Positive Goats Research Articles

Cattle, sheep, and goat humoral immune responses against SARS-CoV-2

Following the emergence of SARS-CoV-2 in late 2019, several species of domestic and wild animals have been found to be susceptible to SARS-CoV-2 infection through experimental inoculation and animal surveillance activities. Detection of SARS-CoV-2 specific antibodies in animals is an important surveillance tool since viral shedding in animals can only be detected for a short period of time. In this study, convenience serum samples were collected from 691 cattle, 698 sheep, and 707 goats from several regions in the United States, between 2019 to 2022. The samples were evaluated for the presence of SARS-CoV-2 specific antibodies using two commercial enzyme-linked immunosorbent assays (ELISA); one based on the inhibition of the SARS-CoV-2 receptor-binding domain (sVNT) and the other based on the nucleocapsid protein (N-ELISA) of SARS-CoV-2. Positive samples from the sVNT were additionally evaluated using a conventional virus neutralization test (VNT) employing the Wuhan-like SARS-CoV-2 USA/WA1/2020 isolate. Our results indicate that ∼1% (6/691) of cattle, ∼2% (13/698) of sheep, and ∼2.5% (18/707) of goat serum samples were positive when using the sVNT, whereas ∼4% of cattle (25/691) and sheep (27/698), and 2.5% (18/707) of goat serum samples tested positive with the N-ELISA. None of the sVNT positive cattle, sheep, or goat serum samples had detectable neutralizing antibody activity (<1:8) against the SARS-CoV-2 USA/WA1/2020 isolate by the VNT. Our results indicate low seropositivity in cattle, sheep, and goats in the U.S., indicating the importance to continue monitoring for SARS-CoV-2 prevalence in animal species that are in close contact with humans.

A pilot study on the epidemiology, diagnosis and characterization of Echinococcus granulosus sensu lato in sheep, goats and dogs in Siirt province of Türkiye revealed remarkable adaptation of Echinococcus canadensis (G6/G7) in goats

Cystic echinococcosis (CE), caused by Echinococcus granulosus sensu lato (s.l.), represents one of the most significant zoonotic diseases globally, affecting both humans and animals. The objective of this study was to ascertain the prevalence of E. granulosus sensu lato in sheep and goats in a pilot region with a one-year slaughterhouse follow-up period and to determine the genetic differences and haplotypes among sheep, goat, and dog isolates. To this end, the prevalence of CE cysts was determined by monitoring the slaughter of sheep and goats at least three days a week at a slaughterhouse in the Siirt province of Türkiye during 2023. Additionally, faecal samples were collected from stray dogs and analysed using both flotation and molecular techniques. The presence of CE cysts was identified in 569 (11.12 %) of the 5119 sheep and 66 (2.31 %) of the 2860 goats after slaughtering. The highest positivity was observed in November (20.39 %), while the lowest was recorded in July (5.62 %). Of the sheep that detected positive, 25 (4.39 %) were less than one year old, while 544 (95.61 %) were older than one year. Of the infected sheep, 26 (4.57 %) were male and 543 (95.43 %) were female. 204 (35.85 %) sheep exhibited fluid-filled CE cysts, 338 (59.40 %) displayed calcification, and 27 (4.75 %) demonstrated the presence of newly developed cysts. The highest positivity was observed in December (5.83 %), while the lowest was recorded in May (0.62 %) in goats. Of the positive goats, two (3 %) were less than one year old, while the remaining 64 (97 %) were older than one year. Of the goats infected with CE cysts, 10 (15.15 %) were male and 56 (84.85 %) were female. Of the cysts, 56.1 % were fluid-filled, 42.4 % were calcified and 1.5 % were newly developed. Following DNA sequence analysis of CE cyst isolates obtained from the slaughterhouse, all 61 sheep sequences were identified as E. granulosus s.s. (G1/G3). Of the 13 goat isolates, seven were identified as E. granulosus s.s. (G1/G3), while the remaining six were classified as E. canadensis (G6/G7). The centrifugal flotation method was employed to detect the presence of Isospora spp. oocysts in eight dogs, Toxocara canis and hookworm eggs in three dogs each, and Dipyllidium caninum eggs in one dog. A total of 54 dog faeces were examined. No Taeniid eggs were observed in any of the dogs. Following PCR analysis of the mt-CO1 gene region in the dog faecal samples, four samples were positive for a 875 bp band. Only one of these bands was suitable for sequence analysis, which confirmed it as E. granulosus s.s. (G1/G3).

