Evaluation of Fresh and Chilled Sahel bucks Semen Extended with two different Avian egg yolks (Chicken and Guinea fowl) based extenders preserved at 5 °c in Maiduguri, Nigeria

2022 ◽  
Vol 22 (1) ◽  
pp. 82
Author(s):  
Abdulhamid Abba ◽  
Abdurahman Mustapha ◽  
Mustapha Bamanga ◽  
Dauda Iliyasu ◽  
Ramatu Ali ◽  
...  
Keyword(s):  
Zoo Biology ◽  
2009 ◽  
Vol 28 (2) ◽  
pp. 137-143 ◽  
Author(s):  
Corinne P. Kozlowski ◽  
Joan E. Bauman ◽  
D. Caldwell Hahn

1990 ◽  
Vol 53 (1) ◽  
pp. 15-21 ◽  
Author(s):  
PAMELA J. SIONKOWSKI ◽  
LEORA A. SHELEF

The viability of Listeria monocytogenes strain Brie-1 was studied in raw and heat-treated (121°C, 15 min) whole eggs, albumen, or yolks during storage at 5 and 20°C. Studies with raw eggs showed that the organism grew only in egg yolks, where initial numbers (106 cells/g) increased to 108 cells/g (generation times of 1.7 d and 2.4 h at 5 and 20°C, respectively). Cell numbers in whole eggs initially declined and then leveled off. A sharp decline in cell numbers was observed in the raw albumen (to 102 cells/g after 22 d at 5°C and to <10 after 55 h at 20°C). In contrast, the organism grew in all heat-treated egg samples. Generation times for cooked whole eggs, yolks, and albumen were 1.9, 2.3, and 2.4 d at 5°C, and 2.6, 2.6, and 3.5 h at 20°C, respectively. The rapid initial decline in populations was observed in raw albumen (pH 8.9), and after adjustments to pH 7.0 or 8.0. Numbers of surviving cells/g after 35 d at 5°C were reduced to 104, 103, and <10, at pH 7, 8, and 9 respectively. With the exception of the raw albumen, refrigerated raw and cooked eggs supported survival and growth of L. monocytogenes, and hence can serve as vehicle of transmission of listeriosis.


2010 ◽  
Vol 47 (3) ◽  
pp. 256-261 ◽  
Author(s):  
Hae-duck Bae ◽  
Hiroyuki Honda ◽  
Rie Murota ◽  
Misato Kobayashi ◽  
Fumihiko Horio ◽  
...  
Keyword(s):  

2012 ◽  
Vol 3 (8) ◽  
pp. 476-478
Author(s):  
Vineetha P.G Vineetha P.G ◽  
◽  
Simmi Tomar ◽  
Deepthi Vijay ◽  
Sreelekshmy Mohandas
Keyword(s):  

2014 ◽  
Vol 43 (6) ◽  
pp. 58-62 ◽  
Author(s):  
V.A. Zabiiakin ◽  
◽  
T.V. Zabiiakina ◽  
A.L. Kropotova ◽  
◽  
...  

2016 ◽  
Vol 5 (04) ◽  
pp. 4974
Author(s):  
Ayoh Stephen O. ◽  
Olanrewaju Comfort A*

