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Journal articles on the topic 'Mycoplasma meleagridis'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Basak, Parinita, Banya Banowary, Safeth Arju, and Mohammad Zakir Hossain. "Isolation and molecular detection of avian mycoplasmosis in selected areas of Mymensingh district in Bangladesh." Asian Journal of Medical and Biological Research 7, no. 2 (June 30, 2021): 182–90. http://dx.doi.org/10.3329/ajmbr.v7i2.54998.

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Avian mycoplasmosis caused by several species of Mycoplasma including Mycoplasma gallisepticum, M synoviae, M. meleagridis and M. iowae. Among these Mycoplasma gallisepticum is the most important poultry pathogen in Bangladesh. For effective control of Mycoplasmosis, proper early diagnosis is the corner stone. The research work was designed, a total of 20 samples, lung exudates, swabs from trachea and air sacs were collected from dead birds of different poultry farms in Mymensingh district during October-December, 2007. Samples were collected in 10% buffered formalin for histopathological study. Swabs were collected in mycoplasma broth supplemented with supplement-G. Additionally Kanamycin solution was added to prevent the growth of gram–Ve bacteria and then the organisms were transferred into mycoplasma agar for isolation. Histopathological studies were conducted using routine procedure in Hematoxylin and Eosin stain. Isolated Mycoplasma were subjected to DNA extraction, Nested PCR was done using a commercial PCR kit. The histopathological study revealed the presence of mycoplasmal related tissue changes, such as severe congestion and infiltration of mononuclear cells in different organs. The extracted DNA accumulated at the upper position of DNA ladder as band without any smear formation. The DNA from avian mycoplasmas was amplified and gave amplified product of 975 bp by outer primer and 395 bp by inner primer which was much smaller than the expected size. In this study, preliminary results from field samples suggest that culture using mycoplasma agar and broth supplement with Supplement-G and Kanamycin solution could be useful for the isolation of pathogenic avian mycoplasmas. Asian J. Med. Biol. Res. 2021, 7 (2), 182-190

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2

Khiari, A. Béjaoui, A. Landoulsi, H. Aissa, B. Mlik, F. Amouna, A. Ejlassi, and B. Ben Abdelmoumen Mardassi. "Isolation of Mycoplasma meleagridis from Chickens." Avian Diseases Digest 6, no. 1 (March 2011): e32-e33. http://dx.doi.org/10.1637/9621-936511-digest.1.

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3

Lam, K. M. "Pathogenicity of Mycoplasma meleagridis for Chicken Cells." Avian Diseases 48, no. 4 (December 2004): 916–20. http://dx.doi.org/10.1637/7217-060304r.

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4

Boussetta, M., N. Chaouachi, and B. Mlik. "Etude sérologique et bactériologique des mycoplasmoses aviaires dans la région du Cap Bon en Tunisie." Revue d’élevage et de médecine vétérinaire des pays tropicaux 50, no. 2 (February 1, 1997): 93–96. http://dx.doi.org/10.19182/remvt.9592.

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Une enquête séroépidémiologique et bactériologique a été effectuée en Tunisie dans une région à forte concentration aviaire pour le dépistage des mycoplasmoses à Mycoplasma gallisepticum, M. synoviae chez la poule et chez la dinde. Au cours de l'enquête, 63 élevages ont été visités et 780 prélèvements de sang et écouvillons trachéaux ont été effectués et analysés pour la recherche sérologique d'anticorps anti-Mycoplasma gallisepticum, -M. synoviae et -M. meleagridis. La recherche bactériologique a porté sur M. gallisepticum et M. synoviae. Les taux d'infection des troupeaux déterminés par sérologie étaient de 36,5 % pour M. gallisepticum, de 19 % pour M. synoviae et de 0 % pour M. meleagridis. Les élevages positifs en bactériologie pour M. gallisepticum et M. synoviae étaient respectivement au nombre de 15 et 5, soit 23,8 et 7,9 % des élevages visités.

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5

Singh, P., Christine A. Yavari, John A. Newman, and Janet M. Bradbury. "Identification of Mycoplasma Iowae by Colony Immunoblotting Utilizing Monoclonal Antibodies." Journal of Veterinary Diagnostic Investigation 9, no. 4 (October 1997): 357–62. http://dx.doi.org/10.1177/104063879700900403.

