scholarly journals Characterization of a variant vlhA gene of Mycoplasma synoviae, strain WVU 1853, with a highly divergent haemagglutinin region

2010 ◽  
Vol 10 (1) ◽  
pp. 6 ◽  
Author(s):  
Awatef Béjaoui Khiari ◽  
Ibtissem Guériri ◽  
Radhia Ben Mohammed ◽  
Boutheina Ben Abdelmoumen Mardassi
Keyword(s):  
1998 ◽  
Vol 35 (3) ◽  
pp. 178-190 ◽  
Author(s):  
S. B. Lockaby ◽  
F. J. Hoerr ◽  
L. H. Lauerman ◽  
S. H. Kleven

Six isolates of Mycoplasma synoviae, identified as WVU 1853, K1968, K1858, 92D8034, F10–2AS, and FMT, were compared for pathogenicity in broiler chickens. Specific-pathogen-free chickens were inoculated, in two groups of 20, with each isolate by footpad or eyedrop inoculation at 1 day of age and were examined at necropsy 7, 14, 28, and 42 days postinoculation. Specimens were taken for histopathology, culture, polymerase chain reaction assay, and hemagglutination-inhibition serology. Isolates were grouped according to pathogenicity on the basis of differences in lesion development and tissue distribution in the respiratory system, other viscera, and the skeletal system. K1968 (pathogenic) induced lesions in all sites examined in both the footpad and eyedrop inoculation groups. It was detected in all sites following footpad inoculation and in all sites except viscera following eyedrop inoculation. WVU 1853, K1858, and 92D8034 (moderately pathogenic) induced lesions and were detected in all sites following footpad inoculation. With eyedrop inoculation, lesions were identified only in upper and lower respiratory sites, and organisms were detected only in upper respiratory sites. F10–2AS (moderately pathogenic) was similar; however, footpad inoculation failed to induce visceral lesions or permit organism detection in any site. F10–2AS was detected in upper and lower respiratory tissues following eyedrop inoculation. FMT (mildly pathogenic) induced only upper respiratory lesions when either footpad or eyedrop inoculation was used, and detection was restricted to upper respiratory sites following eyedrop inoculation. These results are useful in comparative evaluations of the virulence of other M. synoviae isolates and form a basis for characterization of virulence factors of M. synoviae.


2020 ◽  
Vol 99 (2) ◽  
pp. 719-724 ◽  
Author(s):  
Viviana Felice ◽  
Caterina Lupini ◽  
Giulia Mescolini ◽  
Flavio Silveira ◽  
Alessandro Guerrini ◽  
...  

2012 ◽  
Vol 156 (3-4) ◽  
pp. 322-329 ◽  
Author(s):  
Awatef Béjaoui Khiari ◽  
Boutheina Ben Abdelmoumen Mardassi

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Khalda A. Khalifa ◽  
Egbal Sidahmed Abdelrahim ◽  
Magdi Badwi ◽  
Amal M. Mohamed

The current study described the isolation and molecular detection of Mycoplasma gallisepticum (Mg) and Mycoplasma synoviae from tracheal swabs of diseased birds showing signs of respiratory distress in selected commercial (layer and broiler) farms and from yolk and an open air of pens of vaccinated breeder flocks in Sudan. A number of 45 Mycoplasma isolates were recovered from chickens in Khartoum, Gezira, and Equatoria states in Sudan. Of these, eight Mg and three Ms isolates were identified using growth inhibition and rapid serum agglutination (RSA) tests. The conventional PCR technique was applied to amplify 140 bp and 720 bp DNA fragments for the Mg and Ms, respectively. This research confirmed vertical and horizontal transmission of Mg from breeder farms through detection of Mg in yolk of fertile eggs and an air of pens despite previous vaccination. PCR is considered a rapid, sensitive, and cheap method and it will improve the diagnosis of Mycoplasma in chickens.


2013 ◽  
Vol 57 (7) ◽  
pp. 3072-3077 ◽  
Author(s):  
I. Lysnyansky ◽  
I. Gerchman ◽  
I. Mikula ◽  
F. Gobbo ◽  
S. Catania ◽  
...  

ABSTRACTThein vitroactivity of enrofloxacin against 73Mycoplasma synoviaefield strains isolated in Israel and Europe was determined by broth microdilution. Decreased susceptibility to enrofloxacin was identified in 59% of strains, with the MICs ranging from 1 to >16 μg/ml. The estimated MIC50and MIC90values for enrofloxacin were 2 and 8 μg/ml, respectively. Moreover, this study showed that 92% of recent Israeli field isolates (2009 to 2011) ofM. synoviaehave MICs of ≥2 μg/ml to enrofloxacin. Comparison of the quinolone resistance-determining regions (QRDRs) inM. synoviaeisolates revealed a clear correlation between the presence of one of the amino acid substitutions Asp79-Asn, Thr80-Ala/Ile, Ser81-Pro, and Asp84-Asn/Tyr/His of the ParC QRDR and decreased susceptibility to enrofloxacin (MIC, ≥1 μg/ml). Amino acid substitutions at positions GyrA 87, GyrB 401/402, and ParE 420/454 were also identified, but there was no clear-cut correlation with susceptibility to enrofloxacin. Comparison ofvlhAmolecular profiles revealed the presence of 9 different genotypes in the IsraeliM. synoviaefield isolates and 10 genotypes in the European isolates; only onevlhAgenotype (type 4) was identified in both cohorts. Based on results ofvlhAmolecular typing, several mechanisms for emergence and dissemination of Israeli enrofloxacin-resistantM. synoviaeisolates are suggested.


2020 ◽  
Vol 51 (5) ◽  
pp. 1321-1328
Author(s):  
Ali & et al.

The aim of this study was to investigate the presence of Mycoplasma synoviae in broiler and layer chickens infected with respiratory signs. A total of 80 samples were collected randomly from layer and broiler chickens with respiratory signs in Baghdad from the period between January to May 2017 from the trachea, Lung, Air sac, oviduct, tracheal swabs, conjunctiva swabs, choanal swabs, and nasal swabs and cultured in PPLO medium with supplements, then positive culture subjected to DNA extracted and Polymerase Chain Reaction assay (PCR) to detect Mycoplasma as a genus and Mycoplasma spp by using specific primers targeting16S rRNA gene. The results of culture revealed that the total rate of Mycoplasma isolates was19/80(23.75%). DNA was extracted from 19  positive isolates, all nineteen isolates were positive for Mycoplasma genus by conventional PCR assay, and a product of 270 bp was generated by amplification of the 16SrRNA gene, while a 210 bp region of 16S rRNA gene was amplified for the Mycoplasma synoviae in 19 isolates. The products of amplification of Mycoplasma synoviae16SrRNA gene was sent to MACROGEM (Korea) for sequencing, then submitted in the Gene bank database and have accession number:ID: MG846121.1. Sequencing alignment showed that local MS isolates had highly identical with standard references at gene bank, analysis the phylogenetic tree revealed the presence of 100% identity of the Iraqi isolate to the USA: West Virginia, United Kingdom, Australia, and Brazil, also had 99% identity to South Africa, China, Sweden, USA, and  VitNamHatey. This result was concluded that circulation of the Mycoplasma synoviae among birds of the flock and caused respiratory signs in chickens.


Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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