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PLoS Pathog. Oct 2009; 5(10): e1000507.
Published online Oct 30, 2009. doi:  10.1371/journal.ppat.1000507
PMCID: PMC2763215

Systematic Genetic Nomenclature for Type VII Secretion Systems

Glenn F. Rall, Editor

Mycobacteria, such as the etiological agent of human tuberculosis, Mycobacterium tuberculosis, are protected by an impermeable cell envelope composed of an inner cytoplasmic membrane, a peptidoglycan layer, an arabinogalactan layer, and an outer membrane. This second membrane consists of covalently linked, tightly packed long-chain mycolic acids [1],[2] and non-covalently bound shorter lipids involved in pathogenicity [3][5]. To ensure protein transport across this complex cell envelope, mycobacteria use various secretion pathways, such as the SecA1-mediated general secretory pathway [6],[7], an alternative SecA2-operated pathway [8], a twin-arginine translocation system [9],[10], and a specialized secretion pathway variously named ESAT-6-, SNM-, ESX-, or type VII secretion [11][16]. The latter pathway, hereafter referred to as type VII secretion (T7S), has recently become a large and competitive research topic that is closely linked to studies of host–pathogen interactions of M. tuberculosis [17] and other pathogenic mycobacteria [16]. Molecular details are just beginning to be revealed [18][22] showing that T7S systems are complex machineries with multiple components and multiple substrates. Despite their biological importance, there has been a lack of a clear naming policy for the components and substrates of these systems. As there are multiple paralogous T7S systems within the Mycobacteria and orthologous systems in related bacteria, we are concerned that, without a unified nomenclature system, a multitude of redundant and obscure gene names will be used that will inevitably lead to confusion and hinder future progress. In this opinion piece we will therefore propose and introduce a systematic nomenclature with guidelines for name selection of new components that will greatly facilitate communication and understanding in this rapidly developing field of research.

The first T7S-associated protein to be identified was the 6-kD early secreted antigenic target ESAT-6 [23]. This small, highly immunogenic protein lacks a classical N-terminal signal sequence and is present in large amounts in the culture filtrate of M. tuberculosis [23], but is missing from the closely related attenuated live vaccine Mycobacterium bovis bacille Calmette-Guérin (BCG) [24] due to the deletion of region of difference 1 (RD1) [25]. ESAT-6 and its protein partner, the 10-kD culture filtrate protein CFP-10 [26], form a 1[ratio]1 protein complex [27] that involves hydrophobic interaction [18],[28]. Secretion of ESAT-6 and CFP-10 is required for the pathogenicity of M. tuberculosis [29][31]. The absence of ESAT-6 secretion is responsible in part for the attenuation of the BCG and Mycobacterium microti vaccines [13],[32],[33], as well as for the decrease in virulence of the attenuated M. tuberculosis H37Ra strain [34].

In M. tuberculosis, ESAT-6 and CFP-10 belong to the WXG100 family of 23 small secreted proteins that share a size of approximately 100 amino acids, a helical structure, and a characteristic hairpin bend formed by the conserved Trp-Xaa-Gly (W-X-G) motif [35]. The genes encoding these proteins, many of which represent immunodominant T cell antigens [36], are called esx genes in M. tuberculosis (esxA-W, Table 1) and are arranged in tandem pairs at 11 genomic loci [37]. In five of these genomic loci (ESX-1–ESX-5), the esx genes are flanked by genes coding for components of secretion machineries involved in the export of the corresponding ESX proteins (Figure 1). These proteins constitute the major building blocks of the T7S systems [11],[12],[15],[16],[19]. Four of these regions are also characterized by the presence of genes encoding PE and/or PPE proteins (Figure 1, Table 2), named after their characteristic N-terminal motifs proline-glutamic acid (PE) and proline-proline-glutamic acid (PPE) [38]. Apart from genes localized in these core ESX regions, additional genes situated elsewhere on the chromosome may be required for the function of T7S systems. For example, the rv3616c-rv3614c genes are required for secretion of ESAT-6 and CFP-10 by ESX-1 [39][41].

