Thursday 12 October 2017

West African donkey's liveweight estimation using body measurements

Research (Published online: 12-10-2017)
10. West African donkey's liveweight estimation using body measurements
Pierre Claver Nininahazwe, Adama Sow, Rakiswende Constant Roamba, Miguiri Kalandi, Hachi Dirir Ahmed, Georges Anicet Ouedraogo and Germain Jerome Sawadogo
Veterinary World, 10(10): 1221-1226
ABSTRACT
Aim: The objective of this study was to determine a formula for estimating the liveweight in West African donkeys.
Materials and Methods: Liveweight and a total of 6 body measurements were carried out on 1352 donkeys from Burkina Faso, Mali, Niger, and Senegal. The correlations between liveweight and body measurements were determined, and the most correlated body measurements with liveweight were used to establish regression lines.
Results: The average weight of a West African donkey was 126.0±17.1 kg, with an average height at the withers of 99.5±3.67 cm; its body length was 104.4±6.53 cm, and a heart girth (HG) of 104.4±6.53 cm. After analyzing the various regression lines and correlations, it was found that the HG could better estimate the liveweight of West African donkeys by simple linear regression method. Indeed, the liveweight (LW) showed a better correlation with the HG (R2=0.81). The following formulas (Equations 1 and 2) could be used to estimate the LW of West Africa donkeys. Equation 1: Estimated LW (kg) = 2.55 x HG (cm) - 153.49; Equation 2: Estimated LW (kg) = Heart girth (cm)2.68 / 2312.44.
Conclusion: The above formulas could be used to manufacture weighing tape to be utilized by veterinary clinicians and farmers to estimate donkey's weight in the view of medication and adjustment of load.
Keywords: body measurements, donkey, estimated liveweight, West Africa.

Wednesday 11 October 2017

Protective efficacy of combined trivalent inactivated ISA 71 oil adjuvant vaccine against avian influenza virus subtypes (H9N2 and H5N1) and Newcastle disease virus

Research (Published online: 11-10-2017)
9. Protective efficacy of combined trivalent inactivated ISA 71 oil adjuvant vaccine against avian influenza virus subtypes (H9N2 and H5N1) and Newcastle disease virus
Zeinab Mohamed Ali, Mervat Abd El Monaem Hassan, Hussein Ali Hussein, Basem Mohamed Ahmed and Ahmed Abd El-Ghany El Sanousi
Veterinary World, 10(10): 1212-1220
ABSTRACT
Aim: The objective of the present study was to prepare a trivalent inactivated vaccine of Newcastle disease virus (NDV), H5N1, and H9N2 viruses.
Materials and Methods: Three monovalent and a trivalent vaccines were prepared by emulsifying inactivated NDV (LaSota strain), reassortant H5N1, and H9N2 viruses with Montanide ISA 71 oil adjuvant. Parameters used for evaluation of the efficacy of the prepared vaccines in specific pathogen-free chickens were cellular immunity assays (blastogenesis, interferon gamma, interleukin 1 [IL1], and IL6), humoral immunity by hemagglutination inhibition, protection percentage, and shedding.
Results: A single immunization with trivalent vaccine-enhanced cell-mediated immunity as well as humoral immune response with 90% protection against challenges with highly pathogenic avian influenza (HPAI) H5N1 and low pathogenic (LP) avian influenza H9N2 viruses with 100% protection after challenge with NDV.
Conclusion: Development and evaluation of the trivalent vaccine in the study reported the success in preparation of a potent and efficacious trivalent vaccine which is a promising approach for controlling HPAI H5N1, LP H9N2, and ND viral infections.
Keywords: avian influenza, immunization, Newcastle disease virus, shedding, trivalent vaccine.