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The utility of monoclonal antibody Mab-2C in identification of Mycoplasma iowae (MI) by colony immunoblotting technique was explored. Colony immunoblots of reference MI strains, field isolates, and mycoplasmas recovered from experimentally inoculated turkey embryos were probed with Mab-2C. The monoclonal antibody identified colonies of all the MI isolates tested and did not cross-react with colonies of M. gallisepticum, M. synoviae, or M. meleagridis. In western immunoblots of 22 MI field isolates, Mab-2C showed immunoreactivity with an antigen of approximately 45 kD molecular weight. No phenotypic variation of the epitope recognized by Mab-2C was observed in colony immunoblots of MI colonies. The monoclonal antibody reported here can be used for identification of MI colonies by a simple and rapid colony immunoblot method.

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6

Shaohua Zhao and Richard Yamamoto. "Species-specific recombinant DNA probes for Mycoplasma meleagridis." Veterinary Microbiology 35, no. 1-2 (May 1993): 179–85. http://dx.doi.org/10.1016/0378-1135(93)90124-p.

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7

Zhao, Shaohua, and Richard Yamamoto. "Detection of Mycoplasma meleagridis by polymerase chain reaction." Veterinary Microbiology 36, no. 1-2 (July 1993): 91–97. http://dx.doi.org/10.1016/0378-1135(93)90131-p.

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8

Dufour-Gesbert, Fabienne, Isabelle Kempf, Franco De Simone, and Marylène Kobisch. "Antigen heterogeneity and epitope variable expression in Mycoplasma meleagridis isolates." Veterinary Microbiology 78, no. 3 (February 2001): 261–73. http://dx.doi.org/10.1016/s0378-1135(00)00337-0.

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9

Lam, K. M., A. J. DaMassa, and G. Yan Ghazikhanian. "Interactions Between the Membranes of Turkey Cells and Mycoplasma meleagridis." Avian Diseases 47, no. 3 (July 2003): 611–17. http://dx.doi.org/10.1637/6089.

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10

Edson, Robert K., R. Yamamoto, and T. B. Farver. "Mycoplasma meleagridis of Turkeys: Probability of Eliminating Egg-Borne Infection." Avian Diseases 31, no. 2 (April 1987): 264. http://dx.doi.org/10.2307/1590871.

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11

Mardassi, B. Ben Abdelmoumen, A. Béjaoui, L. Oussaeif, B. Mlik, and F. Amouna. "A Recombinant Antigen-Based Elisa For The Simultaneous Differential Serodiagnosis Of Mycoplasma Gallisepticum, Mycoplasma Synoviae, And Mycoplasma Meleagridis Infections." Avian Diseases 52, no. 2 (June 2008): 214–21. http://dx.doi.org/10.1637/8071-071207-reg.1.

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12

Mardassi, B. Ben Abdelmoumen, A. Béjaoui, L. Oussaeif, B. Mlik, and F. Amouna. "A Recombinant Antigen-Based Elisa For the Simultaneous Differential Serodiagnosis of Mycoplasma gallisepticum, Mycoplasma synoviae, and Mycoplasma meleagridis Infections." Avian Diseases Digest 3, no. 2 (June 2008): e4-e4. http://dx.doi.org/10.1637/8319-807108-digest.1.

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13

Lam, K. M., A. J. DaMassa, and G. Yan Ghazikhanian. "Mycoplasma meleagridis-Induced Lesions in the Tarsometatarsal Joints of Turkey Embryos." Avian Diseases 48, no. 3 (September 2004): 505–11. http://dx.doi.org/10.1637/7144.

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14

Zhao, Shaohua, R. Yamamoto, G. Yan Ghazikhanian, and M. I. Khan. "Antigenic analysis of three strains of Mycoplasma meleagridis of varying pathogenicity." Veterinary Microbiology 18, no. 3-4 (December 1988): 373–77. http://dx.doi.org/10.1016/0378-1135(88)90102-2.

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15

Lierz, M., R. Schmidt, L. Brunnberg, and M. Runge. "Isolation of Mycoplasma meleagridis from Free-ranging Birds of Prey in Germany." Journal of Veterinary Medicine Series B 47, no. 1 (February 2000): 63–67. http://dx.doi.org/10.1046/j.1439-0450.2000.00309.x.

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16

Moalic, Pierre-Yves, Fabienne Gesbert, Frédéric Laigret, and Isabelle Kempf. "Evaluation of polymerase chain reaction for detection of Mycoplasma meleagridis infection in turkeys." Veterinary Microbiology 58, no. 2-4 (November 1997): 187–93. http://dx.doi.org/10.1016/s0378-1135(97)00177-6.

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17

Moalic, Pierre-Yves, Fabienne Gesbert, and Isabelle Kempf. "Utility of an internal control for evaluation of a Mycoplasma meleagridis PCR test." Veterinary Microbiology 61, no. 1-2 (March 1998): 41–49. http://dx.doi.org/10.1016/s0378-1135(98)00173-4.

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18

Cardona, C. J., and A. A. Bickford. "Wry Necks Associated with Mycoplasma meleagridis Infection in a Backyard Flock of Turkeys." Avian Diseases 37, no. 1 (January 1993): 240. http://dx.doi.org/10.2307/1591482.

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19

Gethöffer, Friederike, Nele Curland, Ulrich Voigt, Benno Woelfing, Tobias Ludwig, Ursula Heffels-Redmann, Hafez Mohamed Hafez, Michael Lierz, and Ursula Siebert. "Seroprevalences of specific antibodies against avian pathogens in free-ranging ring-necked pheasants (Phasianus colchicus) in Northwestern Germany." PLOS ONE 16, no. 8 (August 4, 2021): e0255434. http://dx.doi.org/10.1371/journal.pone.0255434.

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Infectious diseases in captive pheasants (Phasianus colchicus) are well known, but there is a lack of knowledge about occurrence and distribution of pathogens in free-ranging pheasants in Germany. We investigated 604 sera from hunted pheasants and 152 sera from wild caught pheasants between 2011 to 2015, with the aim to determine the prevalence of specific antibodies against different viruses: Avian influenza virus (AIV) of subtypes H5, H7, H9, paramyxovirus type 1 (PMV-1), avian encephalomyelitis virus (AEV), infectious bursitis disease virus (IBDV), infectious bronchitis virus (IBV), infectious laryngotracheitis virus (ILTV), avian metapneumovirus (aMPV) and Salmonella sp., Mycoplasma synoviae (MS) and Mycoplasma gallisepticum (MG). In addition, 178 caeca were investigated for Histomonas meleagridis. The study reveals an ongoing circulation of IBV in the wild pheasant population during the study. Also high seroprevalences of specific antibodies against aMPV depending on the area and a strong increase in prevalence of IBDV antibodies in sera of pheasants in Lower Saxony were detected. ILTV antibody prevalences differed between areas and AEV antibody detection differed between years significantly, whereas specific antibodies against PMV-1 could not be detected and antibodies against AIV-H5, -H7 and -H9 and Mycoplasma spp. were detected in very few cases.

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20

Mardassi, B. Ben Abdelmoumen, A. Béjaoui Khiari, L. Oussaief, A. Landoulsi, C. Brik, B. Mlik, and F. Amouna. "Molecular cloning of a Mycoplasma meleagridis-specific antigenic domain endowed with a serodiagnostic potential." Veterinary Microbiology 119, no. 1 (January 2007): 31–41. http://dx.doi.org/10.1016/j.vetmic.2006.08.008.

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21

Dufour-Gesbert, Fabienne, Isabelle Kempf, and Marylène Kobisch. "Development of a blocking enzyme-linked immunosorbent assay for detection of turkey antibodies to Mycoplasma meleagridis." Veterinary Microbiology 78, no. 3 (February 2001): 275–84. http://dx.doi.org/10.1016/s0378-1135(00)00280-7.

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22

Yacoub, Elhem, and Boutheina Ben Abdelmoumen Mardassi. "Mm19, a Mycoplasma meleagridis Major Surface Nuclease that Is Related to the RE_AlwI Superfamily of Endonucleases." PLOS ONE 11, no. 3 (March 24, 2016): e0152171. http://dx.doi.org/10.1371/journal.pone.0152171.