Serological evidence of Maedi-Visna and Caprine Arthritis Encephalitis in sheep and goats in the Korça region in Albania

Lentiviruses infect small ruminants and cause similar but different two significant diseases: Maedi-Visna in sheep and Caprine Arthritis Encephalitis in goats. In the current study, 91 of 413 adult sheep and goats from the Korça region tested positive for small ruminant lentiviruses. Furthermore, 11 of the 25 small ruminant herds have at least one positive animal for small ruminant lentiviruses. The overall observed herd prevalence was 44.0% (95% CI: 29–59) for both diseases, 38.6% (95% CI: 18.6-55.1) for Maedi-Visna in sheep, and 66.7% (95% CI: 43.1-90.2) for Caprine Arthritis Encephalitis in goats. The average observed prevalence rate ranges from 20% to 82.9% (95% CI: 12–89.2) within positive goat’s herds, while within sheep-positive herds, it varies from 23.1% to 57.1% (95% CI: 11.7–70.4). There was a positive correlation between seroprevalence rate and animal species; goats seem to have an odd 2.36 (OR 95% CI: 1.48-3.76) higher than sheep to test positive in ELISA. Other risk factors, such as farm size, indoor versus outdoor rearing, and close farm biosecurity, may play a role in disease transmission between and within small ruminant animals’ herds. This is the first study on the prevalence of Maedi-Visna infection in sheep and one of the few published Caprine Arthritis Encephalitis studies in Albania. These findings support the presence of Small Ruminant Lentiviruses (SRLV) in the Korça district emphasize the need for monitoring and controlling SRLV infection in sheep and goats. According to the study’s conclusions, a yearly monitoring program is essential and must be developed in the future to keep the disease under control. This initiative aims to help owners understand SRLV and the need to raise seronegative animals

Two Years after Coxiella burnetii Detection: Pathogen Shedding and Phase-Specific Antibody Response in Three Dairy Goat Herds.

The infection dynamics of Coxiella (C.) burnetii were investigated in three dairy goat herds (A, B, and C) 2 years after the first pathogen detection. A total of 28 and 29 goats from herds A and B, and 35 goats from herd C, were examined. Sera were analyzed on three sampling dates using phase-specific serology. Pathogen shedding was assessed using post-partum vaginal swabs and monthly bulk tank milk (BTM) samples. Dust samples from a barn and milking parlor were also collected monthly. These samples were analyzed with PCR (target IS1111). In herd A, individual animals tested seropositive, while vaginal swabs, BTM, and most dust samples tested negative. Herds B and C exhibited high IgG phase I activity, indicating a past infection. In herd B, approximately two-thirds of the goats shed C. burnetii with vaginal mucus, and irregular positive results were obtained from BTM. Herd C had two positive goats based on vaginal swabs, and BTM tested positive once. Dust samples from herds B and C contained C. burnetii DNA, with higher quantities typically found in samples from the milking parlor. This study highlights the different infection dynamics in three unvaccinated dairy goat herds and the potential use of dust samples as a supportive tool to detect C. burnetii at the herd level.

Multi-omics in vitro study of the salivary modulation of the goat rumen microbiome.

