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IDENTIFICATION OF MAJALAYA COMMON CARP STRAINS RESISTANT TO KHV INFECTION USING CYCA-DAB1*05 ALLELE AS THE MARKER Alimuddin Alimuddin; Mubinun Mubinun; Ayi Santika; Odang Carman; Irvan Faizal; Komar Sumantadinata
Indonesian Aquaculture Journal Vol 6, No 2 (2011): (December 2011)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (124.642 KB) | DOI: 10.15578/iaj.6.2.2011.157-163

Abstract

The Cyca-DAB1*05 allele of major histocompatibility complex class II genes is recently suggested to have a link with the European common carp strain resistant to koi herpesvirus (KHV). In this study, a set of specific primers for Cyca-DAB1*05 was designed and applied as a marker to identify broodstocks of majalaya common carp strain subsequently used as a candidate resistant to KHV infection. From a total of 23 broodstock subjected to PCR analysis, two female and male fish, both having (P) and no Cyca-DAB1*05 (N), were selected and then diallelly mated. Disease resistance of progenies from 10 crosses was determined by a survival analysis in pond rearing and a laboratory challenge-test using cohabitation method. The results have revealed that the average survivals of PxP progenies for pond rearing and KHV challenge test were 86% and 100% higher (P < 0.05) respectively compared to that of NxN fish. Survival rate of PxN/NxP progenies was significantly lower (P < 0.05) than that of PxP fish. Furthermore, PCR analysis showed that almost 91% progenies of PxP crosses seemed to have a KHV resistant gene marker. Thus, this study suggests that the marker is associated with the KHV resistance in majalaya common carp strain, and farming of PxP progenies can be useful to increase common carp production.
IDENTIFICATION OF SNP SPESIFIC MARKER FOR CRUSTACEAN HYPERGLYCEMIC HORMONE GENE: A SOMATIC GROWTH-RELATED IN GIANT FRESHWATER PRAWN (Macrobrachium rosenbergii) Asep Sopian; Alimuddin Alimuddin; Imron Imron; Harry Krettiawan; Fajar Anggraeni; Desy Nurul Astuti
Indonesian Aquaculture Journal Vol 12, No 1 (2017): (June 2017)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (336.842 KB) | DOI: 10.15578/iaj.12.1.2017.7-13

Abstract

High size variation of giant freshwater prawn was found in harvest and resulting in low productivity. Marker assisted selection may be useful to generate broodstock that produces progeny with high growth and homogeneity. This study was conducted to obtain growth related molecular marker in giant freshwater prawn. Genomic DNA was extracted from swimming leg (pleiopods) of 10 giant freshwater prawns fifth Generation for existence of SNP identification, consisted of 5 fast growth (FG) and 5 slow growth (SG).  While for SNP confirmation and resolving power of specific primer studies. The pleiopods sample was taken from six generation of 201 giant freshwater prawns, consisted of 129 fast-growth (FG) with 16.06 ± 2.48 g body weight and 72 slow-growth (SG) with 6.05 ± 0.90 g body weight. Oligonucleotide primers were designed according to Gene Bank database of crustacean hyperglycemic hormone (CHH) gene sequence. The amplified DNA fragment was then sequenced. The results of sequencing showed there was one base different in nucleotides of FG and SG prawns. Six set of primers were designed based on those CH gene sequence. PCR analysis resulted one set of primers which showed a specific amplification product of 280 bp for growth. The result of sequence analysis using the basic local alignment search tools showed that the nucleotide sequence of those PCR products had similarity of 99%-100% with CHH gen of M. rosenbergii. Thus, a candidate of growth related molecular marker have been identified for giant freshwater prawn.
SHORT COMMUNICATION: THE EFFECT OF TANNIN SOLUTION IN PERFORMING SUCCESFULL EGG MICROINJECTION ON AFRICAN CATFISH (Clarias gariepinus) Muhammad Hunaina Fariduddin Ath-thar; Komar Sumantadinata; Alimuddin Alimuddin
Indonesian Aquaculture Journal Vol 4, No 2 (2009): (December 2009)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (119.102 KB) | DOI: 10.15578/iaj.4.2.2009.153-157

