Nature Biotechnology 21, 1307 - 1313 (2003)
Published online: 5 October 2003 | doi:10.1038/nbt886

The genome sequence of the entomopathogenic bacterium Photorhabdus luminescens

Eric Duchaud1, Christophe Rusniok1, Lionel Frangeul2, Carmen Buchrieser1, Alain Givaudan5, Séad Taourit1, Stéphanie Bocs6, Caroline Boursaux-Eude2, Michael Chandler7, Jean-François Charles3, Elie Dassa4, Richard Derose8, Sylviane Derzelle3, Georges Freyssinet8, Sophie Gaudriault5, Claudine Médigue6, Anne Lanois5, Kerrie Powell9, Patricia Siguier7, Rachel Vincent5, Vincent Wingate9, Mohamed Zouine1, Philippe Glaser1, Noël Boemare5, Antoine Danchin3 & Frank Kunst1

This article is distributed under the terms of the Creative Commons Attribution-Non-Commercial-Share Alike license (, which permits distribution, and reproduction in any medium, provided the original author and source are credited. This license does not permit commercial exploitation, and derivative works must be licensed under the same or similar license.

Photorhabdus luminescens is a symbiont of nematodes and a broad-spectrum insect pathogen. The complete genome sequence of strain TT01 is 5,688,987 base pairs (bp) long and contains 4,839 predicted protein-coding genes. Strikingly, it encodes a large number of adhesins, toxins, hemolysins, proteases and lipases, and contains a wide array of antibiotic synthesizing genes. These proteins are likely to play a role in the elimination of competitors, host colonization, invasion and bioconversion of the insect cadaver, making P. luminescens a promising model for the study of symbiosis and host-pathogen interactions. Comparison with the genomes of related bacteria reveals the acquisition of virulence factors by extensive horizontal transfer and provides clues about the evolution of an insect pathogen. Moreover, newly identified insecticidal proteins may be effective alternatives for the control of insect pests.

Photorhabdus luminescens is an enterobacterium that is symbiotic with soil entomopathogenic nematodes and pathogenic to a wide range of insects. P. luminescens promotes its own transmission among susceptible insect populations using its nematode host as vector1. Its life cycle comprises a symbiotic stage in the nematode's gut and a virulent stage in the insect larvae, which it kills through toxemia and septicemia. After the nematode attacks a prey insect and P. luminescens is released, the bacterium produces a wide variety of virulence factors ensuring rapid insect killing. Bioconversion of the insect cadaver by exoenzymes produced by the bacteria allows the bacteria to multiply and the nematode to reproduce. During this process P. luminescens produces antibiotics to prevent invasion of the insect cadaver by bacterial or fungal competitors. Finally, elimination of competitors allows P. luminescens and the nematode to reassociate specifically before leaving the insect cadaver2, 3.

To better understand this complex life style, we determined the genome sequence of P. luminescens subspecies laumondii strain TT014, a symbiont of the nematode Heterorhabditis bacteriophora isolated on Trinidad and Tobago.



General features

Strain TT01 possesses a single circular chromosome of 5,688,987 bp with an average GC content of 42.8%. No plasmid replicon was found. A total of 4,839 protein-coding genes, including 157 pseudogenes, seven complete sets (23S, 5S and 16S) of ribosomal RNA operons and 85 tRNA genes, were predicted (Fig. 1; Supplementary Table 1 online).

Figure 1: Circular representation of the P. luminescens genome.

Figure 1 : Circular representation of the P. luminescens genome.

The outer scale is marked in megabases. Circle 1 and 2 (from outside to inside), genes transcribed clockwise and counterclockwise. Circle 3, transposases (red) and phage-related genes (green). Circle 4, GC bias (G − C/G + C). Circle 5, GC content with <32% G + C in light yellow, between 32% and 53.6% G + C in yellow and with >53.6% G + C in dark yellow. Shifts in GC bias correspond to positions of the predicted origin and terminus of replication or to putative prophage regions (green).

