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Journal of Bacteriology logoLink to Journal of Bacteriology
. 2012 Dec;194(24):6930–6931. doi: 10.1128/JB.01828-12

Full Genome Sequences of All Nine Chlamydia psittaci Genotype Reference Strains

Sarah Van Lent a, Jurgen R Piet b, Delphine Beeckman a, Arie van der Ende b, Filip Van Nieuwerburgh c, Patrik Bavoil d, Garry Myers e, Daisy Vanrompay a, Yvonne Pannekoek b,
PMCID: PMC3510619  PMID: 23209198

Abstract

Chlamydia psittaci primarily infects birds, but zoonotic transmission occurs in people in close contact with infected birds. The clinical outcome ranges from inapparent disease to pneumonia. Here we report the genome sequences of all 9 Chlamydia psittaci genotype reference strains.

GENOME ANNOUNCEMENT

Chlamydia psittaci is a Gram-negative, obligate intracellular bacterium causing respiratory disease in birds but also in mammals. Sequencing of the C. psittaci major outer membrane protein (ompA) gene identified 9 genotypes (A to F, E/B, M56, and WC) (4). Strains with genotypes A to F are isolated from birds, and genotypes WC and M56 represent mammalian isolates (1, 7, 8). The genotypes cluster with host species (5). Genotypes A and B are associated with psittacine birds (cockatoos, parrots, parakeets, and lories) and pigeons, respectively. Genotype C has been isolated from ducks and geese, whereas genotype D was found mainly in turkeys. The host range of genotype E is more diverse, since it has been isolated from pigeons, ratites, ducks, turkeys, and occasionally humans. Genotype F was isolated from psittacine birds and turkeys. Genotype E/B has been isolated mainly from ducks (4). Genotypes WC and M56 represent isolates from epizootics in cattle and muskrats, respectively (2, 6).

Here we report the genome sequences of all C. psittaci genotype reference strains (84/55, genotype A; CP3, genotype B; GR9, genotype C; NJ1, genotype D; MN, genotype E; VS225, genotype F; WS/RT/E30, genotype E/B; M56, genotype M56; WC, genotype WC). Table 1 is a summary of the features of the genomes. Comparative genomics analysis of these genomes will give us insight into the differences in pathogenicity, host tropism, and tissue specificity. Sequencing was performed using shotgun 454 Titanium (Roche) pyrosequencing according to the manufacturer's recommendations. De novo and reference mapping assemblies were performed with the software program Newbler (version 2.3; 454 Life Sciences, Branford, CT). If necessary, subsequent gap closure was done by conventional Sanger sequencing. Genome annotation was performed using the IGS prokaryotic annotation pipeline (3).

Table 1.

Features of the genome sequences

Genotype Strain Host Length (bp) No. of putative coding sequences % GC Plasmidb Reference
A 84/55 Amazona sp. 1,172,064 1,124 39 Y 9
B CP3 Columba liviaa 1,168,150 1,121 39 Y 8
C GR9 Anas platyrhynchos 1,147,152 1,045 39.1 N 7
D NJ1 Meleagris gallapavo 1,161,434 1,049 39 Y 8
E MN Homo sapiens 1,168,490 1,040 39 Y 4
F VS225 Parakeet 1,157,385 1,113 39 Y 2
E/B WS/RT/E30 Anas platyrhynchos 1,140,789 1,048 39 Y 4
M56 M56 Ondatra zibethicus 1,161,385 1,046 38.7 Y 6
WC WC Bos taurus 1,172,265 1,050 39.1 Y 2
a

Isolated from an urban pigeon.

b

Y, yes; N, no.

Nucleotide sequence accession numbers.

The genome sequences and plasmids of C. psittaci 84/55, CP3, GR9, NJ1, MN, VS225, WS/RT/E30, M56, and WC have been deposited at GenBank under the following accession numbers: CP003790 and CP003812; CP003797 and CP003813; CP003791; CP003798 and CP003816; CP003792 and CP003815; CP003793 and CP003817; CP003794 and CP003819; CP003795 and CP003814; and CP003796 and CP003818, respectively.

ACKNOWLEDGMENTS

We thank M. Giglio and S. Daugherty at the Institute of Genome Sciences for their support in annotating the genomes and depositing them in GenBank.

This study was partly funded by an Academic Medical Center Ph.D. scholarship (2008) to J. R. Piet and by FWO Vlaanderen (to D. Beeckman).

REFERENCES

  • 1. Andersen AA. 1991. Serotyping of Chlamydia psittaci isolates using serovar-specific monoclonal antibodies with the microimmunofluorescence test. J. Clin. Microbiol. 29:707–711 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Everett KD, Bush RM, Andersen AA. 1999. Emended description of the order Chlamydiales, proposal of Parachlamydiaceae fam nov. and Simkaniaceae fam. nov., each containing one monotypic genus, revised taxonomy of the family Chlamydiaceae, including a new genus and five new species, and standards for the identification of organisms. Int. J. Syst. Bacteriol. 49(Pt 2):415–440 [DOI] [PubMed] [Google Scholar]
  • 3. Galens K, et al. 2011. The IGS standard operating procedure for automated prokaryotic annotation. Stand. Genomic Sci. 4:244–251 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Geens T, et al. 2005. Sequencing of the Chlamydophila psittaci ompA gene reveals a new genotype, E/B, and the need for a rapid discriminatory genotyping method. J. Clin. Microbiol. 43:2456–2461 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Pannekoek Y, et al. 2010. Multi locus sequence typing of Chlamydia reveals an association between Chlamydia psittaci genotypes and host species. PLoS One 5:e14179 doi:10.1371/journal.pone.0014179 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Spalatin J, Fraser CE, Connell R, Hanson RP, Berman DT. 1966. Agents of psittacosis-lymphogranuloma venereum group isolated from muskrats and snowshoe hares in Saskatchewan. Can. J. Comp. Med. Vet. Sci. 30:260–264 [PMC free article] [PubMed] [Google Scholar]
  • 7. Vanrompay D, Andersen AA, Ducatelle R, Haesebrouck F. 1993. Serotyping of European isolates of Chlamydia psittaci from poultry and other birds. J. Clin. Microbiol. 31:134–137 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Vanrompay D, Butaye P, Sayada C, Ducatelle R, Haesebrouck F. 1997. Characterization of avian Chlamydia psittaci strains using omp1 restriction mapping and serovar-specific monoclonal antibodies. Res. Microbiol. 148:327–333 [DOI] [PubMed] [Google Scholar]
  • 9. Vanrompay D, Ducatelle R, Haesebrouck F. 1994. Pathogenicity for turkeys of Chlamydia psittaci strains belonging to the avian serovars A, B and D. Avian Pathol. 23:247–262 [DOI] [PubMed] [Google Scholar]

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