Differential diagnosis and surgical management of cecal dilatation vis-a-vis cecal impaction in bovine

Research (Published online: 11-09-2018)

7. Differential diagnosis and surgical management of cecal dilatation vis-a-vis cecal impaction in bovine

Gurnoor Singh, Rahul Kumar Udehiya, Jitender Mohindroo, Ashwani Kumar, Tarunbir Singh, Pallavi Verma, Nameirakpam Umeshwori Devi and Arun Anand

Veterinary World, 11(9): 1244-1249

ABSTRACT

Aim: The present study was undertaken to study the clinical and hemato-biochemical alterations, ultrasonography, and surgical treatment of bovine suffering from cecal dilatation and cecal impaction.

Materials and Methods: The present study was conducted on 11 bovines (9 buffaloes and 2 cattle) suffering from cecal dilatation (n=6) and cecal impaction (n=5). The diagnosis of surgical affections of cecum was made on the basis of clinical examination, hematobiochemistry, ultrasonography, and exploratory laparotomy.

Results: A marked decrease in serum total protein, albumin, chloride, potassium, and calcium levels while an increase in lactate concentrations was recorded. Peritoneal fluid examination revealed an increase in total protein concentration. Per rectal examination along with ultrasonography was used as a confirmatory diagnostic tool for cecal dilatation and cecal impaction. Ultrasonographic features of cecal dilatation and cecal impaction were recorded. Left flank laparorumenotomy was performed in six animals with dilated cecum along with colonic fecalith. Post-rumenotomy, these animals were treated with massage of cecum along with kneading of colonic fecalith. Right flank typhlotomy was done in the remaining five animals having impacted cecum for decompression of the dilated cecum. 9 of 11 animals survived which underwent surgery and remained healthy up to 3-month follow-up.

Conclusion: Ultrasonography was reliable in the diagnosis of cecal dilatation and cecal impaction in bovine. Left flank exploration after laparorumenotomy is an ideal surgical technique for the management of cecal dilatation, while right flank typhlotomy is ideal for the management of cecal impaction in bovine.

Keywords: buffalo, cattle, cecum, percussion, typhlotomy, ultrasonography.

The neuroprotective effect of Ocimum sanctum Linn. ethanolic extract on human embryonic kidney-293 cells as in vitro model of neurodegenerative disease

Research (Published online: 11-09-2018)

6. The neuroprotective effect of Ocimum sanctum Linn. ethanolic extract on human embryonic kidney-293 cells as in vitro model of neurodegenerative disease

Puspa Hening, Made Bagus Auriva Mataram, Nastiti Wijayanti, Dwi Liliek Kusindarta and Hevi Wihadmadyatami

Veterinary World, 11(9): 1237-1243

ABSTRACT

Aim: This study aimed to analyze the neuroprotective effect of Ocimum sanctum Linn. ethanolic extract (OSE) on human embryonic kidney-293 (HEK-293) cells as the in vitro model of neurodegenerative diseases.

Materials and Methods: In this research, HEK-293 cells divided into five groups consisting of normal and healthy cells (NT), cells treated with Camptothecin 500 μM as the negative control, cells treated with trimethyltin 10 μM (TMT), cells treated with OSE 75 μg/ml, and cells pre-treated with OSE 75 μg/ml then induced by TMT 10 μM (OSE+TMT). MTT assay and phase contrast microscopy were applied to observe the cell viability quantitatively and morphological after Ocimum sanctum Linn extract treatment. Finally, the reverse transcription polymerase chain reaction was employed to study the expression of choline acetyltransferase (ChAT).

Results: The MTT assay and phase contrast microscopy showed that OSE pre-treatment significantly increased the viability of TMT-induced apoptotic cells and maintained cell viability of the normal HEK-293 cells. Expression of ChAT markedly reduced on TMT treatment group, but OSE administration stabilized ChAT expression in TMT-induced HEK-293 cells.

Conclusion: This present study proved that OSE administration has neuroprotective effect by increased HEK-293 cells viability and maintain ChAT expression.

Keywords: choline acetyltransferase, human embryonic kidney-293, neurodegenerative diseases, Ocimum sanctum Linn. ethanolic extract.

