Serological Survey Of Salmonella gallinarum Antibody In Chickens Around Jos, Plateau State, Nigeria

A serological survey of the prevalence of antibodies to Salmonella gallinarum among chickens under two different management systems around Jos, Plateau State, Nigeria was carried out using the standard plate agglutination test. The objective of this study was to determine serologically the prevalence of antibodies against Salmonella gallinarum among apparently healthy chickens around Jos. A total of 700 serum samples made up of 450 exotic and 250 local breed of chickens were used for this study with 37.9% seropositvity. In the free range system (19.3%) of the flocks sampled were seropositive for Salmonella gallinarium antibodies while in the semi intensive, 18.6% of the flock tested positive. The serum agglutination test (SAT) was adapted to the microtitre format used to determine somatic and flagella titres. The antigen used for this study was specific for S. gallinarum, hence differentiation between species infection was assessed in this study. Perhaps the most feasible way to eradicate the disease is to encourage farmers (both small and large scale) to break the disease cycle at their levels by embarking on prompt and regular vaccination programmes. It is thus concluded that Salmonella gallinarum (fowl typhoid) is present in the area investigated. Fowl typhoid may continue to have a negative effect on the economy of poultry production in Nigeria if not controlled. A statistical analysis was precluded due to inadequate data sets

Ultrastuctural study of the phagocytic activities of splenic macrophages in tilapia (Oreochromis niloticus)

The main stages of the phagocytic process after the intraperitoneal injection of colloidal carbon to tilapia (Oreochromis niloticus), was ultra-structurally documented. Carbon particles were initially indiffuse form in the cytoplasm but they gradually formed discrete electron dense bodies that later fused with cytoplasmic granules to form phagolysosomes. Ultra structural results demonstrate that colloidalcarbon is actively phagocytized by cytoplasmic granules (lysosomes) in the spleen of O. niloticus. Direct phagocytic reaction of cells in the presence of an antigen is therefore very important in immunity

The antimicrobial properties of Ocimum gratissimumextracts on some selected bacterial gastrointestinal isolates

The antimicrobial efficacy of cold and hot water, hexane and methanolic extracts of fresh and dried leaf of Ocimum gratissimum against Salmonella typhimurium, E. coli, Yersinia enterocolitica, Bacilluscereus, and Aeromonas hydrophila were determined using the Agar gel diffusion method. The zones of inhibition, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) andPhytochemistry of the extracts were also determined. Results obtained revealed that the cold water extracts of the fresh leaf was most potent, inhibiting all isolates with diameter zones of inhibition ranging from 5 mm to 18 mm, followed by hexane extract of the fresh leaf with zone range of 6mm to 14 mm, but E. coli showed no resistance to the hexane extract, methanol extract of the fresh leaf showed no inhibitory effect on all isolates. The extracts inhibited the growth of the bacterial isolates in a concentration dependent manner with MICs ranging between (12.5 - 150) mg/ml, while MBCs gave a range of (3.13 - 100) mg/ml. Phytochemical analysis of fresh and dried leaf extracts revealed thepresence of antimicrobial principles such as resins, tannins, glycosides, alkaloids, flavonoids saponin, anthraquinone, cardiac glycoside, steroidal ring, steroidal terpens and carbohydrates at differentconcentrations. The findings from this study seem to provide the in vitro evidence that might justify O. gratissimum as a good candidate medicinal plant for further investigations, and that the activeprinciples of the plant may be more polar in nature

Elderly musculoskeletal disease burden in Karachi, Pakistan: Associations and implications for developing countries

Objective: The global rise in the older population has increased the rates of osteoporosis and osteoarthritis, conditions that impact mobility and functionality. There is limited data on musculoskeletal disease in older populations residing in developing countries.Methods: A community-based study using multistage cluster random sampling of older individuals was conducted in Karachi. Predefined criteria were used for osteoporosis and osteoarthritis. Gait assessment was performed.Results: More than half of the participants were females and 53% reported illiteracy. Around 30% had osteoporosis and two-thirds had osteoarthritis. Multivariate analysis showed associations of female sex, Pashtun ethnicity, illiteracy, and hypertension with the combined variable of osteoporosis and osteoarthritis.Conclusions: The prevalence of osteoarthritis was higher than in other regional studies. Presence of both osteoporosis and osteoarthritis increased the risk of certain geriatric syndromes. High rates of musculoskeletal morbidity are seen in the elderly in Pakistan. Measures at a health-system level are required for better outcomes in older adults

Studies on Prevalence and Risk Factors for Hepatitis B Surface Antigen among Secondary School Students in North-central, Nigeria