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Toxins against insects

More toxin genes were predicted in the P. luminescens genome than in any other bacterial genome sequenced yet. A large number of these toxins may be involved in the killing of a wide variety of insects. Some may act synergistically or use redundancy for 'overkill'5, ensuring a quick death of the host. In addition, some may kill insects by interfering with their development. In the TT01 genome, two paralogs, plu4092 and plu4436, encode proteins similar to juvenile hormone esterases (JHEs) of the insect Leptinotarsa decemlineata6. Juvenile hormone maintains the insect in a larval state. Its inactivation by JHE allows metamorphosis to proceed. JHEs may be used to trigger the insect endocrine machinery at an inappropriate time and thus represents a promising approach for insect control7. These genes are located downstream of highly related orphan genes (plu4093 and plu4437), suggesting a locus duplication.

The toxicity of the proteins encoded by these two loci was verified experimentally. Two Escherichia coli clones, containing the recombinant BAC1A02 and BAC8C11, were shown to be toxic toward insects. BAC1A02, which contains the locus plu4093–plu4092, exhibited substantial oral toxicity toward three mosquito species, Aedes aegypti, Culex pipiens and Anopheles gambiae, as well as toward the lepidopteran Plutella xylostella; BAC8C11, which contains the locus plu4437–plu4436, showed insecticidal activity toward P. xylostella (data not shown). Ingestion of undiluted recombinant E. coli, in which both plu4093 and plu4092 were expressed under the control of the Plac promoter (pDIA700), led to killing of 96% of P. xylostella and 100% of C. pipiens larvae after 48 h8 (Table 1). Partial deletion of plu4092 (pDIA701) abolished toxicity for both insects, indicating that the JHE-like product of plu4092 is required for toxicity. This is the first time that a protein lethal for mosquitoes has been found in P. luminescens.


Mcf, a gene previously identified in the P. luminescens strain W14, encodes a cytotoxin that is able to kill the insect Manduca sexta5. Strain TT01 possesses this gene as well as the paralog plu3128.

Four toxin-complex loci, tca, tcb, tcc and tcd, have been identified in the P. luminescens strain W14 (ref. 9). The tca locus encodes complexes with high oral toxicity for the insect Manduca sexta10, 11. Strain TT01 contains the tcc and tcd loci, an incomplete tca locus and five newly identified tc loci (Fig. 2; Supplementary Table 2 online). The physical linkage of the tcdAB and tccC genes was found in three other insect-associated bacteria, Xenorhabdus nematophila, Serratia entomophila and Yersinia pestis. This organization may be due to gene transfer events between bacteria sharing the same niche, namely insects.

Figure 2: Toxin complex loci identified in strain TT01.

Figure 2 : Toxin complex loci identified in strain TT01.

Related genes are shown in the same color. Similarities of predicted proteins to previously known Tc proteins are reported in Supplementary Table 2 online. Nomenclature is according to Waterfield et al.39 (a) Locus similar to the toxin complex a (tca) locus from strain W14 (GenBank accession no. AF046867). (b) Locus similar to the toxin complex d (tcd) island from strain W14 (GenBank accession no. AY144119). The W14 tcdA3 counterpart is only weakly similar, and thus the corresponding TT01 gene has been designated tcdA5. (c) Locus similar to the toxin complex c (tcc) locus from strain W14 (GenBank accession no. AF047028). (d) Loci weakly similar to the toxin complex c (tcc) locus from strain W14 (GenBank accession no. AF047028). (e) Other loci plu2333, plu2334 and plu2335 correspond to a single pseudogene.

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The putative tcc and rhs gene products belong to one protein superfamily9. They contain repeated Tyr-Asp motifs, previously found in teneurins, transmembrane proteins of invertebrates and vertebrates12. An in silico search for the presence of Arg-Tyr × Tyr-Asp motifs (at least three, no more than one mismatch) in the TTO1 proteome identified 14 putative proteins of a superfamily including the 7 TccC paralogs, putative nematicidal proteins (Plu2222 and Plu2442) and hypothetical rhs-like elements as well as Mcf and its paralog (see Supplementary Fig. 1 and Supplementary Table 3 online). It has been suggested that Tyr-Asp-repeat proteins bind carbohydrates12. One could speculate that proteins belonging to this superfamily are exposed at the surface of the bacteria where they are important for evasion of defenses from a broad spectrum of insects.

