The strength of the sacrouterine ligament is determined by fibroblasts and extracellular matrix. Fibroblasts are the most cells making up the ligament, where the ligament is a connective tissue consisting of most collagen fibers that provide a structure with high tensile strength. Women with POP have a picture of changes that occur in the supporting tissues, where the extracellular matrix plays an important role because of accelerated remodeling in POP patients caused by biochemical changes in extracellular matrix such as collagen, elastin and stromal cells. Myofibroblasts play an important role in extracellular matrix remodeling and its regulation by matrix cell regulators such as metalloprotease (MMP) matrix, transformation growth factor (TGF) -β, and thrombospondin (TSP)-1. The purpose of this study was to prove the low expression of fibroblast cells in the sacrouterine ligament as a risk factor for stage III-IV uterine prolapse.Method: This study was an observational design with case control. There were 22 cases of grade III-IV uterine prolapse as a group of cases and 22 cases of non-prolapse as a control group. This research was carried out at Sanglah General Hospital and the Integrated Biomedical Laboratory of Faculty of Medicine, Universitas Udayana. Samples were taken from sacrouterine ligament of uterine prolapsed patients with stage III-IV and uterine non-prolapse who had performed total hysterectomy at Sanglah Hospital.Results: The results showed that low expression of fibroblasts became a risk 9 times higher of uterine prolapse grade III-IV compared to high level of fibroblast expressin (OR = 9.1; IK95% = 2.3-35.7; p = 0.001).Conclusion: From the results of this study it can be concluded that the low expression of fibroblasts in the sacrouterine ligament is a risk factor for stage III-IV uterine prolapse. Pendahuluan: Prolaps uterus adalah turunnya uterus ke dalam liang vagina atau keluar liang vagina sebagai akibat gagalnya ligamentum penyokong dasar panggul. Prolaps uterus memiliki faktor risiko yang bersifat multifaktorial, namun pada setiap kasus prolaps uterus, selalu ditemukan kelemahan pada jaringan penyangga dasar panggul, termasuk ligamentum sakrouterina. Kekuatan ligamentum sakrouterina ditentukan oleh fibroblas dan matriks ekstraselular. Fibroblas adalah sel terbanyak penyusun ligamentum, dimana ligamentum merupakan jaringan ikat yang terdiri dari sebagian besar serat kolagen yang menyediakan struktur dengan daya tarik yang tinggi. Wanita dengan POP memiliki gambaran perubahan yang terjadi pada jaringan penyokong, dimana matriks ekstraseluler memegang peranan penting karena akselerasi remodeling pada pasien POP yang disebabkan oleh perubahan biokimia pada matriks ekstraseluler seperti kolagen, elastin dan sel stromal. Miofibroblas berperan penting dalam remodeling matriks ekstraseluler dan pengaturannya oleh regulator sel matriks seperti matriks metalloprotease (MMP), transformation growth factor (TGF)-β, dan thrombospondin (TSP)-1. Tujuan penelitian ini adalah untuk membuktikan ekspresi sel fibroblas yang rendah pada ligamentum sakrouterina sebagai faktor risiko terjadinya prolaps uterus derajat III-IV.Metode: Penelitian ini merupakan rancangan observasional dengan kasus kontrol. Terdapat 22 kasus prolaps uterus derajat III-IV sebagai kelompok kasus dan 22 kasus non prolaps sebagai kelompok kontrol. Penelitian ini dikerjakan di RSUP Sanglah dan Laboratorium Biomedik Terpadu FK Universitas Udayana. Sampel diambil dari ligamentum sakrouterina pasien prolaps uterus derajat III-IV dan non-prolaps uterus yang telah dilakukan histerektomi total di RSUP Sanglah.Hasil: Hasil penelitian didapatkan bahwa ekspresi fibroblas yang rendah menjadi risiko terjadinya prolaps uterus derajat III-IV sebesar 9 kali (OR=9,1; IK95%=2,3-35,7; p=0,001).Simpulan: Dari hasil penelitian ini dapat disimpulkan bahwa ekspresi fibroblas yang rendah pada ligamentum sakrouterina menjadi faktor risiko terjadinya prolaps uterus derajat III-IV.
