Contagious Agalactia In Sheep And Goats: Current Perspectives

References

• Lambert M. Contagious agalactia of sheep and goats. Rev Sci Tech. 1987;6:699–711. doi:10.20506/rst.6.3.308
   Google Scholar
• Madanat A, Zendulkova D, Pospísil Z. Contagious agalactia of sheep and goats. A review. Acta Vet Brno. 2001;70:403–412. doi:10.2754/avb200170040403
   Web of Science ®Google Scholar
• Thiaucourt F, Bolske G. Contagious caprine pleuropneumonia and other pulmonary mycoplasmoses of sheep and goats. Rev Sci Tech. 1996;15(4):1397–1414. doi:10.20506/rst.issue.15.4.24939190020
   PubMed Web of Science ®Google Scholar
• Bridré J, Donatien A. Le microbe de l’agalaxie contagieuse et sa culture in vitro. C R Acad Des Sci. 1923;177:841–843.
   Google Scholar
• Nicholas RAJ, Ayling RD, McAuliffe L. Contagious agalactia In: Mycoplasma Diseases of Ruminants. Oxfordshire, UK: CAB International; 2008:98–113.
   Google Scholar
• Cottew GS, Breard A, DaMassa AJ, et al. Taxonomy of the Mycoplasma mycoides cluster. Isr J Med Sci. 1987;23(6):632–635.3312102
   PubMedGoogle Scholar
• Manso-Silvan L, Perrier X, Thiaucourt F. Phylogeny of the Mycoplasma mycoides cluster based on analysis of five conserved protein-coding sequences and possible implications for the taxonomy of the group. Int J Syst Evol Microbiol. 2007;57(10):2247–2258. doi:10.1099/ijs.0.64918-017911291
   PubMedGoogle Scholar
• Manso-Silvan L, Vilei EM, Sachse K, Djordjevic SP, Thiaucourt F, Frey J. Mycoplasma leachii sp. nov. as a new species designation for Mycoplasma sp. bovine group 7 of Leach, and reclassification of Mycoplasma mycoides subsp. mycoides LC as a serovar of Mycoplasma mycoides subsp. capri. Int J Syst Evol Microbiol. 2009;59(6):1353–1358. doi:10.1099/ijs.0.005546-019502315
   PubMedGoogle Scholar
• Le Grand D, Saras E, Blond D, Solsona M, Poumarat F. Assessment of PCR for routine identification of species of the Mycoplasma mycoides cluster in ruminants. Vet Res. 2004;35(6):635–649. doi:10.1051/vetres:200403715535954
   PubMed Web of Science ®Google Scholar
• Poumarat F, Longchambon D, Martel JL. Application of dot immunobinding on membrane filtration (MF dot) to the study of relationships within “M. mycoides cluster” and within “glucose and arginine-negative cluster” of ruminant mycoplasmas. Vet Microbiol. 1992;32(3–4):375–390. doi:10.1016/0378-1135(92)90159-Q1455631
   PubMed Web of Science ®Google Scholar
• Kinde H, DaMassa AJ, Wakenell PS, Petty R. Mycoplasma infection in a commercial goat dairy caused by Mycoplasma agalactiae and Mycoplasma mycoides subsp. mycoides (caprine biotype). J Vet Diagn Invest. 1994;6(4):423–427. doi:10.1177/1040638794006004047858021
   PubMed Web of Science ®Google Scholar
• Gil MC, Pena FJ, Hermoso De Mendoza J, Gomez L. Genital lesions in an outbreak of caprine contagious agalactia caused by Mycoplasma agalactiae and Mycoplasma putrefaciens. J Vet Med B Infect Dis Vet Public Health. 2003;50(10):484–487. doi:10.1046/j.0931-1793.2003.00709.x14720185
   PubMedGoogle Scholar
• De La Fe C, Gutiérrez A, Poveda JB, Assunção P, Ramirez AS, Fabelo F. First isolation of Mycoplasma capricolum subsp capricolum, one of the causal agents of caprine contagious agalactia, on the island of Lanzarote (Spain). Vet J. 2005;173(2):440–442. doi:10.1016/j.tvjl.2005.09.01116324858
   PubMed Web of Science ®Google Scholar
• Gomez-Martin A, Amores J, Paterna A, De la Fe C. Contagious agalactia due to Mycoplasma spp. in small dairy ruminants: epidemiology and prospects for diagnosis and control. Vet J. 2013;198(1):48–56. doi:10.1016/j.tvjl.2013.04.01523759248
   PubMed Web of Science ®Google Scholar
• Corrales JC, Esnal A, De la Fe C, et al. Contagious agalactia in small ruminants. Small Rumin Res. 2007;68(1–2):154–166. doi:10.1016/j.smallrumres.2006.09.010
   Web of Science ®Google Scholar
• Kumar A, Rahal A, Chakraborty S, Verma AK, Dhama K. Mycoplasma agalactiae, an etiological agent of contagious agalactia in small ruminants: a review. Vet Med Int. 2014;2014:286752. doi:10.1155/2014/28675225097796
   PubMedGoogle Scholar
• World Organization for Animal Health (OIE). Volume 1, Chapter 3.7.3 Contagious agalactia In: Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (Terrestrial Manual), 8th Edition, 2018; Paris: OIE; 2019:1430–1440. https://www.oie.int/fileadmin/Home/eng/Health_standards/tahm/3.07.03_CONT_AGALACT.pdf
   Google Scholar
• Heller M, Schwarz R, Noe G, et al. First human case of severe septicaemia associated with Mycoplasma capricolum subsp. capricolum infection. JMM Case Rep. 2015;2(5). doi:10.1099/jmmcr.0.000101.
   Google Scholar
• Truscott RB, Finley GG. Studies on Mycoplasma mycoides subsp. mycoides (LC) in lambs and calves. Can J Comp Med. 1985;49(2):233–234.3893663
   PubMedGoogle Scholar
• Taoudi A, Kirchhoff H. Isolation of Mycoplasma capricolum from cows with mastitis. Vet Rec. 1986;119(10):247. doi:10.1136/vr.119.10.2473765306
   PubMed Web of Science ®Google Scholar
• Kapoor PK, Garg DN, Mahajan SK. Isolation of Mycoplasma mycoides subsp. mycoides (LC variant, Y-Goat) from naturally aborted bovine fetuses. Theriogenology. 1989;32(4):683–691. doi:10.1016/0093-691X(89)90289-616726715
   PubMed Web of Science ®Google Scholar
• Hung AL, Alvarado A, Lopez T, Perales R, Li O, Garcia E. Detection of antibodies to mycoplasmas in South American camelids. Res Vet Sci. 1991;51(3):250–253. doi:10.1016/0034-5288(91)90072-V1780576
   PubMed Web of Science ®Google Scholar
• Nicolas MM, Stalis IH, Clippinger TL, et al. Systemic disease in Vaal rhebok (Pelea capreolus) caused by mycoplasmas in the mycoides cluster. J Clin Microbiol. 2005;43(3):1330–1340. doi:10.1128/JCM.43.3.1330-1340.200515750104
   PubMed Web of Science ®Google Scholar
• Ur-Rahman S, Siddique M, Rasool M. Seroprevalence of Mycoplasma mycoides subspecies capri in ruminants and camel. Small Rumin Res. 2006;63(1–2):28–31. doi:10.1016/j.smallrumres.2005.01.012
   Web of Science ®Google Scholar
• Verbisck-Bucker G, Gonzalez-Candela M, Galian J, Cubero-Pablo MJ, Martin-Atance P, Leon-Vizcaino L. Epidemiology of Mycoplasma agalactiae infection in free-ranging Spanish ibex (Capra pyrenaica) in Andalusia, southern Spain. J Wildl Dis. 2008;44(2):369–380. doi:10.7589/0090-3558-44.2.36918436669
   PubMed Web of Science ®Google Scholar
• De La Fe C, Assunção P, Gutiérrez C, et al. Survey of antibodies to Mycoplasma agalactiae and Mycoplasma mycoides subsp. mycoides (large colony type) in dromedaries (Camelus dromedarius) in close contact with an infected goat population. J Arid Environ. 2009;73(4–5):594–595. doi:10.1016/j.jaridenv.2008.09.022
   Web of Science ®Google Scholar
• Giangaspero M, Orusa R, Nicholas RA, et al. Characterization of Mycoplasma isolated from an ibex (Capra ibex) suffering from keratoconjunctivitis in northern Italy. J Wildl Dis. 2010;46(4):1070–1078. doi:10.7589/0090-3558-46.4.107020966258
   PubMed Web of Science ®Google Scholar
• Ostrowski S, Thiaucourt F, Amirbekov M, et al. Fatal outbreak of Mycoplasma capricolum pneumonia in endangered markhors. Emerg Infect Dis. 2011;17(12):2338–2341. doi:10.3201/eid1712.11018722172532
   PubMed Web of Science ®Google Scholar
• Tardy F, Baranowski E, Nouvel LX, et al. Emergence of atypical Mycoplasma agalactiae strains harboring a new prophage and associated with an alpine wild ungulate mortality episode. Appl Environ Microbiol. 2012;78(13):4659–4668. doi:10.1128/AEM.00332-1222522685
   PubMed Web of Science ®Google Scholar
• Catania S, Gobbo F, Schiavon E, Nicholas RAJ. Severe otitis and pneumonia in adult cattle with mixed infection of Mycoplasma bovis and Mycoplasma agalactiae. Vet Rec Case Rep. 2016;4(2):e000366. doi:10.1136/vetreccr-2016-000366
   Google Scholar
• Nicholas RAJ. Improvements in the diagnosis and control of diseases of small ruminants caused by mycoplasmas. Small Rumin Res. 2002;45(2):145–149. doi:10.1016/S0921-4488(02)00095-0
   Web of Science ®Google Scholar
• Loria GR, Puleio R, Nicholas RAJ. Contagious Agalactia: economic losses and good practice. J Bacteriol Mycol. 2018;5(5):1076.