P. luminescens contains eight genes predicted to encode hemolysin- or hemagglutinin-related proteins secreted by the two-partner secretion (TPS) pathway. These comprise the secreted PhlA protein and the PhlB protein, which allows secretion and activation of PhlA13. We identified six other TPS gene pairs and ten incomplete loci (Supplementary Table 3 online).

Repeats-in-toxin (RTX) proteins constitute another family of toxins, including cytolytic toxins, metalloproteases and lipases. We identified eight genes whose deduced protein sequence is homologous to the Vibrio cholerae RtxA toxin (4,558 amino acids), which causes cross-linking and depolymerization of actin stress fibers in an in vivo model14. The rtxA homologs are clustered in two chromosomal regions and are tandemly organized. Four are complete genes and four are disrupted by frameshifts or insertion sequences (ISs; Supplementary Table 2 online). Furthermore, the organization of the genes predicted to encode the RTX secretion system is identical to that in V. cholerae (Fig. 3). Plu4117 and Plu3668 belong to another subfamily of RTX proteins. This large set of putative RTX toxins and related proteins probably contributes to the insect pathogenicity of P. luminescens. In addition to the RTX family we identified a new family of putative proteins containing Gly-Asp repeats (Supplementary Fig. 2 online). Genes encoding proteins similar to toxins from other bacteria were also predicted, including Plu0840, similar to the heat-stable cytotonic enterotoxin from Aeromonas hydrophila15, and Plu1537, similar to a component of the Bacillus thuringiensis δ-endotoxin16.

Figure 3: Schematic representation of tandemly repeated genes.

Figure 3 : Schematic representation of tandemly repeated genes.

Related genes are color coded: blue-purple, genes encoding putative secretion systems; gray, genes belonging to the core genome; white, genes of unknown function; dashed, pseudogenes. ↓ IS indicates insertion-sequence element. (a) Red, tandemly repeated rtxA genes and genes encoding the RTX secretory machinery as compared to V. cholerae. (b) Yellow, genes encoding unknown proteins, probably secreted by the Type I secretory system encoded by plu0634 and plu0635. (c) Green, luxR gene clusters. (d) Red, clusters encoding putative pyocin- and colicin-like factors; yellow, immunity proteins. (e) Orange, highly related genes of unknown function. (f) Brown, putative O-methyltransferase-encoding genes.

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Toxins against competitors

One of the most important questions about the ecology of this bacterium is how P. luminescens defends the insect cadaver against different microbial competitors. The TT01 genome contains 33 genes, clustered in 20 loci, encoding proteins similar to polyketide and nonribosomal peptide synthases that may be part of the biosynthetic pathway of antibiotics known to be produced by P. luminescens (Supplementary Table 4 online). As observed in strain W14 (ref. 17), ten genes of TT01 are similar to genes for the biosynthesis of syringomycin by Pseudomonas syringae, which acts as a pore-forming host cell cytolysin18. One gene, plu2670, encodes a 16,367-amino-acid putative peptide synthase that is, to our knowledge, the largest protein reported for a prokaryote to date. In our work here, we frequently identified genes that were adjacent to antibiotic biosynthetic genes and that presumably encode transporters involved in antibiotic efflux. Four genes (plu0250, plu2474, plu2475, plu2476) are similar to Burkholderia glumae genes involved in the biosynthesis of toxoflavin. Compounds belonging to this family are active against a variety of Gram-positive bacteria and fungi19.

Toxin-antitoxin systems are efficient in killing related bacteria, including other P. luminescens strains that invade the host20. The TT01 genome encodes three putative colicin-like factors and 17 putative immunity proteins involved in self-protection. These genes are located in three clusters, which may encode pyocin S3–like factors (plu0884, plu4177) and a colicin-like factor (plu1894) (Fig. 3 and Supplementary Table 3 online). This complex pattern of immunity-protein-coding genes may provide a selective advantage to TT01 against related bacteria producing similar toxins.