Abstract

In order to successfully perform a gene transfer activity using microinjection, an individual egg is needed. The common standard operating procedure to collect the individual egg is by applying chemical solution to remove the sticky layer covering the egg surface. Among several available solutions, tannin is one of alternative substances that can be used in performing egg microinjection on African catfish. In this study, the effect of different dosages of tannin solution to remove the sticky layer of eggs was observed. The study was conducted at the Laboratory of Fish Breeding and Genetics, Bogor Agricultural University. Prior to microinjection, the eggs were treated with different dosages of tannin solution right after fertilization. There were four different levels of dosage used as the treatments i.e.: 0.3, 0.5, 0.7, and 0.9 ppm. After the treatments, each individual egg was injected using DNA pmâactin-hrGFP plasmid with a concentration of 20 μg/mL. The results showed that the dosage of 0.5 ppm of tannin was the most effective treatment compared to the other dosages. This dosage produced 71.4% hatching rate and 57.1% transgenic embryos respectively.
IDENTIFICATION OF GROWTH HORMONE GENE OF Pangasionodon hypophthalmus Raden Roro Sri Pudji Sinarni Dewi; Agus Oman Sudrajat; Alimuddin Alimuddin; Komar Sumantadinata
Indonesian Aquaculture Journal Vol 4, No 1 (2009): (June 2009)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (383.557 KB) | DOI: 10.15578/iaj.4.1.2009.9-17

Abstract

Identification of growth hormone (GH) gene in a target fish is the first step in the construction of “all fish genes transfer vector” to generate transgenic fish. The research was done to identify and characterize the GH gene of Pangasionodon hypophthalmus. There were several activities performed in identifying the GH gene: RNA extraction, cDNA synthesis, PCR amplification, and DNA fragment isolation. The characterizations were done using the nucleotide sequencing engine ABIPRISM 3100. The results were then analyzed using BLASTN/P and GENETYX version 7 program. The full-length GH gene of P. hypophthalmus was 1151 bp in length, coding for an open reading frame (ORF) of 603 bp. The 5’ and 3’ untranslated regions of the GH gene were 22 bp and 526 bp long, respectively. The GH gene of P. hypophthalmus had some common characteristics that are owned by GH genes, such as single tryptophan residue (W) on the 104th amino acid, 5 cysteine residues (C) on the amino acid 71, 135, 173, 190, and 198 and a motif of Asn-Xaa-Thr on C terminus which is the potential location for N-linked glycosilation. Polyadenylation signal (aataaa) was on the 14 bp at the upstream of polyadenylation location. Growth hormone of P. hypophthalmus consisted of over 200 amino acids from GH cDNA deduction. The highest proportion of amino acid composition was leusin (14%) while the lowest was tryptophan (0.5%).
DEVELOPMENTS OF DIGESTIVE TRACT IN LARVAE OF CLIMBING PERCH, Anabas testudineus (Bloch) Yulintine Yulintine; Enang Harris; Dedi Jusadi; Ridwan Affandi; Alimuddin Alimuddin
Indonesian Aquaculture Journal Vol 5, No 2 (2010): (December 2010)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (349.29 KB) | DOI: 10.15578/iaj.5.2.2010.109-116

Abstract

Climbing perch, Anabas testudineus (Bloch) is a potential species for aquaculture in Kalimantan, Indonesia and belongs to Anabantidae family. The development of its digestive tract was evaluated on larvae reared under culture conditions of 28oC-30oC, from hatching to 30 days after hatching using histological and morphological methods. The larvae were kept in six 100-L tanks. They were fed with rotifers and microalgae from day 2nd after hatching to day 10th; Artemia nauplii from day 7th to day 15th; Artemia meta-nauplii from day 15th to day 20th; and Tubifex worm from day 20th onwards. The development of digestive tract in climbing perch followed the general pattern described for other species. Shortly after hatching, its digestive system was found to be consisted of an undifferentiated straight tube laying dorsally to the yolk sac. At first feeding (day 2nd), both mouth and anus had opened and the yolk sac was partially absorbed. On day 3, the digestive tract was fully differentiated into buccopharynx, esophagus, intestine and rectum. The two pyloric caeca appeared on day 25th after hatching, indicating the transition from larval to juvenile stage and acquisition of an adult type of digestion.
OVER-EXPRESSION OF GENE ENCODING FATTY ACID METABOLIC ENZYMES IN FISH Alimuddin Alimuddin; Goro Yoshizaki; Toshio Takeuchi; Odang Carman
Indonesian Aquaculture Journal Vol 3, No 2 (2008): (December 2008)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (259.282 KB) | DOI: 10.15578/iaj.3.2.2008.89-106