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23

Jirjis, F. F., S. L. Noll, D. A. Halvorson, K. V. Nagaraja, and D. P. Shaw. "Pathogenesis of Avian Pneumovirus Infection in Turkeys." Veterinary Pathology 39, no. 3 (May 2002): 300–310. http://dx.doi.org/10.1354/vp.39-3-300.

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Avian pneumovirus (APV) is the cause of a respiratory disease of turkeys characterized by coughing, ocular and nasal discharge, and swelling of the infraorbital sinuses. Sixty turkey poults were reared in isolation conditions. At 3 weeks of age, serum samples were collected and determined to be free of antibodies against APV, avian influenza, hemorrhagic enteritis, Newcastle disease, Mycoplasma gallisepticum, Mycoplasma synoviae, Mycoplasma meleagridis, Ornithobacterium rhinotracheale, and Bordetella avium. When the poults were 4 weeks old, they were inoculated with cell culture–propagated APV (APV/Minnesota/turkey/2a/97) via the conjunctival spaces and nostrils. After inoculation, four poults were euthanatized every 2 days for 14 days, and blood, swabs, and tissues were collected. Clinical signs consisting of nasal discharge, swelling of the infraorbital sinuses, and frothy ocular discharge were evident by 2 days postinoculation (PI) and persisted until day 12 PI. Mild inflammation of the mucosa of the nasal turbinates and infraorbital sinuses was present between days 2 and 10 PI. Mild inflammatory changes were seen in tracheas of poults euthanatized between days 4 and 10 PI. Antibody to APV was detected by day 7 PI. The virus was detected in tissue preparations and swabs of nasal turbinates and infraorbital sinuses by reverse transcription polymerase chain reaction, virus isolation, and immunohistochemical staining methods between days 2 and 10 PI. Virus was detected in tracheal tissue and swabs between days 2 and 6 PI using the same methods. In this experiment, turkey poults inoculated with tissue culture-propagated APV developed clinical signs similar to those seen in field cases associated with infection with this virus.

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24

Boyle, J. S., R. T. Good, and C. J. Morrow. "Detection of the turkey pathogens Mycoplasma meleagridis and M. iowae by amplification of genes coding for rRNA." Journal of clinical microbiology 33, no. 5 (1995): 1335–38. http://dx.doi.org/10.1128/jcm.33.5.1335-1338.1995.

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25

Fan, H. H., S. H. Kleven, and M. W. Jackwood. "Studies of Intraspecies Heterogeneity of Mycoplasma synoviae, M. meleagridis, and M. iowae with Arbitrarily Primed Polymerase Chain Reaction." Avian Diseases 39, no. 4 (October 1995): 766. http://dx.doi.org/10.2307/1592413.

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26

Wood, B. J., and S. J. Wilson. "Mycoplasma iowae in turkeys (Meleagris gallopavo)." World's Poultry Science Journal 69, no. 4 (December 1, 2013): 909–16. http://dx.doi.org/10.1017/s0043933913000913.

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27

Abdelrahman, Abdelrahman A., Salama A. S. Shany, Mansy A. A. Dardeer, Kareem E. Hassan, Ahmed Ali, and Magdy F. El-Kady. "Avian Mycoplasma gallisepticum and Mycoplasma synoviae: Advances in diagnosis and control." German Journal of Veterinary Research 1, no. 2 (July 2021): 46–55. http://dx.doi.org/10.51585/gjvr.2021.2.0019.

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Both of Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS) infections are the most common Mycoplasma infection in domestic poultry. The disease is associated with economic losses in poultry. MG and MS are commonly spread within chickens (Gallus gallus domesticus) and turkeys (Meleagris gallopavo domesticus) flocks; however, they are frequently isolated from quails (Coturnix coturnix) and several avian species. Diagnosis of MG or MS infections is confirmed by isolating the organism in a cell-free medium or directly detecting its DNA in infected tissues or swab samples. Serological tests are also widely used for diagnosis. However, advances in molecular biology represented a rapid and sensitive alternative to the traditional culture methods requiring specialized techniques and sophisticated reagents. Several Mycoplasma molecular diagnostic tests are implemented: including polymerase chain reaction (PCR), Random Amplified Polymorphic DNA (RAPD), arbitrary primed polymerase chain reactions (AP‐PCR), and Multiplex real-time polymerase chain reaction (Multiplex MGMS). Current control practices against Mycoplasma infection include intense biosecurity, biosurveillance, medication, and vaccination. However, the egg-borne nature of avian Mycoplasma infection complicates controlling the infection. This review focuses on the advances in diagnosis and control of avian Mycoplasma infection, especially MG and MS infections.

