2010
DOI: 10.1007/s10327-010-0284-8
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Asian-common strains of ‘Candidatus Liberibacter asiaticus’ are distributed in Northeast India, Papua New Guinea and Timor-Leste

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Cited by 10 publications
(4 citation statements)
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“…The presence of HLB in the North-Eastern region of India (Sikkim, West Bengal, Meghalaya, Assam) has been confirmed by PCR analyses, which identified Las not only in suspicious plant samples but also in psyllids from affected orchards in the regions visited (Das et al, 2007;Miyata et al, 2011). Las has also been reported from Vidarbha in Maharashtra (Das, 2009).…”
Section: Indian Subcontinentmentioning
confidence: 88%
See 1 more Smart Citation
“…The presence of HLB in the North-Eastern region of India (Sikkim, West Bengal, Meghalaya, Assam) has been confirmed by PCR analyses, which identified Las not only in suspicious plant samples but also in psyllids from affected orchards in the regions visited (Das et al, 2007;Miyata et al, 2011). Las has also been reported from Vidarbha in Maharashtra (Das, 2009).…”
Section: Indian Subcontinentmentioning
confidence: 88%
“…None of the sixteen samples collected in five locations from the eastern part of the country was positive, and the psyllid vector was not detected in these locations. Las was again identified in three leaf samples from East Timor by Miyata et al (2011).…”
Section: Timor Islandmentioning
confidence: 96%
“…In addition to these genes, the rplKAJL-rpoBC operon sequence, nusG-rplK , and bacteriophage-type DNA polymerase region [30], [31], [32], [33] have been used for genetic differentiation of C Las. The completion of the C Las genome sequence [34] has allowed identifying different regions of the genome with variable number of tandem repeats (VNTRs) [35], [36], [37], [38], [39].…”
Section: Introductionmentioning
confidence: 99%
“…A few single nucleotide changes have been identified in the sequences of 16S rDNA, the omp gene, the wserAtrmU-tufB-secE-nusG-rplKAJL-rpoB gene cluster, and the flanking regions in various Las isolates (Adkar- Purushothama et al 2009;Furuya et al 2010;Miyata et al 2011). Due to their many mutations, this upstream region and the DNA pol region are not suitable for detection and diagnosis using PCR or LAMP methods.…”
mentioning
confidence: 98%