Host interactions

Another intriguing question is how P. luminescens interacts with the nematode midgut and the insect hemocytes. We identified a large number of genes that could be involved in adhesion. plu2096 encodes a protein similar to the Pseudomonas aeruginosa lectin PA-I, which recognizes specific carbohydrates exposed on the host cells and functions as an adhesin and a cytotoxin that plays a role in the initiation of infection21. The putative plu1561 gene product is similar to a Ca2+-dependent adhesion molecule of the cadherin family in Dictyostelium discoideum22. We have further identified one gene, plu2057, encoding a protein 45% similar to inv and three ail-like paralogs (plu2480, plu2481 and plu1967). In Yersinia species, Inv and Ail play a role in surface adhesion or invasion23, 24. Another P. luminescens gene, plu2433, may encode an adhesin required for insect colonization, because Plu2433 is similar to the recently discovered Erwinia carotovora virulence factor (Evf) allowing this bacterium to colonize the gut epithelium of Drosophila melanogaster25.

P. luminescens TT01 has a large repertoire of fimbrial genes. Eleven clusters could be distinguished (see Supplementary Fig. 3 online). Among these, two gene clusters encode proteins similar to MR/P (mannose-resistant) fimbriae of Proteus mirabilis26 as well as type IV pili of pathogenic E. coli and Salmonella enterica27. This large repertoire of pili may help P. luminescens colonize the nematode gut and invade the different insect compartments, as the ngrA gene (an ngrA homolog has previously been identified in Photorhabdus luminescens strain W14; see ref. 28), belonging to cluster VIII, is important for bacterial-nematode interactions28.

Secreted proteins

P. luminescens secretes many enzymes that contribute to insect death and result in bioconversion of the insect cadaver29. In X. nematophila a zinc metalloprotease, PrtA, is involved in the immunosuppression of the insect30. In P. luminescens, the protein is encoded by the operon prtA-inh-prtBCD and is secreted by a type I secretory system31. Other putative proteases were identified, such as Plu2820, similar to a serine protease of the subtilisin family, Plu1382, similar to an extracellular metalloproteinase, and Plu2455, similar to calpain.

Lipases are another class of secreted proteins. TT01 encodes ten triacylglycerol lipase-, phospholipase A- and D-like proteins. For example, the proteins predicted to be encoded by genes plu3370 and plu3369 are similar to phospholipase A and its accessory protein, respectively. Gene plu0830 encodes a similar protein that is more distantly related to phospholipase A. Both contain the lipase-specific consensus sequence G-x-S-x-G-G in their amino-terminal moiety. Yersinia enterocolitica phospholipase A contributes to pathogenesis in a mouse model32, suggesting a role in virulence for the TT01 homolog. Plu1971 is remarkably similar to the Y. pestis plasmid (pMT1)-encoded Yersinia murine toxin (Ymt). It contains the two phospholipase D motifs H-x-K-x4-D-x6-G-G. Genes plu1971 and ymt are 56% identical, with the same GC content (38%), substantially different from the 50% GC content of the pMT1 plasmid; this suggests that ymt has been acquired by Y. pestis from P. luminescens or a close relative. Because Ymt is essential for flea colonization by Y. pestis33, P. luminescens and Y. pestis may use similar genes for insect colonization.

Besides the lip-1 gene, encoding a triacylglycerol lipase34, we predicted four triacylglycerol lipases unrelated to Lip-1, encoded by the tandemly repeated paralogs plu1519, plu1518, plu1517 and plu1516. Another unrelated lipase, Plu2266, is similar to LipP (carboxylesterase) of Pseudomonas sp. strain B11-135, and Plu2313 is highly similar to the extracellular lipase, LipA, from Serratia marcescens36. Plu2313 lacks an N-terminal signal peptide but contains instead, in its C terminus, four almost exact repeats of the glycine-rich motif L-x-G-G-x-G-x-D of RTX toxins, suggestive of a similar secretion pathway37. We predicted a chitin-binding-like protein (Plu2352) and chitinase-like proteins (Plu2235, Plu2458 and Plu2461) as expected for an insect pathogen.


