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Jurnal Sain Veteriner
ISSN : 012660421     EISSN : 24073733     DOI : -
Core Subject : Health,
Arjuna Subject : -
Articles 824 Documents
Efektivitas Larutan Desinfektan Dalam Menginaktivasi Virus Avian Influenza pada Bulu Unggas Bagus Nanang Luwito; I Wayan Teguh Wibawan; Retno Damayanti Soejoedono
Jurnal Sain Veteriner Vol 36, No 2 (2018): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (8406.954 KB) | DOI: 10.22146/jsv.26934

Abstract

Avian Influenza (AI) virus  is pathogenic agent that can spread from one area to another area through the transportation of infected animals or their products such as feathers. This research was aimed to inactivated AI virus with 775 ppm sodium hypochlorite and 0.1% chloroxylenol to examine the difference of treatment by time (day) for inactivation AI virus on the feathers. AI virus isolate A/chicken/sidrap/ 07160336‐2/2016 used in this research was obtained from Balai Besar Veteriner Maros. The treatment of disinfectants were performed on the first day (the day of disinfectan solutions were prepared), the third day and the seventh day by soaked the feathers in disinfectant solution for 10 minutes. The effectiveness of disinfectans were evaluated by inactivation index. The result show that the average of inactivation index of 775 ppm of sodium hypochlorit was 4.17 for the first day, 5.17 for the third day, and 4.20 for the seventh day, while the average of inactivation index of 0.1% chloroxylenol was 5.50 for the first day, 6.43 for the third day, and 5.77 for the seventh day. Our result indicated that the sodium hypochlorit and chloroxylenol were effective for inactivation of AI virus. The 0.1% of chloroxylenol was more effective for inactivation AI virus than 775 ppm of sodium hypochlorit, whilst the most effective duration for the treatment is the three days.
Penggunaan Antigen Mycoplasma gallisepticum Freeze-Thawing dalam Teknik Enzyme-Linked Immunosorbent Assay Faidah Rachmawati Rachmawati; I Wayan Teguh Wibawan; Ni Luh Putu Ika Mayasari
Jurnal Sain Veteriner Vol 36, No 2 (2018): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (10370.559 KB) | DOI: 10.22146/jsv.27021

Abstract

Chronic Respiratory Disease (CRD) is a bacterial infection in chickens caused by Mycoplasma gallisepticum. CRD may result in economic loss in the livestock industry, decreasing of egg production and feed efficiency, increasing of  medication costs, downgrading of carcass and egg qualities. The aim of this study was to develop the Enzyme-Linked Immunosorbent Assay (ELISA) kit for detecting antibodies of M. gallisepticum using freeze-thawing antigens. The cut-off point was determined by S/N method. Chicken antiserum againts M. gallisepticum was collected every week on 1st – 6th week post immunization of whole cell antigen of M. gallisepticum. Optimization of antigen, serum and conjugate were 10 μg/ml protein concentrations, 1:800 serum dilution and 1:10000 conjugate dilution. The validation results on developed ELISA kit (MyGELISA) analyzed  by ROC curve using MedCalc statistical software revealed that developed ELISA kit (MyGELISA) had 100% sensitivity and 86.21% specificity with 95% confidence interval. The results of RSA, MyGELISA and commercial ELISA kit showed antibodies positif againts M. gallisepticum.  In conclusion, MyGELISA using freeze-thawing antigen can be used to detect antibodies of M. gallisepticum.
Ancaman Masuknya Virus Penyakit Mulut dan Kuku Melalui Daging Ilegal di Entikong, Perbatasan Darat Indonesia dan Malaysia Risma JP Silitonga
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (6919.491 KB) | DOI: 10.22146/jsv.27222