Epizootiological study on spatiotemporal clusters of Schmallenberg virus and Lumpy skin diseases: The case of Russia

Research (Published online: 08-09-2018)

5. Epizootiological study on spatiotemporal clusters of Schmallenberg virus and Lumpy skin diseases: The case of Russia

Fayssal Bouchemla, Valery Alexandrovich Agoltsov, Sergey Vasilievich Larionov, Olga Mikhailovna Popova and Ekaterina Vladimirovna Shvenk

Veterinary World, 11(9): 1229-1236

ABSTRACT

Aim: The submitted article attempts to highlight and specify the development of Schmallenberg virus (SBV) and lumpy skin disease (LSD) in cartographic illustrations, as well as to assess the epizootic situation of these diseases in the world, especially in Russia.

Materials and Methods: Outbreaks (samples were collected from clinically healthy as well as suspected animals in infected areas) were confirmed and reported to the World Organization for Animal Health by veterinary officials representing countries in different geographical regions in the world. The reports showed that ELISA and polymerase chain reaction were used to identify SBV and LSD, taking into account number of infected, dead, and susceptible animals in infection foci since their first registration including in Russia. Once conventional statistical population (arrange data according to the main goal by regions, infected, and dead animals) was defined, a model was installed. A geo-information system, QuickMAP, was used to clarify the disease distribution map, and through the illustrations, analysis values were obtained.

Results: Using information clusters of some epizootological criteria in various territories has demonstrated 1.302 focus of infection of SBV, of which 63.22% were registered in Europe and 36.78% in Russia. The seroprevalence in Russia was about 7.92% of the examined animals. According to the morbidity structure, the causative agent mainly affected cattle (64.76%), small ruminants (33.68%), and goats (1.56%). A global assessment of the effectiveness of primary epizootic diagnosis by practicing veterinarians was 63.19%, i.e., of 100 suspicion reports of SBV, 63.19 cases are confirmed by laboratory methods. A detailed assessment of the types of animals affected by the disease showed that it was easily diagnosed in sheep (70.38%), cattle (60.4%), and goats (48.57%), respectively. In the wild animal species, a significant prevalence was recorded as- 54.5%. In 2016, 1.209 foci of LSD were registered in the world, with 20.548 heads of cattle affected, while 8.5% of them identified in Russia (in 2017, the figure was 7.5%). Different maps had been generated in QuickMAP. Cluster analysis of the infected livestock in different regions in Russia showed that, in 2016, the Chechen Republic, Krasnodar, and Volgograd regions were, respectively, severely, moderately, and mildly affected. In 2017, the situation changed and Saratov, Orenburg regions, and Bashkiria were severely affected. However, the number of outbreaks decreased by 84.81% by contribution to the previous year. Eritrea, Namibia, and South Africa were leading in a cluster of most infected areas in 2017.

Conclusion: Infectious diseases do not know borders. The emergence of SBV and LSD in the territory of the Russian Federation has followed the most common general dynamics of transborder diseases without ignoring details. The epizootic risk from wild animals and favorable climatic conditions is critical to fight against transmission of these diseases in Russia.

Keywords: geographic area, prevalence, Russia, Schmallenberg and lumpy skin disease.

Assessment of in vitro potency of inactivated Newcastle disease oil adjuvanted vaccines using hemagglutination test and blocking ELISA

Research (Published online: 06-09-2018)

4. Assessment of in vitro potency of inactivated Newcastle disease oil adjuvanted vaccines using hemagglutination test and blocking ELISA

Saleh E. Aly, Hussein Ali Hussein, Abdel-Hakim M. Aly, Mansour H. Abdel-Baky and Ahmed A. El-Sanousi

Veterinary World, 11(9): 1222-1228

ABSTRACT

Aim: The present study was aimed to establish a protocol for the evaluation of the in vitro potency of commercial inactivated Newcastle disease virus (NDV) oil-adjuvanted vaccines using hemagglutination test (HA) and blocking ELISA (B-ELISA) based on polyclonal antibodies.