   Google Scholar
• FAOSTAT Statistical Database. Data extracted from FAOSTAT, Livestock Primary. Rome, Italy: Food and Agriculture Organization of the United Nations. 2019 Available from: http://www.fao.org/faostat/en/#data/QL. Accessed July 4, 2019.
   Google Scholar
• De La Fe C, Assunção P, Antunes T, Rosales RS, Poveda JB. Microbiological survey for Mycoplasma spp. in a contagious agalactia endemic area. Vet J. 2005;170(2):257–259. doi:10.1016/j.tvjl.2004.05.00215964226
   PubMed Web of Science ®Google Scholar
• Dore S, Liciardi M, Amatiste S, et al. Survey on small ruminant bacterial mastitis in Italy, 2013–2014. Small Rumin Res. 2016;141:91–93. doi:10.1016/j.smallrumres.2016.07.010
   Web of Science ®Google Scholar
• Lima MC, Souza MCC, Espeschit IF, et al. Mastitis in dairy goats from the state of Minas Gerais, Brazil: profiles of farms, risk factors and characterization of bacteria. Pesqui Vet Bras. 2018;38:1742–1751. doi:10.1590/1678-5150-pvb-5698
   Google Scholar
• Mishra AK, Sharma N, Singh DD, et al. Prevalence and bacterial etiology of subclinical mastitis in goats reared in organized farms. Vet World. 2018;11(1):20–24. doi:10.14202/vetworld.29479152
   PubMed Web of Science ®Google Scholar
• Contreras A, Corrales JC, Sierra D, Marco J. Prevalence and aetiology of non-clinical intramammary infection in Murciano-Granadina goats. Small Rumin Res. 1995;17(1):71–78. doi:10.1016/0921-4488(95)00651-Z
   Web of Science ®Google Scholar
• Contreras A, Sierra D, Sánchez A, et al. Mastitis in small ruminants. Small Rumin Res. 2007;68(1):145–153. doi:10.1016/j.smallrumres.2006.09.011
   Web of Science ®Google Scholar
• Giadinis ND, Arsenos G, Tsakos P, et al. “Milk-drop syndrome of ewes”: investigation of the causes in dairy sheep in Greece. Small Rumin Res. 2012;106(1):33–35. doi:10.1016/j.smallrumres.2012.04.018
   Web of Science ®Google Scholar
• Paterna A, Contreras A, Gómez-Martín A, et al. The diagnosis of mastitis and contagious agalactia in dairy goats. Small Rumin Res. 2014;121(1):36–41. doi:10.1016/j.smallrumres.2013.12.002
   Web of Science ®Google Scholar
• Dore S, Amatiste S, Bergagna S, et al. Survey on contagious agalactia of small ruminants in Italy, 2014–2017. IDF Mastitis Conference 2019; 5 16 2019; Copenhagen.
   Google Scholar
• Al-Momani W, Halablab MA, Abo-Shehada MN, Miles K, McAuliffe L, Nicholas RAJ. Isolation and molecular identification of small ruminant mycoplasmas in Jordan. Small Rumin Res. 2006;65(1):106–112. doi:10.1016/j.smallrumres.2005.05.022
   Web of Science ®Google Scholar
• Chazel M, Tardy F, Le Grand D, Calavas D, Poumarat F. Mycoplasmoses of ruminants in France: recent data from the national surveillance network. BMC Vet Res. 2010;6:32. doi:10.1186/1746-6148-6-3220525406
   PubMed Web of Science ®Google Scholar
• Goçmen H, Rosales R, Ayling R, Ülgen M. Comparison of PCR tests for the detection of Mycoplasma agalactiae in sheep and goats. Turk J Vet Anim Sci. 2016;40:421–427. doi:10.3906/vet-1511-65
   Web of Science ®Google Scholar
• Maksimovic Z, Bacic A, Rifatbegovic M. Mycoplasmas isolated from ruminants in Bosnia and Herzegovina between 1995 and 2015. Veterinaria. 2016;65:27–-31
   Google Scholar
• De La Fe C, Sánchez A, Gutierrez A, et al. Effects on goat milk quality of the presence of Mycoplasma spp. in herds without symptoms of contagious agalactia. J Dairy Res. 2009;76(1):20–23. doi:10.1017/S002202990800366X18922196
   PubMed Web of Science ®Google Scholar
• Bergonier D, Berthelot X, Poumarat F. Contagious agalactia of small ruminants: current knowledge concerning epidemiology, diagnosis and control. Rev Sci Tech. 1997;16(3):848–873. doi:10.20506/rst.issue.16.3.69567311
   PubMed Web of Science ®Google Scholar
• Amores J, Sánchez A, Gómez-Martín Á, Corrales JC, Contreras A, de la Fe C. Surveillance of Mycoplasma agalactiae and Mycoplasma mycoides subsp. capri in dairy goat herds. Small Rumin Res. 2012;102(1):89–93. doi:10.1016/j.smallrumres.2011.09.008
   Web of Science ®Google Scholar
• Dos Santos SB, De Melo RPB, Da Silva LTR, et al. Epidemiology of Mycoplasma agalactiae and Mycoplasma mycoides cluster in flocks of northeastern Brazil. Cienc Rural. 2018;48:4.
   Web of Science ®Google Scholar
• Hajizadeh A, Ghaderi R, Ayling RD. Species of mycoplasma causing contagious agalactia in small ruminants in northwest Iran. Vet Ital. 2018;54(3):205–210. doi:10.12834/VetIt.831.4072.230574997
   PubMed Web of Science ®Google Scholar
• Matos RAT, Santos SB, Alves RV, et al. Occurrence and risk factors associated with Mycoplasma agalactiae infection in dairy goat herds of Paraíba State, Brazil. Pesqui Vet Bras. 2019;39(2):93–98. doi:10.1590/1678-5150-pvb-5538
   Web of Science ®Google Scholar
• Filioussis G, Giadinis ND, Petridou EJ, Karavanis E, Papageorgiou K, Karatzias H. Congenital polyarthritis in goat kids attributed to Mycoplasma agalactiae. Vet Rec. 2011;169(14):364. doi:10.1136/vr.d4627
   PubMed Web of Science ®Google Scholar
• Agnello S, Chetta M, Vicari D, et al. Severe outbreaks of polyarthritis in kids caused by Mycoplasma mycoides subspecies capri in Sicily. Vet Rec. 2012;170(16):416. doi:10.1136/vr.100481
   PubMed Web of Science ®Google Scholar
• Johnson GC, Fales WH, Shoemake BM, et al. An outbreak of Mycoplasma mycoides subspecies capri arthritis in young goats: a case study. J Vet Diagn Invest. 2019;31(3):453–457. doi:10.1177/104063871983524330852958
   PubMed Web of Science ®Google Scholar
• Hernandez L, Lopez J, St-Jacques M, Ontiveros L, Acosta J, Handel K. Mycoplasma mycoides subsp. capri associated with goat respiratory disease and high flock mortality. Can Vet J. 2006;47(4):366–369.16642877
   PubMed Web of Science ®Google Scholar
• Poumarat F, Jarrige N, Tardy F. Purpose and overview of results of the Vigimyc Network for the epidemiological surveillance of mycoplasmoses in ruminants in France. EuroRéférence. 2014;12:24–28.
