scholarly journals Mycoplasma gallisepticum: A devastating organism for the poultry industry in Egypt

2021 ◽  
pp. 101658
Author(s):  
Sherif Marouf ◽  
Mahmoud A. Khalf ◽  
Mohammed Alorabi ◽  
Ahmed M. El-Shehawi ◽  
Amira M. El-Tahan ◽  
...  
2009 ◽  
Vol 28 (3) ◽  
pp. 1015-1023 ◽  
Author(s):  
K.M. OSMAN ◽  
M.M. ALY ◽  
Z.M.S. AMIN ◽  
B.S. HASAN

2017 ◽  
Vol 61 (4) ◽  
pp. 439-444 ◽  
Author(s):  
Syed Ehtisham-ul-Haque ◽  
Madiha Kiran ◽  
Usman Waheed ◽  
Muhammad Younus

AbstractIntroduction:Mycoplasma gallisepticum is considered the most pathogenic and economically significant avian Mycoplasma spp. for the worldwide poultry industry. The aim of this study was to develop a novel and sensitive real-time loop-mediated isothermal amplification (LAMP) assay based on the amplification of its mgc2 gene sequence for its rapid molecular detection in poultry.Material and Methods: Blood samples from 300 broiler and layer chickens were screened using a rapid serum agglutination (RSA) test. A real-time LAMP reaction was conducted with seropositive swab samples at 60°C for 90 min in an ESEQuant tube scanner using 6-carboxyfluorescein as the reporting dye.Results: The sensitivity of the developed assay was 10 fg/μL of DNA. The assay was found 100% specific, showing no cross-reactivity with other avian Mycoplasma species. The proportion found of the positive samples by the real-time LAMP was 58%. In comparison, the RSA was found to detect 52% of positive cases.Conclusion: The mgc2 real-time LAMP emerged as a more sensitive and accurate method for molecular detection of M. gallisepticum than RSA. Robustness and precision give it applicability as a potential field diagnostic tool for M. gallisepticum control. The study will be beneficial in reducing economic losses that M. gallisepticum inflicts on the poultry industry. This is the first reported development of a real-time LAMP assay based on the amplification of the mgc2 gene sequence using an ESEQuant tube scanner for galline M. gallisepticum detection.


2020 ◽  
Vol 22 (4) ◽  
pp. 45-47
Author(s):  
S.S. Kozak ◽  
◽  
N.L. Dogadova ◽  
N.A. Gorodnaya ◽  
A.G. Sleza ◽  
...  
Keyword(s):  

Author(s):  
V. Kumar ◽  
N. Pazhanivel ◽  
K. Gopal ◽  
R. Thangathurai ◽  
C. Balachandran

Mareks diseases (MD) is a lymphoproliferative disease of chicken affecting all organs including skin. Mareks disease is become a menace to the poultry industry owing to the serious economic loss. MD is caused by herpes virus with three serotype of MDV (Carter et al., 2006). MD is a very serious problem and it produces up to 60% of mortality in layers and 10% of mortality in broilers. Epidemiological data recorded average about 10–40% flock mortality (Arulmozi et al. 2011). The clinical feature of MD is characterized by paralysis of the wings, legs and neck with lameness, depression and death occurred. The present paper reports the occurrence of MD in Aseel chicken.


2000 ◽  
Vol 68 (2) ◽  
pp. 871-876 ◽  
Author(s):  
Li Liu ◽  
Kevin Dybvig ◽  
Victor S. Panangala ◽  
Vicky L. van Santen ◽  
Christopher T. French

ABSTRACT Mycoplasma gallisepticum, the cause of chronic respiratory infections in the avian host, possesses a family of M9/pMGA genes encoding an adhesin(s) associated with hemagglutination. Nucleotide sequences of M9/pMGA gene family members indicate extensive sequence similarity in the promoter regions of both the transcribed and silent genes. The mechanism that regulates M9/pMGA gene expression is unknown, but studies have revealed an apparent correlation between gene expression and the number of tandem GAA repeat motifs located upstream of the putative promoter. In this study, transposon Tn4001was used as a vector with the Escherichia coli lacZ gene as the reporter system to examine the role of the GAA repeats in M9/pMGA gene expression in M. gallisepticum. A 336-bp M9 gene fragment (containing the GAA repeat region, the promoter, and the translation start codon) was amplified by PCR, ligated with alacZ gene from E. coli, and inserted into the Tn4001-containing plasmid pISM2062. This construct was transformed into M. gallisepticum PG31. Transformants were filter cloned on agar supplemented with 5-bromo-4-chloro-3-indolyl-β-d-galactopyranoside (X-Gal) to monitor lacZ gene expression on the basis of blue/white color selection. Several cycles of filter cloning resulted in cell lineages in which lacZ gene expression alternated between the On and Off states in successive generations of progeny clones. The promoter regions of the M9-lacZ hybrid genes of individual progeny clones were amplified by PCR and sequenced. The only differences between the promoter regions of the blue and white colonies were in the number of GAA repeats. Clones that expressedlacZ had exactly 12 tandem copies of the GAA repeat. Clones that did not express lacZ invariably had either more than 12 (14 to 16) or fewer than 12 (5 to 11) GAA repeats. Southern analysis of M. gallisepticum chromosomal DNA confirmed that the phase-variable expression of the lacZ reporter gene was not caused by Tn4001 transposition. These data strongly indicate that changes in the length of the GAA repeat region are responsible for regulating M9/pMGA gene expression.


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