Materials and Methods: Aqueous phases from a total of 47 batches of inactivated NDV vaccines manufactured by 20 different companies were extracted with isopropyl myristate. The viral antigen in each sample was detected and quantified by a standard HA test and a B-ELISA assay. To verify the efficiency of the antigen extraction method used in the batches which showed HA and to test the validity of using in vitro antigen quantification by HA and B-ELISA tests, a subset of 13 batches (selected from the total 47 batches) was inoculated in groups of 3-4-week-old specific pathogen-free chickens using the recommended vaccine dose. The immunogenicity of the selected vaccine batches was assessed by the NDV-hemagglutination inhibition antibody titers in individual serum samples collected 4 weeks after vaccination. Further, the efficacy of the vaccines and their protection rates were determined by a challenge test carried out for the vaccinated chickens with the Egyptian 2012 isolate of the virulent NDV genotype VII.

Results: A strong correlation was observed between HA titers and B-ELISA mean titers in the tested 47 batches (R2=0.817). This indicated the possibility of using the latter in vitro assays for vaccine potency assessment. The recommended protective NDV antigen titer measured by B-ELISA was determined to be 28 ELISA units per dose. The comparison between the HA titers of the aqueous extracts of test vaccines and the corresponding results of in vivo potency assays (i.e., immunogenicity and efficacy), including antibody titers in the serum of vaccinated birds, indicated that the efficiency of the antigen extraction used may interfere with obtaining a strong correlation between the in vitro and in vivo results.

Conclusion: HA or B-ELISA tests can be used as rapid and cost-effective alternatives to traditional in vivo potency tests for vaccine potency assessment by quantifying the NDV antigen present in aqueous phase extracts of the tested vaccines. The latter in vitro protocol, however, requires efficient extraction of the antigen to be able to obtain good correlation with the traditional in vivo potency tests.

Keywords: blocking ELISA, inactivated vaccines, in vitro, Newcastle disease virus, vaccine potency.

Prevalence, toxigenic potential and antimicrobial susceptibility profile of Staphylococcus isolated from ready-to-eat meats

Research (Published online: 05-09-2018)

3. Prevalence, toxigenic potential and antimicrobial susceptibility profile of Staphylococcus isolated from ready-to-eat meats

Chinwe E. Okoli, Emmanuel Okechukwu Njoga, Simon I. Enem, Enid E. Godwin, John A. Nwanta and Kennedy F. Chah

Veterinary World, 11(9): 1214-1221

ABSTRACT

Aim: An epidemiological surveillance for Staphylococci contamination of ready-to-eat (RTE) meats from Enugu State, Nigeria, was carried out to determine the prevalence, species distribution, toxigenic potential and antimicrobial susceptibility profile of the organisms and hence the microbiological and toxicological safety of the meats.

Materials and Methods: Isolation and phenotypic Staphylococcus detection were done according to standard microbiological methods. Phenotypic resistance to 17 commonly used antimicrobial agents was determined by disc diffusion method. Molecular characterization of the isolates to species level and detection of selected toxigenic and antimicrobial-resistance genes were done by PCR methods.

Results: Twenty-four (9.4%) of the 255 meat samples investigated were contaminated with Staphylococcus species. Twenty-four Staphylococcus isolates belonging to six species of coagulase-negative Staphylococcus(CoNS) were identified. Four (16.7%) isolates harbored genes coding for exfoliative toxin-A. Ten (41.7%) isolates were multidrug resistant, while mecA, tetK, mphC, ermT and ermC were the antimicrobial-resistance genes detected in the isolates. Meat samples sourced from motor parks (16.7%) and open markets (8.5%) were the most contaminated.

Conclusion: 9.4% of RTE meats sampled were contaminated with toxigenic and multidrug resistance CoNS. Beef was the most contaminated RTE meat type and harbored all the toxigenic and most of the antibiotic-resistant genes detected. Meat samples from motor parks had the highest staphylococcal contamination (16.7%), while those from mechanic village had the least (2.4%). Majority (79.2%) of the isolates were not susceptible to fusidic acid but none exhibited antimicrobial-resistance to chloramphenicol, ciprofloxacin, linezolid or teicoplanin. Food safety authorities in the study area should work proactively to massively improve the hygienic practices of meat vendors; in order to limit staphylococcal contamination of RTE meats and the associated public health problems.

Keywords: antibiotic resistance, food safety, Nigeria, polymerase chain reaction, ready-to-eat meats, Staphylococcus.

