Abortifacient pathogens such as bacterial [Brucella spp., Listeria spp., Leptospira interrogans ser., Coxiella burnetii, Campylobacter spp., Anaplasma spp., Chlamydia spp], mycotic [Aspergillus species and Candida species], protozoan [Toxoplasma gondii, Neospora spp.], and viral [Bluetongue virus (BTV), Schmallenberg virus (SBV), Bovine viral Diarrhea Virus (BVDV), and Peste des petits ruminants virus (PPRV)] pathogens are challenges for the productive and reproductive performance of ruminants (cattle, sheep, and goats) globally. No comprehensive report on epidemiology, associated risk factors, or economic burden of these infectious pathogens is available for Nigeria. This review estimated the distribution and burden of abortive pathogens in ruminants in Nigeria for the last twenty-two years (2000-2022). Research articles reporting the detection of any of the above-mentioned abortive pathogens in ready-to-slaughter ruminants (RTSR), sick ruminants (SR), and ruminants with abortive history (RWAH) in Nigeria were accessed using different repositories, including Google Scholar, Proquest, PubMed, ResearchGate and Scopus to determine the prevalence, spatial distribution, and associated risk factors. From a total of 140 articles selected for this review, eight bacterial, four viral, two parasitic, and two mycotic infectious agents were reported for Nigeria. This study reveals a prevalence of 28.2% viral agents, 14.43% bacterial pathogens, 14.24% protozoans, and 28.1% fungal agents in the reported tested samples. Brucellosis was the most often reported among bacterial diseases, followed by leptospirosis and listeriosis. Peste des petits ruminants virus infection was the most common viral disease, followed by bluetongue virus disease. Additionally, two parasitic diseases, neosporosis and toxoplasmosis, and two mycotic diseases, aspergillosis and candidiasis, were reported. In this study, stillbirth and abortion were recorded in 49.2% of sheep with PPRV, 58.95% in goats with Chlamydophila abortus and PPRV, and 6.4% in cattle with Brucella abortus and Histophilus somni infections. Lack of vaccines, open markets, and extensive husbandry systems were among the risk factors associated with different abortive pathogens. This study is a useful tool for researchers and government officers in risk assessment and management of livestock to improve livestock production in Nigeria.

Abortifacient pathogens such as bacterial [Brucella spp., Listeria spp., Leptospira interrogans ser., Coxiella burnetii, Campylobacter spp., Anaplasma spp., Chlamydia spp.], mycotic [Aspergillus spp. and Candida spp.], protozoan [Toxoplasma gondii, Neospora spp.], and viral [Blue tongue virus (BTV), Schmallenberg virus (SBV), Bovine viral diarrhea virus (BVDV), and Peste des petits ruminants virus (PPRV)] pathogens are challenges for the productive and reproductive performance of ruminants (cattle, sheep, and goats) globally. No comprehensive report on epidemiology, associated risk factors, or economic burden of these infectious pathogens is available for Nigeria. This review estimated the distribution and burden of abortive pathogens in ruminants in Nigeria for the last twenty-two years (2000-2022). Research articles reporting the detection of any of the above-mentioned abortive pathogens in ready-to-slaughter ruminants (RTSR), sick ruminants (SR), and ruminants with abortive history (RWAH) in Nigeria were accessed using different repositories, including Google Scholar, Proquest, PubMed, ResearchGate and Scopus to determine the prevalence, spatial distribution, and associated risk factors. From a total of 140 articles selected for this review, eight bacterial, four viral, two parasitic, and two mycotic infectious agents were reported for Nigeria. This study reveals a prevalence of 28.2% viral agents, 14.43% bacterial pathogens, 14.24% protozoans, and 28.1% fungal agents in the reported tested samples. Brucellosis was the most often reported among bacterial diseases, followed by leptospirosis and listeriosis. PPRV infection was the most common viral disease, followed by BTV. Additionally, two parasitic diseases, neosporosis and toxoplasmosis, and two mycotic diseases, aspergillosis and candidiasis, were reported. In this study, stillbirth and abortion were recorded in 49.2% of sheep with PPRV, 58.95% in goats with Chlamydophila abortus and PPRV, and 6.4% in cattle with Brucella abortus and Histophilus somni infections. Lack of vaccines, open markets, and extensive husbandry systems were among the risk factors associated with different abortive pathogens. This study is a useful tool for researchers and government officers in risk assessment and management of livestock to improve livestock production in Nigeria