Ruminants are able to produce large quantities of saliva which enter into the rumen and salivary components exert different physiological functions. Although previous research has indicated that salivary immunoglobulins can partially modulate the rumen microbial activity, the role of the salivary components other than ions on the rumen microbial ecosystem has not been thoroughly investigated in ruminants. To investigate this modulatory activity, a total of 16 semi-continuous in vitro cultures with oats hay and concentrate were used to incubate rumen fluid from four donor goats with autoclaved saliva (AUT) as negative control, saliva from the same rumen fluid donor (OWN) as positive control, and either goat (GOAT) or sheep (SHEEP) saliva as experimental interventions. Fermentation was monitored throughout 7days of incubation and the microbiome and metabolome were analysed at the end of this incubation by Next-Generation sequencing and liquid chromatography coupled with mass spectrometry, respectively. Characterisation of the proteome and metabolome of the different salivas used for the incubation showed a high inter-animal variability in terms of metabolites and proteins, including immunoglobulins. Incubation with AUT saliva promoted lower fermentative activity in terms of gas production (-9.4%) and highly divergent prokaryotic community in comparison with other treatments (OWN, GOAT and SHEEP) suggesting a modulatory effect derived from the presence of bioactive salivary components. Microbial alpha-diversity at amplicon sequence variant (ASV) level was unaffected by treatment. However, some differences were found in the microbial communities across treatments, which were mostly caused by a greater abundance of Proteobacteria and Rikenellacea in the AUT treatment and lower of Prevotellaceae. These bacteria, which are key in the rumen metabolism, had greater abundances in GOAT and SHEEP treatments. Incubation with GOAT saliva led to a lower protozoal concentration and propionate molar proportion indicating a capacity to modulate the rumen microbial ecosystem. The metabolomics analysis showed that the AUT samples were clustered apart from the rest indicating different metabolic pathways were promoted in this treatment. These results suggest that specific salivary components contribute to host-associated role in selecting the rumen commensal microbiota and its activity. These findings could open the possibility of developing new strategies to modulate the saliva composition as a way to manipulate the rumen function and activity.

Oxidative Stress in Goats with Peste des Petits Ruminants (PPR)

Background: Goats in India are endangered by various disease outbreaks. A limited number of disease conditions in goats have been investigated with regard to the effect of oxidative stress. Oxidative stress is an active field of research implicated in numerous disease processes including sepsis, enteritis, pneumonia, mastitis, joint diseases etc. The present work was undertaken to study the oxidative stress contributing pathological changes in naturally occurring Peste des petits ruminant virus (PPRV) in goats of Jabalpur region. Methods: A total of 30 positive PPR samples (19 plasma and 11 lung tissues) were processed for oxidative stress assessment by oxidative stress markers malondialdehyde (MDA) and glutathione (GSH). The oxidative stress was revealed among 30 PPR positive goats when compared with 10 healthy animals. Necropsy examination was conducted to observed gross pathology and lung tissues were collected for histopathological examination. Result: Oxidative stress was observed with decreased GSH and increased MDA concentration among PPRV positive goats in plasma and in lung tissues respectively. Nineteen PPR positive goats revealed different degree of clinical signs and were devided into three groups viz group I mild, group II moderate and group III severe. Grossly, eleven positive goat carcasses revealed pneumonic lesions. Microscopically, lung sections revealed broncho-interstitial pneumonia. These findings are suggestive of oxidative stress induces pathological changes and lead to dehydration and death of goats.

Clinicopathological and Sero-Molecular Detection of Mycoplasma capricolum subsp. capripneumoniae in Goats in Southern Areas of Pakistan.

Contagious caprine pleuropneumonia (CCPP) is a highly fatal infectious disease of goats, caused by Mycoplasma capricolum subsp. capripneumoniae (Mccp). This disease is causing huge economic losses to the goat industry in Pakistan. However, little is known about the epidemiology of CCPP, especially in the hard areas of Khyber Pakhtunkhwa (KP), Pakistan, despite having a huge population of goats. Therefore, this study aimed to elucidate sero-molecular epidemiology and pathology associated with Mccp infection in goats in southern areas of KP including Dera Ismail Khan (DI Khan), Bannu, Karak, and Kohat. A total of 200 (50 from each area) serum samples were collected from clinically infected goats, whereas 600 various samples (nasal swab n = 50, pleural fluid n = 50, lungs n = 50 at each selected area of study) were collected from live goats showing respiratory clinical signs and dead/slaughter goats having lesions in the lungs/pleura. A commercial competitive ELISA kit confirmed anti-Mccp antibodies in altogether 17% of serum samples, while area-wise seroprevalence was recorded as follows: Kohat, 28%, Bannu, 18%, DI Khan, 14%, and Karak, 8%. Moreover, a total of 5.5% of samples collected from clinically positive live and dead goats for Mccp were found by species-specific PCR, whereas area-wise molecular prevalence of Mccp was found in 3% samples from Kohat, 7.33%, Bannu, 6%, Khan, 5.33%, and Karak, 3.33%. Of 400 clinically examined goats, 242 (60%) had nasal discharge, 207 (51%) had pyrexia, 50.75% (203) had coughing, 48.25% (193) had pneumonia, 23% (92) had lacrimation, 7.75% (31) had pneumonia with lacrimation, and 10 (2.5%) showed all signs. Of the total 200 dead/slaughtered goats, pleural fluid was found in 36 goats and consolidation and red hepatization were observed in 40 and 42 goats, respectively. The present study found the presence of prevailing Mccp strain in the goat population of the study area. The highest prevalence of Mccp was found in collected samples from Kohat by PCR. The highest seroprevalence of Mccp was found in serum samples collected from Kohat by ELISA.

