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. 2007 Aug 31;73(20):6660–6668. doi: 10.1128/AEM.01131-07

TABLE 1.

Samples of C. columbae examined in this study, results of diagnostic PCR detection, and sequence accession numbers

Sample code Collection locality Collection date, collectora Infection frequencyb
Accession no. for:
No sexingc Female Male Total 16S rRNA gene fusA gene
FKK99 Ropponmatsu, Fukuoka, Japan 27 August 1999, KY AB303383
SPR06 Sapporo, Hokkaido, Japan 16 August 2006, KY 100% (10/10) 100% (10/10) 100% (10/10) 100% (30/30) AB303382
SMY06 Sumiyoshi, Osaka, Japan 19 October 2006, TW 90% (9/10) 90% (9/10) AB303384
TTR06 Tsuchiura, Ibaraki, Japan 10 November 2006, KSF and TF 100% (10/10) 100% (10/10) AB303385
NNW07 Naniwa, Osaka, Japan 5 March 2007, NU 100% (20/20) 95% (19/20) 97.5% (39/40)
BNS06 Buenos Aires, Argentina 19 October 2006, TF 100% (10/10) 100% (10/10) AB303386
UTH98 Utah, United States 29 June 1998, DC 100% (3/3) 100% (3/3) EU021695
UTH99 Utah, United States 1999, DC EU021696
BRB02 Brisbane, Australia 2002, DC EU021697
BRB07 Brisbane, Australia 16 February 2007, TF 80% (8/10) 80% (8/10) AB303387
Total 94.3% (50/53) 100% (30/30) 96.7% (29/30) 96.5% (109/113)
a

DC, Dale Clayton; KSF, Kayoko Sasaki-Fukatsu; KY, Kazunori Yoshizawa; NU, Nobutaka Urano; TF, Takema Fukatsu; TW, Takeshi Wada.

b

Percentage of infected insects; numbers in parentheses are numbers of insects infected/number examined by diagnostic PCR.

c

Including female adults, male adults, and nymphs.