Abstract

Eicosapentaenoic acid (EPA, 20:5n-3) and docosahexaenoic acid (DHA, 22:6n-3) have important nutritional benefits in humans. EPA and DHA are mainly derived from fish, but the decline in the stocks of major marine capture fishes could result in these fatty acids being consumed less. Farmed fish could serve as promising sources of EPA and DHA, but they need these fatty acids in their diets. Generation of fish strains that are capable of synthesizing enough amounts of EPA/DHA from the conversion of α-linolenic acid (LNA, 18:3n-3) rich oils can supply a new EPA/DHA source. This may be achieved by over-expression of genes encoding enzymes involved in HUFA biosynthesis. In aquaculture, the successful of this technique would open the possibility to reduce the enrichment of live food with fish oils for marine fish larvae, and to completely substitute fish oils with plant oils without reducing the quality of flesh in terms of EPA and DHA contents. Here, three genes, i.e. Δ6-desaturase-like (OmΔ6FAD), Δ5-desaturase-like (OmΔ5FAD) and elongase-like (MELO) encoding EPA/DHA metabolic enzymes derived from masu salmon (Oncorhynchus masou) were individually transferred into zebrafish (Danio rerio) as a model to increase its ability for synthesizing EPA and DHA. Fatty acid analysis showed that EPA content in whole body of the second transgenic fish generation over-expressing OmΔ6FAD gene was 1.4 fold and that of DHA was 2.1 fold higher (P<0.05) than those in non-transgenic fish. The EPA content in whole body of transgenic fish over-expressing OmΔ5FAD gene was 1.21-fold, and that of DHA was 1.24-fold higher (P<0.05) than those in nontransgenic fish. The same patterns were obtained in transgenic fish over-expressing MELO gene. EPA content was increased by 1.30-fold and DHA content by 1.33-fold higher (P<0.05) than those in non-transgenic fish. The results of studies demonstrated that fatty acid content of fish can be enhanced by over-expressing gene encoding enzymes involved in fatty acid biosynthesis, and perhaps this could be applied to tailor farmed fish as even better sources of valuable human food.
MORPHOLOGICAL CHARACTERISTIC OF SPERMATOGONIA AND TESTES DISSOCIATION : A Preliminary Study for the Germ Cell Transplantation in Giant Gouramy (Osphronemus gouramy) Irma Andriani; Ita Djuwita; Komar Sumantadinata; Muhammad Zairin Junior; Harton Arfah; Alimuddin Alimuddin
Indonesian Aquaculture Journal Vol 5, No 2 (2010): (December 2010)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (200.767 KB) | DOI: 10.15578/iaj.5.2.2010.163-172

Abstract

The recent study were attempting to develop spermatogonial germ cell transplantation as a tool to preserve and propagate male germ-plasm from endangered fish species, as well as to produce surrogate broodstock of commercially valuable fish. Spermatogonia identification and testes dissociation were the first necessary steps to obtain highly amount and viable population of spermatogonia as donor cells for transplantation. Using giant gouramy testes as a model, spermatogonia was histological characterized and two methods of testes dissociations were compared (i.e. medium A contained 0.5% trypsin in PBS and medium B contained 0.5% trypsin and DNase 10 IU/μL in PBS complemented with CaCl2, Hepes and FCS). Optimal incubation times (1, 2, 3, 4 and 5 hours) in dissociation medium were also determined. Freshly isolated testes of immature giant gouramy were minced in dissociation medium and then incubated to get monodisperce cell suspension. Parameters observed were number and viability of spermatogonia (ø > 10 μm). The viability was analyzed using trypan blue exclusion dye. The results showed that the average number of spermatogonia observed in medium B was higher than in medium A (P<0.05), meanwhile the viability of spermatogonia between medium A and B were not significantly different (P>0.05). The viability of spermatogonia decreased by the increasing duration time of dissociation. The viability of spermatogonia started to decrease significantly in 2 hours incubation time in medium A and 4 hours incubation time in medium B (P<0.05). In conclusion, application of dissociation medium B yielded higher number of viable spermatogonia than dissociation medium A.
VARIATIONS OF RED COLOR COVERAGE OF CULTURED NEON TETRA (Paracheirodon innesi) FOR BREEDING IMPROVEMENT STRATEGIES Ruby Vidia Kusumah; Dinar Tri Soelistyowati; Alimuddin Alimuddin; Melta Rini Fahmi
Indonesian Aquaculture Journal Vol 16, No 1 (2021): (June, 2021)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15578/iaj.16.1.2021.1-11