Molecular and Seroprevalence of Toxoplasmosis in Goats' Blood and Milk in Iraq.

Toxoplasmosis is one of the most acute parasitic and zoonotic infections, which causes severe economic losses in animals due to abortion and reproductive problems worldwide. Therefore, this study was conducted in Baghdad province to detect the prevalence of Toxoplasmosis in blood and milk samples of 384 adult female goats using the serological indirect-enzyme-linked immunosorbent assay (iELISA) and the molecular polymerase chain reaction (PCR) test. The positive iELISA results were 20.57% in sera and 5.99% in milk samples. Regarding cross-classification results, the iELISA results revealed that 5.73% of goats were positive by testing both sera and milk samples, 14.32% and 0.26% were positive for testing sera and milk only, respectively, and 79.69% were negative by testing sera and milk. Targeting the B1 gene, the total positive results of the PCR assay showed that 13.92% and 30.43% of blood and milk samples, respectively, were positive at 546bp. Concerning cross-classification results, the total positive goats by testing of both sera and milk was 8.86%, while 5.06% of goats were positive only for testing of blood, and 86.08% were negative for testing of both samples. At the same time, no positive PCR results were detected in milk samples. In conclusion, there is a wide prevalence and incidence of Toxoplasmosis among goats in study areas. Furthermore, studies are essential to detect the parasite in different ages and sexes of goats and other domestic and wild animals using ELISA as a reliable, automated, and rapid test and PCR as a highly confirmative test.

Field evaluation of the tuberculin skin test for the detection of Mycobacterium tuberculosis complex infection in communal goats (Capra hircus) in KwaZulu-Natal, South Africa

In South Africa, animal tuberculosis (TB) control programs predominantly focus on domestic cattle and African buffaloes (Syncerus caffer) despite increasing global reports of tuberculosis in goats (Capra hircus). Left undetected, Mycobacterium tuberculosis complex (MTBC) infected goats may hinder TB eradication efforts in cattle and increase zoonotic risk to humans. Since the publication of animal TB testing guidelines in 2018, prescribing the use of the tuberculin skin test (TST) for goats in South Africa by the Department of Agriculture, Land Reform, and Rural Development (DALRRD), there have been no published reports of any field application of the prescribed test criteria in goat herds. Therefore, this study aimed to evaluate the performance of these DALRRD guidelines using the single intradermal cervical tuberculin test (SICT) and the single intradermal comparative cervical tuberculin test (SICCT). Between October and December 2020, 495 goats from communal pastures of Kwa-Zulu Natal (KZN), where M. bovis infection has been identified in cattle and where cattle and goats cohabitate, were tested using the SICT and SICCT (M. bovis-exposed group). Additionally, 277 goats from a commercial Saanen dairy herd, with no history of M. bovis, were also tested (M. bovis-unexposed group). Estimated apparent prevalence of TST positive goats was determined based on published test interpretation criteria as described by DALRRD. When proportions of test-positive goats were compared between different DALRRD criteria, the ≥ 4 mm cut-off criterion for the SICCT resulted in the lowest proportion of positive results in the presumably uninfected group (1/277 positive in the unexposed group). The apparent prevalence of TB in the exposed group was estimated at 3.0% (95% CI: 1.7–4.9%), which is similar to previous reports of M. bovis prevalence in cattle from this area (6%). The detection of a significantly greater proportion of SICCT positive goats in the M. bovis-exposed group compared to the unexposed group suggests that MTBC infection is present in this population. Further investigations should be undertaken, in conjunction with confirmatory molecular tests, mycobacterial culture, and advanced pathogen sequencing to establish whether MTBC infection in domestic goats is a true under-recognized threat to the eradication of animal TB in South Africa.

