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To treat resistant Escherichia coli infection in chicks, Ampicillin was stabilized with a synthetic aluminum-magnesium silicate (AMS) to prolong its bioavailability. Its dose was also reduced to minimize adverse side effects. Vitamins A, C, E and Selenium levels in the chicks' feeds were increased to enhance immune response of the chicks. E. coli coloning forming units, per ml of bile of the chicks, treated with Ampicillin and with Ampicillin in AMS, were: 228800.00 ± 90103.50 and 134500.00 ± 44937.97 at 10 mg/kg, 104400.00 ± 36024.44 and 34800.00 ± 8014.97 at 7.5 mg/kg, 198400.00 ± 129301.80 and 156800.00 ± 109392.70 at 5 mg/kg. Mean bacterial loads of the untreated groups, fed normal feed and those fed the fortified feed were 824400.00 ± 322424.80 and 534800.00 ± 277832.80. At 7.5 mg/kg. Ampicillin in the AMS, effectively (P < 0.05) treated resistant E. coli infection in chicks, fed immunestimulants, with the infection rate reduced by 95.8%.

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Peste des petits ruminants (PPR) is a disease of economic and veterinary importance leading to considerable economic losses. PPR affects small domestic and wild ruminants. Sheep and goats are the natural hosts of PPR but cattle, pigs, African buffaloes and camels are also affected by the PPR virus. Clinical signs seen are mainly fever, mucopurulent nasal and ocular discharges, cough, dyspnoea, gastroenteritis leading to severe diarrhoea. The post mortem lesions seen are congested lungs, congestion of gastrointestinal tract, especially the discontinuous streaks of congestion, which is referred to as Zebra stripes or Zebra markings, oedematous and congested retropharyngeal and mesenteric lymph nodes, linear haemorrhages in the intestinal mucosa and splenomegaly. PPR infection is characterized by a rise in packed cell volume (PCV), increase in haemoglobin concentration (HbC), leukopenia with lymphopenia. The serum alkaline phosphatase, alanine aminotransferase and aspartate aminotransferase activities are elevated, blood urea nitrogen and creatinine concentrations are also elevated. The disease is also characterized by disseminated intravascular coagulopathy (DIC) evidenced by prolonged prothrombin time (PT), prolonged activated thromboplastin time (APTT), thrombocytopenia, and hypofibrinogenemia. In PPR infection, serum biomarkers of oxidative stress such as vitamins A, C, E and glutathione activity decreases while serum catalase, superoxide dismutase, glutathione reductase and xanthine oxidase increase. Diagnostic techniques include histopathology, virus isolation, immunocapture enzyme-linked immunosorbent assay (icELISA), Competitive Enzyme Linked Imunnosorbent Assay (cELISA) and Combined Indirect ELISA (CI-ELISA) agar gel immunodiffusion, real-time polymerase chain reaction (RT-PCR), reverse transcription-loop mediated isothermal amplification assay (RT-LAMP), Luciferase immunoprecipitation system (LIPS) and immunohistochemistry. Therefore, this review focused on the aetiology, epidemiology, pathology, immunology, and disease status in Africa, diagnosis, control, prevention, treatment and control of this disease.

Background and Aim: Peste des petits ruminants (PPR) is an acute, extremely contagious transboundary viral disease of small ruminants with severe economic consequences, caused by PPR virus. Cost-effective and rapid diagnosis of the disease is essential for prompt management and control. This study aimed to compare the application of a commercial colorimetric loop-mediated isothermal amplification (cLAMP) kit and reverse transcriptase-polymerase chain reaction (RT-PCR) in the diagnosis of PPR in sheep and goats in Southeast Nigeria. Materials and Methods: Nasal swab samples were collected from West African Dwarf sheep and goats showing clinical signs suggestive of PPR (n=80) and those without any clinical signs (n=140) of the disease. The diagnosis was achieved through detection of PPR viral genome in the samples using a cLAMP kit and RT-PCR. cLAMP assay was done directly on nasal swab samples without ribosomal nucleic acid extraction. A set of six primers targeting the matrix gene protein was used for the cLAMP assay. Results: PPR viral genome was detected by both cLAMP and RT-PCR in 51 (63.8%) of the 80 samples from sheep and goats with signs suggestive of PPR while 14 (10%) of those without signs tested positive for PPR by both assay methods. There was a 100% agreement in the cLAMP and RT-PCR results. However, cLAMP was a faster, easier, and less expensive method compared to RT-PCR. Conclusion: The cLAMP assay demonstrates the potential for a point of care diagnosis in the field and a valuable diagnostic tool in areas with poor electricity supply as well as in a less equipped diagnostic laboratory. Since the reagents are affordable, cLAMP can be a diagnostic tool of choice in the detection and surveillance of PPR virus in countries with limited resources.

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Aims: Peste des petits Ruminants (PPR) is a major viral disease that poses a challenge to small ruminant farming. Its natural occurrence has been complicated by secondary bacterial infection which has led to an increase in morbidity and mortality rates. This study reports the management outcome of natural PPR-infected goats using two types of antibiotics in Nsukka metropolis of Enugu State Nigeria. Methodology: Goats (N=24) were confirmed to be suffering from PPR based on clinical signs and using polymerase chain reaction (PCR). The animals were divided into two groups. Group A was treated with 20% oxytetracycline (N= 10) and group B with procaine penicillin and streptomycin combination (penstrept) (N= 14) injection. Clinical signs, recovery and survivability, temperature, haematology [Packed cell volume (PCV); haemoglobin concentration (Hbconc); red blood cell (RBC) and white blood cell (WBC) counts] and some serum biochemical profiles [alanine aminotransferase (ALT); aspartate transaminase (AST); total protein (TP); Albumin; urea; creatinine; potassium and sodium] were used to assess the efficacy of the antibiotics using standard techniques. Results: The mean temperature, RBC, WBC and urea values of the PPR-infected goats were above their reference ranges, mean albumin values were below the reference range while mean Hbconc, PCV, AST, ALT, TP and creatinine values were within their reference range before the commencement of treatment. Following treatment, clinical signs cleared in 20% and 35.7% of the goats treated with oxytetracycline and penstrep respectively. Death was recorded in 20% and 15% of goats treated with oxytetracycline and penstrep respectively before the end of treatment. Penstrep-treated group showed improvement in their haematological profile. Conclusion: Based on our findings, the use of penstrep in the management of PPR-infected goats gave a better result.