Hepatitis B virus (HBV) Infection is one of the major global public health problems, with its attendant risks especially among the young adults. This study was therefore carried out to assess the sero-prevalence of hepatitis B surface antigen (HBsAg) and associated risk factors among students of a secondary school in Jagindi Tasha, Kaduna State, Nigeria. One hundred and ninety (190) apparently healthy students were screened and sera samples obtained were separated and analysed for HBsAg using a commercially available Enzyme Linked Immunosorbent Assay (ELISA)-based kit (Dialab). Information was obtained for risk factors using structured questionnaire. Out of the 190 samples screened, 35 (18.4%) were sero-positive. Subjects aged 13-15 years recorded 6.8% positivity (x2 = 1.084; p>0.05) and male subjects had 25.5% positivity compared to 10.9% positivity for females (x2 = 6.768; p<0.05). Risk factors such as blood transfusion was 32.0% among male subjects compared to 30.0% in females (x2 =18.07; p-value = 0.113). Furthermore, alcoholic consumption, the predominant lifestyle of the youths in this community was 20.0% among male subjects as compared to none in females. Unfortunately, the prevalence of HBV appears high among the studied population. This suggests that public awareness on the virus be accorded urgent attention, while vaccination programme should be improved in the community

Delivery of thermostable Newcastle disease (ND) vaccine to chickens with broken millet grains as the vehicle

The efficacy of treated broken millet grains as a carrier for delivery of thermostable Newcastle disease (ND) vaccine HRV4 to free-range chickens in three locations was assessed by haemagglutinationinhibition (HI) test and challenge experiment. Out of 256 birds fed with first dose of the vaccine, 130 (50.8%) produced detectable HI antibody but only 16 (6.3%) attained serum antibody level of log2 3.0adjudged protective. From the locations, Igumale (74 birds), Kuru (88 birds) Riyom (94 birds), only 1 (1.4%), 8 (9.1%) and 7 (7.4%) attained log2 titre 3.0, respectively. A booster vaccine dose 2 weeks lateron 236 of the birds led to 126 (53.4%) attaining HI (log2) titre 3.0 [Igumale (63 birds), Kuru (86 birds) Riyom (87 birds) had 33 (53.5%), 46 (53.5%) and 42 (48.3%) respectively attaining log2 titres of 3.0]. Out of a total of 70 buy-back chickens challenged, 49 (70.0%) survived. The break down showed that from Igumale (20 birds), Kuru (25 birds) Riyom (25 birds), the survivors were 13 (65.0%), 19 (76.0%) and 17 (68.0%), respectively. Out of 28 unvaccinated control birds challenged, only 4 survived. The overall results showed that millet, if properly treated, could be a good vaccine carrier and that the method of vaccination was relatively efficacious.

Diagnosis of enteric fever in the emergency department: a retrospective study from Pakistan

Background:Enteric fever is one of the top differential diagnoses of fever in many parts of the world. Generally, the diagnosis is suspected and treatment is initiated based on clinical and basic laboratory parameters.Aims: The present study identifies the clinical and laboratory parameters predicting enteric fever in Patients visiting the emergency department of a tertiary care hospital in Pakistan.Methods:This is a retrospective chart review of all adult Patients with clinically suspected enteric fever admitted to the hospital through the emergency department during a 5-year period (2000-2005).Results:A total of 421 emergency department Patients were admitted to the hospital with suspected enteric fever. There were 53 cases of blood culture-positive enteric fever and 296 disease-negative cases on culture. The mean age in the blood culture-positive group was 27 years (SD: 10) and in the group with negative blood culture for enteric fever, 35 years (SD: 15) with a male to female ratio of 1:0.6 in both groups. Less than half (48%) of all Patients admitted with suspected enteric fever had the discharge diagnosis of enteric fever, of which only 13% of the Patients had blood culture/serologically confirmed enteric fever. None of the common clinical and laboratory parameters differed between enteric fever-positive Patients and those without it.Conclusion:Commonly cited clinical and laboratory parameters were not able to predict enteric fever

A Common and Unstable Copy Number Variant Is Associated with Differences in Glo1 Expression and Anxiety-Like Behavior

Glyoxalase 1 (Glo1) has been implicated in anxiety-like behavior in mice and in multiple psychiatric diseases in humans. We used mouse Affymetrix exon arrays to detect copy number variants (CNV) among inbred mouse strains and thereby identified a ∼475 kb tandem duplication on chromosome 17 that includes Glo1 (30,174,390–30,651,226 Mb; mouse genome build 36). We developed a PCR-based strategy and used it to detect this duplication in 23 of 71 inbred strains tested, and in various outbred and wild-caught mice. Presence of the duplication is associated with a cis-acting expression QTL for Glo1 (LOD>30) in BXD recombinant inbred strains. However, evidence for an eQTL for Glo1 was not obtained when we analyzed single SNPs or 3-SNP haplotypes in a panel of 27 inbred strains. We conclude that association analysis in the inbred strain panel failed to detect an eQTL because the duplication was present on multiple highly divergent haplotypes. Furthermore, we suggest that non-allelic homologous recombination has led to multiple reversions to the non-duplicated state among inbred strains. We show associations between multiple duplication-containing haplotypes, Glo1 expression and anxiety-like behavior in both inbred strain panels and outbred CD-1 mice. Our findings provide a molecular basis for differential expression of Glo1 and further implicate Glo1 in anxiety-like behavior. More broadly, these results identify problems with commonly employed tests for association in inbred strains when CNVs are present. Finally, these data provide an example of biologically significant phenotypic variability in model organisms that can be attributed to CNVs