Co-Authors A. A. G. P. Wiraguna A.A. Wiradewi Lestari A.A.G. Sudewa AAG Budhitresna AAG Putra Ahmad Hamim Sadewa Aida Lousie Tenden Rompis Alberto Agustinho Pereira Da Costa Joao Anak Agung Ayu Mirah Adi Anak Agung Bagus Bramardipa Anak Agung Gede Sudewa Djelantik Anak Agung Keswari Krisnandika Anak Agung Ngurah Subawa Anak Agung Oka Wijaya Anak Agung Sagung Kendran and R. Kusnandi Andika Budi Kurnianto Anwar Santoso Arthawan Arthawan Bayu Setiabudi Berata , I Ketut Chandra Yowani Dewa Ayu Agus Sri Laksmi DWI SURYANTO Dyah Kanya Wati Faiziah - G.A.M.K. Dewi Gusti Ayu Mayani Kristina Dewi Gusti Ayu Yuniati Kencana Gusti Ngurah Narendra Putra Harjana, Ngakan Putu Anom HARTANINGSIH - Hartaningsih . I D. N. Wibawa I Dewa Made Sukrama I Gede Ngurah Harry Wijaya Surya I GEDE PUTU WIRAWAN I Gusti Agung Arta Putra I Gusti Agung Ayu Suartini I Gusti Agung Dewi Sarihati I Gusti Agung Trisna Windiani I Gusti Ayu Putu Eka Pratiwi I Gusti Ketut Suarjana I Gusti Made Krisna Erawan I Gusti Ngurah Kade Mahardika I Gusti Ngurah Sudisma I K. Sukardika I Kadek Swastika I Ketut Berata I Ketut Eli Supartika I Ketut Junitha I Ketut Suada I Ketut Suada I Ketut Suastika I Ketut Suastika I KETUT SUATA I Ketut Suatha I Ketut Suwiyoga I Made Bakta I Made Damriyasa I Made Dwinata I Made Galih Diparayoga I Made Jawi I Made Kardena I Made Subrata I Made Sudarmaja I Made Sukada i Nengah Wandia I Nyoman Agus Bagiada I Nyoman Budi Hartawan I Nyoman Polos I Nyoman Suarsana I Nyoman Suartha I Putu Cahyadi Putra, I Putu Cahyadi I Putu Sudiarta I W. Wita, I W. I Wayan Bebas I Wayan Gorda I Wayan Masa Tenaya I Wayan Masa Tenaya, I Wayan Masa I Wayan Megadhana I Wayan Putu Sutirta Yasa I Wayan Suardana I Wayan Wita I.A.P. Apsari I.B.K. Suardana I.H. Utama I.W. Batan Ida Ayu Pasti Apsari Ida Bagus Gede Suparyatha Ida Bagus Kade Suardana Ida Bagus Komang Ardana Ida Bagus Made Oka Ida Bagus Ngurah Swacita Ida Bagus Oka Winaya Ida Bagus Suardana Ida Bagus Subanada Ignatius Ferdi Yuatmadja Inna Narayani K. Sri Marhaeni Julyasih K. Suata K. Sukardika Kadek Karang Agustina Ketut Budiasa Ketut ELI Supartika Ketut Santhia Adhy Putra KETUT SUADA Ketut Suata Ketut Tirtayasa Luh Dewi Anggreni Luh Putu Agustini LUH PUTU AGUSTINI Luh Putu Wrasiati M.D. Rudyanto M.Pd S.T. S.Pd. I Gde Wawan Sudatha . Made Damriyasa, Made Made Oka Ari kamayani, Made Oka Ari Made Wiryana Marissa Divia Dayanti Marson, Fransiska Gratia Sonita Mudinillah, Adam Mufa, Romy Muhammad Dary N. T. Suryadhi Ngakan Putu Anom Harjana Ni Luh Putu Eka Diarthini NI LUH PUTU MANIK WIDIYANTI Ni Made Krisna Dewi Ni Made Suaniti NINING HARTANINGSIH Nyoman Agus Bagiada Nyoman Suartha Nyoman Tigeh Suryadi Oka Lely Palagan Senopati Sewoyo Purwitasari, Made Santi Putri, Dilyanti Maya Putri, Rindar Mentari Nusanti Putu Ayu Asri Damayanti Putu Ayu Sisyawati Putriningsih Rasmaya Niruri Rasmaya Niruri S. Soetjiningsih, S. S. Sotjiningsih S.K. Widyastuti sang gede purnama Sewoyo, Palagan Senopati Siti Maryam Soetjiningsih - Soetjiningsih . Sri Kayati Widyastuti Sri Wahjuni Sukada, Made SUMARNO Suryadi, Nyoman Tigeh Sutjahjo Suherman, Sutjahjo Suwarno - T. Sari Nindia Tjok Gede Oka Pemayun, Tjok Gede Oka Tjokorda Gde Agung Suwardewa TRI KOMALA SARI Wayan Tunas Artama Widyasanti, Ni Wayan Helpina Wimpie I Pangkahila Wirata, Ketut Yasunobu Matsumoto Yosevangelika Hutabarat Yoshihiro Hayashi