Fraserbentsen7406

Conclusion An SNP at intron 4 of the IGF1 gene was associated with the growth trait and was usable as a genetic marker candidate for improvement of growth traits of Kejobong goats while von Bertalanffy model provides proper and accurate estimates of parameters to describe the growth performance of Kejobong goats. PJ34 in vitro Copyright © Lestari, et al.Aim This study was aimed to investigate antimicrobial and cytotoxicity effect of nano ZnO in in vitro for the application of livestock feed supplement. Materials and Methods Nano ZnO was synthesized by wet chemical precipitation method using zinc acetate as a precursor and sodium hydroxide was used for reducing the precursor salt. The properties of synthesized powder were characterized using ultraviolet (UV)-visible spectroscopy, Fourier transform infrared (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD), respectively. In vitro antimicrobial activities were analyzed against the pathogenic bacteria in poultry Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, and Streptococcus aeruginosa. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was conducted to analyze the cytotoxicity effect of nano ZnO. Results SEM showed a spherical ZnO particle in the range of 70-100 nm. The size of the particle and purity of the sample were confirmed by XRD. The nano-sized ZnO particles exhibited the UV absorption peak at 335 nm. In FTIR spectroscopy, pure ZnO nanoparticles showed stretching vibrations at 4000-5000 cm-1. ZnO nanoparticles exhibited remarkable antibacterial activity against E. coli, S. aureus, K. pneumoniae, and S. aeruginosa bacterial strains. Cell viability was significantly reduced in a dose-dependent manner in the cytotoxicity study. Conclusion From the broad-spectrum antibacterial activity and the lower cytotoxicity observed at the prescribed dose, it is concluded that nano ZnO powder is a potential alternate zinc supplement for livestock. Copyright © Geetha, et al.Background and Aim Camel farming remains a part of the culture of the Arabian Peninsula although modern methods have greatly increased camel densities in the entire region. In the United Arab Emirates (UAE), camel production is threatened by tick parasitism. However, no study has considered assessing the magnitude of the problem in the UAE. We conducted a study evaluating tick richness, abundance, and spatial distribution of ticks on camels in farms near Al Ain, UAE. In addition, we conducted a survey of farm owners to determine the control methods used to eliminate camel ticks. Materials and Methods Tick counts were made on 502 camels (Camelus dromedarius). For each examined animal, visual counts of ticks were made on the entire body segregating the counts by head, neck, forelegs, hump, abdomen, back legs, and tail area. In addition, a total of 70 camel owners from the study area were randomly selected and surveyed about the tick control methods. Results Hyalomma dromedarii was the only species found during the study. The prevalence of ticks was 98% among the sampled animals. The mean intensity (tick load) was 25.8±2.4 ticks/host and the maximum number of ticks per animal was 102. Ticks were found in five vicinities that are on the border with Oman. The highest number of ticks on the body of the camel occurred on the tail area followed by the abdomen. Cypermethrin was the most commonly used acaricide (46.9%). Conclusion The high abundance of ticks reported in this study calls for the establishment of a good management strategy. In addition, finding ticks in vicinities in the UAE that are on the border with Oman suggests a cross-border movement between the two countries. Therefore, studying this movement is important to understand its role in the global circulation of some H. dromedarii tick-borne diseases and the movement of acaricide resistance alleles among tick populations. Copyright © Al-Deeb and Muzaffar.Background and Aim Bovine tuberculosis (bTB) is a chronic bacterial disease of cattle caused by Mycobacterium bovis. bTB causes severe economic losses resulting from livestock deaths, chronic disease, and trade restrictions. Determination of serum levels of adenosine deaminase (ADA), an enzyme produced by monocytes/macrophages and lymphocytes, has been used in the diagnosis of human TB. This study aimed to evaluate the role of ADA enzyme activity in the diagnosis of bTB. Materials and Methods In this study, a total of 100 animals (cattle and buffaloes) were screened for bTB by comparative intradermal tuberculin test (CITT) and interferon-γ (IFN-γ) test and in serum samples obtained from 100 screened animals, ADA seric activity was evaluated using ADA-MTB kit procured from Tulip Diagnostics. Results A total of 18 animals were positive TB reactors by CITT, 8 were positive by IFN-γ, and 4 animals were positive by both CITT and IFN-γ. The average ADA value of bTB-positive animals either by CITT, IFN-γ, or both CITT and IFN-γ was 12.55 U/L, 14.8 U/L, and 18.36 U/L, respectively, in CID negative, it was 10.57 U/L and in IFN-γ negative, it was 10.59 U/L. Conclusion The average ADA value of bTB-positive animals positive either by CITT, IFN-γ, or both CITT and IFN-γ was more than the average ADA value in animals negative for bTB by either of the tests. Copyright © Dhaliwal, et al.Aim This study aimed to determine the molecular characteristics of Pasteurella multocida isolates originated from Sumba Island, East Nusa Tenggara Province. Materials and Methods The isolates of P. multocida stored in frozen storage were cultured in blood agar as a selective medium and identified conventionally. Molecular tests were initiated by DNA isolation and then followed by polymerase chain reaction tests with specific primers for the determination of P. multocida serotype A or B. Positive strain of serotype B was then confirmed molecularly using 16S rRNA gene primer and followed by the sequencing of nucleotides. Results The study showed that both P. multocida isolates from Sumba island, i.e. PM1 is isolated from East Sumba district, while PM2 isolated from West Sumba district have 99.6% homology. Both isolates also known have 99% similarities with P. multocida originated from India, Britain, and Japan, respectively. The isolates share the same clade in the phylogenetic tree. Conclusion The 16S rRNA sequencing revealed a high similarity of P.