Clinical, molecular detection and phylogenetic analysis study of local foot-and-mouth disease virus in Al-Qadisiyah province of Iraq

Research (Published online: 04-09-2018)

2. Clinical, molecular detection and phylogenetic analysis study of local foot-and-mouth disease virus in Al-Qadisiyah province of Iraq

Khalefa Ali Mansour, Hassan Hachim Naser and Muthanna Hadi Hussain

Veterinary World, 11(9): 1210-1213

ABSTRACT

Aim: This study was directed during an outbreak of suspected foot-and-mouth disease (FMD) in cattle in Al-Qadisiyah province, Iraq 2016. The disease has made a huge economic loss in livestock. It was suspected that the vaccination has failed to protect the animals from the infection because of the difference in the strains. Consequently, we designed the study to make the diagnosis and detect the strain of the causative virus.

Materials and Methods: The extraction of the DNA was done on 73 samples and Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) was used in the detection of FMD virus (FMDV) for primary diagnosis, and serotype-specific diagnosis was done with universal primer sets 1F/1R, A-1C612, and O-ARS4 with the expected band of 329, 865, and 1301 bp, respectively.

Results: Universal primer pair 1F/1R detected FMD in 55 of 73 (75.3%); of these, 37 (67.3%) were females and 18 (32.7%) were males, with high significance (p<0.01) between males and females in the PCR positivity ratio. The tested samples with positive universal primer were amplified with specific primers A-IC612 with no reaction for serotype O-ARS4.

Conclusion: The products of RT-PCR were sent for RNA sequencing, and the results were 100% positive to serotype A which means that it is the predominant type in Iraq. It may help in the importing or production of the vaccine to make a preventive plan for the disease. The virus of FMD is contagious and dangerous due to its role in the huge economic loses. The detection of this virus is widely explained in lots of articles, but it is more specific and sensitive in RT-PCR and sequencing. Consequently, the authorities responsible for importing and/or production vaccines have to avoid the importing of other serotypes because it will be losing money and more outbreaks will explode.

Keywords: cattle, clinical, foot-and-mouth disease, Iraq, polymerase chain reaction.

An innovative approach to predict immune-associated genes mutually targeted by cow and human milk microRNAs expression profiles

Research (Published online: 01-09-2018)

1. An innovative approach to predict immune-associated genes mutually targeted by cow and human milk microRNAs expression profiles

Kaj Chokeshaiusaha, Thanida Sananmuang, Denis Puthier and Catherine Nguyen

Veterinary World, 11(9): 1203-1209

ABSTRACT

Aim: Milk is rich in miRNAs - the endogenous small non-coding RNA responsible for gene post-transcriptional silencing. Milk miRNAs were previously evidenced to affect consumer's immune response. While most studies relied on a few well-characterized milk miRNAs to relate their immunoregulatory roles on target genes among mammals, this study introduced a procedure to predict the target genes based on overall milk miRNA expression profiles - the miRNome data of cow and human.

Materials and Methods: Cow and human milk miRNome expression datasets of cow and human milk lipids at 2, 4, and 6 months of lactation periods were preprocessed and predicted for their target genes using TargetScanHuman. Enrichment analysis was performed using target genes to extract the immune-associated gene ontology (GO) terms shared between the two species. The genes within these terms with more than 50 different miRNAs of each species targeting were selected and reviewed for their immunological functions.

Results: A total of 146 and 129 miRNAs were identified in cow and human milk with several miRNAs reproduced from other previous reports. Enrichment analysis revealed nine immune-related GO terms shared between cow and human (adjusted p≤0.01). There were 14 genes related to these terms with more than 50 miRNA genes of each species targeting them. These genes were evidenced for their major roles in lymphocyte stimulation and differentiation.

Conclusion: A novel procedure to determine mutual immune-associated genes targeted by milk miRNAs was demonstrated using cow and human milk miRNome data. As far as we know, this was the 1st time that milk miRNA target genes had been identified based on such cross-species approach. Hopefully, the introduced strategy should hereby facilitate a variety of cross-species miRNA studies in the future.

Keywords: immune-associated target gene, microRNAs, milk, miRNome.