A Q fever outbreak on a dairy goat farm did not result in Coxiella burnetii shedding on neighboring sheep farms – An observational study

Q fever is a zoonotic airborne disease caused by the bacterium Coxiella burnetii. Small ruminants shed tremendous amounts of bacteria during abortion or parturition, resulting in high environmental contamination. From January 2018 to April 2018, a Q fever outbreak occurred on a dairy goat farm with 360 does located on a peninsula in the North Sea. The sheep density on the peninsula was high (108.8 sheep per km2 agricultural land). Therefore, epidemiological investigations were conducted to assess the possible C. burnetii transmission from the positive dairy goat farm to the neighboring sheep flocks. For this purpose, vaginal swabs and serum samples were collected from freshly lambed sheep on twelve sheep farms during the lambing season in 2019. These farms were located within a 10 km radius around the outbreak. Additionally, dust samples from one windowsill of each lambing shed were taken to evaluate the environmental contamination. Sera were examined by ELISA, vaginal swabs and dust samples by qPCR (insertion sequence 1111). Data on wind velocity and direction, precipitation, and humidity from the local weather station were included in the assessment. All vaginal swabs tested negative by qPCR. Only in one dust sample from one farm (8.11 km away) was a low amount of C. burnetii DNA (Cq 38.6) detected. In two flocks, seropositive sheep were present [intra-flock prevalence: 4.5 % (0.94 km away), 7.5 % (3.09 km away)]. The prevailing wind directions came from a westerly direction, with an average wind speed of ≥ 5 m/s. During the Q fever outbreak (January to April 2018), the precipitation was at least equal to the 10-year monthly average, and the humidity was above 80 %. Taken together, the Q fever outbreak on the dairy goat farm did probably not spread to the sheep flocks in the proximity. The precipitation and high humidity during the kidding period possibly prevented C. burnetii from spreading and high wind speeds might have a dilution effect. In the future, the pathogen-animal-environment interface has to be taken into account for future Q fever risk assessments, which is in line with the One Health approach.

First molecular confirmation of Coenurus cerebralis in sheep and goats with neurological behaviors in Iraq.

Background and Aim:Coenurus cerebralis is the intermediate stage of the canine cestode, which infect sheep and goats, resulting mainly in neurological signs and causing direct and indirect economic losses. This study aimed to demonstrate the existence of C. cerebralis and to elucidate the role of this parasite in inducing neurological behaviors in sheep and goats.Materials and Methods:On the basis of historical data on neurological signs, we subjected 76 animals (49 sheep and 27 goats) of different ages, sexes, and geographical areas for molecular examination of their blood samples using the polymerase chain reaction assay.Results:Of the 76 animals, 23.68% tested positive for C. cerebralis infection. We found significant increases in infection (p<0.05) in sheep (26.53%) more than in goats (18.52%). Circling movement was prevalent significantly among both C. cerebralis-positive sheep and goats. The Nineveh region had a significant (p<0.05) increase in positive sheep and goats, and the sheep of all study regions were infected significantly (p<0.05) more than were the goats. We found no significant (p>0.05) variation between sheep ages ≥1-3 years and ≥3 years; however, both groups had a significantly (p≤0.043) higher positivity rate than did sheep ages <1 year. The findings of sheep ages <1 year and ≥1-3 years were significantly higher than those of the goats, but not for goats ages ≥3 years. Female sheep and goats showed a significant increase in positivity versus that for the males.Conclusion:To the best of our knowledge, this study is the first report in Iraq targeting detection of C. cerebralis in sheep and goats with neurological behaviors; therefore, additional studies involving different animals in other regions using molecular techniques are needed.

Haemato-biochemical alterations in caprine theileriosis

Theileriosis is an important haemoparasitic disease of goats which causes serious economic losses to farmers. There is a paucity of information on the clinico-haemato-biochemical aspects of caprine theileriosis in Kerala. The present study was undertaken to evaluate the haemato-biochemical alterations associated with clinical cases of caprine theileriosis in twenty five smear positive goats in Thrissur district, Kerala. Major clinical signs observed were anaemia, fever, lymphnode enlargement, anorexia, respiratory distress. Haemato-biochemical analysis revealed macrocytic hypochromic anaemia with low Hb, Volume of Packed Red Cells (VPRC), platelet, Total Erythrocyte Count (TEC) and hyperproteinaemia with hyperglobulinaemia in the affected goats.

