Duck plague (DP) is the most feared duck disease in the world. For isolation, identification, molecular detection and characterization of DP virus (DPV), a total of 94 samples were collected from commercial farms (n=6) and households (n=13) from Rajshahi (n=37), Netrokona (n=35) and Mymensingh (n=22) districts of Bangladesh. The samples were processed and inoculated into 11-13 days old embryonated duck eggs for virus propagation. Virus was identified using agar gel immunodiffusion test (AGIT) and passive hemagglutination (PHA) test, and was confirmed by polymerase chain reaction (PCR) targeting DNA polymerase and gC genes, followed by sequencing. Pathogenicity tests were performed using duck embryos, ducklings and ducks. Among the 94 samples, 17 isolates were confirmed as DPV by PCR amplification of partial DNA polymerase (446-bp) and gC genes (78-bp), respectively. One of the isolates (Anatid herpes 1 BAU DMH) was sequenced and found to be closely related with a Chinese variant of DPV (GenBank: JQ647509.1). Thus, we assume that both Bangladeshi and Chinese isolates of DPV may have a common ancestor.http://dx.doi.org/10.5455/javar.2015.b90

Duck plague (DP) is the most feared duck disease in the world. For isolation, identification, molecular detection and characterization of DP virus (DPV), a total of 94 samples were collected from commercial farms (n=6) and households (n=13) from Rajshahi (n=37), Netrokona (n=35) and Mymensingh (n=22) districts of Bangladesh. The samples were processed and inoculated into 11-13 days old embryonated duck eggs for virus propagation. Virus was identified using agar gel immunodiffusion test (AGIT) and passive hemagglutination (PHA) test, and was confirmed by polymerase chain reaction (PCR) targeting DNA polymerase and gC genes, followed by sequencing. Pathogenicity tests were performed using duck embryos, ducklings and ducks. Among the 94 samples, 17 isolates were confirmed as DPV by PCR amplification of partial DNA polymerase (446-bp) and gC genes (78-bp), respectively. One of the isolates (Anatid herpes 1 BAU DMH) was sequenced and found to be closely related with a Chinese variant of DPV (GenBank: JQ647509.1). Thus, we assume that both Bangladeshi and Chinese isolates of DPV may have a common ancestor. [J Adv Vet Anim Res 2015; 2(3.000): 296-303]

The objective of this study was to evaluate the effect of exogenous fibrolytic enzyme (EFE) and/or live yeast culture supplementation in total mixed ration (TMR) on rumen fermentation patterns in buffalo. For this, four adult buffalo bulls weighing 377.05±43.36 kg were randomly allotted to four dietary treatments viz., TMR containing R:C ratio of 70:30 (T1), T1 supplemented with EFE at 15 g/animal/day (T2), T1 supplemented with live yeast culture at 10 g/animal/day (T3), and T1 supplemented with EFEs at 15 g/animal/day and live yeast culture at 10 g/animal/day (T4). Rumen liquor from the fistulated animals was collected at 0, 1, 2, 4, 6 and 8 h post-feeding, and was analyzed. This study revealed that rumen pH values were highest at 0 h, and were declined to minimum by 4 h post-feeding, while total volatile fatty acids (TVFA), ammonia nitrogen (NH3-N), and nitrogen (N) fractions reached to peak at 4 h post-feeding, and later followed a decreasing trend in all the treatments. Supplementation of EFE in TMR (T2) had no effect (P>0.05) on rumen pH and food and protozoal N concentration, while it influenced to increase (P<0.01) the concentration of TVFA, NH3-N and other N fractions as compared to the T1. Yeast culture supplementation in TMR (T3) increased (P<0.01) rumen pH, TVFA, NH3-N, total N, TCA-insoluble N and residual N. However, no effect (P>0.05) on food and protozoal N in buffalo bulls was found. This study indicated that, supplementation of EFE and/or live yeast culture in TMR (T4) increased (P<0.01) the rumen pH, TVFA, NH3-N and N fractions in buffalo bulls as compared to the control group. Therefore, it is concluded that supplementation of EFE and/or live yeast culture in TMR can increase the concentration of rumen metabolites in buffalo bulls.  http://dx.doi.org/10.5455/javar.2015.b98