Ticks transmit a greater variety of pathogenic micro-organisms than any other arthropod vector group, and are among the most important vectors of diseases affecting animals. A survey on the prevalence of tick species infesting domestic birds sold in Gwagwalada main market, Abuja between April and July, 2015. A total of 450 birds were examined by feather separation with fingers and a pair of forceps to expose the skin of the birds for presence of the ticks. An overall prevalence of 25.6% was observed. Out of the 150 domestic fowls examined 62(53.9%) were infested, 44(29.3%) of the 150 Guinea fowl and 9(6.0%) of the 150 Pigeons were infested. Of all the ticks identified, 93(51.4%) were from the Domestic Fowls and 77(42.5%) from the Guinea fowl and 11(6.0%) from Pigeon. Thirty (32.3%) of the ticks from the Domestic fowls were Argas persicus, 25(26.9%) Argas walkerae, 20 (21.5%) Ornithodorus moubata and 18(19.4%) Ornithodorus savignyi. Similarly, 34(44.2%) of the ticks from Guinea fowl were A. walkerae, 20(28.2%) O. moubataand 23(32.4%) O. savignyi. Five (45.5%) of the ticks from Pigeon were A. persicus, 4 (36.4%) were A. walkerae, 2 (18.2%) were O. moubata and no O. savignyi. Observation on the location of tick from the hosts body showed highest prevalence was found under the wings (55.2%) and lowest on the head & neck (5.00%). The result of this research revealed that Gwagwalada market poultry section is endemic of tick infestation. Chemical control with acaricides and improved management and sanitation of the poultry cages in the market should be enforced.


2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 252-253
Author(s):  
Cherrie Nolden ◽  
Abbey Grisham ◽  
Dan Schaefer ◽  
Matt Akins ◽  
Mark Cook

Abstract Antibody production in egg yolks of immunized laying hens is an alternative to conventional mammalian production. Antibody yield peak and duration have not been described for immunoglobulin Y technology using Freund’s incomplete adjuvant (FIA) and C-phosphate-guanosine oligodeoxynucleotides (CpG-ODN) without the inclusion of Freund’s complete adjuvant for enhancing the immune response to an interleukin-10 (IL-10) peptide. This study sought to describe the antibody titer production for an 8 amino acid sequence from the surface of the bovine IL-10 protein (VMPQAENG) as the antigen emulsified with CpG-ODN and FIA in phosphate buffered saline (PBS). 60 hens were assigned to receive the complete vaccine (Peptide), 20 received the vaccine without the IL-10 peptide (Control), and 8 received a PBS injection (Blank). Hens were immunized with 0.25 mL in 4 locations, each breast and each thigh on days 1, 15 and 29. The complete vaccine delivered 0.6 mg IL-10 peptide, 8 µg CpG-ODN, and 0.33 mL FIA per hen on each vaccination day. Eggs were collected regularly until 175 days after the first immunization and the anti IL-10 peptide activities of the yolk were determined by ELISA. Egg titers by treatment were analyzed with a repeated measures ANOVA in SAS. The supplementation of FIA with CpG-ODN produced high titers, of over 100 µg of antibody per mL of yolk (µg Ab/mL yolk), around day 33 through day 76, with a slow decline through day 175 when average titers remained above 40 µg Ab/mL yolk. Peptide egg titers were significantly higher than Blank or Control titers from day 31 though day 175 (P < 0.0001). Titers recovered from Marcq et al. (2015) with similar methods were 1.5 to 7 times lower than these results over the same number of days.


Author(s):  
Quan-Kuan Shen ◽  
Min-Sheng Peng ◽  
Adeniyi C Adeola ◽  
Ling Kui ◽  
Shengchang Duan ◽  
...  

Abstract Domestication of the helmeted guinea fowl (HGF; Numida meleagris) in Africa remains elusive. Here we report a high-quality de novo genome assembly for domestic HGF generated by long and short-reads sequencing together with optical and chromatin interaction mapping. Using this assembly as the reference, we performed population genomic analyses for newly sequenced whole-genomes for 129 birds from Africa, Asia, and Europe, including domestic animals (n = 89), wild progenitors (n = 34), and their closely related wild species (n = 6). Our results reveal domestication of HGF in West Africa around 1,300-5,500 years ago. Scanning for selective signals characterized the functional genes in behavior and locomotion changes involved in domestication of HGF. The pleiotropy and linkage in genes affecting plumage color and fertility were revealed in the recent breeding of Italian domestic HGF. In addition to presenting a missing piece to the jigsaw puzzle of domestication in poultry, our study provides valuable genetic resources for researchers and breeders to improve production in this species.


Sign in / Sign up

Export Citation Format

Share Document