Development and Evaluation of an Indirect Capripoxvirus ELISA Based on Truncated P32 Protein Expressed in E. coli.

As notifiable diseases, lumpy skin disease (LSD), sheep pox (SPP), and goat pox (GTP) are associated with a profound effect on cattle, sheep, and goat farming industries. Development of the ELISA method could effectively facilitate serodiagnosis of the infected animals. This study aimed to develop an ELISA system based on the recombinant full-length and truncated P32 protein (Tr.P32) of goat pox virus. The P32 protein was expressed in Rosetta strain of E. coli using pET24a+ vector and evaluated by SDS-PAGE and Western blotting. Then, Tr.P32 was purified by Ni-NTA affinity chromatography under denaturing conditions and used to develop a capripoxvirus-specific ELISA. Checkerboard titration and receiver-operating characteristic (ROC) analysis were used to optimize the ELISA system and determine diagnostic specificity and sensitivity, respectively. The diagnostic potential of the developed ELISA was evaluated using positive and negative control sera collected from goat, sheep, and cattle. Results showed that the expression level of full-length P32 recombinant protein was negligible, while Tr.P32, a ~ 31 kDa recombinant protein, was expressed up to 0.270-0.300 mg/200 mL of culture media. The results of checkerboard titration revealed that 675 ng/well of Tr.P32 antigen and 1:10 dilution of control sera (anti GTPV HIS and healthy goat sera) caused maximum difference in absorbance between positive and negative goat sera. The recombinant Tr.P32 showed good reactions with antibodies against GTP virus (GTPV), SPP virus (SPPV), and LSD virus (LSDV), whereas no cross-reactions with anti-Orf virus antibodies were detected. By comparing with the neutralization index (NI), cut off, diagnostic sensitivity and specificity of the developed indirect-ELISA were estimated, 0.397, 94% and 96.6%, respectively. These findings indicate that the ELISA system based on Tr.P32 protein could potentially be used in sero-surveillance of all capripoxviruses; however, further investigations are required.

Detection of Brucella Abortus in Caprine and Ovine by Real-Time PCR Assay

A molecular research was carried out in the areas of Lahore in order to confirm the existence of B. abortus antigen in Caprine and ovine by utilizing molecular techniques in this study. Small ruminants can be infected with B. abortus (the causative agent of bovine brucellosis), which complicates brucellosis control efforts because most brucellosis control programmes rely on immunological testing rather than genomic testing to determine the specific species circulating in ruminants. Now at this investigation, n = 1270 goat serum samples and n = 770 sheep serum samples were collected, respectively. After already being tested with the Rose Bengal test, all positive specimens were examined to the real-time PCR technique. RBT confirmed brucellosis prevalence of 21.43±0.37% and 18.11±0.12 in caprine and ovine respectively. Out of 230 positive goat samples, real-time PCR found B. abortus in 150 samples (65.21±0.51) in sheep and goats and 118 samples (71.51±0.21%) out of 165 seropositive sheep samples. Brucella abortus infection in small ruminants could be caused by a combination of factors including mixed farming of small and large ruminants, sharing of the same pasture, and the presence of reservoir hosts on a farm, all of which could be risk factors for Brucella species cross-infection in non-species hosts. It has been determined that B. abortus is the causative agent of caprine and ovine brucellosis in the country of Pakistan. Results of this study can be utilised to develop successful brucellosis eradication and control strategies in small ruminants, which can be applied to other animals.

Kejadian mastitis subklinis pada kambing perah Peranakan Etawa di desa Bangelan kecamatan Wonosari kabupaten Malang

Etawa crossbred goat is one species of goat that is raised for milk production. One of the diseases that often occur in dairy livestock is mastitis, in which there is inflammation of the mammary gland. It is common in goat, that mastitis does not show clinical symptoms (subclinical). This research aims to determine the incidence of subclinical mastitis in Etawa crossbred goats in Bangelan village Wonosari district Malang regency. This research involved 25 respondent farms, which are Etawa crossbred dairy goat farms. In this research, subclinical mastitis cases were directly detected using California Mastitis Test (CMT). The results showed that out of 70 samples collected, 41 (58.6%) samples were positive. These CMT positive goats were from 88% of the respondent farms.

