Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2015 Apr 23;3(2):e00152-15. doi: 10.1128/genomeA.00152-15

Draft Genome Sequences of 53 Genetically Distinct Isolates of Bordetella bronchiseptica Representing 11 Terrestrial and Aquatic Hosts

Karen B Register a, Yury V Ivanov b, Nathan Jacobs b, Jessica A Meyer b, Laura L Goodfield b, Sarah J Muse b, William E Smallridge b, Lauren Brinkac c, Maria Kim c, Ravi Sanka c, Eric T Harvill b, Liliana Losada c,
PMCID: PMC4408323  PMID: 25908122

Abstract

Bordetella bronchiseptica infects a variety of mammalian and avian hosts. Here, we report the genome sequences of 53 genetically distinct isolates acquired from a broad range of terrestrial and aquatic animals. These data will greatly facilitate ongoing efforts to better understand the evolution, host adaptation, and virulence mechanisms of B. bronchiseptica.

GENOME ANNOUNCEMENT

Bordetella bronchiseptica infects a variety of terrestrial and aquatic animals, having a host range that is remarkably broad compared with that of other Bordetella species. Most frequently, it causes respiratory disease in pigs and dogs, but is also an occasional zoonotic pathogen (1, 2). For some hosts, including birds and several species of wild mammals, its colonization has not been associated with disease (3, 4). The characterization of isolates using multilocus enzyme electrophoresis (5), PvuII ribotyping (68), and multilocus sequence typing (8, 9) indicates that some genotypes preferentially infect one or a few hosts. Here, we report the genome sequences of 53 B. bronchiseptica isolates selected to maximally represent geographic, host range, and molecular diversity. The isolates originated from terrestrial and aquatic hosts including 10 mammalian and one avian species, and they collectively represent Australia, Asia, Europe, and North America. They include the 32 PvuII ribotypes so far defined (68) (K. B. Register, unpublished data), 29 of the 60 multilocus sequence types (STs) currently identified among the B. bronchiseptica species (9) (http://pubmlst.org/bordetella/), and 5 STs not previously associated with the bacterium.

Genomic DNA was prepared (10) and sequenced using a combination of 3- or 5-kb mate-pair Illumina MiSeq 2 × 250-bp and HiSeq 2000 1 × 100-bp paired-end reads. After quality trimming, the reads for each strain (between 2,221,299 and 6,288,700) were assembled with the Celera Assembler 6.1 (11) or the Velvet assembler (12). The underlying consensus sequences and gaps were improved using custom scripts to recruit unmapped reads. All the genomes have between 41 and 296 contigs (median, 117 contigs) (Table 1), with N50 values ranging from 41,868 bp to 281,818 bp (median, 100,254 bp). The overall G+C content is ~68.1%, with genome sizes ranging from 5.04 Mb to 5.83 Mb. The genomes were annotated using the J. Craig Venter Institute (JCVI) prokaryotic annotation pipeline and contain between 4,388 and 5,660 predicted protein-coding genes. Due to their high copy number, the rRNA loci were broken in the assemblies, so the exact number of operons could not be confidently enumerated in each strain. All strains have between 50 and 68 tRNAs, consistent with previously published genomes (13). The pangenome of the species was estimated at 10,375 genes, with just over 3,300 genes present in all strains, and an additional 1,084 genes present in >90% of the strains. In contrast, just over 3,300 singleton genes were identified, with a single strain containing as few as 1 and as many as 310 strain-specific genes. The majority of the unique genes encode hypothetical proteins or proteins with functions associated with phage and other mobile elements. These results are typical of species that frequently acquire genes by horizontal transfer.

TABLE 1 .