Abstract

This study was aimed to analyze the risk of FMD virus to enter Indonesia by the presence of illegal meat at Entikong, a borderland between Indonesia and Malaysia. The primary datas were collected using questionnaires method to collect expertise, in-depth interviews, and direct field observations. Secondary datas were obtained from scientific publications and articles or unpublished datas (statistics, goverment documents and reports). The respondents were choosen by purposive sampling. The circulating illegal meat was possibly originate fromdifferent countries, including FMD-endemic countries/zones such as Peninsular Malaysia, Thailand, India and even unidentified countries/zones according to our respondends. The types of illegal meat such as frozen deglanded bonein-meat and frozen deglanded offal that enter Entikong carry the risk of becoming a source of FMD infection. Based on the entry route, delivery frequency, and meat volume, ilegal meat was possibly also entered into Indonesia using non-vehicular transportation. These conditions indicated that the entrance of illegal meat could pose risk of the FMD virus entry to Indonesia, especially at the borderland between Indonesia and Malaysia at Entikong. It is highly recommended to apply strict inspection at the border entraces and increase collaboration with related institutions to prevent the entrance of illegal meat and to reduce the entry risk of FMD virus.
Pengembangan Metode Identifikasi Kerusakan DNA Spermatozoa Ternak Teguh Ari Prabowo; R. Iis Arifiantini; Dondin Sajuthi; Uus Saefullah
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (688.871 KB) | DOI: 10.22146/jsv.27538

Abstract

The success of artificial insemination is very much determined by the quality of spermatozoa. The detection or identification of damaged chromatin of spermatozoa DNA is very important to forsee the adverse clinical outcome. However, the method of identification is still depended on expensive imported kits. Therefore, the objective of this research was to developed an identification kit to determine the quality of livestock spermatozoa DNA chromatin.This study consist of three step. Step 1) Determination of low melting point agarose (LMP-agarose) concentration which is 0,6%, 0,7% and 0,8%. 2) Comparison of three lysis solution (LS) which is LS I (0.4M Tris, 0.8M DTT, 1% SDS, pH 7.5), LS II (0.4M Tris,2 M NaCl, 1% SDS , pH 7.5), and LS III (0.4M Tris-HCl, 2M NaCl, 1% SDS 0,05 M EDTA, pH 7.5). 3) Comparison different staining which is Eosin yellow and Methylene blue. The results showed that 0.6% LMP-agarose demonstrated the best concentration to “trapped the spermatozoa” compared for sheep and goats. whereas the three concentration of spermatozoa cows can not be used to trap spermatozoa cow. The best formulation to lysis the membrane was LS III (0.4M Tris -HCl, 2M NaCl, 1% SDS 0,05 M EDTA). The best staining was eosin yellow and methylene blue with 2:1 ratio.
Peran Makromineral pada Reproduksi Ruminansia Yanuartono Yanuartono; Soedarmanto Indarjulianto; Alfarisa Nururrozi; Hary Purnamaningsih
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (6708.368 KB) | DOI: 10.22146/jsv.27541

Abstract

Macromineral is one component of a nutrient that has an important role in the growth, health, production,reproduction and immune system of animals. Ruminants need makromineral such as Ca, P, Mg, K, Na , Cl and S. Mineral needs of ruminant affected by several factors such as their age, pregnancy and lactation status.Mineral deficiency can cause disturbances in reproduction ruminant. Ca and P have direct influence while Mg, K, Na, Cl and S acted indirectly on reproductive function. A complete understanding of the role macromineral on ruminant reproductive function is indispensable for the prevention of their reproductive disorders due toimproper feeding minerals.
Deteksi Spesies Brucella pada Kambing di Rumah Potong Hewan Jakarta Mujiatun Mujiatun; Retno Damajanti Soejoedono; Etih Sudarnika; Susan Maphilindawati Noor
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1204.201 KB) | DOI: 10.22146/jsv.27546