The facultative intracellular pathogen Brucella and the free-living bacteria Ochrobactrum are both α-proteobacteria and very close to each other. A group of researchers recently clustered Ochrobactrum strains into the genus Brucella according to a BLAST distance approach. Thus, we performed a deeper comparative genetic analysis for eleven Ochrobactrum strains and twelve different Brucella isolates to demonstrate important differences between these bacteria. In addition to the clear differences between Brucella and Ochrobactrum, like the differences in genes contents, and different genome sizes, the Brucella-specific gene bscp31 was not found in Ochrobactrum, as well as other important Brucella-specific proteins and virulence factors. Differences in antimicrobial resistance genes content and the presence or absence of plasmids were obvious between Brucella and Ochrobactrum spp. Genome alignment of Brucella spp. and Ochrobactrum spp. revealed a genome similarity of 85.7% maximum, whereas all analyzed Brucella spp. in this study had a similarity of 97.6-99.9%, and all compared Ochrobactrum spp. 82.6-98.0%. Because of these facts mentioned in this work, Brucella and Ochrobactrum should be considered separate genera.

intracellular pathogen Brucella and the free-living bacteria Ochrobactrum are both α-proteobacteria and very close to each other. A group of researchers recently clustered Ochrobactrum strains into the genus Brucella according to a BLAST distance approach. Thus, we performed a deeper comparative genetic analysis for eleven Ochrobactrum strains and twelve different Brucella isolates to demonstrate important differences between these bacteria. In addition to the clear differences between Brucella and Ochrobactrum, like the differences in genes contents, and different genome sizes, the Brucella-specific gene bscp31 was not found in Ochrobactrum, as well as other important Brucella-specific proteins and virulence factors. Differences in antimicrobial resistance genes content and the presence or absence of plasmids were obvious between Brucella and Ochrobactrum spp. Genome alignment of Brucella spp. and Ochrobactrum spp. revealed a genome similarity of 85.7% maximum, whereas all analyzed Brucella spp. in this study had a similarity of 97.6-99.9%, and all compared Ochrobactrum spp. 82.6-98.0%. Because of these facts mentioned in this work, Brucella and Ochrobactrum should be considered separate genera

This research aimed to determine the accuracy of the progesterone test kit for milk and blood for early pregnancy diagnosis in Ettawa cross goats (PE). Five lactating PE goats were used in this study and were synchronized with PGF2 intramuscularly. The result is that all goats showed a sign of estrus. Four goats were mated naturally, while one other was not mated. The determination of day 0 was when the females were standing heat. The early pregnancy diagnosis using dairy cow test strips was performed 18-22 days after mating or post-estrus. The accuracy of the diagnosis was confirmed by ultrasound on day 35 after mating/post estrus. Diagnosis using the milk progesterone kit showed negative results for five days of examination in all goats, whereas using the blood progesterone kit showed positive results in four goats. When confirmed, the ultrasound showed that one goat was not pregnant, and four other goats were pregnant. It can be concluded that the pregnancy test strip kits containing progesterone are effective in diagnosing early pregnancy in PE goats with high accuracy in blood samples (100%) despite low accuracy in milk samples (20%).

This research aimed to determine the accuracy of the progesterone test kit for milk and blood as means of early pregnancy diagnosis in Ettawa cross goats (PE). Five lactating PE goats were used in this study and were synchronized with PGF2α intramuscularly. The result is that all goats showed a sigh of estrus. Four goats were mated naturally, while one other was not mated. The determination of day-0 was when the females were standing heat. Early pregnancy diagnosis using dairy cow test strips performed 18-22 days after mating or post-estrus. The accuracy of the diagnosis was confirmed by ultrasound examination on day 35 after mating/post estrus. Diagnosis using the milk progesterone kit showed negative results for five days of examination in all goats, whereas using the blood progesterone kit showed positive results in four goats. When confirmed, using ultrasound showed one goat was diagnosed as not pregnant, and four other goats were diagnosed pregnant. It can be concluded that the use of progesterone dairy cow pregnancy test strip kits is effectively used to diagnose early pregnancy in PE goats with high accuracy in blood samples (100%) and low accuracy in milk samples (20%).

This study aims to determine the histomorphometry of the small intestine of turkeys (Meleagris gallopavo) at different age levels. This study used a completely randomized design. This study used 18 male turkeys, divided into 3 groups of ages 8, 16, and 24 weeks, each group comprising 6 turkeys. The necropsied turkey's small intestine was taken into histological preparations and stained with haematoxylin-eosin (HE). The results showed that the histological picture of the small intestine layer of turkeys at different age levels consisted of four layers: tunica mucosa, tunica submucosa, tunica muscular, and tunica serosa. Histomorphometrically, there was an increase in the thickness of all layers of the small intestine from 8 and 16 weeks of age (P0.05), and the height of the intestinal villi increased in all parts of the small intestine at 8, 16, and 24 weeks of age (P0.05). In conclusion, with histomorphometric measurements, it can be seen that there are differences in the three age groups.

