Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2015 Nov 5;3(6):e01316-15. doi: 10.1128/genomeA.01316-15

Draft Genome Sequence of “Candidatus Liberibacter asiaticus” from Diaphorina citri in Guangdong, China

F Wu a,b, Z Zheng a, X Deng a,, Y Cen a, G Liang a, J Chen b,
PMCID: PMC4645217  PMID: 26543132

Abstract

The draft genome sequence of “Candidatus Liberibacter asiaticus” strain YCPsy from an Asian citrus psyllid (Diaphorina citri) in Guangdong, China, is reported here. The YCPsy strain has a genome size of 1,233,647 bp, 36.5% G+C content, 1,171 open reading frames (ORFs), and 53 RNAs.

GENOME ANNOUNCEMENT

Candidatus Liberibacter asiaticus,” an unculturable alphaproteobacterium, inhabits both Asian citrus psyllids (Diaphorina citri Kuwayama) and citrus plants. Infection of the bacterium is associated with citrus huanglongbing (HLB) (yellow shoot disease), a destructive disease in citrus production. D. citri transmits “Ca. Liberibacter asiaticus” (1). HLB was observed in Guangdong, China, >100 years ago (2). Transmission of the HLB pathogen by D. citri was reported in 1977 (3) before the detection of “Ca. Liberibacter asiaticus” in 1996 (4, 5). Because of the lack of in vitro culture, research on “Ca. Liberibacter asiaticus” has been challenging. Thanks to the development of next-generation sequencing technology, genomes of “Ca. Liberibacter asiaticus” strains can be sequenced directly from psyllid or plant hosts for biological study. Zheng et al. (6) sequenced the genome of “Ca. Liberibacter asiaticus” strain A4 from periwinkle in Guangdong. Here, we report a draft genome sequence of “Ca. Liberibacter asiaticus” from D. citri in the same geographical location.

A mandarin citrus tree (Citrus reticulata cv. Shatangju) infected with “Ca. Liberibacter asiaticus” was maintained in a growth chamber (RXZ-380A; Jiangnan Instrument, Inc., Ningbo, China) with the settings of 28 ± 1°C, 60% ± 5% rH, and 14:10 h light/dark (L:D) at South China Agricultural University in Guangzhou, China. The original source of “Ca. Liberibacter asiaticus” was from an HLB Shatangju tree in Boluo City of Guangdong (23°26′07″N, 114°29′56″E). Psyllids were fed on the infected citrus tree for 2 months. An individual psyllid adult was collected for DNA extraction using the DNeasy blood and tissue kit (Qiagen, Shanghai, China). Infection of “Ca. Liberibacter asiaticus” was monitored by the PCR method of Li et al. (7). DNA from a single psyllid sample (threshold cycle [CT], 18.1) was amplified using illustra GenomiPhi version 2 DNA amplification kits (GE Healthcare, Inc., Waukesha, WI, USA). The amplified DNA was sequenced using an Illumina MiSeq format (Illumina, Inc., San Diego, CA).

A total of 3.98 × 107 reads with a mean of 251 bp per read were generated from the psyllid DNA sample. Using the whole genomes of “Ca. Liberibacter asiaticus” strains psy62 (8) and A4 (6) as references, a total of 5,854,876 and 5,886,489 reads, respectively, were identified using the standalone BLAST software (version 2.2.30; e-value, <10-20) (9). The “Ca. Liberibacter asiaticus” reads were collected using a Perl script. The combination of de novo assembly using Velvet (version 1.2.10) (10) and reference assembly using Bowtie2 (version 2.2.6) (11) generated 9 contigs ranging from 1,587 bp to 755,458 bp, with an average coverage of 1,120×. The draft genome of “Ca. Liberibacter asiaticus” strain YCPsy comprises 1,233,647 bp, with a G+C content of 36.5%. Annotation was performed using the RAST server (http://rast.nmpdr.org/) (12), and the YCPsy genome was predicted to have 1,171 open reading frames (ORFs) and 53 RNAs.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession no. LIIM00000000. The version described in this manuscript is the first version LIIM01000000.

ACKNOWLEDGMENTS

This research was supported by Chinese Modern Agricultural Technology Systems (CARS-27) and the Special Fund for Agro-Scientific Research in the Public Interest, China (grant 2010003067) and the California Citrus Research Board.

The mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture.

Footnotes

Citation Wu F, Zheng Z, Deng X, Cen Y, Liang G, Chen J. 2015. Draft genome sequence of “Candidatus Liberibacter asiaticus” from Diaphorina citri in Guangdong, China. Genome Announc 3(6):e01316-15. doi:10.1128/genomeA.01316-15.

REFERENCES

  • 1.Bové JM. 2006. Huanglongbing: a destructive, newly emerging, century-old disease of citrus. J Plant Pathol 88:7–37. [Google Scholar]
  • 2.Lin KH. 1956. Observations on yellow shoot of citrus. Etiological study of yellow shoot of citrus. Acta Phytopathol Sinica 2:1–11. [Google Scholar]
  • 3.Plant Pathology Teaching and Research Group of Guangdong Agricultural and Forestry College 1977. Preliminary report on huanglongbing transmission by citrus psyllid. Guangdong. J Agric Sci 6:50–53. [Google Scholar]
  • 4.Deng X, Tang W. 1996. The studies on detection of citrus huanglongbing pathogen by polymerase chain reaction. J South China Agric Univ 17:119–120. [Google Scholar]
  • 5.Tian Y, Ke S, Ke C. 1996. Detection and quantitation of citrus huanglongbing pathogen by polymerase chain reaction. Acta Phytopathol Sin 26:243–250. [Google Scholar]
  • 6.Zheng Z, Deng X, Chen J. 2014. Whole-genome sequence of “Candidatus Liberibacter asiaticus” from Guangdong, China. Genome Announc 2(2):e00273-14. doi: 10.1128/genomeA.00273-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Li W, Hartung JS, Levy L. 2006. Quantitative real-time PCR for detection and identification of Candidatus Liberibacter species associated with citrus huanglongbing. J Microbiol Methods 66:104–115. doi: 10.1016/j.mimet.2005.10.018. [DOI] [PubMed] [Google Scholar]
  • 8.Duan Y, Zhou L, Hall DG, Li W, Doddapaneni H, Lin H, Liu L, Vahling CM, Gabriel DW, Williams KP, Dickerman A, Sun Y, Gottwald T. 2009. Complete genome sequence of citrus huanglongbing bacterium, “Candidatus Liberibacter asiaticus” obtained through metagenomics. Mol Plant Microbe Interact 22:1011–1020. doi: 10.1094/MPMI-22-8-1011. [DOI] [PubMed] [Google Scholar]
  • 9.Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL. 2009. BLAST+: architecture and applications. BMC Bioinformatics 10:421. doi: 10.1186/1471-2105-10-421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18:821–829. doi: 10.1101/gr.074492.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Langmead B, Salzberg SL. 2012. Fast gapped-read alignment with bowtie 2. Nat Methods 9:357–359. doi: 10.1038/nmeth.1923. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: Rapid Annotations using Subsystems Technology. BMC Genomics 9:75. doi: 10.1186/1471-2164-9-75. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES