Objective: The study aims to prepare the ash filtrate (AF) from household ashes using an in-house-designed handmade filtration system and to observe the antimicrobial efficacy and sanitizing effects. Materials and Methods: Household ashes from various plant sources were collected, and AF was prepared through a handmade filtration system after adding water. The pH of stock AF was measured, and 20%, 40%, 60%, and 80% AF solutions were prepared by adding distilled water in appropriate proportions to obtain a wide range of pH values. The antimicrobial efficacy of AF against Salmonella spp. in vitro, Newcastle disease virus (NDV), and low pathogenic avian influenza virus (LPAIV) H9 N2 in ovo were analyzed. Contaminated eggs were individually sprayed or dipped with AF to detect the bacterial load on the eggshell surface. Further experimental use of AF as an egg sanitizer in routine biosecurity operations in broiler sheds was also evaluated. Results: The prepared AF showed high alkalinity; pH varied from 10.7 to 8.20 and contained a higher amount of K, Na, and Cl. The alkaline AF and its dilution gradually inhibited Salmonella growth and showed gradual pH-dependent antibacterial efficacy. Similarly, AF and its dilution showed a gradual decrease in viral titer against the LPAIV (H9N2); however, antiviral activity against the velogenic strain of NDV was quite steady. Applying AF as an egg sanitizer also reduced the bacterial loads significantly on the eggshell surface compared to untreated eggs. Moreover, AF having pH 10.5 experimentally used in routine sanitization practices of a boiler shed resulted in low bird mortality (10/210), higher body weight gain, and a low feed conversion ratio compared to the untreated control flock. Conclusion: The higher alkalinity of the AF is responsible for the antimicrobial activity of commercial disinfectants. Consequently, we can use AF as a low-cost, effective, natural antimicrobial agent to replace chemical disinfectants. J. Adv. Vet. Anim. Res., 11(4): 1007–1016, December 2024 http://doi.org/10.5455/javar.2024.k851

Objective: The study aims to prepare the ash filtrate (AF) from household ashes using an in-house-designed handmade filtration system and to observe the antimicrobial efficacy and sanitizing effects. Materials and Methods: Household ashes from various plant sources were collected, and AF was prepared through a handmade filtration system after adding water. The pH of stock AF was measured, and 20%, 40%, 60%, and 80% AF solutions were prepared by adding distilled water in appropriate proportions to obtain a wide range of pH values. The antimicrobial efficacy of AF against Salmonella spp. in vitro, Newcastle disease virus (NDV), and low pathogenic avian influenza virus (LPAIV) H9N2 in ovo were analyzed. Contaminated eggs were individually sprayed or dipped with AF to detect the bacterial load on the eggshell surface. Further experimental use of AF as an egg sanitizer in routine biosecurity operations in broiler sheds was also evaluated. Results: The prepared AF showed high alkalinity; pH varied from 10.7 to 8.20 and contained a higher amount of K, Na, and Cl. The alkaline AF and its dilution gradually inhibited Salmonella growth and showed gradual pH-dependent antibacterial efficacy. Similarly, AF and its dilution showed a gradual decrease in viral titer against the LPAIV (H9N2); however, antiviral activity against the velogenic strain of NDV was quite steady. Applying AF as an egg sanitizer also reduced the bacterial loads significantly on the eggshell surface compared to untreated eggs. Moreover, AF having pH 10.5 experimentally used in routine sanitization practices of a boiler shed resulted in low bird mortality (10/210), higher body weight gain, and a low feed conversion ratio compared to the untreated control flock. Conclusion: The higher alkalinity of the AF is responsible for the antimicrobial activity of commercial disinfectants. Consequently, we can use AF as a low-cost, effective, natural antimicrobial agent to replace chemical disinfectants. [J Adv Vet Anim Res 2024; 11(4.000): 1007-1016]