Antigenic distribution, pathological changes, antibody response and serological detection in non‐pregnant goats following experimental infection by Brucella melitensis

This study describes the pathological changes, antibody response, isolation and distribution patterns following exposure of non-pregnant goats to live Brucella melitensis. Eighteen healthy adult female goats were divided into two equal groups. Group 1 was infected via conjunctival sac with 109 cfu/ml of B.melitensis, while Group 2 was similarly exposed to sterile PBS. Serum and swabs from the eyes and vagina were collected at 5-day intervals. On days 15, 30 and 75 post-infection, 3 goats from each group were killed before the conjunctiva, ovary, oviduct, uterine horn, uterine body and vagina, the submandibular, prescapular and supramammary lymph nodes, the mammary gland, liver, spleen, urinary bladder and synovial membranes were collected for bacterial isolation and pathological study. Exposure of non-pregnant goats to B.melitensis did not produce clinical signs and gross lesions but produced mild necrosis and inflammation in the lymph nodes, the organs of reproductive tract, the mammary gland and urinary bladder. In general, microscopic lesions were most severe in the D75 goats, followed by D30 and D15 goats. Brucella melitensis was most frequent and significantly (p<.05) isolated from the D30 (64.4±25.2%) and least from D15 goats (39.3±26.0%) goats. The organs that were most frequently isolated were the uterus, followed by the mammary gland, supramammary lymph node and urinary bladder. Earliest isolation from the ocular swabs was on day 5, while the vaginal swabs were on day 20 post-infection. The antibody response showed first significant (p<.05) increase on day 15 and reached peak on day 45 post-infection, corresponding with the first detection of sero-converter goats by the RBPT at 15days and by the CFT at 40days post-infection. In conclusion, infected non-pregnant goats shed B.melitensis through the vagina by day 20. The sero-positive goats were detectable by RBPT after 15days but by CFT after 40days. Since both serological tests detected positive goats at different time period of infection, paired-serum samplings might reduce this discrepancy.

Milk As a New Diagnostic Tool for Rapid Detection of Fascioliasis in Dairy Goats Using Excretory/Secretory Antigen

Fascioliasis is a serious livestock illness of particular importance for dairy goats; the objectives of this study were to describe effects of F. gigantica on milk composition and to use this information to estimate economic damages linked with Fasciola spp. infections. Furthermore, the study sought to standardize the use of milk instead of serum for early diagnosis of fascioliasis in dairy goats. One-hundred samples of goat milk along with corresponding blood samples were obtained at random from flocks in Cairo and Giza Governorates. The ELISA and DOT-ELISA were performed in both serum and milk of dairy goats. Total mesophilic count (mean value) was 2.12 × 106 ± 1.63 × 105CFU/ml in enzyme-linked immunosorbent assay (ELISA) positive samples and 1.46 × 104 ± 8.58 × 102CFU/ml in ELISA-negative samples. The mean values were significantly different (P < 0.05). The mean values of percentages of fat, SNF, protein, salts, lactose, pH, and MSCC/ml in ELISA-positive samples were 2.3 ± 0.17, 8.21 ± 0.63, 3.08 ± 0.18, 0.90 ± 0.06, 3.64 ± 0.28, 6.93 + 0.53, and 1.18 × 106 ± 9.07 × 104cells/ml, respectively. A significant difference (P < 0.05) between the mean values of two composition parameters, i.e., percent of fat and MSCC/ml in ELISA-positive and -negative samples, for Fasciola gigantica was observed. The antigen used for the diagnosis of F. gigantica was excretory/secretory (E/S) antigen. The dilutions of (E/S) concentrations after checkerboard titration for indirect ELISA were 20μg/ml protein and for dot-ELISA, 300ng/μl. Sera dilution was 1:100 in the two tests, and milk dilution was 1:50 for indirect ELISA, and 1:25 for dot-ELISA. The two tests were performed using known F. gigantica positive and negative goat sera and known rat hyper immunized negative and positive sera against E/S antigen of F. gigantica as well as known sera for paramphistomes without F. gigantica infection. The cutoff values in indirect ELISA were 0.45 for sera and 0.35 for milk. The application of different serological technique in goat farms reveals a good test in rapid diagnosis of fascioliasis especially the uses of dot ELISA when using the milk instead of the serum.

Prevalence and Spatial Distribution of Animal Brucellosis in Central Punjab, Pakistan.

Brucellosis is an important zoonotic disease of animals and humans caused by bacteria of the genus Brucella. Brucellae are Gram-negative intracellular bacteria which infect a wide variety of animals including goats, sheep, buffaloes, cows, pigs, and wildlife. The objectives of this study were to determine the seroprevalence and spatial distribution of brucellosis in Central Punjab, Pakistan. A total of 1083 blood samples of goats, sheep, buffaloes, and cows were collected from 38 villages of four districts (Kasur, Faisalabad, Lahore, and Okara) of Punjab, Pakistan, and screened for brucellosis by Rose Bengal Plate test (RBPT) and PCR confirmed. Epidemiological, demographic data and GPS coordinates for every sample were collected. By using interpolation of the Aeronautical Reconnaissance Coverage Geographic Information System (Arc GIS), a surface plot was generated applying inverse distance weight (IDW). It was found that 35 (3.23%) serum samples were positive for brucellosis. In eight (61.5%), six (75%), seven (87.5%), and eight (89%) villages, positive goats, sheep, buffaloes, and cattle were detected, respectively. In general, older animals are more often positive for brucellosis. In goats bucks were more often RBPT positive than females while in sheep, buffaloes, and cattle more females were positive. The spatial distribution of brucellosis shows that it is widely distributed in the western region of the study area in goats and in the South-West region in sheep. Similarly, for buffaloes it is restricted to the south-east and north-west regions, and in cattle brucellosis is present in western region of study area only. Reflected by this study, brucellosis poses a risk for livestock in developing countries due to lack of awareness by officials, owners, and consumers, and control measures are missing. A risk map of brucellosis was generated to develop effective strategies for awareness rising and to improve the quality of control programs in Pakistan.

Histopathological Observation of The Qurban Goat’s (Capra Aegagrus Hircus) Lung Organs in Tulus Rejo Village, Pekalongan District, East Lampung 2019 Suspected Of Being Infected With Pneumonia

Placement of goats of various ages and the number of animals that exceed the maximum limit in one cage can cause the spread of diseases caused by viruses, bacteria, etc. One of them can cause pneumonia. Dirt and extreme temperatures in East Lampung are feared to increase the growth of bacteria that cause pneumonia. The purpose of this research was to determine the type of pneumonia that infects and the differences between the histopathological organs of the healthy qurban goats and those infected with pneumonia. This research was conducted in October-November 2019 at the Pathology Laboratory of the Veterinary Institute of Lampung. About 13 samples of lung organ of goat qurban (Capra aegagrus hircus) were taken from the Baburahman mosque of Tulus Rejo Village, Pekalongan District, East Lampung. The results of the study found 6 samples of positive qurban goat lungs infected with pneumonia, with the characteristics of inflammatory cells accompanied by thickening of the septa alveoli, edema, and the presence of hemorrhage. Based on observations, the most infecting types of pneumonia are pulmonary edema and peri-bronchial edema.

Anaplasma platys-Like Infection in Goats, Beijing, China.

As one of the important tick-borne zoonotic pathogens, Anaplasma has both veterinary and public health significance. Here, we performed a survey of Anaplasma infection in the goats from a farm in Beijing, China, and found 44.6% (41/92) were infected with Anaplasma capra, and 22.8% (21/92) were infected with Anaplasma sp. This Anaplasma sp. bacterium was close to a recently emerging Anaplasma platys strain based on gltA and groEL gene phylogenetic analysis. As to further understand the characteristics of Anaplasma sp., we raised a couple of positive goats (n = 2) in the laboratory with tick-free settings. We observed inappetence, vomiting, high fever, and weakness of limbs in the goat's offspring (n = 3). In addition, the blood samples from all offspring were all positive of this Anaplasma spp. We did not see any intracellular morulae in neutrophils, monocytes, and erythrocytes, but we identified some in the platelets of the blood smears from the positive goats by light microscopy. We named it A. platys-like and suggested it may infect platelets and be transmitted vertically through the placenta of goats. These findings deserve further evaluation.