The use of medicinal plants plays a major role in the primary health care of animals in South Africa. A survey was conducted to document medicinal plants used to control parasites in goats in Kwezi and Ntambethemba villages in the Eastern Cape Province, South Africa. Information from 50 farmers and 3 herbalists was obtained through the use of a structured questionnaire, and a snowball sampling technique was used to identify key informants. The obtained data were analysed using PROC FREQ of SAS (2003), and fidelity level values were determined to estimate the healing potential of the mentioned plants. The survey revealed nine plant species belonging to eight families that were used to control parasites in goats. Asphodelaceae (22.22%) was the most frequently used plant family. Leaves were the most used plant parts, constituting 60.38%. They were prepared either as infusions or decoctions of single plants or in mixtures. Aloe ferox, Acokanthera oppositifolia and Elephantorrhiza elephantina were the plants having the highest fidelity level for their use to control parasites, each scoring 100%, followed by Albuca setosa (83.33%). The study revealed low knowledge about ethnoveterinary medicine in the study area. It also revealed that information on ethno-veterinary medicine in this area is mostly confined to older people and there is danger that this knowledge can be lost before being passed on to other generations. Therefore, there is an urgent need to document information on these plant species so that the future generation can benefit. Further investigation should be carried out to validate the efficacy and safety of the above-mentioned plants so as to provide cheap alternative ways of controlling parasites.Keywords: ailments; ethno-veterinary practices; small ruminant; traditional medicine

The use of medicinal plants plays a major role in the primary health care of animals in South Africa. A survey was conducted to document medicinal plants used to control parasites in goats in Kwezi and Ntambethemba villages in the Eastern Cape Province, South Africa. Information from 50 farmers and 3 herbalists was obtained through the use of a structured questionnaire, and a snowball sampling technique was used to identify key informants. The obtained data were analysed using PROC FREQ of SAS (2003), and fidelity level values were determined to estimate the healing potential of the mentioned plants. The survey revealed nine plant species belonging to eight families that were used to control parasites in goats. Asphodelaceae (22.22%) was the most frequently used plant family. Leaves were the most used plant parts, constituting 60.38%. They were prepared either as infusions or decoctions of single plants or in mixtures. Aloe ferox, Acokanthera oppositifolia and Elephantorrhiza elephantina were the plants having the highest fidelity level for their use to control parasites, each scoring 100%, followed by Albuca setosa (83.33%). The study revealed low knowledge about ethnoveterinary medicine in the study area. It also revealed that information on ethno-veterinary medicine in this area is mostly confined to older people and there is danger that this knowledge can be lost before being passed on to other generations. Therefore, there is an urgent need to document information on these plant species so that the future generation can benefit. Further investigation should be carried out to validate the efficacy and safety of the above-mentioned plants so as to provide cheap alternative ways of controlling parasites. Keywords: ailments; ethno-veterinary practices; small ruminant; traditional medicine

Objective: Lighting requirements of birds have to be considered for choosing the optimal light intensity. Therefore, the experiment was carried out to study the effects of the different light intensities on performance, welfare and behavior of turkey poults. Materials and Methods: A total of 81 turkey poults aging 3 weeks were randomly selected and divided into three equal groups. The birds were subjected for 3 different light intensities (5, 25 and 50 lux) with 12 h photoperiod in 3 separate rooms. The growth performance parameters of the poults were measured; the parameters were body weight (BW), average feed intake (FI), average body weight gain (ABWG), relative growth rate (RGR), and feed conversion ratio (FCR). Besides, blood parameters and behavioral characters were observed. Results: Our results revealed that poults reared in low intensity (5 lux) had better performance (body weight gain, relative growth rate and feed intake). Also, final body weight was significantly higher in 5 lux. The cortisol level was lower in 5 lux than other 25 and 50 lux. Behavior of poults is affected by light intensities in our study, where feather preening, feather pecking and aggressive behaviors were significantly higher in birds housed in the highest intensity (50 lux). In the same way, drinking time was significantly higher in 25 lux. The poults tended to lay and rest on perches more under the lowest intensity (5 lux). Conclusion: It was concluded that, it is better to use moderate light intensity to improve previous parameters with avoiding abnormal behavior.http://dx.doi.org/10.5455/javar.2016.c126

Objective: Lighting requirements of birds have to be considered for choosing the optimal light intensity. Therefore, the experiment was carried out to study the effects of the different light intensities on performance, welfare and behavior of turkey poults. Materials and Methods: A total of 81 turkey poults aging 3 weeks were randomly selected and divided into three equal groups. The birds were subjected for 3 different light intensities (5, 25 and 50 lux) with 12 h photoperiod in 3 separate rooms. The growth performance parameters of the poults were measured; the parameters were body weight (BW), average feed intake (FI), average body weight gain (ABWG), relative growth rate (RGR), and feed conversion ratio (FCR). Besides, blood parameters and behavioral characters were observed. Results: Our results revealed that poults reared in low intensity (5 lux) had better performance (body weight gain, relative growth rate and feed intake). Also, final body weight was significantly higher in 5 lux. The cortisol level was lower in 5 lux than other 25 and 50 lux. Behavior of poults is affected by light intensities in our study, where feather preening, feather pecking and aggressive behaviors were significantly higher in birds housed in the highest intensity (50 lux). In the same way, drinking time was significantly higher in 25 lux. The poults tended to lay and rest on perches more under the lowest intensity (5 lux). Conclusion: It was concluded that, it is better to use moderate light intensity to improve previous parameters with avoiding abnormal behavior. [J Adv Vet Anim Res 2016; 3(1.000): 18-23]

Objectives: The objective of this study was to isolate and identify Staphylococcus aureus and Escherichia coli from raw milk samples of cattle and buffalo, and to evaluate the antibiotic sensitivity pattern. Materials and methods: A total of 34 milk samples were collected twice from 17 different healthy cattle (n=14) and buffaloes (n=3) at one-month interval, and analyzed in laboratory by staining, cultural and biochemical characteristics followed by polymerase chain reaction targeting nuc gene of S. aureus and 16 S rRNA of E. coli. Antibiotic sensitivity pattern of the isolated bacteria was assessed using the disc diffusion method.  Results: Confirmation of the isolates as S. aureus and E. coli were carried out by PCR using nuc gene, 16S rRNA gene specific primers specific for S. aureus and E. coli respectively. A total of 12 samples (35.29%; 11 from cattle, 1 from buffalo) were found to be positive for S. aureus; 5 and 7 during first and second month, respectively. The E. coli were found in three samples (2 from cattle, 1 from buffaloe); one in first month and two in the second month. The antibiotic sensitivity test using 4 commonly used antibiotics indicated that the most of the isolates were resistant to Gatifloxacin and one isolate showed intermediate resistance to Ofloxacin while sensitive to Ciprofloxacin and Levofloxacin.Conclusion: Two different species of bacteria i.e., S. aureus and E. coli are contaminating with milk samples. The pathogenic bacteria can be controlled effectively by using Ciprofloxacin and Levofloxacin in the case of mastitis in cattle and buffaloes in Bangladesh.http://dx.doi.org/10.5455/javar.2016.c133

Objectives: The objective of this study was to isolate and identify Staphylococcus aureus and Escherichia coli from raw milk samples of cattle and buffalo, and to evaluate the antibiotic sensitivity pattern. Materials and methods: A total of 34 milk samples were collected twice from 17 different healthy cattle (n=14) and buffaloes (n=3) at one-month interval, and analyzed in laboratory by staining, cultural and biochemical characteristics followed by polymerase chain reaction targeting nuc gene of S. aureus and 16 S rRNA of E. coli. Antibiotic sensitivity pattern of the isolated bacteria was assessed using the disc diffusion method. Results: Confirmation of the isolates as S. aureus and E. coli were carried out by PCR using nuc gene, 16S rRNA gene specific primers specific for S. aureus and E. coli respectively. A total of 12 samples (35.29%; 11 from cattle, 1 from buffalo) were found to be positive for S. aureus; 5 and 7 during first and second month, respectively. The E. coli were found in three samples (2 from cattle, 1 from buffaloe); one in first month and two in the second month. The antibiotic sensitivity test using 4 commonly used antibiotics indicated that the most of the isolates were resistant to Gatifloxacin and one isolate showed intermediate resistance to Ofloxacin while sensitive to Ciprofloxacin and Levofloxacin. Conclusion: Two different species of bacteria i.e., S. aureus and E. coli are contaminating with milk samples. The pathogenic bacteria can be controlled effectively by using Ciprofloxacin and Levofloxacin in the case of mastitis in cattle and buffaloes in Bangladesh. [J Adv Vet Anim Res 2016; 3(1.000): 62-67]

Objective: This study was constructed to build up the normal dimensions of the digestive tract of domestic Rabbit (Oryctolagus cuniculus).Materials and methods: Five rabbits of both sexes were used in this study. After dissection of the rabbits, the exact positions of different parts of the digestive tract (i.e., esophagus, stomach, small intestine, large intestine) were measured using Metric rule, thread, electronic and normal balance.Results: The mean lengths of the small intestine and large intestine were 169.53±21.65 and 132.3±17.42 cm, respectively, and weight of the whole digestive tract was 263.60±56.80 gm. The mean lengths and mean diameter of esophagus, duodenum, jejunum, ileum, cecum, colon and rectum were 9.62±1.64, 41.26±4.06, 106.60±14.64, 21.64±46.32, 41.14±2.82, 83.16±13.74 and 8.0±1.08 cm and 1.16±0.12, 1.71±0.11, 1.70±0.09, 1.73±0.05, 5.47±0.15, 3.36±0.16 and 2.81±0.24 cm, respectively.Conclusion: These results can be considered as a baseline study that may assist in disease diagnosis and clinical works with rabbits.http://doi.org/10.5455/javar.2016.c144

Objective: This study was constructed to build up the normal dimensions of the digestive tract of domestic Rabbit (Oryctolagus cuniculus). Materials and methods: Five rabbits of both sexes were used in this study. After dissection of the rabbits, the exact positions of different parts of the digestive tract (i.e., esophagus, stomach, small intestine, large intestine) were measured using Metric rule, thread, electronic and normal balance. Results: The mean lengths of the small intestine and large intestine were 169.53+/-21.65 and 132.3+/-17.42 cm, respectively, and weight of the whole digestive tract was 263.60+/-56.80 gm. The mean lengths and mean diameter of esophagus, duodenum, jejunum, ileum, cecum, colon and rectum were 9.62+/-1.64, 41.26+/-4.06, 106.60+/-14.64, 21.64+/-46.32, 41.14+/-2.82, 83.16+/-13.74 and 8.0+/-1.08 cm and 1.16+/-0.12, 1.71+/-0.11, 1.70+/-0.09, 1.73+/-0.05, 5.47+/-0.15, 3.36+/-0.16 and 2.81+/-0.24 cm, respectively. Conclusion: These results can be considered as a baseline study that may assist in disease diagnosis and clinical works with rabbits. [J Adv Vet Anim Res 2016; 3(2.000): 145-151]

Objective: An attempt was undertaken for the detection and characterization of Avibacterium paragallinarum from clinically sick broiler chickens during field outbreaks.Materials and methods: Nasal and ocular discharges (n=6), tracheal swab (n=6), tracheal washing (n=4) and infraorbital sinus exudates (n=4) were collected aseptically from broiler chickens (n=10). To isolate A. paragallinarum, the clinical samples were cultured onto blood agar and chocolate agar enriched with Nicotinamide Adenine Dinucleotide (NAD) and feeder organism (Staphylococcus aureus). Identification of A. paragallinarum was performed by Gram staining reaction, sugar fermentation profiles using five basic sugars (Dextrose, Maltose, Sucrose, Lactose and Mannitol) and biochemical tests (Indole, Voges Proskauer and Methyl red tests). Antibiogram of the bacterial isolates of infected chicken was performed against five antibiotics namely Ciprofloxacin, Azithromycin, Gentamicin, Ampicillin and Cefalexin using disk diffusion method.Results: Results of colonial morphology, Gram staining reaction, sugar fermentation and biochemical tests confirmed one isolate as A. paragallinarum. The overall prevalence of IC in broiler chicken was 10% (1 of 10). This isolate was found to be sensitive to Ciprofloxacin, Azithroycin and Gentamicin and resistant to Ampicillin and Cefalexin.Conclusion: This is the first report of detection of A. paragallinarum from broiler chicken in Bangladesh.http://doi.org/10.5455/javar.2016.c149