Objective: This study aimed to explore the viability of nitrogen distribution in milk to detect adulteration in market milk. Materials and Methods: Raw cow milk was obtained from the dairy farm at Bangladesh Agricultural University Dairy Farm (BAUDF). Fluid market milk, nonbranded bulk powdered milk, and local brand powdered milk were bought from the Mymensingh city area. The milk samples were T1 (milk from a known source—BAUDF, control group), T2 (reconstituted nonbranded bulk powdered milk), T3 (reconstituted local brand powdered milk), T4 (fluid market milk from Goala), T5 (mixture of 75% T1 and 25% T2), and T6 (mixture of 50% T1 and 50% T2). There were four replications in each variable, and the samples were tested for their physicochemical properties (specific gravity and acidity), gross composition (total solids, ash, milk fat, lactose, and total protein), and nitrogen distribution [casein nitrogen, noncasein nitrogen (NCN), and nonprotein nitrogen (NPN)]. Results: Statistical analysis revealed a significant difference (p < 0.05) among the milk samples about their physicochemical properties and gross composition. The T2 and T6 samples imparted lower protein content (p < 0.05). Much lower (p < 0.05) casein content was found in T2 and T6 than in T1. The NCN content among the samples also differed significantly (p < 0.05). All groups showed similar NPN values (p > 0.05) but the T1 (p < 0.05). Conclusion: The results from this study show the potential of the nitrogen distribution of milk to detect adulterated and reconstituted market milk; however, a hefty dataset is required before being adopted at the field level. J. Adv. Vet. Anim. Res., 11(4): 1023-1029, December 2024 http://doi.org/10.5455/javar.2024.k853

Objective: This study aimed to explore the viability of nitrogen distribution in milk to detect adulteration in market milk. Materials and Methods: Raw cow milk was obtained from the dairy farm at Bangladesh Agricultural University Dairy Farm (BAUDF). Fluid market milk, nonbranded bulk powdered milk, and local brand powdered milk were bought from the Mymensingh city area. The milk samples were T1 (milk from a known source—BAUDF, control group), T2 (reconstituted nonbranded bulk powdered milk), T3 (reconstituted local brand powdered milk), T4 (fluid market milk from Goala), T5 (mixture of 75% T1 and 25% T2), and T6 (mixture of 50% T1 and 50% T2). There were four replications in each variable, and the samples were tested for their physicochemical properties (specific gravity and acidity), gross composition (total solids, ash, milk fat, lactose, and total protein), and nitrogen distribution [casein nitrogen, noncasein nitrogen (NCN), and nonprotein nitrogen (NPN)]. Results: Statistical analysis revealed a significant difference (p < 0.05) among the milk samples about their physicochemical properties and gross composition. The T2 and T6 samples imparted lower protein content (p < 0.05). Much lower (p < 0.05) casein content was found in T2 and T6 than in T1. The NCN content among the samples also differed significantly (p < 0.05). All groups showed similar NPN values (p > 0.05) but the T1 (p < 0.05). Conclusion: The results from this study show the potential of the nitrogen distribution of milk to detect adulterated and reconstituted market milk; however, a hefty dataset is required before being adopted at the field level. [J Adv Vet Anim Res 2024; 11(4.000): 1023-1029]

Objective: Orangutans (Pongo abelii), as endemic primates of Indonesia, are characterized by a predominantly arboreal lifestyle. Klebsiella pneumoniae (K. pneumonia) and other Gram-negative bacteria are present in the Indigenous flora of many mammals, including orangutans. This study aimed to investigate the antibiotic resistance and virulence profile of K. pneumonia isolated from wild Sumatran orangutans. Materials and Methods: This study investigated 10 fecal samples from wild Sumatran orangutans from the Gunung Leuser National Park, Aceh, Indonesia. Biochemical and molecular identification of K. pneumoniae using the RNA polymerase subunit b gene and detection of virulence-associated genes. In addition, molecular detection of antibiotic resistance genes was performed to characterize the resistance mechanisms in the isolates. Results: K. pneumonia was detected in 6 out of 10 fecal samples from wild Sumatran orangutans. The virulence genes mrkD and entB were detected in all (100%) of the isolates, whereas wabG was identified in 83.33% of the strains. Antibiotic susceptibility testing against K. pneumoniae revealed that three isolates were susceptible to streptomycin (S) and nalidixic acid (NA), while all six isolates were susceptible to chloramphenicol and ciprofloxacin. One isolate demonstrated intermediate resistance to NA, while the remaining two exhibited intermediate resistance to S. Six isolates were resistant to ampicillin, tetracycline, and erythromycin, indicating multidrug resistance. Furthermore, antibiotic resistance genes were detected in the isolates with the following prevalence: blaTEM gene (six isolates; 100%), blaSHV (six isolates; 100%), blaCTX-M gene (four isolates; 66.67%), and tetA gene (four isolates; 66.67%). Conclusion: This study revealed the virulence and resistance profile of K. pneumoniae bacterium isolated from wild Sumatran orangutans, which is essential for formulating effective conservation and healthcare strategies.  J. Adv. Vet. Anim. Res., 11(4): 1066–1075, December 2024 http://doi.org/10.5455/javar.2024.k858