The objective of this study was to evaluate the effect of exogenous fibrolytic enzyme (EFE) and/or live yeast culture supplementation in total mixed ration (TMR) on rumen fermentation patterns in buffalo. For this, four adult buffalo bulls weighing 377.05+/-43.36 kg were randomly allotted to four dietary treatments viz., TMR containing R:C ratio of 70:30 (T1), T1 supplemented with EFE at 15 g/animal/day (T2), T1 supplemented with live yeast culture at 10 g/animal/day (T3), and T1 supplemented with EFEs at 15 g/animal/day and live yeast culture at 10 g/animal/day (T4). Rumen liquor from the fistulated animals was collected at 0, 1, 2, 4, 6 and 8 h post-feeding, and was analyzed. This study revealed that rumen pH values were highest at 0 h, and were declined to minimum by 4 h post-feeding, while total volatile fatty acids (TVFA), ammonia nitrogen (NH3-N), and nitrogen (N) fractions reached to peak at 4 h post-feeding, and later followed a decreasing trend in all the treatments. Supplementation of EFE in TMR (T2 and not;) had no effect (P>0.05) on rumen pH and food and protozoal N concentration, while it influenced to increase (P<0.01) the concentration of TVFA, NH3-N and other N fractions as compared to the T1. Yeast culture supplementation in TMR (T3) increased (P<0.01) rumen pH, TVFA, NH3-N, total N, TCA-insoluble N and residual N. However, no effect (P>0.05) on food and protozoal N in buffalo bulls was found. This study indicated that, supplementation of EFE and/or live yeast culture in TMR (T4) increased (P<0.01) the rumen pH, TVFA, NH3-N and N fractions in buffalo bulls as compared to the control group. Therefore, it is concluded that supplementation of EFE and/or live yeast culture in TMR can increase the concentration of rumen metabolites in buffalo bulls. [J Adv Vet Anim Res 2015; 2(3.000): 310-315]

The aim of the present study was morphological and histochemical analysis of the lacrimalgland (LG) in African black ostrich Struthio camelus domesticus in the embryonic and postnatalperiod. Studies were conducted on 50 ostriches aged between the 28th day of incubation until7 months old. Tissue sections were stained with haematoxylin and eosin, Azan trichrome,periodic acid-Schiff, Alcian blue pH 2.5, aldehyde fuchsin and Hale’s dialysed iron. The LGin ostrich was classified as a tubulo-acinar type. The primordia of the lobes were determinedin the LG structure on the 28th day of incubation, whilst the weakly visible lobes with aciniand tubules were observed on the 40th day of incubation. Morphometric studies of the LGshowed steady growth, characterised by an increase in both length and width. Histometricmeasurements of lobe size showed little difference between the first, second and third agegroups, whilst in the fourth age group a marked increase in size of lobes was observed.The study showed that, apart from morphological changes, during the growth of the LGthe character of acid mucopolysaccharides changed. Sulphated acid mucopolysaccharideswere indicated, particularly with aldehyde fuchsin (AF) staining in the fourth age group.The Hale’s dialysed iron (HDI) staining showed a low concentration of carboxylated acidmucopolysaccharides in the first and second age groups and a higher concentration in thethird and fourth age groups. Periodic acid-Schiff staining (PAS)-positive cells were observedin each age group, but only a small number of cells with a weakly PAS-positive reaction weredemonstrated in the first age group.

The aim of the present study was morphological and histochemical analysis of the lacrimalgland (LG) in African black ostrich Struthio camelus domesticus in the embryonic and postnatalperiod. Studies were conducted on 50 ostriches aged between the 28th day of incubation until7 months old. Tissue sections were stained with haematoxylin and eosin, Azan trichrome,periodic acid-Schiff, Alcian blue pH 2.5, aldehyde fuchsin and Hale’s dialysed iron. The LGin ostrich was classified as a tubulo-acinar type. The primordia of the lobes were determinedin the LG structure on the 28th day of incubation, whilst the weakly visible lobes with aciniand tubules were observed on the 40th day of incubation. Morphometric studies of the LGshowed steady growth, characterised by an increase in both length and width. Histometricmeasurements of lobe size showed little difference between the first, second and third agegroups, whilst in the fourth age group a marked increase in size of lobes was observed.The study showed that, apart from morphological changes, during the growth of the LGthe character of acid mucopolysaccharides changed. Sulphated acid mucopolysaccharideswere indicated, particularly with aldehyde fuchsin (AF) staining in the fourth age group.The Hale’s dialysed iron (HDI) staining showed a low concentration of carboxylated acidmucopolysaccharides in the first and second age groups and a higher concentration in thethird and fourth age groups. Periodic acid-Schiff staining (PAS)-positive cells were observedin each age group, but only a small number of cells with a weakly PAS-positive reaction weredemonstrated in the first age group.

This study was conducted to determine the effect of maternally derived antibody (MDA) on live vaccine against infectious bursal disease. A total of 140 chicks selected from vaccinated parent stock were used in this investigation. In a preset vaccination schedule, blood samples were collected to check for the actual effect. It was noticed that on day 1 the chicks contained a high level (6400.54 ± 2993.67) of maternally derived antibody that gradually decreased below a positive level within 21 days (365.86 ± 634.46). It was found that a high level of MDA interferes with the vaccine virus, resulting in no immune response. For better immune response, it is suggested that the chickens should be vaccinated at day 21, as the uniformity of MDA is poor (coefficient of the variation [CV] 30%), and boosted at day 28. Indeed, two vaccinations are necessary to achieve good protection against infectious bursal disease virus of the entire flock.

This study was conducted to determine the effect of maternally derived antibody (MDA) on live vaccine against infectious bursal disease. A total of 140 chicks selected from vaccinated parent stock were used in this investigation. In a preset vaccination schedule, blood samples were collected to check for the actual effect. It was noticed that on day 1 the chicks contained a high level (6400.54 ± 2993.67) of maternally derived antibody that gradually decreased below a positive level within 21 days (365.86 ± 634.46). It was found that a high level of MDA interferes with the vaccine virus, resulting in no immune response. For better immune response, it is suggested that the chickens should be vaccinated at day 21, as the uniformity of MDA is poor (coefficient of the variation [CV] > 30%), and boosted at day 28. Indeed, two vaccinations are necessary to achieve good protection against infectious bursal disease virus of the entire flock.

Eperythrozoonosis is a small ruminant disease caused by the bacterium Mycoplasma ovis (formerly known as Eperythrozoon ovis). Whilst acute infection in sheep may result in an anaemia and ill thrift syndrome, most animals do not develop clinical signs. Molecular methods were used to compare and evaluate the prevalence of infection with M. ovis in sheep and goats in Tunisia. A total of 739 whole blood samples from 573 sheep and 166 goats were tested for the M. ovis 16S rRNA gene using PCR. The overall prevalence was 6.28% ± 0.019 (36/573). Only sheep were infected with M. ovis (p 0.001), and the prevalence was significantly higher in central Tunisia (29.2%) compared with other regions (p 0.05). The prevalence revealed significant differences according to breed and bioclimatic zones (p 0.001). Furthermore, the prevalence in young sheep (35/330; 10.6%) was higher than in adults (1/243; 0.41%) (p 0.001). Only sheep of the Barbarine breed were infected, with a prevalence of 11.8% (p 0.001). This is the first molecular study and genetic characterisation of M. ovis in North African sheep breeds.

Eperythrozoonosis is a small ruminant disease caused by the bacterium Mycoplasma ovis (formerly known as Eperythrozoon ovis). Whilst acute infection in sheep may result in an anaemia and ill thrift syndrome, most animals do not develop clinical signs. Molecular methods were used to compare and evaluate the prevalence of infection with M. ovis in sheep and goats in Tunisia. A total of 739 whole blood samples from 573 sheep and 166 goats were tested for the M. ovis 16S rRNA gene using PCR. The overall prevalence was 6.28% ± 0.019 (36/573). Only sheep were infected with M. ovis (p < 0.001), and the prevalence was significantly higher in central Tunisia (29.2%) compared with other regions (p < 0.05). The prevalence revealed significant differences according to breed and bioclimatic zones (p < 0.001). Furthermore, the prevalence in young sheep (35/330; 10.6%) was higher than in adults (1/243; 0.41%) (p < 0.001). Only sheep of the Barbarine breed were infected, with a prevalence of 11.8% (p < 0.001). This is the first molecular study and genetic characterisation of M. ovis in North African sheep breeds.

Eperythrozoonosis is a small ruminant disease caused by the bacterium Mycoplasma ovis (formerly known as Eperythrozoon ovis). Whilst acute infection in sheep may result in an anaemia and ill thrift syndrome, most animals do not develop clinical signs. Molecular methods were used to compare and evaluate the prevalence of infection with M. ovis in sheep and goats in Tunisia. A total of 739 whole blood samples from 573 sheep and 166 goats were tested for the M. ovis 16S rRNA gene using PCR. The overall prevalence was 6.28% ± 0.019 (36/573). Only sheep were infected with M. ovis (p < 0.001), and the prevalence was significantly higher in central Tunisia (29.2%) compared with other regions (p < 0.05). The prevalence revealed significant differences according to breed and bioclimatic zones (p < 0.001). Furthermore, the prevalence in young sheep (35/330; 10.6%) was higher than in adults (1/243; 0.41%) (p < 0.001). Only sheep of the Barbarine breed were infected, with a prevalence of 11.8% (p < 0.001). This is the first molecular study and genetic characterisation of M. ovis in North African sheep breeds.