Abstract

Brucellosis is a zoonosis and occupational diseases transmision. The diseases caused by bacterial and attack multiple species of animals. Common species that infects goats as the most pathogenic species (zoonotic) is Brucella melitensis; however, the species B. abortus could also infect goats. The study purposed to find out the brucellosis seropositive in goat in Jakarta slaughterhouse and to detect caused agent of brucellosis. Sampling was done through slaughtered goats that come from brucellosis endemic area. The samples were collected fromslaughtered mature female goats i.e serum, goat milk, vaginal swab, mamary gland, limphoglandula supramamary, limph, and uterus. The detection method was used i.e patological lession, serological, culture and PolymeraseChain Reaction (PCR) technique. The serological detection of brucellosis in goats was done parallelly between Rose Bengal Test (RBT), Complement Fixation Test (CFT) and Enzyme Linked Immunosorbent Assay (ELISA). The results of this study demonstrated that out of the 119 serum samples serologically tested, negative for RBT, one was positive for CFT and none were positive with ELISA. Patological observation in the Brucella predilection organs, there were 5 goat carcases showed pathological lession (vagina discharge, hemoragy at limphand limphoglandula, crumbly limph and there were pus in uterus). The serum samples that had reacted positively and the organs with pathological lesion were confirmed further with PCR, bacterial isolation and identification.The PCR test results and the culture of milk samples, vaginal swabs and organs did not reveal any Brucella spp bacteria (B. abortus, B. melitensis, B. ovis dan B. suis) and also vaccine strains of RB51. Based on these results, it was concluded that brucellosis in goats on Java Island was a 0.84% seropositive (confidence interval 95%; 0.00826 - 0.00854) (1/119), although the species of Brucella that had infected them remains unknown.
Efek Antikariogenik Ekstrak Daun Beluntas (Pluchea indica) sebagai Penghambat Pertumbuhan Streptococcus Mutans penyebab Karies Gigi Nungki Fatimatuzzahra; Nourmalita Safitri Ningsih; Feny Feny; Adam Darsono; Siti Isrina Oktavia Salasia
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (7139.244 KB) | DOI: 10.22146/jsv.27547

Abstract

Anti-plaque agents are known to reduce the formation of dental biofilms such as fluoride and chlorhexidine. However, excessive use of fluoride causes fluorosis and chlorhexidine side effects caused genotoxic. Pluchea indica L is one of the abundance of tropical herbs in the Asia-Pacific reported to have antiinflammatoryproperties and reduces the incidence of gastric necrosis, antinociception, neutralizing toxic venom, antioxidant, antiulcerative, hepatoprotective, antimoeba and broad-spectrum antimicrobial. This study examinesthe effectiveness anticariogenic Pluchea indica leaf extract in inhibiting the growth of Streptococcus mutans causing dental caries in vitro. Determination of Minimum Inhibitoric Concentration (MIC) on Pluchea indica leafextract is by diffusion test on the growth of Streptococcus mutans by Kirby Bauer Test. S. mutans concentration Mc Farland 0.5 standard (108 CFU ml-1) were inoculated in media Müller-Hinton agar (MHA). Paper diskcontaining Pluchea indica leaf extract at each concentration of 10%, 20%, 30%, 40%, 50%, 60%, and 70% were placed in an agar medium inoculated bacteria then incubated at 37°C on condition microaerophilia using candlejar. Determination of significance various Pluchea indica leaf extract concentration using one-way ANOVA test. The result of the diffusion method showed Pluchea indica leaf extract at a minimum concentration of 10% beenable to establish inhibited zone of Streptococcus mutans growth in MHA media. By one-way ANOVA test to various concentrations of extracts using Microsoft Excel 2007 have been obtained with F=4.85, Fcrit = 2.85 andP-value = 0.0071. Based on this research, it was concluded that Inhibitoric Minimum Concentration Pluchea indica leaf extract is capable of effective concentration of 10% and it has a significant (P-value< 0,05) of variousconcentration.
Sonogram Pemeriksaan Kebuntingan Dini pada Kambing Kacang (Capra hircus) Santoso Santoso; Amrozi Amrozi; Bambang Purwantara; Herdis Herdis
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (529.297 KB) | DOI: 10.22146/jsv.27548