This study aims to determine the histomorphometry of the small intestine of turkeys (Meleagris gallopavo) at different age levels. This study used a completely randomized design. This study used 18 male turkeys, divided into 3 groups of ages 8, 16, and 24 weeks, each group comprising 6 turkeys. The necropsied turkey's small intestine was taken into histological preparations and stained with haematoxylin-eosin (HE). The results showed that the histological picture of the small intestine layer of turkeys at different age levels consisted of four layers: tunica mucosa, tunica submucosa, tunica muscular, and tunica serosa. Histomorphometrically, there was an increase in the thickness of all layers of the small intestine from 8 and 16 weeks of age (P0.05), and the height of the intestinal villi increased in all parts of the small intestine at 8, 16 and 24 weeks of age (P0.05 ). In conclusion, with histomorphometric measurements, it can be seen that there are differences in the three age groups.

One of the fishery products that decomposes very rapidly is shrimp. Utilizing natural preservatives, such asAverrhoa bilimbiL. juice, is one method for maintaining the quality of food ingredients. This study aims to determine the effect of addingA. bilimbiL. juice with different concentrations and soaking times on vannamei shrimp decay. In this study, an experimental laboratory was used to examine decay using the Postma and H2S tests. As much as 500 g of vannamei shrimp were divided into four treatment groups and two repetitions, with 5 g of each sample soaked inA. bilimbiL. juice with concentrations of 0%, 2.5%, 5%, 7.5%, and 10% for 0, 3, 6, and 9 hours. Early decay was observed at 0 and 3 hours after soaking vannamei shrimp in solutions with concentrations of 0%, 2.5%, 5%, 7.5%, and 10%. At concentrations of 5%, 7.5%, and 10%, there was no initial decay after soaking vannamei shrimp for six hours at a concentration of 0% and 2.5%. During 9 hours of soaking at concentrations of 0%, 2.5%, and 5%, initial decay occurred, whereas there was no initial decay at concentrations of 7.5% and 10%. The conclusion of this research isA. bilimbiL. juice with concentrations of 7.5% and 10% for 6 and 9 hours inhibits the decomposition of vannamei shrimp.

One of the fishery products that decomposes very rapidly is shrimp. Utilizing natural preservatives, such as Averrhoa bilimbi L. juice, is one method for maintaining the quality of food ingredients. This study aims to determine the effect of adding A. bilimbi L. juice with different concentrations and soaking times on vannamei shrimp decay. In this study, an experimental laboratory was used to examine decay using the Postma and H2S tests. As much as 500 g of vannamei shrimp were divided into four treatment groups and two repetitions, with 5 g of each sample soaked in A. bilimbi L. juice with concentrations of 0%, 2.5%, 5%, 7.5%, and 10% for 0, 3, 6, and 9 hours. Early decay was observed at 0 and 3 hours after soaking vannamei shrimp in solutions with concentrations of 0%, 2.5%, 5%, 7.5%, and 10%. At concentrations of 5%, 7.5%, and 10%, there was no initial decay after soaking vannamei shrimp for six hours at a concentration of 0% and 2.5%. During 9 hours of soaking at concentrations of 0%, 2.5%, and 5%, initial decay occurred, whereas there was no initial decay at concentrations of 7.5% and 10%. The conclusion of this research is A. bilimbi L. juice with concentrations of 7.5% and 10% for 6 and 9 hours inhibits the decomposition of vannamei shrimp.

The impact of free radicals on testicular Leydig cells can result in the disruption of male reproductive health. The present study aimed to evaluate the effects of a high-fat diet on Leydig cells and the potential of kepok banana peel extract as a medication to mitigate these effects. In total of 20 adult male Wistar rats were assigned to five groups and treated with standard feed (P1), high-fat feed (P2), high-fat feed with simvastatin (P3), and high-fat feed with banana peel extract at doses of 100 and 200 mg/kg BW (P4 and P5). After 60 days of treatment, the number of Leydig cells was determined using HE staining methods. Data were analyzed using an One Way ANOVA test. The results showed that the administration of 100 mg/kg BW of kepok banana peel extract (P4) was able to maintain the number of Leydig cells and counteract the negative effects of a high-fat diet. These findings suggest that kepok banana peel extract may have the potential as a herbal medicine for supporting male reproductive health.

The impact of free radicals on testicular Leydig cells can result in the disruption of male reproductive health. The present study aimed to evaluate the effects of a high-fat diet on Leydig cells and the potential of kepok banana peel extract as a medication to mitigate these effects. In total of 20 adult male Wistar rats were assigned to five groups and treated with standard feed (P1), high-fat feed (P2), high-fat feed with simvastatin (P3), and high-fat feed with banana peel extract at doses of 100 and 200 mg/kg BW (P4 and P5). After 60 days of treatment, the number of Leydig cells was determined using HE staining methods. Data were analyzed using an One Way ANOVA test. The results showed that the administration of 100 mg/kg BW of kepok banana peel extract (P4) was able to maintain the number of Leydig cells and counteract the negative effects of a high-fat diet. These findings suggest that kepok banana peel extract may have the potential as a herbal medicine for supporting male reproductive health.