Figure 1
Genetic organization of the 5 ESX loci and the espA operon in M. tuberculosis H37Rv with the proposed nomenclature and predicted cellular localization of the conserved ESX gene products and their interactions.
Table 1
Overview of esx Genes (WXG100 Family) of M. tuberculosis H37Rv, Also Showing Previously Used Gene Names in Brackets.
Table 2
New and Old Nomenclature of the Different Esx Conserved Components (ecc Genes) and Genes Encoding ESX-1 Secretion-Associated Proteins (esp Genes) of the T7S Systems of M. tuberculosis H37Rv.

Apart from members of the M. tuberculosis complex, the ESX-1 cluster is also present in a range of mycobacteria, including Mycobacterium kansasii [23] and Mycobacterium leprae [42]. However, experimental work has mainly focused on the ESX-1 system of Mycobacterium marinum [21], [22], [43][47], a fish pathogen that shows high homology in its ESX loci with M. tuberculosis [48], and the fast grower Mycobacterium smegmatis [49][51]. M. marinum has also been used to define a role for the paralogous system ESX-5, which is required for the secretion of PE and PPE proteins [16],[52],[53]. For the remaining ESX-2, ESX-3, and ESX-4 systems, only very limited predictions of their putative functions can be made. ESX-3 transcriptome data suggest that this system is involved in iron/zinc homeostasis [54],[55], which would be consistent with the essential role of ESX-3 in M. tuberculosis [56]. The putative functions of ESX-2 and ESX-4 remain unknown. ESX-4, which harbors a smaller number of genes than other ESX loci (Table 2), appears to represent the most ancestral T7S system in mycobacteria [12]. This hypothesis is based on the observation that ESX-4-like loci are the only ESX clusters that are found in other high GC Gram-positive bacteria, suggesting that the last common ancestor of mycobacteria already harbored an ESX-4 T7S system. Other ESX clusters may have evolved later by gene duplication and gene diversification events. However, the finding that Nocardia farcinica (http://nocardia.nih.go.jp/) contains two T7S systems, one orthologous to ESX-4 and one locus that shows some similarity to all the conserved components of larger T7S systems, suggests that evolution of T7S systems is more complex than previously anticipated. This second T7S locus in N. farcinica even contains two PPE-like genes that were originally thought to be specific for the mycobacteria [38].

T7S-like systems are also found outside the high GC Gram-positive bacteria, since a number of Firmicutes have WXG100 members [35]. However, the loci containing these WXG100 genes are only weakly similar to the mycobacterial T7S systems: in fact, only the gene encoding the FtsK/SpoIIIE-like protein is present. Therefore, these systems should be called WXG100 systems to differentiate them from true T7S systems. Both Staphylococcus aureus and Bacillus anthracis have an active WXG100 system, and the WXG100 system encoded by S. aureus is important for virulence [57],[58].

Research in the T7S/ESX field is relatively new, but is now rapidly expanding and we therefore would like to propose a systematic nomenclature for all components involved. Until now a small number of genes within the different ESX loci of mycobacteria have been named, but for most genes the original genome annotation numbers are used. These gene numbers vary between different species and even between different strains of the same species, and therefore make comparative studies confusing. Our nomenclature is appropriate for all T7S systems in high GC-Gram-positive species. Extending this nomenclature to the T7S-like systems of Firmicutes is not recommended, since there are only a very few conserved components.

As a starting point for the new nomenclature, we focus on the most studied system, the ESX-1 system of M. tuberculosis, which is the paradigm T7S system. The new nomenclature is given for ESX-1 in M. tuberculosis (Figure 1 and Table 2) and for all ESX systems in various Mycobacteria (Table S1). The proposed rules for the nomenclature are as follows:

  • Only genes that have homologues in at least four of the mycobacterial ESX systems will get a general name, whereas the locus-specific genes have a more restricted name reflecting their specificity. The reason for this distinction is that the conserved genes are most likely to represent the core components of the secretion system. Moreover, all of the conserved ESX-1 components have been shown to be essential for ESAT-6/CFP-10 secretion in at least one of the mycobacterial species studied (See below). In contrast, many of the locus-specific genes encode secreted proteins, as has been shown for the ESX-1 system (see below). Furthermore, in M. leprae, an organism with an extreme reductive evolution of its genome, almost all of the non-conserved ESX-1 components are pseudogenes, whereas all of the conserved components seem to be intact [42].
  • The three letter acronym for the conserved components will be ecc, for esx conserved component (Figure 1, Table 2). This abbreviation has not been used for other genes in bacteria.
  • The ESAT-6 and CFP-10 encoding genes, esxA and esxB, respectively, and the other esx genes (Table 1) will not be renamed. These gene names are informative, well-accepted, and frequently used in the literature. Furthermore, the esx gene products seem to be secreted proteins and do not seem to be components of the secretion system itself, although their presence is required for the secretion of other substrates. The same reasoning is used for the pe and ppe genes. Four of the five systems harbor pe and ppe genes, but for the moment their functions within the T7S systems remain uncertain. Furthermore, various mycobacterial species contain a large number of genes belonging to the pe and ppe families, and it would be confusing to rename some of them. Finally, the subtilisin-like proteases already have an established and descriptive name in literature, i.e., the mycosins [59]. Therefore, we will not change this name.
  • The alphabetic suffix of conserved genes will be based on the gene order in the paradigm ESX-1 system (see Figure 1). This decision is mainly based on the fact that the ESX-1 system is the most studied. The gene order of the different T7S systems is highly variable and it is therefore difficult to propose a logical ordering that would be satisfactory for all systems. The genes of ESX-2/-3/-4 and -5 will therefore be named according to their paralogue in ESX-1 (Table 2 and Table S1), allowing for a direct and relevant comparison. The gene names of each mycobacterial T7S will include a numeral suffix indicating the ESX cluster to which this gene belongs. In order to avoid confusion with numbering of alleles, the ESX cluster number is indicated in subscript. As shown in Figure 1, the first conserved gene of the ESX-1 cluster will be eccA1.
  • In some of the T7S clusters, the gene encoding the FtsK/SpoIIIE-like protein is split in two genes. Since these gene products clearly form a functional unit, as has also been shown for the two FtsK/SpoIIIE-like proteins of the ESX-1 system [14], the split genes will get a lower case alphabetic suffix, i.e., eccCa1 and eccCb1 for the ESX-1 system of M. tuberculosis (Figure 1 and Table 2).
  • When working with several different organisms, it can also be useful to indicate the origin of the respective genes. For this we recommend using a two-letter subscript at the end of the gene name. For example, the orthologues of the M. tuberculosis genes eccCa1mt and eccCb1mt would be eccCa1ms and eccCb1ms in M. smegmatis.
  • The gene names can be converted into their proteins by capitalization, e.g., EccCa1. Alternatively, once the true function of a protein is known, the name could be changed to indicate this function, as has been done for the secretins of type II and type III secretion systems. If in the future new genes are identified that are essential for the functioning of several T7S systems, these genes could be named similarly using the next alphabetical suffix (eccG, eccH, etc.).
  • As discussed above, in addition to the conserved genes, there are also region-specific genes. The role of these genes in ESAT-6/CFP-10 secretion is not entirely clear: some of the encoded proteins seem to be involved in the secretion of T7S substrates in M. marinum, whereas their orthologues show less or no effect on secretion in M. tuberculosis. Recently, it has been shown that a subset of these proteins are in fact also substrates of the ESX-1 system. Thus far, four ESX-1 substrates have been identified in addition to ESAT-6 and CFP-10. These substrates are called EspA [39], EspB [46], EspR [41], and the M. marinum homologue of Rv3864 [22]. The acronym Esp stands for ESX-1 secretion-associated protein. Both rv3864 and espB are located within the ESX-1 cluster, whereas EspA and the secreted regulatory protein EspR are encoded by genes outside the ESX-1 locus. However, the espA gene is part of an operon (rv3616-3614) that has paralogues in the 5′ region of the ESX-1 locus. Therefore, we propose naming all the region-specific genes of the ESX-1 system and the rest of the espA operon esp genes with alphabetical suffixes (see Table 2 and Figure 1). We will follow the espA operon and ESX-1 gene order, with the exception of espB and espR, which are already named. This means that the first gene in the esx-1 operon, whose gene product was recently shown to be secreted protein in M. marinum, will be named espE. One of the new esp genes, espG, is present with low but significant homology in two other ESX systems (ESX-2 and ESX-3) and should therefore also have a numeral suffix (Figure 1, Table 2).
  • The nomenclature of esp genes in M. marinum is more complicated, in particular for espA. The genome of M. marinum contains a large gene cluster upstream of the ESX-1 locus, among which are 15 espA-like genes [48]. In addition, there are three more paralogues at other locations in the genome. These genes should all be named espA with a superscript numeral suffix to indicate the exact gene and a subscript “mm” to indicate the species.
  • Region-specific genes or genes encoding secreted proteins of the other ESX loci and T7S systems should not be called esp, as this name should be reserved for ESX-1 related genes. If there are important region-specific genes for ESX-2/-3/-4 or -5, a new name has to be introduced.

In order to ensure wide visibility for this new nomenclature it will be included in the most extensively used mycobacterial genome databases. As a first step, selected genome browsers available at the Institut Pasteur (http://genolist.pasteur.fr/) and/or the Ecole Polytechnique Federale de Lausanne (http://tuberculist.epfl.ch/) will adopt these new rules; other databases could follow this example.

In conclusion, we would like to emphasize that the introduction of a uniform gene nomenclature for other secretion systems in Gram-negative bacteria (type II, type III) has facilitated comparative analysis of these systems. We anticipate that the acceptance/implementation of this proposal will provide similar advantages for the T7S systems.

Supporting Information

Table S1

New and old nomenclature of the different conserved components of the T7S systems in selected mycobacteria (M. tuberculosis H37Rv, M. marinum M, M. smegmatis mc2155, M. leprae TN, M. avium paratuberculosis K10). The numeral suffices to indicate the ESX clusters to which the genes belong are omitted. Note that the ESX-2 genes of M. avium paratuberculosis are located in two separate genomic loci. TM, transmembrane domain.

(0.09 MB DOC)

Table S2

Comparison of the transmembrane topologies and signal sequence predictions of the M. tuberculosis H37Rv Ecc membrane proteins. Amongst the different topology prediction programs that were used (TMHMM Server v. 2.0, MEMSAT3, Philius, SCAMPI, HMMTOP and Phobius) MEMSAT3 gave the correct prediction for the highest number of Ecc membrane proteins. Therefore, only the topology prediction results of TMHMM (used on the TubercuList server) and MEMSAT3 are shown. The clearly incorrect predictions are depicted in gray. TM, transmembrane domain; in, cytoplasmic location; out, periplasmic location; C, C-terminus; N, N-terminus; ss, signal sequence.

(0.07 MB DOC)

Acknowledgments

We are grateful to our many collaborators and colleagues, who have contributed to the rapid progress in this field.

Footnotes

The authors have declared that no competing interests exist.

This work has received funding from the European Community's Seventh Framework Programme ([FP7/2007–2013]) under grant agreement n°201762. In addition, the authors acknowledge their individual external funding for T7S/ESX related research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