   Google Scholar
• Shah MK, Saddique U, Ahmad S, et al. Isolation rate and antimicrobial susceptibility profiles of Mycoplasma mycoides subspecies capri field isolates from sheep and goats in Pakistan. Small Rumin Res. 2017;153:118–122. doi:10.1016/j.smallrumres.2017.06.002
   Web of Science ®Google Scholar
• Rahman H, Saddique U, Hassan Z, et al. The predominant incidence of Mycoplasma mycoides subsp. capri in suspected cases of contagious caprine pleuropneumonia in sheep and goats of northern Pakistan. Pak J Zool. 2018;50:50.
   Web of Science ®Google Scholar
• Bergonier D, Poumarat F. Contagious agalactia of small ruminants: epidemiology, diagnosis and control. Rev Sci Tech. 1996;15(4):1431–1475. doi:10.20506/rst.15.4.9889527414
   PubMed Web of Science ®Google Scholar
• Szeredi L, Tenk M, Dan A. Infection of two goatherds with Mycoplasma mycoides subsp. capri in Hungary, evidence of a possible faecal excretion. J Vet Med B Infect Dis Vet Public Health. 2003;50(4):172–177. doi:10.1046/j.1439-0450.2003.00654.x12916690
   PubMedGoogle Scholar
• Azevedo EOD, Alcântara MDBD, Nascimento ERD, et al. Contagious agalactia by Mycoplasma agalactiae in small ruminants in Brazil: first report. Braz J Microbiol. 2006;37:576–581. doi:10.1590/S1517-83822006000400033
   Web of Science ®Google Scholar
• Rodriguez J, Poveda J, Gutierrez C, Acosta B, Fernandez A. Polyarthritis in kids associated with Mycoplasma putrefaciens. Vet Rec. 1994;135(17):406–407. doi:10.1136/vr.135.17.4067856032
   PubMed Web of Science ®Google Scholar
• Bajmocy E, Turcsanyi I, Bolske G, Bacsadi A, Kiss I. Disease caused by Mycoplasma mycoides subspecies mycoides LC in Hungarian goat herds. Acta Vet Hung. 2000;48(3):277–283. doi:10.1556/AVet.48.2000.3.411402711
   PubMed Web of Science ®Google Scholar
• DaMassa AJ, Holmberg CA, Brooks DL. Comparison of caprine mycoplasmosis caused by Mycoplasma capricolum, Mycoplasma mycoides subsp. mycoides, and Mycoplasma putrefaciens. Isr J Med Sci. 1987;23(6):636–640.3667229
   PubMedGoogle Scholar
• DaMassa AJ, Brooks DL, Adler HE. Caprine mycoplasmosis: widespread infection in goats with Mycoplasma mycoides subsp mycoides (Large-Colony type). Am J Vet Res. 1983;44(2):322–325.6338774
   PubMed Web of Science ®Google Scholar
• Gil MC, Hermoso de Mendoza M, Alonso JM, Rey J, Poveda JB, Hermoso de Mendoza J. Mastitis caused by Mycoplasma mycoides subspecies mycoides (Large Colony Type) in goat flocks in Spain. J Vet Med B Infect Dis Vet Public Health. 1999;46(10):741–743. doi:10.1046/j.1439-0450.1999.00303.x
   Google Scholar
• Kwantes LJ, Harby HAM. Caprine mycoplasmal arthritis in the Sultanate of Oman. Small Rumin Res. 1995;16(3):287–289. doi:10.1016/0921-4488(95)00619-V
   Web of Science ®Google Scholar
• Giadinis ND, Petridou EJ, Sofianidis G, et al. Mortality in adult goats attributed to Mycoplasma capricolum subspecies capricolum. Vet Rec. 2008;163(9):278–279. doi:10.1136/vr.163.9.27818757908
   PubMed Web of Science ®Google Scholar
• DaMassa AJ, Brooks DL, Holmberg CA, Moe AI. Caprine mycoplasmosis: an outbreak of mastitis and arthritis requiring the destruction of 700 goats. Vet Rec. 1987;120(17):409–413. doi:10.1136/vr.120.17.4093603972
   PubMed Web of Science ®Google Scholar
• Mondal D, Srivastava MK. Ovine pneumonia due to Mycoplasma agalactiae. Indian J Anim Sci. 2004;74(3):253–255.
   Web of Science ®Google Scholar
• Kidanemariam A, Gouws J, van Vuuren M, Gummow B. Ulcerative balanitis and vulvitis of dorper sheep in South Africa: a study on its aetiology and clinical features. J S Afr Vet Assoc. 2005;76(4):197–203. doi:10.4102/jsava.v76i4.42616642715
   PubMed Web of Science ®Google Scholar
• Loria GR, Casalone C, Sparacino L, et al. Mycoplasma agalactiae in sheep brains: a new site of infection? Large Anim Rev. 2007;13:65–68.
   Google Scholar
• Schumacher VL, Hinckley L, Liao X, Tulman E, Geary SJ, Smyth JA. Meningitis caused by Mycoplasma mycoides subspecies capri in a goat. J Vet Diagn Invest. 2011;23(3):565–569. doi:10.1177/104063871140341321908292
   PubMed Web of Science ®Google Scholar
• Rosales RS, Puleio R, Loria GR, Catania S, Nicholas RAJ. Mycoplasmas: brain invaders? Res Vet Sci. 2017;113:56–61. doi:10.1016/j.rvsc.2017.09.00628889017
   PubMed Web of Science ®Google Scholar
• Zavagli V. L’agalactie contagieuse des brebis et des chèvres. Bull Off Int Epizoot. 1951;36:336–362.
   Google Scholar
• Levisohn S, Davidson I, Caro Vergara MR, Rapoport E. Use of an ELISA for differential diagnosis of Mycoplasma agalactiae and M. mycoides subspecies mycoides (LC) in naturally infected goat herds. Res Vet Sci. 1991;51(1):66–71. doi:10.1016/0034-5288(91)90033-K1716774
   PubMed Web of Science ®Google Scholar
• Villalba EJ, Poveda JB, Fernandez A, Rodriguez JL, Gutierrez C, Gomez-Villamandos J. An outbreak caused by Mycoplasma mycoides species in goats in the Canary Islands. Vet Rec. 1992;130(15):330–331. doi:10.1136/vr.130.15.3301595163
   PubMed Web of Science ®Google Scholar
• Castro-Alonso A, Rodríguez F, De la Fé C, et al. Correlating the immune response with the clinical–pathological course of persistent mastitis experimentally induced by Mycoplasma agalactiae in dairy goats. Res Vet Sci. 2009;86(2):274–280. doi:10.1016/j.rvsc.2008.06.00418703207
   PubMed Web of Science ®Google Scholar
• Todaro M, Puleio R, Sabelli C, Scatassa ML, Console A, Loria GR. Determination of milk production losses in Valle del Belice sheep following experimental infection of Mycoplasma agalactiae. Small Rumin Res. 2015;123(1):167–172. doi:10.1016/j.smallrumres.2014.10.005
   Web of Science ®Google Scholar
• Kheirabadi KH, Ebrahimi A. Investigation of Mycoplasma agalactiae in milk and conjunctival swab samples from sheep flocks in west central, Iran. Pak J Biol Sci. 2007;10(8):1346–1348. doi:10.3923/pjbs.2007.1346.134819069942
   PubMedGoogle Scholar
• Tardy F, Mercier P, Solsona M, Saras E, Poumarat F. Mycoplasma mycoides subsp. mycoides biotype large colony isolates from healthy and diseased goats: prevalence and typing. Vet Microbiol. 2007;121(3–4):268–277. doi:10.1016/j.vetmic.2006.12.00217224248
   PubMed Web of Science ®Google Scholar
• Ariza-Miguel J, Rodriguez-Lazaro D, Hernandez M. A survey of Mycoplasma agalactiae in dairy sheep farms in Spain. BMC Vet Res. 2012;8:171. doi:10.1186/1746-6148-8-17123006445
   PubMed Web of Science ®Google Scholar
• Olaogun OM, Kanci A, Barber SR, et al. Survey of Victorian small ruminant herds for mycoplasmas associated with contagious agalactia and molecular characterisation of Mycoplasma mycoides subspecies capri isolates from one herd. Aust Vet J. 2017;95(10):392–400. doi:10.1111/avj.2017.95.issue-1028948623
   PubMed Web of Science ®Google Scholar
• Tardy F, Treilles M, Gay E, et al. Contagious agalactia monitoring in caprine herds through regular bulk tank milk sampling. J Dairy Sci. 2019;102(6):5379–5388. doi:10.3168/jds.2018-1588930981487
   PubMed Web of Science ®Google Scholar
• Tardy F, Maigre L, Tricot A, Poumarat F, Nguyen L, Le Grand D. Comparison of isolates of Mycoplasma mycoides subspecies capri from asymptomatic and septicaemic goats. J Comp Pathol. 2011;144(1):70–77. doi:10.1016/j.jcpa.2010.06.00420708197
   PubMed Web of Science ®Google Scholar
• Haapala V, Pohjanvirta T, Vahanikkila N, et al. Semen as a source of Mycoplasma bovis mastitis in dairy herds. Vet Microbiol. 2018;216:60–66. doi:10.1016/j.vetmic.2018.02.00529519526
   PubMed Web of Science ®Google Scholar
• De la Fe C, Amores J, Martín AG, Sánchez A, Contreras A, Corrales JC. Mycoplasma agalactiae detected in the semen of goat bucks. Theriogenology. 2009;72(9):1278–1281. doi:10.1016/j.theriogenology.2009.07.02419773063
   PubMed Web of Science ®Google Scholar
• De la Fe C, Martín AG, Amores J, et al. Latent infection of male goats with Mycoplasma agalactiae and Mycoplasma mycoides subspecies capri at an artificial insemination centre. Vet J. 2010;186(1):113–115. doi:10.1016/j.tvjl.2009.07.01019665400
   PubMed Web of Science ®Google Scholar
• Amores J, Gómez-Martín A, Corrales JC, Sánchez A, Contreras A, De la Fe C. Presence of contagious agalactia causing mycoplasmas in Spanish goat artificial insemination centres. Theriogenology. 2011;75(7):1265–1270. doi:10.1016/j.theriogenology.2010.11.04021220162
   PubMed Web of Science ®Google Scholar
• Gómez-Martín A, Corrales JC, Amores J, et al. Controlling contagious agalactia in artificial insemination centers for goats and detection of Mycoplasma mycoides subspecies capri in semen. Theriogenology. 2012;77(6):1252–1256. doi:10.1016/j.theriogenology.2011.10.00622115814
   PubMed Web of Science ®Google Scholar
• Gómez-Martín A, Uc N, Vieira LA, et al. Survival capacity of Mycoplasma agalactiae and Mycoplasma mycoides subsp capri in the diluted semen of goat bucks and their effects on sperm quality. Theriogenology. 2015;83(5):911–919. doi:10.1016/j.theriogenology.2014.11.02925543157
   PubMed Web of Science ®Google Scholar
• Paterna A, Gómez-Martín Á, Van Der Ham MP, et al. Mycoplasma excretion in reproductive male and female goats. Jpn J Vet Res. 2017;65(2):83–88.