Enzymatic Analysis of Recombinant Japanese Encephalitis Virus NS2B(H)-NS3pro Protease with Fluorogenic Model Peptide Substrates

Background Japanese encephalitis virus (JEV), a member of the Flaviviridae family, causes around 68,000 encephalitis cases annually, of which 20–30% are fatal, while 30–50% of the recovered cases develop severe neurological sequelae. Specific antivirals for JEV would be of great importance, particularly in those cases where the infection has become persistent. Being indispensable for flaviviral replication, the NS2B-NS3 protease is a promising target for design of anti-flaviviral inhibitors. Contrary to related flaviviral proteases, the JEV NS2B-NS3 protease is structurally and mechanistically much less characterized. Here we aimed at establishing a straightforward procedure for cloning, expression, purification and biochemical characterization of JEV NS2B(H)-NS3pro protease. Methodology/Principal Findings The full-length sequence of JEV NS2B-NS3 genotype III strain JaOArS 982 was obtained as a synthetic gene. The sequence of NS2B(H)-NS3pro was generated by splicing by overlap extension PCR (SOE-PCR) and cloned into the pTrcHisA vector. Hexahistidine-tagged NS2B(H)-NS3pro, expressed in E. coli as soluble protein, was purified to >95% purity by a single-step immobilized metal affinity chromatography. SDS-PAGE and immunoblotting of the purified enzyme demonstrated NS2B(H)-NS3pro precursor and its autocleavage products, NS3pro and NS2B(H), as 36, 21, and 10 kDa bands, respectively. Kinetic parameters, Km and kcat, for fluorogenic protease model substrates, Boc-GRR-amc, Boc-LRR-amc, Ac-nKRR-amc, Bz-nKRR-amc, Pyr-RTKR-amc and Abz-(R)4SAG-nY-amide, were obtained using inner filter effect correction. The highest catalytic efficiency kcat/Km was found for Pyr-RTKR-amc (kcat/Km: 1962.96±85.0 M−1 s−1) and the lowest for Boc-LRR-amc (kcat/Km: 3.74±0.3 M−1 s−1). JEV NS3pro is inhibited by aprotinin but to a lesser extent than DEN and WNV NS3pro. Conclusions/Significance A simplified procedure for the cloning, overexpression and purification of the NS2B(H)-NS3pro was established which is generally applicable to other flaviviral proteases. Kinetic parameters obtained for a number of model substrates and inhibitors, are useful for the characterization of substrate specificity and eventually for the design of high-throughput assays aimed at antiviral inhibitor discovery

CYP17, GSTP1, PON1 and GLO1 gene polymorphisms as risk factors for breast cancer: an Italian case-control study

<p>Abstract</p> <p>Background</p> <p>Estrogens, environmental chemicals with carcinogenic potential, as well as oxidative and carbonyl stresses play a very important role in breast cancer (BC) genesis and progression. Therefore, polymorphisms of genes encoding enzymes involved in estrogen biosynthesis pathway and in the metabolic activation of pro-carcinogens to genotoxic intermediates, such as cytochrome P450C17α (CYP17), endogenous free-radical scavenging systems, such as glutathione S-transferase (GSTP1) and paraoxonase 1 (PON1), and anti-glycation defenses, such as glyoxalase I (GLO1), could influence individual susceptibility to BC. In the present case-control study, we investigated the possible association of CYP17 A1A2, GSTP1 ILE105VAL, PON1 Q192R or L55M, and GLO1 A111E polymorphisms with the risk of BC.</p> <p>Methods</p> <p>The above-said five polymorphisms were characterized in 547 patients with BC and in 544 healthy controls by PCR/RFLP methods, using DNA from whole blood. To estimate the relative risks, Odds ratios and 95% confidence intervals were calculated using unconditional logistic regression after adjusting for the known risk factors for BC.</p> <p>Results</p> <p>CYP17 polymorphism had no major effect in BC proneness in the overall population. However, it modified the risk of BC for certain subgroups of patients. In particular, among premenopausal women with the A1A1 genotype, a protective effect of later age at menarche and parity was observed. As to GSTP1 and PON1 192 polymorphisms, the mutant Val and R alleles, respectively, were associated with a decreased risk of developing BC, while polymorphisms in PON1 55 and GLO1 were associated with an increased risk of this neoplasia. However, these findings, while nominally significant, did not withstand correction for multiple testing.</p> <p>Conclusion</p> <p>Genetic polymorphisms in biotransformation enzymes CYP17, GSTP1, PON1 and GLO1 could be associated with the risk for BC. Although significances did not withstand correction for multiple testing, the results of our exploratory analysis warrant further studies on the above mentioned genes and BC.</p