Objective: Orangutans (Pongo abelii), as endemic primates of Indonesia, are characterized by a predominantly arboreal lifestyle. Klebsiella pneumoniae (K. pneumonia) and other Gram-negative bacteria are present in the Indigenous flora of many mammals, including orangutans. This study aimed to investigate the antibiotic resistance and virulence profile of K. pneumonia isolated from wild Sumatran orangutans. Materials and Methods: This study investigated 10 fecal samples from wild Sumatran orangutans from the Gunung Leuser National Park, Aceh, Indonesia. Biochemical and molecular identification of K. pneumoniae using the RNA polymerase subunit b gene and detection of virulence-associated genes. In addition, molecular detection of antibiotic resistance genes was performed to character¬ize the resistance mechanisms in the isolates. Results: K. pneumonia was detected in 6 out of 10 fecal samples from wild Sumatran orangutans. The virulence genes mrkD and entB were detected in all (100%) of the isolates, whereas wabG was identified in 83.33% of the strains. Antibiotic susceptibility testing against K. pneumoniae revealed that three isolates were susceptible to streptomycin (S) and nalidixic acid (NA), while all six isolates were susceptible to chloramphenicol and ciprofloxacin. One isolate demonstrated intermediate resistance to NA, while the remaining two exhibited intermediate resistance to S. Six isolates were resistant to ampicillin, tetracycline, and erythromycin, indicating multidrug resis¬tance. Furthermore, antibiotic resistance genes were detected in the isolates with the following prevalence: blaTEM gene (six isolates; 100%), blaSHV (six isolates; 100%), blaCTX-M gene (four isolates; 66.67%), and tetA gene (four isolates; 66.67%). Conclusion: This study revealed the virulence and resistance profile of K. pneumoniae bacterium isolated from wild Sumatran orangutans, which is essential for formulating effective conservation and healthcare strategies. [J Adv Vet Anim Res 2024; 11(4.000): 1066-1075]

Objective: The aim of the current work is studying the effect of antioxidants and nano-antioxidants on in vitro development and mitochondrial function of buffalo oocytes. Materials and Methods: Good and excellent Buffalo oocytes were in vitro matured: (1) tissue culture medium-199 (control group), (2) TCM-199 + melatonin (Mel) 10−9 M (Mel group), (3) TCM-199 + zinc 10−6 M (Zn group), (4) TCM-199 + nano- Mel 10−6 M (N-Mel group), and (5) TCM199 + nano-zinc-oxide 10−6 M (N-ZnO group) and incubated with CO2 5% and 38.5°C for 22 hr. In vitro-matured oocytes were either stained for mitochondrial function or cultured for detection of embryo development. Results: The maturation rate of buffalo oocytes in the N-Mel and N-ZnO groups had a significant (p < 0.05) increase (91.89% and 93.64%, respectively) compared to the Mel group (85.78%) and Zn group (81.37%), and all groups were significantly higher than the control (73.16%). Mitochondrial intensity was significantly elevated (p < 0.05) in the N-Mel and N-ZnO groups than in oocytes matured in the Mel, Zn, or control groups. Rates of fertilization, cleavage, and transferable embryos of buffalo oocytes matured in vitro were significantly raised in the N-ZnO group (88.35%, 85.93%, and 30.71%, respectively) and the N-Mel group (86.74%, 82.75%, and 28.32%, respectively) (p < 0.05) when compared with the Mel group (82.46%, 77.25%, and 21.29%, respectively) and the Zn group (79.98%, 75.19%, and 19.68%, respectively), and all were increased significantly (p < 0.05) compared to the control group (71.76%, 68.7%, and 11.98%, respectively). Conclusion: Supplementation of maturation medium with Mel 10−9 M and zinc sulfate 10−6 M and nano-Mel 10−6 M and nano-zinc oxide 10−6 M improves buffalo oocyte maturation rates, mitochondrial function, and embryo development. J. Adv. Vet. Anim. Res., 11(4): 1093–1104, December 2024 http://doi.org/10.5455/javar.2024.k860