   Web of Science ®Google Scholar
• Pourbakhsh SA, Abtin A, Ashtari A, Kheirkhah B, Bayatzadeh MA, Ahangaran S. Isolation and detection of Mycoplasma agalactiae from semen samples of goats. Arch Razi Inst. 2017;72(3):159–164. doi:10.22092/ari.2017.11161030341936
   PubMedGoogle Scholar
• Gregory L, Rizzo H, Gaeta NC, et al. Interference of Mycoplasma spp. or Ureaplasma spp. in ovine semen quality. J Microbiol Res. 2012;2(5):118–122. doi:10.5923/j.microbiology.20120205.01
   Google Scholar
• Prats-van der Ham M, Tatay-Dualde J, de la Fe C, et al. Detecting asymptomatic rams infected with Mycoplasma agalactiae in ovine artificial insemination centers. Theriogenology. 2017;89:324–328. doi:10.1016/j.theriogenology.2016.09.01427863702
   PubMed Web of Science ®Google Scholar
• Bergonier D, Crémoux R, Rupp R, Lagriffoul G, Berthelot X. Mastitis of dairy small ruminants. Vet Res. 2003;34(5):689–716. doi:10.1051/vetres:200303014556701
   PubMed Web of Science ®Google Scholar
• Crawford TB, Adams DS. Caprine arthritis-encephalitis: clinical features and presence of antibody in selected goat populations. J Am Vet Med Assoc. 1981;178(7):713–719.6259112
   PubMed Web of Science ®Google Scholar
• Chakraborty S, Kumar A, Tiwari R, et al. Advances in diagnosis of respiratory diseases of small ruminants. Vet Med Int. 2014;2014:508304. doi:10.1155/2014/50830425028620
   PubMedGoogle Scholar
• Nicholas RAJ, Ayling RD, Loria GR. Ovine mycoplasmal infections. Small Rumin Res. 2008;76(1):92–98. doi:10.1016/j.smallrumres.2007.12.014
   Web of Science ®Google Scholar
• Rifatbegovic M, Maksimovic Z, Hulaj B. Mycoplasma ovipneumoniae associated with severe respiratory disease in goats. Vet Rec. 2011;168(21):565. doi:10.1136/vr.d886
   PubMed Web of Science ®Google Scholar
• Contreras A, Miranda RE, Sánchez A, et al. Presence of Mycoplasma species and somatic cell counts in bulk-tank goat milk. Small Rumin Res. 2008;75(2):247–251. doi:10.1016/j.smallrumres.2007.11.007
   Web of Science ®Google Scholar
• Tolone M, Sutera AM, Borrello S, et al. Effect of Mycoplasma agalactiae mastitis on milk production and composition in Valle dell Belice dairy sheep. Ital J Anim Sci. 2019;18(1):1067–1072. doi:10.1080/1828051X.2019.1617044
   Web of Science ®Google Scholar
• Corrales JC, Sanchez A, Luengo C, Poveda JB, Contreras A. Effect of clinical contagious agalactia on the bulk tank milk somatic cell count in Murciano-Granadina goat herds. J Dairy Sci. 2004;87(10):3165–3171. doi:10.3168/jds.S0022-0302(04)73451-715377594
   PubMed Web of Science ®Google Scholar
• Gonzalo C, Carriedo JA, Blanco MA, et al. Factors of variation influencing bulk tank somatic cell count in dairy sheep. J Dairy Sci. 2005;88(3):969–974. doi:10.3168/jds.S0022-0302(05)72764-815738231
   PubMed Web of Science ®Google Scholar
• Gelasakis AI, Angelidis A, Giannakou R, Arsenos G. Bacterial subclinical mastitis and its effect on milk quality traits in low-input dairy goat herds. Vet Rec. 2018;183(14):449. doi:10.1136/vr.10480430045996
   PubMed Web of Science ®Google Scholar
• Marogna G, Rolesu S, Lollai S, Tola S, Leori G. Clinical findings in sheep farms affected by recurrent bacterial mastitis. Small Rumin Res. 2010;88(2):119–125. doi:10.1016/j.smallrumres.2009.12.019
   Web of Science ®Google Scholar
• Tatay-Dualde J, Sánchez A, Prats-van der Ham M, et al. Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk. Ir Vet J. 2015;68(1):21. doi:10.1186/s13620-015-0049-y26351565
   PubMedGoogle Scholar
• Cottew GS, Yeats FR. Occurrence of mycoplasmas in clinically normal goats. Aust Vet J. 1981;57(1):52–53. doi:10.1111/j.1751-0813.1981.tb07094.x7236149
   PubMed Web of Science ®Google Scholar
• Cottew GS, Yeats FR. Mycoplasmas and mites in the ears of clinically normal goats. Aust Vet J. 1982;59(3):77–81. doi:10.1111/j.1751-0813.1982.tb02731.x7159311
   PubMed Web of Science ®Google Scholar
• Gil MC, Hermoso De Mendoza M, Rey J, et al. Isolation of mycoplasmas from the external ear canal of goats affected with contagious agalactia. Vet J. 1999;158(2):152–154. doi:10.1053/tvjl.1999.038310489272
   PubMed Web of Science ®Google Scholar
• Pereyre S, Tardy F, Renaudin H, et al. Identification and subtyping of clinically relevant human and ruminant mycoplasmas by use of matrix-assisted laser desorption ionization-time of flight mass spectrometry. J Clin Microbiol. 2013;51(10):3314–3323. doi:10.1128/JCM.01573-1323903545
   PubMed Web of Science ®Google Scholar
• Becker CA, Ramos F, Sellal E, Moine S, Poumarat F, Tardy F. Development of a multiplex real-time PCR for contagious agalactia diagnosis in small ruminants. J Microbiol Methods. 2012;90(2):73–79. doi:10.1016/j.mimet.2012.04.02022579581
   PubMed Web of Science ®Google Scholar
• Wong YP, Othman S, Lau YL, Radu S, Chee HY. Loop-mediated isothermal amplification (LAMP): a versatile technique for detection of micro-organisms. J Appl Microbiol. 2018;124(3):626–643. doi:10.1111/jam.1364729165905
   PubMed Web of Science ®Google Scholar
• Rekha V, Rana R, Thomas P, et al. Development of loop-mediated isothermal amplification test for the diagnosis of contagious agalactia in goats. Trop Anim Health Prod. 2015;47(3):581–587. doi:10.1007/s11250-015-0767-x25616985
   PubMed Web of Science ®Google Scholar
• Loria GR, Puleio R, Nicholas R, Arcoleo G, Drago C. A novel LAMP field test for the diagnosis of contagious agalactia caused by Mycoplasma. agalactiae. Anim Husb Dairy Vet Sci. 2018;2(3):1076.