Strain descriptions and genome assembly characteristics

B. bronchiseptica strain Host No. of contigs Length (bp) GenBank accession no. Repository
00-P-2730 Human 296 5,831,418 JGWG00000000 NRRL
00-P-2796 Human 179 5,551,792 JGWH00000000 NRRL
345 Human 79 5,286,504 JGWJ00000000 Harvill Lab
3E44 Rabbit 104 5,255,953 JGWK00000000 NRRL
7E71 Horse 109 5,163,549 JGWL00000000 NRRL
980 Unknown 70 5,535,898 JGWM00000000 Harvill Lab
A1-7 Rabbit 184 5,265,200 JGWO00000000 Harvill Lab
B18-5 Rabbit 99 5,219,442 JGWP00000000 Harvill Lab
B20-10725633 Rabbit 124 5,316,022 JGWQ00000000 Harvill Lab
CA90 BB02 Turkey 170 5,126,467 JHBU00000000 Harvill Lab
CA90 BB1334 Turkey 120 5,269,162 JGWR00000000 NRRL
CARE970018BB Pig 121 5,240,190 JGWS00000000 NRRL
D756 Human 102 5,233,656 JGWT00000000 Harvill Lab
D989 Human 75 5,326,241 JGWU00000000 Harvill Lab
D993 Human 197 5,278,699 JGWV00000000 Harvill Lab
E010 Human 187 5,179,093 JGWW00000000 Harvill Lab
E012 Human 156 5,175,924 JGWX00000000 Harvill Lab
E013 Human 119 5,099,096 JGWY00000000 Harvill Lab
E014 Human 111 5,210,402 JGWZ00000000 Harvill Lab
F-1 Turkey 96 5,377,336 JGXA00000000 NRRL
F2 Turkey 164 5,380,523 JGXB00000000 NRRL
F4563 Human 162 5,263,073 JGXC00000000 NRRL
GA96-01 Human 158 5,292,152 JGXD00000000 NRRL
M435/02/3 Seal 182 5,157,766 JGXE00000000 NRRL
M85/00/2 Seal 159 5,157,897 JGXF00000000 NRRL
MBORD591 Dog 271 5,151,134 JGXG00000000 NRRL
MBORD595 Dog 107 5,214,983 JGXH00000000 NRRL
MBORD624 Horse 213 5,306,540 JGXI00000000 NRRL
MBORD632 Horse 164 5,148,641 JGXJ00000000 NRRL
MBORD635 Cat 55 5,092,496 JGXK00000000 NRRL
MBORD665 Guinea pig 51 5,147,090 JGXL00000000 NRRL
MBORD668 Guinea pig 59 5,149,790 JGXM00000000 NRRL
MBORD670 Guinea pig 80 5,169,029 JGXN00000000 NRRL
MBORD675 Human 41 5,173,023 JGXO00000000 NRRL
MBORD678 Guinea pig 50 5,184,788 JHBQ00000000 NRRL
MBORD681 Koala 70 5,158,310 JGXP00000000 NRRL
MBORD698 Koala 52 5,151,735 JGXQ00000000 NRRL
MBORD707 Turkey 56 5,138,088 JGXR00000000 NRRL
MBORD731 Horse 52 5,132,633 JGXS00000000 NRRL
MBORD762 Guinea pig 63 5,280,420 JHBR00000000 NRRL
MBORD782 Cat 90 5,134,438 JGXT00000000 NRRL
MBORD785 Dog 102 5,152,034 JGXU00000000 NRRL
MBORD839 Dog 103 5,190,832 JGXV00000000 NRRL
MBORD849 Pig 68 5,216,172 JGXW00000000 NRRL
MBORD901 Turkey 109 5,096,955 JGXX00000000 NRRL
MO211 Human 140 5,258,097 JHOJ00000000 Harvill Lab
MO275 Human 131 5,032,460 JHBS00000000 NRRL
OSU054 Turkey 131 5,400,773 JHBZ00000000 Harvill Lab
OSU095 Turkey 54 5,460,040 JGXY00000000 NRRL
OSU553 Turkey 250 5,685,971 JGXZ00000000 NRRL
RB630 Rabbit 48 5,312,681 JGYA00000000 NRRL
SBL-F6116 Human 121 5,060,248 JHBT00000000 NRRL
SO10328 Sea otter 115 5,116,835 JGYB00000000 NRRL

Whole-genome single-nucleotide polymorphism (SNP) analysis clusters isolates into two main groups corresponding to complexes I and IV (9). All avian isolates cluster in complex IV, while most other nonhuman isolates cluster in complex I. In contrast, the human isolates from North America and Europe are evenly dispersed between complexes I and IV. The results of this study provide a wealth of information useful for understanding the evolution, host adaptation, and virulence mechanisms of B. bronchiseptica.

Nucleotide sequence accession numbers.

The sequences of the B. bronchiseptica isolates have been deposited in GenBank under the accession numbers listed in Table 1; the source of each strain is also listed.

ACKNOWLEDGMENTS

This project was supported in part by federal funds from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services under contract no. HHSN272200900007C.

All isolates were collected in agreement with each institution’s institutional review board (IRB) requirements for patient safety and confidentiality.

We thank William Boatwright for his excellent technical assistance.

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 Register KB, Ivanov YV, Jacobs N, Meyer JA, Goodfield LL, Muse SJ, Smallridge WE, Brinkac L, Kim M, Sanka R, Harvill ET, Losada L. 2015. Draft genome sequences of 53 genetically distinct isolates of Bordetella bronchiseptica representing 11 terrestrial and aquatic hosts. Genome Announc 3(2):e00152-15. doi:10.1128/genomeA.00152-15.

REFERENCES

  • 1.Mattoo S, Cherry JD. 2005. Molecular pathogenesis, epidemiology, and clinical manifestations of respiratory infections due to Bordetella pertussis and other Bordetella subspecies. Clin Microbiol Rev 18:326–382. doi: 10.1128/CMR.18.2.326-382.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Register KB, Sukumar N, Palavecino EL, Rubin BK, Deora R. 2012. Bordetella bronchiseptica in a paediatric cystic fibrosis patient: possible transmission from a household cat. Zoonoses Public Health 59:246–250. doi: 10.1111/j.1863-2378.2011.01446.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Farrington DO, Jorgenson RD. 1976. Prevalence of Bordetella bronchiseptica in certain wild mammals and birds in central Iowa. J Wildl Dis 12:523–525. doi: 10.7589/0090-3558-12.4.523. [DOI] [PubMed] [Google Scholar]
  • 4.Boot R, Hinz K-H. 2005. Antigenic relationship of avian strains of three Bordetella species determined by ELISA. Vet Rec 157:447–448. doi: 10.1136/vr.157.15.447. [DOI] [PubMed] [Google Scholar]
  • 5.Musser JM, Bemis DA, Ishikawa H, Selander RK. 1987. Clonal diversity and host distribution in Bordetella bronchiseptica. J Bacteriol 169:2793–2803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Register KB, Boisvert A, Ackermann MR. 1997. Use of ribotyping to distinguish Bordetella bronchiseptica isolates. Int J Syst Bacteriol 47:678–683. doi: 10.1099/00207713-47-3-678. [DOI] [PubMed] [Google Scholar]
  • 7.Register KB, Magyar T. 1999. Optimized ribotyping protocol applied to Hungarian Bordetella bronchiseptica isolates: identification of two novel ribotypes. Vet Microbiol 69:277–285. doi: 10.1016/S0378-1135(99)00118-2. [DOI] [PubMed] [Google Scholar]
  • 8.Register KB, Ivanov YV, Harvill ET, Davison N, Foster G. Novel, host-restricted genotypes of Bordetella bronchiseptica associated with phocine respiratory tract isolates. Microbiology 161:580–592. doi: 10.1099/mic.0.000035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Diavatopoulos DA, Cummings CA, Schouls LM, Brinig MM, Relman DA, Mooi FR. 2005. Bordetella pertussis, the causative agent of whooping cough, evolved from a distinct, human-associated lineage of B. bronchiseptica. PLoS Pathog 1:e45. doi: 10.1371/journal.ppat.0010045. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Chomczynski P, Sacchi N. 1987. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  • 11.Miller JR, Delcher AL, Koren S, Venter E, Walenz BP, Brownley A, Johnson J, Li K, Mobarry C, Sutton G. 2008. Aggressive assembly of pyrosequencing reads with mates. Bioinformatics 24:2818–2824. doi: 10.1093/bioinformatics/btn548. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.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]
  • 13.Park J, Zhang Y, Buboltz AM, Zhang X, Schuster SC, Ahuja U, Liu M, Miller JF, Sebaihia M, Bentley SD, Parkhill J, Harvill ET. 2012. Comparative genomics of the classical Bordetella subspecies: the evolution and exchange of virulence-associated diversity amongst closely related pathogens. BMC Genomics 13:545. doi: 10.1186/1471-2164-13-545. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES