Phenotypic and genotypic characterization of Clavibacter michiganensis subsp michiganensis causing tomato bacterial canker and wilt disease in Turkey


BASIM H., BASIM E.

EUROPEAN JOURNAL OF PLANT PATHOLOGY, cilt.151, sa.2, ss.355-369, 2018 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 151 Sayı: 2
  • Basım Tarihi: 2018
  • Doi Numarası: 10.1007/s10658-017-1378-3
  • Dergi Adı: EUROPEAN JOURNAL OF PLANT PATHOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.355-369
  • Anahtar Kelimeler: Bacterial canker, Clavibacter michiganensis subsp., michiganensis, FAME, Rep-PCR, PFGE, CAMPESTRIS PV VESICATORIA, GREENHOUSE TOMATOES, GENETIC DIVERSITY, POPULATIONS, PLASMIDS, SPREAD, PCR, RESISTANCE, SEQUENCE, IDENTIFICATION
  • Akdeniz Üniversitesi Adresli: Evet

Özet

Tomato bacterial canker and wilt disease caused by Clavibacter michiganensis subsp. michiganensis (Cmm) is among one of the major bacterial diseases associated with tomato (Solanum lycopersicum L.) in the western Mediterranean region of Turkey. A total of 118 Cmm isolates were obtained from the petiole and the main vein of leaves of different cultivars of diseased tomato plants, and these isolates were cultured in semiselective medium (mSCM). The identity of Cmm isolates was confirmed through gas chromatography-fatty acid methyl-esters (GC-FAME) analysis and polymerase chain reaction (PCR) using the primers, CMM5 and CMM6. The fatty acid analysis of all the Turkish isolates yielded major components that included anteisoheptadeconic acid (a15:0), palmitic acid (i16:0) and anteisoheptadeconic acid (a17:0); the analysis detected and categorized all the isolates into 10 different FAME groups. Among repetitive element sequence PCR (rep-PCR) analysis, Box primer yielded the most reproducible genomic profiles with band sizes that ranged from 200 bp to 2 kb. The isolates were also separated into 12 groups by pulsed-field gel electrophoresis (PFGE) after digesting the total genomic DNA with SpeI, a rare cutting enzyme. The genome sizes of the different strains of Cmm were also determined after running unrestricted total genomic DNA, which yielded average values between 3.0 and 3.5 MB. All the Cmm isolates had pCM1 and pCM2 plasmids. This is the first report on the detailed characterization of the Cmm population in Turkey.