   Google Scholar
• Assunção P, De la Fe C, Ramirez AS, Poveda JB, Andrada M. Serological study of contagious agalactia in herds of goats in the Canary Islands. Vet Rec. 2004;154(22):684–687. doi:10.1136/vr.154.22.68415200073
   PubMed Web of Science ®Google Scholar
• Al-Momani W, Nicholas RA, Abo-Shehada MN. Risk factors associated with Mycoplasma agalactiae infection of small ruminants in northern Jordan. Prev Vet Med. 2008;83(1):1–10. doi:10.1016/j.prevetmed.2007.08.00317881071
   PubMed Web of Science ®Google Scholar
• Lambert M, Calamel M, Dufour P, Cabasse E, Vitu C, Pepin V. Detection of false-positive sera in contagious agalactia with a multiantigen ELISA and their elimination with a protein G conjugate. J Vet Diagn Invest. 1998;10(4):326–330. doi:10.1177/1040638798010004039786519
   PubMed Web of Science ®Google Scholar
• Poumarat F, Le Grand D, Gaurivaud P, et al. Comparative assessment of two commonly used commercial ELISA tests for the serological diagnosis of contagious agalactia of small ruminants caused by Mycoplasma agalactiae. BMC Vet Res. 2012;8:109. doi:10.1186/1746-6148-8-10922776779
   PubMed Web of Science ®Google Scholar
• Hasso SA, Al-Omran AH. Antibody response patterns in goats experimentally infected with Mycoplasma agalactiae. Small Rumin Res. 1994;14(1):79–81. doi:10.1016/0921-4488(94)90014-0
   Web of Science ®Google Scholar
• Nicholas RAJ, Ayling RD, McAuliffe L. Antigenic Analysis of Mycoplasmas In: Mycoplasma Diseases of Ruminants. Oxfordshire, UK: CAB International; 2008:98–113.
   Google Scholar
• Arun TR, Rana R, Singh P, et al. Development of a gold nanoparticle based lateral flow assay for rapid diagnosis of contagious agalactia in goats. Asian J Anim Vet Adv. 2014;9:405–413. doi:10.3923/ajava.2014.405.413
   Google Scholar
• OIE. Animal health information WAHIS interface; 2005–2019 Available from: https://www.oie.int/wahis_2/public/wahid.php/Diseaseinformation/Diseasetimelines/index/newlang/en?header_disease_type_hidden=0&header_disease_id_hidden=0&header_selected_disease_name_hidden=0&header_disease_type=0&header_disease_id_terrestrial=47&header_disease_id_aquatic=−999&header_firstyear=2005&header_lastyear=2019. Accessed November 26, 2019.
   Google Scholar
• Hosein Abadi E, Saadati D, Najimi M, Hassanpour M. A Study on Mycoplasma agalactiae and chlamydophila abortus in aborted ovine fetuses in Sistan and Baluchestan region, Iran. Arch Razi Inst. 2019;74(3):295–301. doi:10.22092/ari.2018.120393.119331592595
   PubMedGoogle Scholar
• Verbisck G, Gonzalez-Candela M, Cubero MJ, Leon L, Serrano E, Perales A. Mycoplasma agalactiae in Iberian ibex (Capra pyrenaica) in Spain. Vet Rec. 2010;167(11):425–426. doi:10.1136/vr.c4908
   PubMed Web of Science ®Google Scholar
• Cokrevski S, Crcev D, Loria GR, Nicholas RAJ. Outbreaks of contagious agalactia in small ruminants in the Republic of Macedonia. Vet Rec. 2001;148(21):667. doi:10.1136/vr.148.21.66711400990
   PubMed Web of Science ®Google Scholar
• Hanedan B, Kirbas A, Kandemir FM, Aktas MS, Yildiz A. Evaluation of arginase activity, nitric oxide and oxidative stress status in sheep with contagious agalactia. Acta Vet Hung. 2017;65(3):394–401. doi:10.1556/004.2017.03728956486
   PubMed Web of Science ®Google Scholar
• World Organisation for Animal Health (OIE). Available from: https://www.oie.int/wahis_2/public/wahid.php/Diseaseinformation/Diseasedistributionmap/index/newlang/en?disease_type_hidden=0&disease_id_hidden=47&selected_disease_name_hidden=Contagious+agalactia+%28-+-%29+&disease_type=0&disease_id_terrestrial=47&species_t=0&disease_id_aquatic=-999&species_a=0&sta_method=semesterly&selected_start_year=2014&selected_report_period=1&selected_start_month=1&date_submit=OK. Accessed September 9, 2019.
   Google Scholar
• Loria GR, Nicholas RA. Contagious agalactia: the shepherd’s nightmare. Vet J. 2013;198(1):5–6. doi:10.1016/j.tvjl.2013.06.01723891425
   PubMed Web of Science ®Google Scholar
• Fusco M, Corona L, Onni T, et al. Development of a sensitive and specific enzyme-linked immunosorbent assay based on recombinant antigens for rapid detection of antibodies against Mycoplasma agalactiae in sheep. Clin Vaccine Immunol. 2007;14(4):420–425. doi:10.1128/CVI.00439-0617287317
   PubMedGoogle Scholar
• Loria GR, Puleio R, Agnello S, Marogna G, Nicholas RAJ. Can vaccines for contagious agalactia reduce disease progression in infected animals: a preliminary study? Vet Rec Case Rep. 2018;6:4. doi:10.1136/vetreccr-2018-000715
   Google Scholar
• Corona L, Cillara G, Tola S. Proteomic approach for identification of immunogenic proteins of Mycoplasma mycoides subsp. capri. Vet Microbiol. 2013;167(3):434–439. doi:10.1016/j.vetmic.2013.08.02424090811
   PubMed Web of Science ®Google Scholar
• Cillara G, Manca MG, Longheu C, Tola S. Discrimination between Mycoplasma mycoides subsp. capri and Mycoplasma capricolum subsp. capricolum using PCR-RFLP and PCR. Vet J. 2015;205(3):421–423. doi:10.1016/j.tvjl.2015.05.01326088269
   PubMed Web of Science ®Google Scholar
• Carta T, Mannu F, Fadda M, et al. Development of a real-time PCR for detection of Mycoplasma agalactiae in bulk tank milk samples and epidemiology of infection in Sardinia [Conference poster]. XVII Congresso Nazionale S.I.Di.L.V.; 9 28–30, 2016; Parma.
   Google Scholar
• Filioussis G, Ioannou I, Petridou E, Avraam M, Giadinis ND, Kritas SK. Isolation and analysis of tetracycline-resistant Mycoplasma agalactiae strains from an infected goat herd in Cyprus. Acta Vet Hung. 2013;61(3):291–296. doi:10.1556/AVet.2013.01823921341
   PubMed Web of Science ®Google Scholar
• Filioussis G, Petridou E, Giadinis ND, Kritas SK. In vitro susceptibilities of caprine Mycoplasma agalactiae field isolates to six antimicrobial agents using the E test methodology. Vet J. 2014;202(3):654–656. doi:10.1016/j.tvjl.2014.08.02425439442
   PubMed Web of Science ®Google Scholar
• Lo WS, Gasparich GE, Kuo CH. Convergent evolution among ruminant-pathogenic mycoplasma involved extensive gene content changes. Genome Biol Evol. 2018;10(8):2130–2139. doi:10.1093/gbe/evy17230102350
   PubMed Web of Science ®Google Scholar
• Brown DR, Whitcomb RF, Bradbury JM. Revised minimal standards for description of new species of the class mollicutes (division Tenericutes). Int J Syst Evol Microbiol. 2007;57(Pt 11):2703–2719. doi:10.1099/ijs.0.64722-017978244
   PubMedGoogle Scholar
• Yus E, Maier T, Michalodimitrakis K, et al. Impact of genome reduction on bacterial metabolism and its regulation. Science. 2009;326(5957):1263–1268. doi:10.1126/science.117726319965476
   PubMed Web of Science ®Google Scholar
• Askaa G, Erno H. Elevation of Mycoplasma agalactiae subsp. bovis to Species Rank: Mycoplasma bovis (Hale et al.) comb. nov. Int J Syst Bacteriol. 1976;26(3):323–325. doi:10.1099/00207713-26-3-323
   Google Scholar
• Ambroset C, Pau-Roblot C, Game Y, Gaurivaud P, Tardy F. Identification and characterization of mycoplasma feriruminatoris sp. nov. Strains isolated from alpine ibex: a 4th Species in the Mycoplasma mycoides cluster hosted by non-domesticated ruminants? Front Microbiol. 2017;8:939. doi:10.3389/fmicb.2017.0093928611743
   PubMed Web of Science ®Google Scholar
• Breton M, Tardy F, Dordet-Frisoni E, et al. Distribution and diversity of mycoplasma plasmids: lessons from cryptic genetic elements. BMC Microbiol. 2012;12:257. doi:10.1186/1471-2180-12-25723145790
   PubMed Web of Science ®Google Scholar
• Sirand-Pugnet P, Lartigue C, Marenda M, et al. Being pathogenic, plastic, and sexual while living with a nearly minimal bacterial genome. PLoS Genet. 2007;3(5):e75. doi:10.1371/journal.pgen.003007517511520
   PubMed Web of Science ®Google Scholar
• Pereyre S, Sirand-Pugnet P, Beven L, et al. Life on arginine for Mycoplasma hominis: clues from its minimal genome and comparison with other human urogenital mycoplasmas. PLoS Genet. 2009;5(10):e1000677. doi:10.1371/journal.pgen.100067719816563
   PubMed Web of Science ®Google Scholar
• Dordet Frisoni E, Marenda MS, Sagne E, et al. ICEA of Mycoplasma agalactiae: a new family of self-transmissible integrative elements that confers conjugative properties to the recipient strain. Mol Microbiol. 2013;89(6):1226–1239. doi:10.1111/mmi.2013.89.issue-623888872
   PubMed Web of Science ®Google Scholar
• Dordet-Frisoni E, Sagne E, Baranowski E, et al. Chromosomal transfers in mycoplasmas: when minimal genomes go mobile. MBio. 2014;5(6). doi:10.1128/mBio.01958-14.