Objective: The aim of the current work is studying the effect of antioxidants and nano-antioxidants on in vitro development and mitochondrial function of buffalo oocytes. Materials and Methods: Good and excellent Buffalo oocytes were in vitro matured: (1) tissue culture medium-199 (control group), (2) TCM-199 + melatonin (Mel) 10−9 M (Mel group), (3) TCM-199 + zinc 10−6 M (Zn group), (4) TCM-199 + nano- Mel 10−6 M (N-Mel group), and (5) TCM-199 + nano-zinc-oxide 10−6 M (N-ZnO group) and incubated with CO2 5% and 38.5°C for 22 hr. In vitro-matured oocytes were either stained for mitochondrial function or cultured for detection of embryo development. Results: The maturation rate of buffalo oocytes in the N-Mel and N-ZnO groups had a significant (p < 0.05) increase (91.89% and 93.64%, respectively) compared to the Mel group (85.78%) and Zn group (81.37%), and all groups were significantly higher than the control (73.16%). Mitochondrial intensity was significantly elevated (p < 0.05) in the N-Mel and N-ZnO groups than in oocytes matured in the Mel, Zn, or control groups. Rates of fertilization, cleavage, and transferable embryos of buffalo oocytes matured in vitro were significantly raised in the N-ZnO group (88.35%, 85.93%, and 30.71%, respectively) and the N-Mel group (86.74%, 82.75%, and 28.32%, respectively) (p < 0.05) when compared with the Mel group (82.46%, 77.25%, and 21.29%, respectively) and the Zn group (79.98%, 75.19%, and 19.68%, respectively), and all were increased significantly (p < 0.05) compared to the control group (71.76%, 68.7%, and 11.98%, respectively). Conclusion: Supplementation of maturation medium with Mel 10−9 M and zinc sulfate 10−6 M and nano-Mel 10−6 M and nano-zinc oxide 10−6 M improves buffalo oocyte maturation rates, mitochondrial function, and embryo development. [J Adv Vet Anim Res 2024; 11(4.000): 1093-1104]

Rabies is endemic in Sudan with continuing outbreaks occurring annually, the most common animals affected are dogs, followed by goats and equids. This work focused on equid rabies, to elucidate the current situation of the disease through analysis of reports of equid rabies outbreaks in Sudan during 2010–2022 supported by laboratory confirmation of the disease. During the study period, 66 animals were affected during 35 equid rabies outbreaks. The highest incidences were found in Al Gezira (30.3%), followed by Darfur (24.2%) and Kordofan (15.2%). The highest incidence rate was observed during 2018 (33.3%), followed by 2015 (16.7%). Within seasons, the highest incidence rate was reported during October – December (33.3%), followed by July – September (30.3%). Chi-square analysis revealed a significant correlation between rabid animals and year, season, and state. Wald statistics demonstrated that year and season had a significant association with the disease. Virus antigen was identified (72.2%) in brain tissues using the fluorescent antibody test. Viral nucleic acid was amplified (n = 6) with a reverse transcriptase polymerase chain reaction assay.Contribution: As equids are kept in close contact with humans and other animals in the country, according to the present investigation, equid rabies in Sudan is a potential public health concern, emphasising the importance of implementing effective control measures.

Rabies is endemic in Sudan with continuing outbreaks occurring annually, the most common animals affected are dogs, followed by goats and equids. This work focused on equid rabies, to elucidate the current situation of the disease through analysis of reports of equid rabies outbreaks in Sudan during 2010–2022 supported by laboratory confirmation of the disease. During the study period, 66 animals were affected during 35 equid rabies outbreaks. The highest incidences were found in Al Gezira (30.3%), followed by Darfur (24.2%) and Kordofan (15.2%). The highest incidence rate was observed during 2018 (33.3%), followed by 2015 (16.7%). Within seasons, the highest incidence rate was reported during October – December (33.3%), followed by July – September (30.3%). Chi-square analysis revealed a significant correlation between rabid animals and year, season, and state. Wald statistics demonstrated that year and season had a significant association with the disease. Virus antigen was identified (72.2%) in brain tissues using the fluorescent antibody test. Viral nucleic acid was amplified (n = 6) with a reverse transcriptase polymerase chain reaction assay. Contribution: As equids are kept in close contact with humans and other animals in the country, according to the present investigation, equid rabies in Sudan is a potential public health concern, emphasising the importance of implementing effective control measures.