Homogeneity of Mycoplasma agalactiae vaccine strains isolated from Taliqan, Lorestan, and Shiraz in Iran

Subject Areas : Molecular Microbiology

Khatereh  Kabiri ¹ (Ph.D. student, Department of Microbiology, Islamic Azad University, Tehran North Branch, Tehran, Iran.)
Keivan  Tadayon ² (Associate Professor, Veterinary Bacterial Vaccines Section, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.)
Seyyed Ali  Pourbakhsh ³ (Professor, Mycoplasma Laboratory, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.)
Jamileh  Nowroozi ⁴ (Professor, Department of Microbiology, Tehran North Branch, Islamic Azad University, Tehran, Iran.)

Received: 2017-08-13 Accepted : 2017-11-01 Published : 2018-08-23

Keywords: genotype, MLVA, Mycoplasma agalactia, Agalaxy, Vaccine strains,

Abstract :

Background & Objectives: Iran continues to hold one of the most currently active world foci of agalaxy in ruminants. The three local strains of Taliqan, Lorestan, and Shiraz have been used for many years in preparation of the only commercially available killed vaccine against agalaxy in the Iranian market. This study was conducted to determine the genetic link between these strains. Materials & Methods: All three strains of Taleghan, Lorestan, and Shiraz were cultivated freshly on PPLO agar media. The genetic material was extracted by boiling method. In order to investigate the genomic relations between these strains, a Multi-Locus Variable Number Tandem Repeat Analysis (MLVA) strategy concentrating on 4 VNTR loci of 5, 9, 17, and 19 was employed. The nucleotide sequences of all PCR products were determined, as well. Results: Nucleotide sequence analysis showed an identical MLVA pattern by all the three strains. When compared to the Mycoplasma agalactiae PG2 laboratory strain, the only VNTR19 locus was different between Iranians and the PG2 strain, with respect to a 3bps addition at this locus in Iranian strain. Conclusion: The identical genetic pattern of the three Iranian strains is likely an indication of the activity of one or more indigenous ancestral clone in the geography of Iran that has been appeared and evolved throughout its livestock history and became homogeneous and predominant due to the absence of efficient disease control policies. The similarity between three Iranian and the PG2 strains might be due to homoplasy or human intervention through animal husbandry activities such as livestock importation. Applying standard genotyping methods to a larger number of local isolates help to better assess this observation.

References:

1. Nouvel LX, Marenda MS, Glew MD, Sagne E, Giammarinaro P, Tardy F, Poumarat F,
   Rosengarten R, Citti C. 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.
   2. Noaman V. Identification of Mycoplasma agalactiae by conventional and molecular methods on
   small ruminants in central zone of Iran. Comp Clin Path. 2015; 24(3): 653-657.
   3. Khezri M, Pourbakhsh SA. A survey of Mycoplasma agalactiae in small ruminants with
   contagious agalactiae syndrome in Iran. Bangladesh J Vet Med. 2014; 12(1): 67-72.
   4. Mohammadpour SH, Pourbakhsh SA, Kheirkhah B. Isolation and identification of Mycoplasma
   agalactiae by polymerase chain reaction (PCR) in suspected sheep samples in Kerman Province,
   Iran. Afr J Microbiol Res. 2013; 7(10): 885-889.
   5. Khezri M, Pourbakhsh SA, Ashtari A, Rokhzad B, Khanbabaie H. Isolation and prevalence of
   Mycoplasma agalactiae in Kurdish sheep in Kurdistan, Iran. Vet World. 2012; 5(12): 727-731.
   6. Bidhendi SM, Khaki PLangroudi RP. Isolation and identification of Mycoplasma agalactiae by
   culture and polymerase chain reaction in sheep and goat milk samples in Kordestan province,
   Iran. Arch Razi Inst. 2011; 66(1): 11-16.
   7. Amir Momen H, Roshdi Maleki M. Identification of Mycoplasma agalactiae in milk by culture
   and PCR methods in Hamedan of Iran. Ind J Fundament Appl Life Sci. 2014; 4 (S4): 2175-2180.
   8. Sotoodehnia A, Moazenijula A, Rad AN, Jabbari A. Preparation of agalactia vaccine in
   fermentor. Arch Razi Inst. 2007; 62(1): 45-48.
   9. Tola S, Idini G, Manunta D, Casciano I, Rocchigiani AM, Angioi ALeori G. Comparison of
   Mycoplasma agalactiae isolates by pulsed field gel electrophoresis, SDS-PAGE and
   immunoblotting. FEMS Microbiol Lett. 1996; 143(2-3): 259-65.
   10. 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.
   11. McAuliffe L, Gosney F, Hlusek M, de Garnica ML, Spergser J, Kargl M, Rosengarten R,
   Ayling RD, Nicholas RA, Ellis RJ. Multilocus sequence typing of Mycoplasma agalactiae. J
   Med Microbiol. 2011; 60(6): 803-811.
   12. 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.
   13. Ataee RA, Golmohammadi R, Alishiri GH, Mirnejad R, Najafi A, Esmaeili D, Jonaidi-Jafari N.
   Simultaneous detection of Mycoplasma pneumoniae, Mycoplasma hominis and Mycoplasma
   arthritidis in synovial fluid of patients with rheumatoid arthritis by Multiplex PCR. Arch Iran
   Med. 2015; 18(6): 345-350.
   
   14. Subramaniam S, Bergonier D, Poumarat F, Capaul S, Schlatter Y, Nicolet J, Frey J. Species
   identification of Mycoplasma bovis and Mycoplasma agalactiae based on the uvrC genes by
   PCR. Mol Cell Probes. 1998; 12(3): 161-169.
   15. Prats-van der Ham M, Tatay-Dualde J, de la Fe C, Paterna A, Sanchez A, Corrales JC,
   Contreras A, Gomez-Martin A. Detecting asymptomatic rams infected with Mycoplasma
   agalactiae in ovine artificial insemination centers. Theriogenol. 2017; 89: 324-328.
   16. Notifiable diseases: Contagious agalactia pathogen confirmed in Wales. Vet Rec. 2014; 175
   (19): 468.
   17. Ruiz-Fons F, Gonzalez-Barrio D, Aguilar-Rios F, Soler AJ, Garde JJ, Gortazar C,
   Fernandez-Santos Mdel R. Infectious pathogens potentially transmitted by semen of the black
   variety of the Manchega sheep breed: Health constraints for conservation purposes. Anim
   Reprod Sci. 2014; 149(3-4): 152-157.
   18. do Nascimento NC, Santos AP, Guimaraes AM, Sanmiguel PJ, Messick JB. Mycoplasma
   haemocanis- the canine hemoplasma and its feline counterpart in the genomic era. Vet Res.
   2012; 43: 66.
   19. Dos Santos LF, Clavijo MJ, Sreevatsan S, Rovira A, Moreira MA, Pieters M. Genotyping of
   Mycoplasma hyorhinis using multiple-locus variable number tandem repeat analysis. J
   Microbiol Methods. 2015; 111: 87-92.
   20. Pantoja LG, Pettit K, Dos Santos LF, Tubbs R, Pieters M. Mycoplasma hyopneumoniae
   genetic variability within a swine operation. J Vet Diagn Invest. 2016; 28(2): 175-179.
   21. Pinho L, Thompson G, Rosenbusch R, Carvalheira J. Genotyping of Mycoplasma bovis
   isolates using multiple-locus variable-number tandem-repeat analysis. J Microbiol Methods.
   2012; 88(3): 377-385.
   22. Hata E, Suzuki K, Hanyu H, Itoh M, Higuchi H, Kobayashi H. Molecular epidemiology of
   cases of Mycoplasma californicum infection in Japan. Appl Environ Microbiol. 2014; 80(24):
   7717-7724.
   23. Ferandon C, Peuchant O, Renaudin H, Bebear C. Diversity of Mycoplasma hominis clinical
   isolates from Bordeaux, France, as assessed by multiple-locus variable-number tandem repeat
   analysis. BMC Microbiol. 2013; 13: 120.
   24. Cazanave C, Charron A, Renaudin H, Bebear C. Method comparison for molecular typing of
   French and Tunisian Mycoplasma genitalium-positive specimens. J Med Microbiol. 2012; 61(Pt
   4): 500-506.
   25. Nwankpa ND, Manso-silvan L, Lorenzon S, Yaya A, Lombin LH, Thiaucourt F. Variable
   Number Tandem Repeat (VNTR) analysis reveals genetic diversity within Mycoplasma
   mycoides mycoides small colony isolates from Nigeria. Vet Microbiol. 2010; 146(3-4):354-355.
   26. Mahdavi S, Salehi TZ, Madani R, Keyvanfar H. Comparative study of homology of
   cytoplasmic membrane protein 40 KDa of Mycoplasma agalactiae in isolated strains in Iran.
   Afr J Microbiol Res. 2009; 3(9): 528-532.
   
   27. Candela MG, Serrano E, Sevila J, Leon L, Caro MR, Verheyden H. Pathogens of zoonotic and
   biological importance in roe deer (Capreolus capreolus): Seroprevalence in an agro-system
   population in France. Res Vet Sci. 2014; 96(2): 254-259.
   28. Murai K, Lehenbauer TW, Champagne JD, Glenn K, Aly SS. Cost-effectiveness of diagnostic
   strategies using quantitative real-time PCR and bacterial culture to identify contagious mastitis
   cases in large dairy herds. Prev Vet Med. 2014; 113(4): 522-535.
   29. Sanna G, Lecca V, Foddai A, Tola S. Development of a specific immunomagnetic
   capture-PCR for rapid detection of viable Mycoplasma agalactiae in sheep milk samples. J
   Appl Microbiol. 2014; 117(6): 1585-1591.
   30. Gomez-Martin A, Uc N, Vieira LA, Gadea J, Cadenas J, Sanchez A, De la Fe C. Survival
   capacity of Mycoplasma agalactiae and Mycoplasma mycoides subsp capri in the diluted semen
   of goat bucks and their effects on sperm quality. Theriogenol. 2015; 83(5): 911-919