Within an insect, P. luminescens needs to get access to the available nutrients and has to deal with low-iron conditions. The overall intermediary metabolism of P. luminescens is similar to that found in most Enterobacteriaceae, but it comprises many degradation pathways that are absent from the laboratory strain E. coli K12, including urease, proline or histidine degradation pathways that may help the bacteria to multiply in the hemocele of the insect larvae, while providing the bacteria and the nematode host with building blocks for their growth.

The TT01 genome contains many genes encoding proteins similar to monooxygenases, dioxygenases and hydroxylases that could be implicated in rapid elimination of insect polyphenols, such as plu4258, adjacent to glutathione transferase (plu4259), or operons such as the hca operon or plu1434–plu1437. Many gene products may be involved in the detoxification of reactive oxygen species generated by the invaded host; the bacterium may take advantage of the reactivity of dioxygen to metabolize insect products. We also identified counterparts of a putative steroid monooxygenase (Plu4232), glycine oxidase (Plu2242) and aromatic monooxygenase (Plu1313) as well as five tandemly organized paralogs (plu4890–plu4895), possibly encoding proteins similar to O-methyltransferase that may play a similar role (Fig. 3).

Iron acquisition seems to be of particular importance for the life cycle of P. luminescens, as this bacterium has the largest known set of iron, heme, hemin and siderophore transporters. Five loci have counterparts in Y. pestis, one of which is similar to the genes involved in biosynthesis of the siderophore yersiniabactin (Supplementary Table 3 and Supplementary Fig. 4 online). A sixth locus (fecIfecE) is similar to the E. coli iron(III)-dicitrate transport system. Two putative binding proteins and six outer membrane receptors of the ISVH (iron-siderophores, vitamin B12 and hemin) family may be involved in iron, heme, hemin or siderophore transport38 (Supplementary Table 3 online).

P. luminescens encodes four complete type I, one type II and one type III secretion systems39. The latter one is highly similar to the plasmid-encoded type III system of Y. pestis and is probably involved in the secretion of virulence proteins or in immunomodulation of the insect response. The phage elements present in the genome may participate in the release of molecules involved in pathogenesis by partial lysis of the bacteria (S.G., unpublished data).


To adapt to invertebrate environments such as the nematode gut, the insect hemolymph and the insect cadaver, P. luminescens needs to sense changes in such conditions as nutrient and cation availability, osmolarity and bacterial density. Strain TT01 encodes homologs of the five E. coli sigma factors RpoD, RpoS, RpoH, FliA and RpoN. In contrast to E. coli, which has only one ECF sigma factor, TT01 possesses five such factors. We predicted 192 transcriptional regulators (Supplementary Table 5 online) from the sequence. Interestingly, the LuxR family of regulators is over-represented (32 genes) and the majority of these genes are tandemly located in two regions (Fig. 3). This tandem organization of the luxR genes may play a role in the response of TT01 to acylhomoserine lactone (AHL) signals produced by TT01 or by closely related bacteria. LuxR regulators may then, in association with AHL-responsive systems, affect diverse biological functions including bioluminescence. Although TT01 contains a complete lux operon responsible for the production of bioluminescence, we could identify only one gene, plu2238, that might be part of an AHL-responsive system. It encodes a protein highly similar (76% identity) to an Agrobacterium tumefaciens N-AHL-lactonase40.

Two other highly represented classes of regulators are phage gene repressors (37) and Ner-like regulators (15), which is consistent with the large number of prophages or prophage remnants present in the genome. Bacteriophages may have affected bacterial-host interactions. It has been shown that overexpression of a Ner-like regulator switches the primary bacterial variant, which supports nematode growth, to the secondary variant, which does not41. Nineteen two-component regulators and 20 LysR–type regulators were identified. A LysR-type regulator, also called HexA or LrhA, was reported to control symbiosis negatively and pathogenicity positively, suggesting that it is involved in the transition from symbiosis to pathogenicity42. However, the relatively low number of two-component regulators identified in the P. luminescens genome (compared to the 89 systems of P. aeruginosa) might be related to the quite stable environment encountered by P. luminescens, obviating the need for metabolic adaptation to a wide range of conditions.

Genome comparison

The P. luminescens life cycle and a number of its phenotypic traits resemble those of Y. pestis. Both transit and colonize insects and both are pathogenic bacteria. However, P. luminescens has been used for biological control of insects without causing any harm to humans. Several common phenotypic characteristics are reflected in the genome. We identified 2,107 genes in P. luminescens that have an ortholog in Y. pestis. In addition, 77% (1,621 out of 2,107) of the orthologous genes of TT01 and Y. pestis CO92 (ref. 43) are syntenic. Interestingly, Y. pestis and P. luminescens share not only the chromosomal backbone of Enterobacteriaceae, which both share also with E. coli, but also many putative mobile regions encoding toxins, virulence factors and proteins of unknown function (Supplementary Fig. 5 online). Orthologs of genes present on the Y. pestis plasmids (pCD1 and pMT1) were also identified in the genome of P. luminescens.

The impressive number of mobile genetic elements or their remnants suggest that the TT01 genome is subject to continuously ongoing gene transfer (Supplementary Table 6 online). We identified phage remnants representing 4% of the genome, 195 ISs or IS fragments, putative transposons, and 711 inverted repeats of the enterobacterial repetitive intergenic consensus (ERIC) sequences44, in contrast to only 21 ERIC sequences present in the E. coli K12 chromosome. In addition, several gene classes are over-represented (Supplementary Table 3 online), suggesting frequent rearrangements (duplication, recombination) and a high degree of genome plasticity. This redundancy may contribute not only to the impressive arsenal of toxins but also to the generation of variability, which is an advantage for a pathogen subject to strong selective constraints. P. luminescens kills a wide variety of insects and thus has to circumvent a multitude of host defenses.



The availability and the functional analysis of the genome sequence of P. luminescens TT01 should lead to several useful applications, such as the development of new entomotoxins for crop protection and the genetic engineering of the bacterium-nematode pair for use as biological control agents. The identification of new antibiotic biosynthetic genes, which could be manipulated to generate new biological activities by domain shuffling, provides a promising resource for fighting microbial infections in the future. Furthermore, the availability of the first genome sequence of a symbiotic as well as entomopathogenic bacterium is an important advance in helping to decipher the relation between pathogenesis and symbiosis.



Cloning, sequencing, assembly and annotation.

Genome sequencing was performed using the whole-genome shotgun strategy45, as described previously46, 47. Two libraries (1–2 kb and 2–3 kb inserts) were generated by random mechanical shearing of genomic DNA and cloning into pcDNA-2.1 (Invitrogen) and a medium-size insert library (5–10 kb) was generated in the low copy number vector pSYX3448. The BAC library was constructed as previously described49. Assembly and annotation are detailed in Supplementary Methods online.

BAC1A02 encompassing the JHE-like toxin locus plu4093–plu4092 extends from position 4,729,455 to position 4,789,585 of the P. luminescens genome; BAC8C11 encompassing the JHE-like toxins locus plu4437–plu4436 extends from position 5,179,747 to position 5,205,606.

To construct the pDIA700 plasmid, a DNA fragment containing the two genes plu4093 and plu4092, was generated by PCR with primers JHE2 (5′-AACTGCAGCATTGAAGCAGAGCGTTGACAT-3′) and JHE3 (5′-CGGGATCCGACGTCGGCAAGTGCATCAAAT-3′). The amplified DNA fragment of 2,060 bp was purified and cloned into the pBluescript SK vector (Stratagene) at the EcoRV site.

To inactivate plu4092, the pDIA700 was digested with EcoRI, leading to a deletion of the DNA region located between an EcoRI site located at the 270th codon of plu4092 and the pBluescript EcoRI site, and self-ligated to yield pDIA701, which contains a 3′ truncated plu4092 gene.

Insecticidal assays.

P. xylostella leaf bioassay. The recombinant E. coli XL1-Blue strain containing pDIA700 or pDIA701 and E. coli DH10B containing BAC1A02 or BAC8C11 were grown for 20 h at 28 °C in 50 ml of LB broth supplemented with 100 μg/ml ampicillin or 12.5 μg/ml chloramphenicol, respectively. For each clone, six cabbage leaves (3 cm diameter) were incubated in undiluted bacterial cultures for 1 h with 0.05% Tween 20 (Sigma). Treated leaves were put onto 6-well plates with agar beds containing 15 g/l of agar (Difco) and 30 mg/l of the fungicide nipagine (Sigma). Five second-instar larvae were placed into each well. All the assays were done at 28 °C with a photoperiod of 11 h:13 h (night/day). After 2 d the treated leaves were replaced by untreated leaves. The larval mortality was recorded at day 2 and day 3.

Recombinant E. coli strains containing the pBluescript SK vector without insert and P. luminescens TT01 cultures were used as negative and positive controls, respectively. The percentage of larval mortality was corrected with respect to the negative control by using the Abbott equation50. The toxicity of each clone was tested on 30 larvae, and each experiment was done in triplicate.

Mosquitocidal activity. Derivatives of E. coli TG1 containing plasmids pDIA700 and pDIA701, or E. coli DH10B containing BAC1A02 or BAC8C11, were grown at 30 °C in 50 ml LB broth supplemented with 100 μg/ml ampicillin or 12.5 μg/ml chloramphenicol, respectively, until the optical density at 600 nm (OD600) reached a value of 2, then harvested by centrifugation and resuspended at the same optical density. Ten second-instar C. pipiens larvae were placed in Petri dishes (2.5 cm diameter) containing 5 ml bacterial suspensions at OD600 = 2 (or water as a control). Yeast cells were given as a food source in all dishes (to avoid mortality in the control), and larval mortality was recorded at days 1 and 2. Two independent experiments were conducted at 24 ± 2 °C, each one in duplicate. The same procedure was used for toxicity assays involving Aedes aegypti and Anopheles gambiae.


The genome sequence has been submitted to EMBL under the accession number BX470251. The complete data set of DNA and protein sequences, linked to the relevant annotations and functional assignments, is available online at

Note: Supplementary information is available on the Nature Biotechnology website.



This work received financial support from the Institut Pasteur, the Centre National de la Recherche Scientifique, the Institut National de la Recherche Agronomique and the Ministère de l'Industrie et des Finances (Après séquençage des Génomes). We wish to thank Tatiana Vallaeys and Evelyne Krin for helpful discussions, Ivan Moszer and Eduardo Rocha for help with bioinformatics, Elisabeth Couvé, Christina Nielsen-Le Roux and Hafed Nedjari for expert technical assistance and Tim Stinear for critical reading of the manuscript.

Competing interests statement

The authors declare no competing financial interests.

Received 7 May 2003; Accepted 18 August 2003; Published online 5 October 2003.



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  1. Laboratoire de Génomique des Microorganismes Pathogènes, Institut Pasteur, 28 rue du Dr. Roux, 75724 Paris Cedex 15, France.
  2. Génopole, Plate-Forme Intégration et Analyse Génomiques, Institut Pasteur, 28 rue du Dr. Roux, 75724 Paris Cedex 15, France.
  3. Unité de Génétique des Génomes Bactériens, Institut Pasteur, 28 rue du Dr. Roux, 75724 Paris Cedex 15, France.
  4. Unité de Programmation Moléculaire et Toxicologie Génétique, Institut Pasteur, 28 rue du Dr. Roux, 75724 Paris Cedex 15, France.
  5. Laboratoire EMIP, Université Montpellier II, IFR122, Institut National de la Recherche Agronomique (UMR 1133), 34095 Montpellier Cedex 5, France.
  6. Atelier de Génomique Comparative, Génoscope/CNRS-UMR 8030, 2, rue Gaston Crémieux, 91006 Evry Cedex 15, France.
  7. Laboratoire de Microbiologie et de Génétique Moléculaire, CNRS, 118 Route de Narbonne, 31062 Toulouse Cedex, France.
  8. Bayer CropScience, 1 rue Pierre Fontaine, 91058 Evry, France.
  9. Bayer CropScience, 2 T.W. Alexander Drive, Research Triangle Park, North Carolina 27709, USA.

Correspondence to: Frank Kunst1 e-mail:


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