1. Hoffmann C, Leis A, Niederweis M, Plitzko JM, Engelhardt H. Disclosure of the mycobacterial outer membrane: cryo-electron tomography and vitreous sections reveal the lipid bilayer structure. Proc Natl Acad Sci U S A. 2008;105:3963–3967. [PMC free article] [PubMed]
2. Zuber B, Chami M, Houssin C, Dubochet J, Griffiths G, et al. Direct visualization of the outer membrane of mycobacteria and corynebacteria in their native state. J Bacteriol. 2008;190:5672–5680. [PMC free article] [PubMed]
3. Camacho LR, Ensergueix D, Perez E, Gicquel B, Guilhot C. Identification of a virulence gene cluster of Mycobacterium tuberculosis by signature-tagged transposon mutagenesis. Mol Microbiol. 1999;34:257–267. [PubMed]
4. Cox JS, Chen B, McNeil M, Jacobs WR., Jr Complex lipid determines tissue-specific replication of Mycobacterium tuberculosis in mice. Nature. 1999;402:79–83. [PubMed]
5. Trivedi OA, Arora P, Vats A, Ansari MZ, Tickoo R, et al. Dissecting the mechanism and assembly of a complex virulence mycobacterial lipid. Mol Cell. 2005;17:631–643. [PubMed]
6. Pugsley AP. The complete general secretory pathway in gram-negative bacteria. Microbiol Rev. 1993;57:50–108. [PMC free article] [PubMed]
7. Wiker HG, Harboe M. The antigen 85 complex: a major secretion product of Mycobacterium tuberculosis. Microbiol Rev. 1992;56:648–661. [PMC free article] [PubMed]
8. Braunstein M, Espinosa BJ, Chan J, Belisle JT, Jacobs WR., Jr SecA2 functions in the secretion of superoxide dismutase A and in the virulence of Mycobacterium tuberculosis. Mol Microbiol. 2003;48:453–464. [PubMed]
9. McDonough JA, McCann JR, Tekippe EM, Silverman JS, Rigel NW, Braunstein M. Identification of functional Tat signal sequences in Mycobacterium tuberculosis proteins. J Bacteriol. 2008;190:6428–6438. [PMC free article] [PubMed]
10. Saint-Joanis B, Demangel C, Jackson M, Brodin P, Marsollier L, et al. Inactivation of Rv2525c, a substrate of the twin arginine translocation (Tat) system of Mycobacterium tuberculosis, increases beta-lactam susceptibility and virulence. J Bacteriol. 2006;188:6669–6679. [PMC free article] [PubMed]
11. Tekaia F, Gordon SV, Garnier T, Brosch R, Barrell BG, et al. Analysis of the proteome of Mycobacterium tuberculosis in silico. Tuber Lung Dis. 1999;79:329–342. [PubMed]
12. Gey Van Pittius NC, Gamieldien J, Hide W, Brown GD, Siezen RJ, et al. The ESAT-6 gene cluster of Mycobacterium tuberculosis and other high G+C Gram-positive bacteria. Genome Biol. 2001;2:RESEARCH0044. [PMC free article] [PubMed]
13. Pym AS, Brodin P, Majlessi L, Brosch R, Demangel C, et al. Recombinant BCG exporting ESAT-6 confers enhanced protection against tuberculosis. Nat Med. 2003;9:533–539. [PubMed]
14. Stanley SA, Raghavan S, Hwang WW, Cox JS. Acute infection and macrophage subversion by Mycobacterium tuberculosis require a specialized secretion system. Proc Natl Acad Sci U S A. 2003;100:13001–13006. [PMC free article] [PubMed]
15. Brodin P, Rosenkrands I, Andersen P, Cole ST, Brosch R. ESAT-6 proteins: protective antigens and virulence factors? Trends Microbiol. 2004;12:500–508. [PubMed]
16. Abdallah A, Gey van Pittius N, Champion P, Cox J, Luirink J, et al. Type VII secretion–mycobacteria show the way. Nat Rev Microbiol. 2007;5:883–891. [PubMed]
17. Simeone R, Bottai D, Brosch R. ESX/type VII secretion systems and their role in host-pathogen interaction. Curr Opin Microbiol. 2009;12:4–10. [PubMed]
18. Brodin P, de Jonge MI, Majlessi L, Leclerc C, Nilges M, et al. Functional analysis of early secreted antigenic target-6, the dominant T-cell antigen of Mycobacterium tuberculosis, reveals key residues involved in secretion, complex formation, virulence, and immunogenicity. J Biol Chem. 2005;280:33953–33959. [PubMed]
19. Champion PA, Stanley SA, Champion MM, Brown EJ, Cox JS. C-terminal signal sequence promotes virulence factor secretion in Mycobacterium tuberculosis. Science. 2006;313:1632–1636. [PubMed]
