How to Kill the Honey Bee Larva: Genomic Potential and Virulence Mechanisms of Paenibacillus larvae

被引:80
作者
Djukic, Marvin [1 ,2 ]
Brzuszkiewicz, Elzbieta [1 ,2 ]
Fuenfhaus, Anne [3 ]
Voss, Joern [1 ,2 ]
Gollnow, Kathleen [1 ,2 ]
Poppinga, Lena [3 ]
Liesegang, Heiko [1 ,2 ]
Garcia-Gonzalez, Eva [3 ]
Genersch, Elke [3 ]
Daniel, Rolf [1 ,2 ]
机构
[1] Univ Gottingen, Dept Genom & Appl Microbiol, Inst Microbiol & Genet, D-37073 Gottingen, Germany
[2] Univ Gottingen, Gottingen Genom Lab, Inst Microbiol & Genet, D-37073 Gottingen, Germany
[3] Inst Bee Res, Dept Mol Microbiol & Bee Dis, Hohen Neuendorf, Germany
关键词
AMERICAN FOULBROOD DISEASE; BACTERIAL PATHOGEN; SUBSP LARVAE; CLOSTRIDIUM-BOTULINUM; DIFFERENT GENOTYPES; SECRETED PROTEASES; SYNERGISTIC FACTOR; GRANULOSIS-VIRUS; ETIOLOGIC AGENT; APIS-MELLIFERA;
D O I
10.1371/journal.pone.0090914
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Paenibacillus larvae, a Gram positive bacterial pathogen, causes American Foulbrood (AFB), which is the most serious infectious disease of honey bees. In order to investigate the genomic potential of P. larvae, two strains belonging to two different genotypes were sequenced and used for comparative genome analysis. The complete genome sequence of P. larvae strain DSM 25430 (genotype ERIC II) consisted of 4,056,006 bp and harbored 3,928 predicted protein-encoding genes. The draft genome sequence of P. larvae strain DSM 25719 (genotype ERIC I) comprised 4,579,589 bp and contained 4,868 protein-encoding genes. Both strains harbored a 9.7 kb plasmid and encoded a large number of virulence-associated proteins such as toxins and collagenases. In addition, genes encoding large multimodular enzymes producing nonribosomally peptides or polyketides were identified. In the genome of strain DSM 25719 seven toxin associated loci were identified and analyzed. Five of them encoded putatively functional toxins. The genome of strain DSM 25430 harbored several toxin loci that showed similarity to corresponding loci in the genome of strain DSM 25719, but were non-functional due to point mutations or disruption by transposases. Although both strains cause AFB, significant differences between the genomes were observed including genome size, number and composition of transposases, insertion elements, predicted phage regions, and strain-specific island-like regions. Transposases, integrases and recombinases are important drivers for genome plasticity. A total of 390 and 273 mobile elements were found in strain DSM 25430 and strain DSM 25719, respectively. Comparative genomics of both strains revealed acquisition of virulence factors by horizontal gene transfer and provided insights into evolution and pathogenicity.
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页数:14
相关论文
共 88 条
[31]   Strain- and genotype-specific differences in virulence of Paenibacillus larvae subsp larvae, a bacterial pathogen causing American foulbrood disease in honeybees [J].
Genersch, E ;
Ashiralieva, A ;
Fries, I .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (11) :7551-7555
[32]   The use of repetitive element PCR fingerprinting (rep-PCR) for genetic subtyping of German field isolates of Paenibacillus larvae subsp larvae [J].
Genersch, E ;
Otten, C .
APIDOLOGIE, 2003, 34 (03) :195-206
[33]   Significance of haemotrophic mycoplasmas in veterinary medicine with particular regard to the M-suis infection in swine [J].
Hoelzle, Ludwig E. .
BERLINER UND MUNCHENER TIERARZTLICHE WOCHENSCHRIFT, 2007, 120 (1-2) :34-41
[34]   Honey bee pathology: current threats to honey bees and beekeeping [J].
Genersch, Elke .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2010, 87 (01) :87-97
[35]   American Foulbrood in honeybees and its causative agent, Paenibacillus larvae [J].
Genersch, Elke .
JOURNAL OF INVERTEBRATE PATHOLOGY, 2010, 103 :S10-S19
[36]   TOTAL HEMOCYTE COUNTS OF HONEY BEE LARVAE (APIS-MELLIFERA L) FROM VARIOUS ELEVATIONS [J].
GILLIAM, M ;
SHIMANUKI, H .
EXPERIENTIA, 1970, 26 (09) :1006-+
[37]  
Graham J.M., 1992, HIVE HONEY BEE
[38]   CRISPRFinder: a web tool to identify clustered regularly interspaced short palindromic repeats [J].
Grissa, Ibtissem ;
Vergnaud, Gilles ;
Pourcel, Christine .
NUCLEIC ACIDS RESEARCH, 2007, 35 :W52-W57
[39]   A guild of 45 CRISPR-associated (Cas) protein families and multiple CRISPR/Cas subtypes exist in prokaryotic genomes [J].
Haft, DH ;
Selengut, J ;
Mongodin, EF ;
Nelson, KE .
PLOS COMPUTATIONAL BIOLOGY, 2005, 1 (06) :474-483
[40]   Serine protease mechanism and specificity [J].
Hedstrom, L .
CHEMICAL REVIEWS, 2002, 102 (12) :4501-4523