Abstract

Red color coverage (RCC) is a commercial trait developed and refined to improve the appearance of many ornamental fish commodities. In neon tetra, the status of variation of RCC is not yet investigated or reported. This study aimed to analyze the RCC variation of cultured neon tetra as a basis for breeding strategies. A total of 900 neon tetras (standard length, SL, of 2.29 ± 0.16 cm) were collected from Bojongsari, Curug, and Pondok Petir fish farms located in Depok Districts, West Java. All fish were relocated and reared in a fish farm specialized in culturing neon tetra for two weeks using nine aquariums with photoperiod set up of 12 hours bright and 12 hours dark. The RCC traits were determined according to the percentages of RCC length (%LRCC), RCC width (%WRCC), and RCC area (%ARCC) and quantified using the digital image method. The result showed that the RCC varied by sex, size, and original location (P<0.05) in a low coefficient of variation (1.89%-11.41%). The RCC values in the male group were higher than that of females based on %LRCC and %ARCC parameters (P<0.05). Males had the highest %LRCC at size LXL, which was correlated with SL (r 0.25, P<0.1), of females at M size. The %LRCC values of the neon tetra population from the Bojongsari farm were higher than those from the other locations. Based on these findings, breeding strategies of the RCC traits should consider sex, size, and population (farm location) variations. Specifically for neon tetra, this strategy should be based on selecting the SL or %LRCC parameter of M for females and LXL for males.
IMMUNE RELATED GENES EXPRESSION ANALYSIS IN KOI FISH AFTER VACCINATED WITH KOI HERPES VIRUS DNA VACCINES Sri Nuryati; Fauzan Wahib Alsani; Hasan Nasrullah; Odang Carman; Yuni Puji Hastuti; Eni Kusrini; Alimuddin Alimuddin
Indonesian Aquaculture Journal Vol 15, No 1 (2020): (June, 2020)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15578/iaj.15.1.2020.25-32

Abstract

Vaccination is a practical step in preventing diseases caused by koi herpes virus (KHV) in koi fish (Cyprinus carpio haematopterus). We have developed two DNA vaccines for KHV named as GP-25 and GP-11 from two local isolates coded as ORF25 and ORF81, respectively. Although both vaccines have been reported to increase survival rates, the evaluation of koi fish immune responses at the molecular level has not been done post-vaccinations. The aim of this research was to determine the effects of koi herpesvirus DNA vaccine on the immune-modulation of koi fish at mRNA level. This recent research used the best vaccine doses of both vaccines determined from our previous study: 7.5 and 12.5 µg per 100 g fish of GP-11, and 12.5 µg per 100 g fish of GP-25. The immune gene expression was analyzed using the RT-qPCR method from the fish liver at 0, 1, 7, 14, and 28 days post-vaccination (dpv). The results showed that, in the vaccinated fish, the immune genes viz. tumor necrosis factor a (TNFa), interleukin-1b (IL1b), interferon-g (IFNg), Mx1, immunoglobulin Mu chain (IgM), and major histocompatibility complex (MHC) class I and class II were induced to significant extents. The higher dose vaccination using the GP-11 vaccine showed higher immune gene expression than that of the lower dose. Furthermore, the GP-25 vaccine had induced lower immune responses than the GP-11 vaccine when using the same dose of vaccination, but relatively the same when the half-dose of GP-11 vaccine was used. In conclusion, the GP-11 and GP-25 vaccine provided the immune-modulatory effects on the koi fish immune response after vaccination.
GROWTH RESPONSE OF CLOWN LOACH (Chromobotia macracanthus Bleeker 1852) JUVENILES IMMERSED IN WATER CONTAINING RECOMBINANT GROWTH HORMONE Asep Permana; Alimuddin Alimuddin; Wartono Hadie; Agus Priyadi
Indonesian Aquaculture Journal Vol 10, No 2 (2015): (December 2015)
Publisher : Center for Fisheries Research, Agency for Marine and Fisheries Research and Human Resource

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (352.365 KB) | DOI: 10.15578/iaj.10.2.2015.125-130

Abstract

The main problem in the culture of clown loach (Chromobotia macracanthus) is the slow growth rate, which takes about six months to reach its market size (two inches total body length). Slow growth eventually cause a long production time and increase the production costs. An alternative solution can be proposed in order to enhance the growth is by using recombinant growth hormone. The aim of this study was to determine the immersion dose of recombinant Epinephelus lanceolatus growth hormone (rElGH) which can generate the highest growth in clown loach. Larvae at seven day after hatching were hyperosmotic treated with NaCl 2.0% for one minute, then immersed for one hour in water containing 0.3% NaCl, 0.01% bovine serum albumin (BSA), and different doses of rElGH, namely: 0.12 (treatment A), 1.2 (B), 12 (C), and 120 mg/L (D). As control, fish were immersed in water without rElGH and NaCl (control-1), water containing 0.3% NaCl and 0.01% BSA (control-2), and 0.3% NaCl water (control-3). Each treatment was replicated three times. The results showed that clown loach juveniles in treatment B, C, and D had longer total body length (P<0.05) than control-1, while fish treatment A was the same as controls. Survival and body weight were similar in all treatments and controls (P>0.05). In addition, the percentage of large size juveniles increased approximately 5% in treatment B, almost the same as in the medium size, while the small size were decrease compared to the control-1. Thus, the best immersion dose of rElGH was 1.2 mg/L water.
Co-Authors . Irmawati . Kurdianto . Suharsono A. Octavera A. Santika Abinawanto ACHIS M. SIREGAR Achmad Sudradjat Ade Sunarma ADITYA BRAHMANDITO Afif Abdurrahman Afpriyaningrum MD AGUS O. SUDRAJAT Agus Oman Sudrajat Agus Priyadi Agus Priyadi Agus Priyadi Ahmad Muzaki AKHMAD TAUFIQ MUKTI Amrullah Amrullah Anang Hari Kristanto Andi Aliah Hidayani Andi Aliah Hidayani Andi Aliah Hidayani Andi Haerul Andi Parenrengi Andi Parenrengi Andi Parenrengi Andi Parenrengi Andi Parenrengi Andi Tenriulo Andi Tenriulo Andi Tenriulo Angela Mariana Lusiastuti Angela Mariana Lusiastuti Angela Mariana Lusiastuti ANNA OCTAVERA Anny Hary Ayu Aras Syazili Arief Boediono Arief Boediono Arief Eko Prasetiyo Aris Tri Wahyudi Asep Permana Asep Permana Asep Sopian Asep Sopian ASMI CITRA MALINA A. R. TASSAKKA Aulia Saputra Aulia Saputra Ayi Santika Ayi Santika Ayi Santika Azis Azis Bagus Rahmat Basuki Bambang Iswanto Beginer Subhan Boyun Handoyo Boyun Handoyo Budimawan DARMAWAN SETIA BUDI Darussalam DEDI JUSADI DENNY KHAIRUDI Deny Sapto Chondro Utomo Desy Nurul Astuti Dewi Yuniati Dian Hardiantho Dian Hardiantho Dian Novita Sari Dian R Herdianto Dinamella Wahjuningrum Dinar Tri Soelistiyowati Dinar Tri Soelistyowati Dinar Tri Sulistyowati Dinar Tri Sulistyowati Dody Dharmawan Trijuno Dody Dharmawan Trijuno Dondy Arafat Dwi Hany Yanti Dwi Hany Yanti Dwi Yanti Emma Suryati Emma Suryati Enang Harris Enang Harris Enang Harris Eni Kusrini Eni Kusrini Eni Kusrini Eni Kusrini Eni Kusrini Eni Kusrini Eni Kusrini Eni Kusrini Eni Kusrini Eny Heriyati ENY SUPARYANI Erma Primanita Hayuningtyas Erma Primanita Hayuningtyas Estu Nugroho Evi Tahapari F.H. Pasaribu Fadhila Maharani Putri FADHILLAH RAHMAWATI Fajar Anggraeni Fajar Maulana Fauzan Wahib Alsani Fitriyah Husnul Khotimah Fredinan Yulianda G. Yoshizaki GEMI TRIASTUTIK Gloria Ika Satriani GORO YOSHIZAKI