   PubMed Web of Science ®Google Scholar
• Citti C, Dordet-Frisoni E, Nouvel LX, Kuo CH, Baranowski E. Horizontal gene transfers in Mycoplasmas (Mollicutes). Curr Issues Mol Biol. 2018;29:3–22. doi:10.21775/cimb.029.00329648541
   PubMed Web of Science ®Google Scholar
• Faucher M, Nouvel L-X, Dordet-Frisoni E, et al. Mycoplasmas under experimental antimicrobial selection: the unpredicted contribution of horizontal chromosomal transfer. PLoS Genet. 2019;15(1):e1007910. doi:10.1371/journal.pgen.100791030668569
   PubMed Web of Science ®Google Scholar
• Calcutt MJ, Foecking MF. Genome sequence of Mycoplasma putrefaciens type strain KS1. J Bacteriol. 2011;193(21):6094. doi:10.1128/JB.06051-1121994925
   PubMed Web of Science ®Google Scholar
• Tardy F, Mick V, Dordet-Frisoni E, et al. Integrative conjugative elements are widespread in field isolates of Mycoplasma species pathogenic for ruminants. Appl Environ Microbiol. 2015;81(5):1634–1643. doi:10.1128/AEM.03723-1425527550
   PubMed Web of Science ®Google Scholar
• Poumarat F, Gautier-Bouchardon AV, Bergonier D, Gay E, Tardy F. Diversity and variation in antimicrobial susceptibility patterns over time in Mycoplasma agalactiae isolates collected from sheep and goats in France. J Appl Microbiol. 2016;120(5):1208–1218. doi:10.1111/jam.2016.120.issue-526835882
   PubMed Web of Science ®Google Scholar
• Tola S, Idini G, Manunta D, et al. Comparison of Mycoplasma agalactiae isolates by pulsed field gel electrophoresis, SDS-PAGE and immunoblotting. FEMS Microbiol Lett. 1996;143(2–3):259–265. doi:10.1111/fml.1996.143.issue-2-38837480
   PubMed Web of Science ®Google Scholar
• Nouvel L-X, Marenda MS, Glew MD, et al. Molecular typing of Mycoplasma agalactiae: tracing European-wide genetic diversity and an endemic clonal population. Comp Immunol Microbiol Infect Dis. 2012;35(5):487–496. doi:10.1016/j.cimid.2012.04.00522584004
   PubMed Web of Science ®Google Scholar
• Ariza-Miguel J, Rodriguez-Lazaro D, Hernandez M. Molecular characterization of Mycoplasma agalactiae reveals the presence of an endemic clone in Spain. J Clin Microbiol. 2013;51(2):656–660. doi:10.1128/JCM.02835-1223224102
   PubMed Web of Science ®Google Scholar
• De la Fe C, Amores J, Tardy F, Sagne E, Nouvel LX, Citti C. Unexpected genetic diversity of Mycoplasma agalactiae caprine isolates from an endemic geographically restricted area of Spain. BMC Vet Res. 2012;8:146. doi:10.1186/1746-6148-8-14622920649
   PubMed Web of Science ®Google Scholar
• Pilo P, Fleury B, Marenda M, Frey J, Vilei EM. Prevalence and distribution of the insertion element ISMag1 in Mycoplasma agalactiae. Vet Microbiol. 2003;92(1–2):37–48. doi:10.1016/S0378-1135(02)00311-512488069
   PubMed Web of Science ®Google Scholar
• McAuliffe L, Churchward CP, Lawes JR, Loria G, Ayling RD, Nicholas RA. VNTR analysis reveals unexpected genetic diversity within Mycoplasma agalactiae, the main causative agent of contagious agalactia. BMC Microbiol. 2008;8:193. doi:10.1186/1471-2180-8-19318992155
   PubMed Web of Science ®Google Scholar
• Tatay-Dualde J, Prats-Van Der Ham M, De La Fe C, et al. Antimicrobial susceptibility and multilocus sequence typing of Mycoplasma capricolum subsp. capricolum. PLoS One. 2017;12:3. doi:10.1371/journal.pone.0174700
   Web of Science ®Google Scholar
• Ghanem M, El-Gazzar M. Development of Mycoplasma synoviae (MS) core genome multilocus sequence typing (cgMLST) scheme. Vet Microbiol. 2018;218:84–89. doi:10.1016/j.vetmic.2018.03.02129685226
   PubMed Web of Science ®Google Scholar
• Delaney NF, Balenger S, Bonneaud C, et al. Ultrafast evolution and loss of CRISPRs following a host shift in a novel wildlife pathogen, Mycoplasma gallisepticum. PLoS Genet. 2012;8(2). doi:10.1371/annotation/b5608bc6-aa54-40a7-b246-51fa7bc4a9db.
   PubMed Web of Science ®Google Scholar
• Marenda MS, Sagne E, Poumarat F, Citti C. Suppression subtractive hybridization as a basis to assess Mycoplasma agalactiae and Mycoplasma bovis genomic diversity and species-specific sequences. Microbiology. 2005;151(2):475–489. doi:10.1099/mic.0.27590-015699197
   PubMedGoogle Scholar
• Browning GF, Noormohammadi AH, Markham PF. Identification and characterization of virulence Genes in Mycoplasmas In: Browning GF, Citti C, editors. Mollicutes: Molecular Biology and Pathogenesis. Caister Academic Press; 2014:77–90.