Abstract

This study was conducted to determine the earliest day of pregnancy diagnosis in kacang goat using transrectal ultrasonography. The goat were synchronized by using prostaglandin in the luteal phase. Pregnancy was determined by isoechogenic visualization surrounded by hypoechogenic. Early pregnancy was detected on days 20 of embryonic vesicle diameter 1.2±0.1 cm. Fetus was detected on days 22 with a long gestation fetus 0.4±0.1 cm. Average increase until days 30 pregnancy was 0.19 ± 0.1 cm per day. Development of fetus was followed by an increasing the diameter and thickness of uterus. The diameter of uterus increased from days 14 (0.8 ± 0.3 cm) until days 30 (3.6 ± 0.2 cm), and thickness of uterus increased from days 14 (0.4 ± 0, 2 cm) until days 30 (1.8 ± 0.2 cm). It could be concluded that the earliest pregnancy diagnosis showed positive sign on days 20 and fetus was earliest observed on days 22.
Studi Respon Imun Humoral Mencit, Tikus, dan Ayam terhadap Infeksi Toxoplasma Gondii Gifti Rosalina Ratnaningrum; Dana Meida; Andhini Mutiara Putri; Hilda Syara Shita Devi; Dwi Priyowidodo
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (6673.961 KB) | DOI: 10.22146/jsv.27556

Abstract

Toxoplasmosis is a disease caused by the protozoan Toxoplasma gondii. T. gondii is an obligate intracellular parasite that is transmitted by congenital and acquisition. T. gondii can infect all warm-blooded animals and are zoonotic. It is estimated that more than a third of the world’s population is infected by T. gondii. Chicken is one of the animals that can be infected with T. gondii and plays an important role in the spread of this disease to humans because it is one of the animals used as a source of animal feed. Mice and rats are also play an important role in the spread of toxoplasmosis in the definitive host, especially in cats. T. gondii infection is usually asymptomatic, but in certain circumstances, such as when the host’s immune system is weakened, this parasite can causeserious illness. This study were aimed to determine the humoral immune response against T. gondii infection in mice, rats and chickens by serological Latex Agglutination Test (LAT) using Pastorex-Toxo® kit. Two weeks oldbroiler chickens were 8 heads, Wistar strain rats aged 8 weeks as many as 18 heads and strain Balb C mice aged 8 weeks as many as 13 cows used in this study. Animals were grouped into two groups, namely the control andinfection groups. Mice, rats, and chickens were infected each with 103, 107 and 105 takizoit by intra-peritoneal injection. Blood samples were taken from the animals and infection control from day to-1, 2, 3, 4, 5, 6 for mice,the to-1, 2, 3, 4, 5, 6, 7, 8 for rats, and day - 2, 4, 14 for chicken by intracardia 3 ml, then put in a non-EDTA tubes and centrifuged at a speed of 10,000 rpm for 5 minutes to collect serum. The results showed a humoral immuneresponse against T. gondii in rats began to appear on day 5 post-infection, chickens began to emerge the 2nd day post infection, whereas mice do not indicate a humoral immune response against T. gondii post infection.
Potensi Ekstrak Daun Sage (Salvia officinalis.L) sebagai anti-Streptococcus suis Penyebab Zoonotik Meningitis Mitra Slipranata; Fajar Budi Lestari; Novra Arya Sandi; Siti Isrina Oktavia Salasia
Jurnal Sain Veteriner Vol 34, No 2 (2016): Desember
Publisher : Fakultas Kedokteran Hewan Universitas Gadjah Mada bekerjasama dengan PB PDHI

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (6908.327 KB) | DOI: 10.22146/jsv.27558

Abstract

The phenomenon of microbial resistance to an antibiotic or some kind of specific antibiotics (multi drugs resistance) greatly complicate the treatment process, one of which is Streptococcus suis (S. suis) which is known to cause meningitis in animals and humans. Today, with rising bacterial resistance to a wide rangeof antibiotics, it takes an effort to assess the potential medicinal plants as an antibiotic that is appropriate and safe. Sage (Salvia officinalis.L) is reported to have antibacterial and fungicidal effect. Phenolic acids such assalvin and ether monomethyl salvin which isolated from the sage thought to have antimicrobial activity against several bacterial strains. The purpose of this study was to prove the ability of sage leaf extract as an antibacterialagainst S. suis causes streptococcal meningitis in vitro. In-vitro method used in this research through a two-stage dilution test and the diffusion test on Mueller Hinton Agar (MHA). S. suis isolates (code 225) were tested in vitro against 8 levels sage leaf extract concentration, ie a concentration of 1%, 3% 5%, 7%, 10%, 20%, 40% and 60%. The results of the test obtained by minimum inhibitory concentrations (MICs) and minimum sage known to potentially inhibit the growth of S. suis.

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