Goro Yoshizaki Goro Yoshizaki Goro Yoshizaki Gunarto Gunarto Gusrina Gusrina H. Arfah Hafidah, Riva Hardiantho D Harton Arfah Hary Krettiawan Haryanti Haryanti HASAN NASRULLAH Hasan Nasrullah Hasan Nasrullah Hasan Nasrullah Hasan Nasrullah Hasan Nasrullah Hasan Nasrullah HAWIS H. MADDUPPA Herjayanto, Muh. Huria Marnis Huria Marnis I.W. Teguh Wibawan Iis Diatin Ika Safitri Ikhsan Khasani Imron Imron Imron Imron INCE AYU KHAIRANA KADRIAH Indah Mastuti Indah Permata Sari Indra Lesmana Intan Febrianti Irin Iriana Kusmini Irma Andriani Irma Andriani IRMA ANDRIYANI Irmawati IRMAWATI IRMAWATI Irmawati, Budimawan Irvan Faizal Irvan Faizal Irvan Faizal Irvan Faizal Irvan Faizal Irvan Faizal IRVAN FAIZAL Irvan Faizal Irzal Effendi Ita Djuwita Ita Djuwita Jasmadi Jasmadi Jean-Christophe Avarre Joko Santoso Joni Haryadi Jr., Muhammad Zairin Julie Ekasari K. Chaitanya Deepti K. Sumantadinata Kamaruddin Ketut Mahardika Ketut Sugama khairuzzazi Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata KOMAR SUMANTADINATA Kukuh Nirmala Kurnia Anggraini Rahmi Lies Emmawati Hadie Luky Adrianto M. SASMITO JATI M. Zairin Junior M.Y. Jamal Maharani, Adinda Maskur Maskur Megawati, Novi MEIMULYA MEIMULYA Melta Rini Fahmi Mia Setiawati Mira Mawardi Mochamad Syaifudin Moh. Tauhid Umar Mohammad Zairin Mohammad Zairin Mubinun Mubinun Muh Alias L. Rajamuddin Muh. Alias L. Rajamuddin MUHAMMAD AGUS SUPRAYUDI Muhammad Firdaus Muhammad Hunaina Fariduddin Ath-thar Muhammad Hunaina Fariduddin Ath-thar Muhammad Husni Amarullah Muhammad Muhammad Muhammad Muttaqin Muhammad Safir Muhammad Yamin Muhammad Zairin Jr Muhammad Zairin Jr Muhammad Zairin Jr. Muhammad Zairin Jr. Muhammad Zairin Jr. Muhammad Zairin Jr. MUHAMMAD ZAIRIN JR. Mulyasari Mulyasari MUNTI YUHANA Muslim Muslim Muzahar N.A. Maswan Nadia Ayuningthias NADIARTI NADIARTI NITA RUKMINASARI Nita Rukminasari Nita Rukminasari Novi Megawati Novi Megawati Nunak Nafiqoh Nunuk Listiyowati Nur Bambang Priyo Utomo Nur Bambang Priyo Utomo NURBETY TARIGAN Nurly Faridah Nurly Faridah O. Carman O.Z. Arifin Odang Carman P. Ratna Kumar Petrus Rani Pong-Masak Priadi Setyawan Pustika Ratnawati Putriku Nadzira Sativa R Rifai R.D. Soejoedono Raden Roro Sri Pudji Sinarni Dewi Raden Roro Sri Pudji Sinarni Dewi Ratu Siti Aliah Ratu Siti Aliah RATU SITI ALIAH Ratu Siti Aliah Rendy Ginanjar Reni Agustina Lubis Ridwan RIDWAN AFFANDI Rommy Suprapto Ruby Vidia Kusumah Rudhy Gustiano RUSTIDJA S. Mariam Samsu Adi Rahman Sari Budi Moria Sembiring Sekar Ayu Chairunnisa Sekar Sulistyaning Hadiwibowo Setiawati M Shabarullah Siska Aliyas Sandra Siti Aslamyah Siti Fadilah Siti Khodijah Siti Subaidah Siti Zuhriyyah Musthofa Sitti Fakhriyyah SLAMET SUBYAKTO Soelistyowati DT Soko Nuswantoro Sri Murtini Sri Nuryati Sri Nuryati St. Hidayah Triana Suci Antoro Sukenda, Sukenda, SUKMARAHARJA A. TARIGAN Sularto Sularto Sularto Sularto Sutanti Sutanti Syuhada Restu Danupratama T. Takeuchi Tatag Budiardi Toshio Takeuchi Tristiana Yuniarti Uswatun Hasanah Uswatun Hasanah Utut Widyastuti Utut Widyastuti Utut Widyastuti Utut Widyastuti Utut Widyastuti Wartono Hadie Wartono Hadie Wartono Hadie Wartono Hadie Wartono Hadie Wedaraningtyas Nugrahani Wicaksono, Aryo Wenang WIDANARNI WIDANARNI Wiwien Mukti Andriyani Wiwien Mukti Andriyani Y. Hadiroseyani Yanti Inneke Nababan yogi Himawan Yulintine Yulintine Yuni Puji Hastuti Yushinta Fujaya Yushinta Fujaya Zairin Jr M Zakki Zainun