Objective: An attempt was undertaken for the detection and characterization of Avibacterium paragallinarum from clinically sick broiler chickens during field outbreaks. Materials and methods: Nasal and ocular discharges (n=6), tracheal swab (n=6), tracheal washing (n=4) and infraorbital sinus exudates (n=4) were collected aseptically from broiler chickens (n=10). To isolate A. paragallinarum, the clinical samples were cultured onto blood agar and chocolate agar enriched with Nicotinamide Adenine Dinucleotide (NAD) and feeder organism (Staphylococcus aureus). Identification of A. paragallinarum was performed by Gram staining reaction, sugar fermentation profiles using five basic sugars (Dextrose, Maltose, Sucrose, Lactose and Mannitol) and biochemical tests (Indole, Voges Proskauer and Methyl red tests). Antibiogram of the bacterial isolates of infected chicken was performed against five antibiotics namely Ciprofloxacin, Azithromycin, Gentamicin, Ampicillin and Cefalexin using disk diffusion method. Results: Results of colonial morphology, Gram staining reaction, sugar fermentation and biochemical tests confirmed one isolate as A. paragallinarum. The overall prevalence of IC in broiler chicken was 10% (1 of 10). This isolate was found to be sensitive to Ciprofloxacin, Azithroycin and Gentamicin and resistant to Ampicillin and Cefalexin. Conclusion: This is the first report of detection of A. paragallinarum from broiler chicken in Bangladesh. [J Adv Vet Anim Res 2016; 3(2.000): 173-177]

Objective: This study was aimed at elucidating the association between Para influenza virus 3 (PIV3) and respiratory infections in domestic ruminants in different areas of Sudan.Materials and methods: During 2010-2013, five hundred sixty five lung samples with signs of pneumonia were collected from cattle (n=226), sheep (n=316) and goats (n=23) from slaughter houses in different areas in Sudan. The existence of PIV3 antigen was screened in the collected samples using ELISA and Fluorescent antibody technique. PIV3 genome was detected by PCR, and sequence analysis was conducted.Results: Positive results were found in 29 (12.8%) cattle, 31 (9.8%) sheep and 11 (47.8%) goat samples. All the studied areas showed positive results. Highest prevalence (66.7%) was detected in the sheep and goats in Khartoum, followed by in goats in Nyala (33.3%) at western Sudan. Sequence analyses of PIV3 of different regions of Sudan indicated that these were similar in sequence and length. The BLAST analysis indicated that the test sequences were closely related to the available annotated sequences at the GenBank. All these sequences matched with Bovine parainfluenza virus 3 except two those were matching with Swine parainfluenza virus 3.Conclusion: The results prove the existence of PIV3 infection in cattle, sheep and goats in the studied areas in Sudan and suggest its possible role in the respiratory infections. Genetic analysis indicate that the virus is mostly similar with bovine PIV3.http://doi.org/10.5455/javar.2016.c160

Objective: This study was aimed at elucidating the association between Para influenza virus 3 (PIV3) and respiratory infections in domestic ruminants in different areas of Sudan. Materials and methods: During 2010-2013, five hundred sixty five lung samples with signs of pneumonia were collected from cattle (n=226), sheep (n=316) and goats (n=23) from slaughter houses in different areas in Sudan. The existence of PIV3 antigen was screened in the collected samples using ELISA and Fluorescent antibody technique. PIV3 genome was detected by PCR, and sequence analysis was conducted. Results: Positive results were found in 29 (12.8%) cattle, 31 (9.8%) sheep and 11 (47.8%) goat samples. All the studied areas showed positive results. Highest prevalence (66.7%) was detected in the sheep and goats in Khartoum, followed by in goats in Nyala (33.3%) at western Sudan. Sequence analyses of PIV3 of different regions of Sudan indicated that these were similar in sequence and length. The BLAST analysis indicated that the test sequences were closely related to the available annotated sequences at the GenBank. All these sequences matched with Bovine parainfluenza virus 3 except two those were matching with Swine parainfluenza virus 3. Conclusion: The results prove the existence of PIV3 infection in cattle, sheep and goats in the studied areas in Sudan and suggest its possible role in the respiratory infections. Genetic analysis indicate that the virus is mostly similar with bovine PIV3. [J Adv Vet Anim Res 2016; 3(3.000): 236-241]