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28

Sá, Sílvio G. de, José W. Pinheiro Júnior, Sineide M. de Oliveira Vilela, Erica P. B. X. Moraes, Pedro P. F. Albuquerque, Débora R. A. Ferreira, and Rinaldo A. Mota. "Occurrence and risk factors assessment associated with Mycoplasma gallisepticum (MG) infection in chickens in the semiarid region of Pernambuco, Brazil." Pesquisa Veterinária Brasileira 35, no. 6 (June 2015): 531–35. http://dx.doi.org/10.1590/s0100-736x2015000600007.

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Abstract: The aim of the present study was to assess the occurrence of Mycoplasma gallisepticum (MG) infection and risk factors of this disease in three hundred serum samples from on 23 familiar agricultural properties in the semiarid region of the state of Pernambuco, Brazil. ELISA was used to study antibodies anti-Mycoplasma gallisepticum. The univariate analysis (chi-squared test or Fischer's exact test) followed by multivariate analysis (logistic regression) were used to assess the risk factors with two variables: management and sanity of the poultry. It was detected a frequence of 53.33% (157/300) of the birds were positive for MG, with 100% foci. The risk factors confirmed by multivariate analysis, in the present study, were the presence of other poultry species on the property, including Numida meleagris (OR=2.22; p=0.005), parrots (OR=1.72; p=0.027), and of passerines (OR=1.88; p=0.007). These results showed that Mycoplasma gallisepticum infection is endemic among backyard poultry in the semiarid region of the state of Pernambuco. These birds could be a source of infection for other wild or domestic poultry. . This is the first report of the occurrence of avian mycoplasmosis in backyard poultry in the state of Pernambuco in northeastern Brazil. The risk factors identified should serve as a parameter for the health authorities to seek solutions related to controlling the disease.

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29

PAPANIKOLAOU (I.N. ΠΑΠΑΝΙΚΟΛΑΟΥ), J. N. "Epidemiological investigation o„f Mycoplasmas, M. gallisepticum, M. synoviae and M. meleagridis i poultry flocks in Greece." Journal of the Hellenic Veterinary Medical Society 53, no. 4 (January 25, 2018): 297. http://dx.doi.org/10.12681/jhvms.15385.

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The results of an investigation for the detection of abs to Mg, Ms and Mm in poultry farms in different regions in Greece are presented. For this purpose during the years of 1997-2000,1449 serum samples were examined, from which 1296 were originated from 72 chicken flocks (27 broiler; 19 layer, 22 breeder and 4 back-yard poultry), 75 from 4 turkey flocks, 58 from 3 flocks of partriges and 20 from 1 ostrich flock. The method used was the R.S.A. test (as a screening test) in combination with HI test. The incidence of Ms for broilers, layers and breeders was over 3 1% of the examined flocks, while the Mg in all the commercial chicken flocks was 17-25%. In back - yard poultry the incidence of Ms was 75% and to Mg 50%. In turkeys and partriges the incidence of Ms was 50% and 66% of the flocks respectively, while the positive flocks for Mg was 25-33%. The turkeys were negative for abs to Mm. The ostrich flock was also negative for abs to Mg and Ms. The results of our investigation indicate that the incidence of mycoplasmas in poultry, especially to Ms, is high in Greece. As a conclusion for the eradication of mycoplasmosis, it is necessary for the poultry industry and for the country, to follow the instruction included in 90/539/EEC directive and to take strickt hygienic measures in order to eliminate the microorganisms from the poultry flocks.

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30

Fritz, B. A., C. B. Thomas, and T. M. Yuill. "SEROLOGICAL AND MICROBIAL SURVEY OF MYCOPLASMA GALLISEPTICUM IN WILD TURKEYS (MELEAGRIS GALLOPAVO) FROM SIX WESTERN STATES." Journal of Wildlife Diseases 28, no. 1 (January 1992): 10–20. http://dx.doi.org/10.7589/0090-3558-28.1.10.

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31

MacDonald, Amanda M., Claire M. Jardine, Evelin Rejman, John R. Barta, Jeff Bowman, Hugh Y. Cai, Leonardo Susta, and Nicole M. Nemeth. "HIGH PREVALENCE OF MYCOPLASMA AND EIMERIA SPECIES IN FREE-RANGING EASTERN WILD TURKEYS (MELEAGRIS GALLOPAVO SILVESTRIS) IN ONTARIO, CANADA." Journal of Wildlife Diseases 55, no. 1 (January 1, 2019): 54. http://dx.doi.org/10.7589/2017-11-273.

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32

Yacoub, Elhem, Pascal Sirand-Pugnet, Aurélien Barré, Alain Blanchard, Christophe Hubert, Florence Maurier, Emmanuel Bouilhol, and Boutheina Ben Abdelmoumen Mardassi. "Genome Sequences of Two Tunisian Field Strains of Avian Mycoplasma , M. meleagridis and M. gallinarum." Genome Announcements 4, no. 3 (June 16, 2016). http://dx.doi.org/10.1128/genomea.00558-16.

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Mycoplasma meleagridis and Mycoplasma gallinarum are bacteria that affect birds, but little is known about the genetic basis of their interaction with chickens and other poultry. Here, we sequenced the genomes of M. meleagridis strain MM_26B8_IPT and M. gallinarum strain Mgn_IPT, both isolated from chickens showing respiratory symptoms, poor growth, reduction in hatchability, and loss of production.

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33

Rocha, Ticiana S., Luigi Bertolotti, Salvatore Catania, Philippe Pourquier, and Sergio Rosati. "Genome Sequence of a Mycoplasma meleagridis Field Strain." Genome Announcements 4, no. 2 (March 3, 2016). http://dx.doi.org/10.1128/genomea.00017-16.

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Mycoplasma meleagridis is a major cause of disease and economic loss in turkeys. Here, we report the genome sequence of an M. meleagridis field strain, which enlarges the knowledge about this bacterium and helps the identification of possible coding sequences for drug resistance genes and specific antigens.

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34

Yacoub, Elhem, Pascal Sirand-Pugnet, Alain Blanchard, and Boutheina Ben Abdelmoumen Mardassi. "Genome Sequence of Mycoplasma meleagridis Type Strain 17529." Genome Announcements 3, no. 3 (May 21, 2015). http://dx.doi.org/10.1128/genomea.00484-15.

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35

Abolnik, Celia. "Complete Genome Sequence of Mycoplasma meleagridis , a Possible Emerging Pathogen in Chickens." Genome Announcements 3, no. 3 (May 7, 2015). http://dx.doi.org/10.1128/genomea.00380-15.

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36

Orosco L., Rocío, Eliana Icochea D., John Guzmán L., Norma Noé M., and Nestor Falcón P. "PREVALENCIA DE ANTICUERPOS CONTRA Mycoplasma meleagridis EN PAVOS REPRODUCTORES DEL DEPARTAMENTO DE LIMA." Revista de Investigaciones Veterinarias del Perú 22, no. 3 (October 25, 2011). http://dx.doi.org/10.15381/rivep.v22i3.271.

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37

Catania, Salvatore, Stefania Rodio, Maria Luisa Moronato, Roger D. Ayling, and Robin A. J. Nicholas. "Outbreak of disease associated with Mycoplasma meleagridis in a free‐range mixed poultry farm." Veterinary Record Case Reports 2, no. 1 (January 2014). http://dx.doi.org/10.1136/vetreccr-2014-000107.

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38

Abolnik, Celia. "Retraction for Abolnik, Complete Genome Sequence of Mycoplasma meleagridis , a Possible Emerging Pathogen in Chickens." Genome Announcements 3, no. 3 (June 4, 2015). http://dx.doi.org/10.1128/genomea.00695-15.

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39

More, Simon, Anette Bøtner, Andrew Butterworth, Paolo Calistri, Klaus Depner, Sandra Edwards, Bruno Garin‐Bastuji, et al. "Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): avian mycoplasmosis (Mycoplasma gallisepticum, M. meleagridis)." EFSA Journal 15, no. 8 (August 2017). http://dx.doi.org/10.2903/j.efsa.2017.4953.

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