Monday 9 October 2017

Polymerase chain reaction detection of genes responsible for multiple antibiotic resistance Staphylococcus aureus isolated from food of animal origin in Egypt

Research (Published online: 09-10-2017)
8. Polymerase chain reaction detection of genes responsible for multiple antibiotic resistance Staphylococcus aureus isolated from food of animal origin in Egypt
Fawzy R. El Seedy, A. A. Samy, Hala S. H. Salam, Eman A. Khairy and Aya A. Koraney
Veterinary World, 10(10): 1205-1211
ABSTRACT
Aim: The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance S. aureus isolated from food of animal origin in Egypt.
Materials and Methods: A total of 125 samples were randomly collected from milk, meat, and their products from Giza and Beni-Suef Governorates markets. The S. aureus isolates were subjected to antimicrobial sensitivity tests using four antibacterial disks (Oxoid), and then the polymerase chain reaction (PCR) was performed for detection of antibiotic resistance genes.
Results: Out of 125 samples, 19 S. aureus isolates were detected. All detected isolates were multiple drug resistance (MDR). The penicillin-, erythromycin-, kanamycin-, and tetracycline-resistant isolates were examined by PCR for resistance genes blaZ, (msrAermB, and ermC), aac(6')aph (2''), and tetK. The isolates harbored these resistance genes with percentage of 100% (100%, 0%, and 100%), 62.5%, and 100%, respectively.
Conclusion: Contaminated foods of animal origin may represent a source of MDR S. aureus that can be a major threat to public health.
Keywords: food of animal origin, multiple antibiotic resistance, polymerase chain reaction, resistance genes, Staphylococcus aureus.

Sunday 8 October 2017

Public health concerns of highly pathogenic avian influenza H5N1 endemicity in Africa

Review (Published online: 08-10-2017)
7. Public health concerns of highly pathogenic avian influenza H5N1 endemicity in Africa
Olubunmi Gabriel Fasanmi, Ismail Ayoade Odetokun, Fatima Adeola Balogun and Folorunso Oludayo Fasina
Veterinary World, 10(10): 1194-1204
ABSTRACT
Highly pathogenic avian influenza virus (HPAIV) H5N1 was first officially reported in Africa in 2006; thereafter this virus has spread rapidly from Nigeria to 11 other African countries. This study was aimed at utilizing data from confirmed laboratory reports to carry out a qualitative evaluation of the factors responsible for HPAI H5N1 persistence in Africa and the public health implications; and to suggest appropriate control measures. Relevant publications were sought from data banks and repositories of FAO, OIE, WHO, and Google scholars. Substantiated data on HPAI H5N1 outbreaks in poultry in Africa and in humans across the world were mined. HPAI H5N1 affects poultry and human populations, with Egypt having highest human cases (346) globally. Nigeria had a reinfection from 2014 to 2015, with outbreaks in Cote d'Ivoire, Ghana, Niger, Nigeria, and Burkina Faso throughout 2016 unabated. The persistence of this virus in Africa is attributed to the survivability of HPAIV, ability to evolve other subtypes through genetic reassortment, poor biosecurity compliance at the live bird markets and poultry farms, husbandry methods and multispecies livestock farming, poultry vaccinations, and continuous shedding of HPAIV, transboundary transmission of HPAIV through poultry trades; and transcontinental migratory birds. There is, therefore, the need for African nations to realistically reassess their status, through regular surveillance and be transparent with HPAI H5N1 outbreak data. Also, it is important to have an understanding of HPAIV migration dynamics which will be helpful in epidemiological modeling, disease prevention, control and eradication measures.
Keywords: Africa, highly pathogenic avian influenza H5N1, public health implications.

Friday 6 October 2017

Seroprevalence of Fasciola gigantica infection in bovines using cysteine proteinase dot enzyme-linked immunosorbent assay

Research (Published online: 06-10-2017)
6. Seroprevalence of Fasciola gigantica infection in bovines using cysteine proteinase dot enzyme-linked immunosorbent assay
Niranjan Kumar, Anju Varghese and J. B. Solanki
Veterinary World, 10(10): 1189-1193
ABSTRACT
Aim: The objective of the present study was to know the seroprevalence status of Fasciola gigantica infection in cattle and buffaloes using cysteine proteinase (CP) antigen in dot enzyme-linked immunosorbent assay (ELISA) format under field conditions.

Materials and Methods: As per the standard protocol, the sera were collected from the blood of 112 cattle and 38 buffaloes of coastal areas of Navsari district, South Gujarat, India. The indirect ELISA was performed on the strip of nitrocellulose paper blotted with 1 μl of CP antigen, to detect F. gigantica seropositive animals.

Results: The native CP of F. gigantica revealed a single visible band on 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis. There was no any noted cross-reaction between the selected antigen and sera of Gastrothylax crumenifer-infected animals in ELISA. Out of 150 screened bovines, the sera of 47 (31.33%) were found to be reactive in dot-ELISA, with a prevalence rate of 31.25% and 31.58% in cattle and buffaloes, respectively. The seropositive bovines with heavy, moderate, and light level of infection were 44.68%, 34.04%, and 21.28%, respectively (p<0.05 between heavy and light; p>0.05 between moderate and heavy or light). The share of F. gigantica seropositive and negative animals was 31% and 69%, respectively. The optical density at 450 nm of pooled sera of seropositive bovines with heavy, moderate, and light reactivity in plate-ELISA was significantly higher with field or reference negative sera.

Conclusion: The CP-based dot-ELISA can be useful for field veterinarians for quick and timely isolation of the animals requiring urgent flukicide therapy.

Keywords: bovines, cysteine proteinase, dot enzyme-linked immunosorbent assay, Fasciola gigantica.

Wednesday 4 October 2017

Effect of antioxidants supplementation on the quality of Beetal buck semen stored at 4°C

Research (Published online: 05-10-2017)
5. Effect of antioxidants supplementation on the quality of Beetal buck semen stored at 4°C
Archana Sarangi, Pardeep Singh, Meenakshi Virmani, A. S. Yadav, Subhasish Sahu, H. M. Ajithakumar, Anuradha Kumari and A. P. Rath
Veterinary World, 10(10): 1184-1188
ABSTRACT
Aim: An experiment was designed to evaluate the role of Vitamin E and glutathione in improving the seminal parameters during hypothermic storage of liquid semen at 4°C for 72 h.

Materials and Methods: Thirty-six semen ejaculates were collected by artificial vagina from 6 bucks (Beetal) during the normal reproduction season (September to November) at weekly interval. The samples were centrifuged, and the seminal plasma was removed. The sperm pellet was diluted with Tris-based extender and divided into three groups. Group T1: Control samples without antioxidants, Group T2: Samples supplemented with tocopherol at 3 mM, and Group T3: Samples supplemented with glutathione at 1 mM. The samples were evaluated for progressive motility, percent liveability, percent abnormal spermatozoa, and acrosome integrity after liquid preservation for 0, 24, 48, and 72 h. The level of lipid peroxidation and antioxidant enzymes, namely, glutathione peroxidase (GPx) and superoxide dismutase (SOD) were estimated after liquid preservation for 0 and 72 h.

Results: It was observed that, after storage of semen at 4°C up to 72 h, the progressive sperm motility, percent liveability, percent abnormal spermatozoa, and percent intact acrosomes were significantly (p<0.05) higher in group T2 and T3 samples as compared to control. However, the level of lipid peroxidation in T2 and T3 groups was significantly (p<0.05) lower after 72 h of incubation at 4°C. Similarly, GPx and SOD values were significantly (p<0.05) increased in T2 and T3 groups after 72 h of storage at 4°C.

Conclusion: Thus, it can be concluded that Vitamin E and glutathione supplementation at 3 mM and 1 mM, respectively, while preserving the semen samples at 4°C helped in maintaining the seminal parameters up to 72 h and protected the spermatozoa from oxidative damage.

Keywords: Beetal buck, glutathione and liquid preservation, oxidative stress, semen, seminal parameters, Vitamin E.