   Google Scholar
• Vogl G, Plaickner A, Szathmary S, Stipkovits L, Rosengarten R, Szostak MP. Mycoplasma gallisepticum invades chicken erythrocytes during infection. Infect Immun. 2008;76(1):71–77. doi:10.1128/IAI.00871-0717954728
   PubMed Web of Science ®Google Scholar
• Raymond BBA, Turnbull L, Jenkins C, et al. Mycoplasma hyopneumoniae resides intracellularly within porcine epithelial cells. Sci Rep. 2018;8(1):17697. doi:10.1038/s41598-018-36054-330523267
   PubMedGoogle Scholar
• Citti C, Nouvel LX, Baranowski E. Phase and antigenic variation in mycoplasmas. Future Microbiol. 2010;5(7):1073–1085. doi:10.2217/fmb.10.7120632806
   PubMed Web of Science ®Google Scholar
• Gaurivaud P, Ganter S, Villard A, et al. Mycoplasmas are no exception to extracellular vesicles release: revisiting old concepts. PLoS One. 2018;13(11):e0208160. doi:10.1371/journal.pone.020816030485365
   PubMed Web of Science ®Google Scholar
• Baranowski E, Bergonier D, Sagné E, et al. Experimental infections with Mycoplasma agalactiae identify key factors involved in host-colonization. PLoS One. 2014;9(4):e93970. doi:10.1371/journal.pone.009397024699671
   PubMed Web of Science ®Google Scholar
• Hegde S, Zimmermann M, Rosengarten R, Chopra-Dewasthaly R. Novel role of Vpmas as major adhesins of Mycoplasma agalactiae mediating differential cell adhesion and invasion of Vpma expression variants. Int J Med Microbiol. 2018;308(2):263–270. doi:10.1016/j.ijmm.2017.11.01029229193
   PubMed Web of Science ®Google Scholar
• Fleury B, Bergonier D, Berthelot X, Peterhans E, Frey J, Vilei EM. Characterization of P40, a cytadhesin of Mycoplasma agalactiae. Infect Immun. 2002;70(10):5612–5621. doi:10.1128/IAI.70.10.5612-5621.200212228289
   PubMed Web of Science ®Google Scholar
• Arfi Y, Minder L, Di Primo C, et al. MIB-MIP is a mycoplasma system that captures and cleaves immunoglobulin G. Proc Natl Acad Sci USA. 2016;113(19):5406–5411. doi:10.1073/pnas.160054611327114507
   PubMed Web of Science ®Google Scholar
• Lartigue C, Vashee S, Algire MA, et al. Creating bacterial strains from genomes that have been cloned and engineered in yeast. Science. 2009;325(5948):1693–1696. doi:10.1126/science.117375919696314
   PubMed Web of Science ®Google Scholar
• Gibson DG, Glass JI, Lartigue C, et al. Creation of a bacterial cell controlled by a chemically synthesized genome. Science. 2010;329(5987):52–56. doi:10.1126/science.119071920488990
   PubMed Web of Science ®Google Scholar
• Jores J, Ma L, Ssajjakambwe P, et al. Removal of a subset of non-essential genes fully attenuates a highly virulent Mycoplasma strain. Front Microbiol. 2019;10:664. doi:10.3389/fmicb.2019.0066431001234
   PubMed Web of Science ®Google Scholar
• Caramelli M, Ru G, Casalone C, et al. Evidence for the transmission of scrapie to sheep and goats from a vaccine against Mycoplasma agalactiae. Vet Rec. 2001;148(17):531–536. doi:10.1136/vr.148.17.53111354646
   PubMed Web of Science ®Google Scholar
• León Vizcaíno L, Garrido Abellán F, Cubero Pablo MJ, Perales A. Immunoprophylaxis of caprine contagious agalactia due to Mycoplasma agalactiae with an inactivated vaccine. Vet Rec. 1995;137(11):266–269. doi:10.1136/vr.137.11.2667502465
   PubMed Web of Science ®Google Scholar
• Buonavoglia D, Fasanella A, Sagazio P, Tempesta M, Iovane G, Buonavoglia C. Persistence of antibodies to Mycoplasma agalactiae in vaccinated sheep. New Microbiol. 1998;21(2):209–212.9579346
   PubMedGoogle Scholar
• Tola S, Manunta D, Rocca S, et al. Experimental vaccination against Mycoplasma agalactiae using different inactivated vaccines. Vaccine. 1999;17(22):2764–2768. doi:10.1016/S0264-410X(99)00070-510438045
   PubMed Web of Science ®Google Scholar
• Greco G, Corrente M, Buonavoglia D, Aliberti A, Fasanella A. Inactivated vaccine induces protection against Mycoplasma agalactiae infection in sheep. New Microbiol. 2002;25(1):17–20.11837386
   PubMedGoogle Scholar
• De La Fe C, Assunção P, Saavedra P, Tola S, Poveda C, Poveda JB. Field trial of two dual vaccines against Mycoplasma agalactiae and Mycoplasma mycoides subsp. mycoides (large colony type) in goats. Vaccine. 2007;25(12):2340–2345. doi:10.1016/j.vaccine.2006.11.05017239497
   PubMed Web of Science ®Google Scholar
• Buonavoglia D, Greco G, Quaranta V, Corrente M, Martella V, Decaro N. An oil-emulsion vaccine induces full-protection against Mycoplasma agalactiae infection in sheep. New Microbiol. 2008;31(1):117–123.18437850
   PubMed Web of Science ®Google Scholar
• Buonavoglia D, Greco G, Corrente M, et al. Long-term immunogenicity and protection against Mycoplasma agalactiae induced by an oil adjuvant vaccine in sheep. Res Vet Sci. 2010;88(1):16–19. doi:10.1016/j.rvsc.2009.07.00619683321
   PubMed Web of Science ®Google Scholar
• Abo El-Yazid H, Soliman R, Wassif I, et al. Protective efficacy of the inactivated adjuvant vaccines against Mycoplasma agalactiae infection in goats. Int J Vet Sci Med. 2018;8:14–19.
   Google Scholar
• Agnone A, Manna M, Sireci G, et al. A comparison of the efficacy of commercial and experimental vaccines for contagious agalactia in sheep. Small Rumin Res. 2013;112:230–234. doi:10.1016/j.smallrumres.2012.12.022
   Web of Science ®Google Scholar
• Lacasta D, Ferrer LM, Ramos JJ, Gonzalez JM, Ortin A, Fthenakis GC. Vaccination schedules in small ruminant farms. Vet Microbiol. 2015;181(1–2):34–46. doi:10.1016/j.vetmic.2015.07.01826220514
   PubMed Web of Science ®Google Scholar
• Kabiri K, Pourbakhsh SA, Norouzi J, Sekhavati M, Tadayon K. Homogeneity of Mycoplasma agalactiae vaccine strains in an agalaxy- high-burden environment. Iran J Microbiol. 2019;11(1):48–54.30996831
   PubMed Web of Science ®Google Scholar
• Campos AC, Azevedo EO, Alcântara MDB, et al. Efficiency of inactive vaccines against contagious agalactia in Brazil. Arq Bras Med Vet Zootec. 2013;65:1394–1402. doi:10.1590/S0102-09352013000500018
   Google Scholar
• Sunder J, Srivastava NC, Singh VP. Preliminary trials on development of vaccine against Mycoplasma mycoides subsp. mycoides type LC infection in goats. J Appl Anim Res. 2002;21(1):75–80. doi:10.1080/09712119.2002.9706359
   Web of Science ®Google Scholar
• Ramirez AS, De La Fe C, Assunçao P, Gonzales M, Poveda C. Preparation and evaluation of an invactivated polyvalent vaccine against Mycoplasma spp. on infected goats In: Eur 19693–COST Action 826 Mycoplasmas of Ruminants : Pathogenicity, Diagnostics, Epidemiology and Molecular Genetics. Brussels: European Commission; 2001:154–157.
   Google Scholar
• Marogna G, A. B, A. F, Schianchi G. Produzione, uso ed efficacia sul campo di un vaccino stabulogeno contro Mycoplasma mycoides subsp. capri nelle capre. Large Anim Rev. 2015;Suppl. 1(5):104–106.
   Google Scholar
• Saléry M. Autogenous vaccines in Europe: national approaches to authorisation. Regul Rapporteur. 2017;14(6):27–32.
   Google Scholar
• Gautier-Bouchardon AV, Ferre S, Le Grand D, Paoli A, Gay E, Poumarat F. Overall decrease in the susceptibility of Mycoplasma bovis to antimicrobials over the past 30 years in France. PLoS One. 2014;9(2):e87672. doi:10.1371/journal.pone.008767224503775
   PubMed Web of Science ®Google Scholar
• Antunes NT, Tavio MA, Mercier P, et al. In vitro susceptibilities of Mycoplasma putrefaciens field isolates. Antimicrob Agents Chemother. 2007;51(9):3452–3454. doi:10.1128/AAC.00420-0717638695
   PubMed Web of Science ®Google Scholar
• Antunes NT, Tavío MM, Assunção P, et al. In vitro susceptibilities of field isolates of Mycoplasma mycoides subsp. mycoides large colony type to 15 antimicrobials. Vet Microbiol. 2007;119(1):72–75. doi:10.1016/j.vetmic.2006.08.01316978803
   PubMed Web of Science ®Google Scholar
• Antunes NT, Tavío MM, Assunção P, et al. In vitro susceptibilities of field isolates of Mycoplasma agalactiae. Vet J. 2008;177(3):436–438. doi:10.1016/j.tvjl.2007.05.00817604191
   PubMed Web of Science ®Google Scholar
• De Garnica ML, Rosales RS, Gonzalo C, Santos JA, Nicholas RAJ. Isolation, molecular characterization and antimicrobial susceptibilities of isolates of Mycoplasma agalactiae from bulk tank milk in an endemic area of spain. J Appl Microbiol. 2013;114(6):1575–1581. doi:10.1111/jam.2013.114.issue-623445345
   PubMed Web of Science ®Google Scholar
• Paterna A, Tatay-Dualde J, Amores J, et al. In vitro assessment of the antimicrobial susceptibility of caprine isolates of Mycoplasma mycoides subsp. capri. Vet J. 2016;214:96–101. doi:10.1016/j.tvjl.2016.05.01027387734
   PubMed Web of Science ®Google Scholar
• Prats-van der Ham M, Tatay-Dualde J, Ambroset C, De la Fe C, Tardy F. The moderate drift towards less tetracycline-susceptible isolates of contagious agalactia causative agents might result from different molecular mechanisms. Vet Microbiol. 2018;220:39–46. doi:10.1016/j.vetmic.2018.05.00129885799
   PubMed Web of Science ®Google Scholar
• Paterna A, Sanchez A, Gomez-Martin A, et al. In vitro antimicrobial susceptibility of Mycoplasma agalactiae strains isolated from dairy goats. J Dairy Sci. 2013;96(11):7073–7076. doi:10.3168/jds.2012-649224035026
   PubMed Web of Science ®Google Scholar
• Al-Momani W, Nicholas RAJ, Janakat S, Abu-Basha E, Ayling RD. The in vitro effect of six antimicrobials against Mycoplasma putrefaciens, Mycoplasma mycoides subsp. mycoides LC and Mycoplasma capricolum subsp. capricolum isolated from sheep and goats in Jordan. Trop Anim Health Prod. 2006;38(1):1–7. doi:10.1007/s11250-006-4334-317405622
   PubMed Web of Science ®Google Scholar
• Hannan PC. Guidelines and recommendations for antimicrobial minimum inhibitory concentration (MIC) testing against veterinary mycoplasma species. International Research Programme on Comparative Mycoplasmology. Vet Res. 2000;31(4):373–395. doi:10.1051/vetres:200010010958240
   PubMed Web of Science ®Google Scholar
• Gautier-Bouchardon AV. Antimicrobial Resistance in Mycoplasma spp. Microbiol Spectr. 2018;6:4. doi:10.1128/microbiolspec.ARBA-0030-2018
   Web of Science ®Google Scholar
• Khalil D, Becker CAM, Tardy F. Monitoring the decrease in susceptibility to ribosomal RNAs targeting antimicrobials and its molecular basis in clinical mycoplasma bovis isolates over time. Microb Drug Resist. 2017;23(6):799–811. doi:10.1089/mdr.2016.026828151090
   PubMed Web of Science ®Google Scholar
• Prats-van der Ham M, Tatay-Dualde J, de la Fe C, et al. Molecular resistance mechanisms of Mycoplasma agalactiae to macrolides and lincomycin. Vet Microbiol. 2017;211:135–140. doi:10.1016/j.vetmic.2017.10.01229102109
   PubMed Web of Science ®Google Scholar
• Ayling RD, Bisgaard-Frantzen S, March JB, Godinho K, Nicholas RA. Assessing the in vitro effectiveness of antimicrobials against Mycoplasma mycoides subsp. mycoides small-colony type to reduce contagious bovine pleuropneumonia infection. Antimicrob Agents Chemother. 2005;49(12):5162–5165. doi:10.1128/AAC.49.12.5162-5165.200516304194
   PubMed Web of Science ®Google Scholar
• Prats-van der Ham M, Tatay-Dualde J, Gómez-Martín Á, et al. 23S rRNA and L22 ribosomal protein are involved in the acquisition of macrolide and lincosamide resistance in Mycoplasma capricolum subsp. capricolum. Vet Microbiol. 2018;216:207–211. doi:10.1016/j.vetmic.2018.02.01429519518
   PubMed Web of Science ®Google Scholar
• Tatay-Dualde J, Prats-van der Ham M, de la Fe C, et al. Resistance mechanisms against quinolones in Mycoplasma capricolum subsp. capricolum. Vet J. 2017;223:1–4. doi:10.1016/j.tvjl.2017.03.00728671064
   PubMed Web of Science ®Google Scholar
• Al-Momani W, Abu-Basha E, Janakat S, Nicholas RAJ, Ayling RD. In vitro antimycoplasmal activity of six Jordanian medicinal plants against three Mycoplasma species. Trop Anim Health Prod. 2007;39(7):515–519. doi:10.1007/s11250-007-9033-117969714
   PubMed Web of Science ®Google Scholar
• Arjoon AV, Saylor CV, May M. In Vitro efficacy of antimicrobial extracts against the atypical ruminant pathogen Mycoplasma mycoides subsp. capri. BMC Complement Altern Med. 2012;12. doi:10.1186/1472-6882-12-169
   PubMed Web of Science ®Google Scholar
• Lopez A, de Tangil MS, Vega-Orellana O, Ramirez AS, Rico M. Phenolic constituents, antioxidant and preliminary antimycoplasmic activities of leaf skin and flowers of Aloe vera (L.) Burm. f. (syn. A. barbadensis Mill.) from the Canary Islands (Spain). Molecules. 2013;18(5):4942–4954. doi:10.3390/molecules1805494223624648
   PubMed Web of Science ®Google Scholar
• Kama-Kama F, Midiwo J, Nganga J, et al. Selected ethno-medicinal plants from Kenya with in vitro activity against major African livestock pathogens belonging to the “Mycoplasma mycoides cluster”. J Ethnopharmacol. 2016;192:524–534. doi:10.1016/j.jep.2016.09.03427649681
   PubMed Web of Science ®Google Scholar
• Kama-Kama F, Omosa LK, Nganga J, et al. Antimycoplasmal Activities of Compounds from Solanum aculeastrum and Piliostigma thonningii against Strains from the Mycoplasma mycoides Cluster. Front Pharmacol. 2017;8:920. doi:10.3389/fphar.2017.0092029311927
   PubMed Web of Science ®Google Scholar
• Shah MK, Sadique U, Ahmad S, et al. Molecular identification and comparative antimycoplasmal activity of three indigenous medicinal plants against Mycoplasma putrefaciens isolated from sheep. J Anim Plant Sci. 2017;27(5):1543–1551.
   Web of Science ®Google Scholar
• Silva NS, Marinho ML, Azevedo EO, Campos AC, Carvalho MGX. Allopathic and homeopathic treatment with contagious agalactia in goats: a comparative study. Arch Vet Sc. 2013;18(4):57–64.
   Google Scholar
• Paterna A, Sanchez A, Amores J, et al. Survival of Mycoplasma agalactiae and Mycoplasma mycoides subspecies capri in heat treated goat colostrum. Vet J. 2013;196(2):263–265. doi:10.1016/j.tvjl.2012.09.01123154071
   PubMed Web of Science ®Google Scholar
• Justice-Allen A, Trujillo J, Corbett R, Harding R, Goodell G, Wilson D. Survival and replication of Mycoplasma species in recycled bedding sand and association with mastitis on dairy farms in Utah. J Dairy Sci. 2010;93(1):192–202. doi:10.3168/jds.2009-247420059918
   PubMed Web of Science ®Google Scholar
• Eterpi M, McDonnell G, Thomas V. Decontamination efficacy against Mycoplasma. Lett Appl Microbiol. 2011;52(2):150–155. doi:10.1111/j.1472-765X.2010.02979.x21198694
   PubMed Web of Science ®Google Scholar
• Miranda-de la Lama GC, Mattiello S. The importance of social behaviour for goat welfare in livestock farming. Small Rumin Res. 2010;90(1):1–10. doi:10.1016/j.smallrumres.2010.01.006
   Web of Science ®Google Scholar
• Zobel G, Neave HW, Webster J. Understanding natural behavior to improve dairy goat (Capra hircus) management systems. Transl Anim Sci. 2019;3(1):212–224. doi:10.1093/tas/txy145
   PubMed Web of Science ®Google Scholar
• Calcutt MJ, Lysnyansky I, Sachse K, Fox LK, Nicholas RAJ, Ayling RD. Gap analysis of Mycoplasma bovis disease, diagnosis and control: an aid to identify future development requirements. Transbound Emerg Dis. 2018;65(1):91–109. doi:10.1111/tbed.2018.65.issue-S129582590
   PubMedGoogle Scholar
• Thiaucourt F, Manso-Silvan L, Salah W. et al. Mycoplasma mycoides, from “mycoides Small Colony” to “capri”. A microevolutionary perspective. BMC Genomics. 2011;12:114. doi:10.1186/1471-2164-12-11421324191
   PubMed Web of Science ®Google Scholar
• Wise KS, Foecking MF, Roske K. et al. Distinctive repertoire of contingency genes conferring mutation- based phase variation and combinatorial expression of surface lipoproteins in Mycoplasma capricolum subsp. capricolum of the Mycoplasma mycoides phylogenetic cluster. J Bacteriol. 2006;188:(13):4926–4941. doi:10.1128/JB.00252-0616788201
   PubMed Web of Science ®Google Scholar