20. de Jonge MI, Pehau-Arnaudet G, Fretz MM, Romain F, Bottai D, et al. ESAT-6 from Mycobacterium tuberculosis dissociates from its putative chaperone CFP-10 under acidic conditions and exhibits membrane-lysing activity. J Bacteriol. 2007;189:6028–6034. [PMC free article] [PubMed]
21. Smith J, Manoranjan J, Pan M, Bohsali A, Xu J, et al. Evidence for pore formation in host cell membranes by ESX-1-secreted ESAT-6 and its role in Mycobacterium marinum escape from the vacuole. Infect Immun. 2008;76:5478–5487. [PMC free article] [PubMed]
22. Carlsson F, Joshi SA, Rangell L, Brown EJ. Polar localization of virulence-related Esx-1 secretion in mycobacteria. PLoS Pathog. 2009;5:e1000285. doi: 10.1371/journal.ppat.1000285. [PMC free article] [PubMed]
23. Sorensen AL, Nagai S, Houen G, Andersen P, Andersen AB. Purification and characterization of a low-molecular-mass T-cell antigen secreted by Mycobacterium tuberculosis. Infect Immun. 1995;63:1710–1717. [PMC free article] [PubMed]
24. Harboe M, Oettinger T, Wiker HG, Rosenkrands I, Andersen P. Evidence for occurrence of the ESAT-6 protein in Mycobacterium tuberculosis and virulent Mycobacterium bovis and for its absence in Mycobacterium bovis BCG. Infect Immun. 1996;64:16–22. [PMC free article] [PubMed]
25. Mahairas GG, Sabo PJ, Hickey MJ, Singh DC, Stover CK. Molecular analysis of genetic differences between Mycobacterium bovis BCG and virulent M. bovis. J Bacteriol. 1996;178:1274–1282. [PMC free article] [PubMed]
26. Berthet FX, Rasmussen PB, Rosenkrands I, Andersen P, Gicquel B. A Mycobacterium tuberculosis operon encoding ESAT-6 and a novel low-molecular-mass culture filtrate protein (CFP-10). Microbiology. 1998;144:3195–3203. [PubMed]
27. Renshaw PS, Panagiotidou P, Whelan A, Gordon SV, Hewinson RG, et al. Conclusive evidence that the major T-cell antigens of the Mycobacterium tuberculosis complex ESAT-6 and CFP-10 form a tight, 1[ratio]1 complex and characterization of the structural properties of ESAT-6, CFP-10, and the ESAT-6*CFP-10 complex. Implications for pathogenesis and virulence. J Biol Chem. 2002;277:21598–21603. [PubMed]
28. Renshaw PS, Lightbody KL, Veverka V, Muskett FW, Kelly G, et al. Structure and function of the complex formed by the tuberculosis virulence factors CFP-10 and ESAT-6. Embo J. 2005;24:2491–2498. [PMC free article] [PubMed]
29. Lewis KN, Liao R, Guinn KM, Hickey MJ, Smith S, et al. Deletion of RD1 from Mycobacterium tuberculosis mimics bacille Calmette-Guerin attenuation. J Infect Dis. 2003;187:117–123. [PMC free article] [PubMed]
30. Hsu T, Hingley-Wilson SM, Chen B, Chen M, Dai AZ, et al. The primary mechanism of attenuation of bacillus Calmette-Guerin is a loss of secreted lytic function required for invasion of lung interstitial tissue. Proc Natl Acad Sci U S A. 2003;100:12420–12425. [PMC free article] [PubMed]
31. Guinn KI, Hickey MJ, Mathur SK, Zakel KL, Grotzke JE, et al. Individual RD1-region genes are required for export of ESAT-6/CFP-10 and for virulence of Mycobacterium tuberculosis. Mol Microbiol. 2004;51:359–370. [PMC free article] [PubMed]
32. Pym AS, Brodin P, Brosch R, Huerre M, Cole ST. Loss of RD1 contributed to the attenuation of the live tuberculosis vaccines Mycobacterium bovis BCG and Mycobacterium microti. Mol Microbiol. 2002;46:709–717. [PubMed]
33. Brodin P, Majlessi L, Marsollier L, de Jonge MI, Bottai D, et al. Dissection of ESAT-6 system 1 of Mycobacterium tuberculosis and impact on immunogenicity and virulence. Infect Immun. 2006;74:88–98. [PMC free article] [PubMed]
34. Frigui W, Bottai D, Majlessi L, Monot M, Josselin E, et al. Control of M. tuberculosis ESAT-6 secretion and specific T cell recognition by PhoP. PLoS Pathog. 2008;4:e33. doi: 10.1371/journal.ppat.0040033. [PMC free article] [PubMed]
35. Pallen MJ. The ESAT-6/WXG100 superfamily – and a new Gram-positive secretion system? Trends Microbiol. 2002;10:209–212. [PubMed]
36. Skjot RL, Oettinger T, Rosenkrands I, Ravn P, Brock I, et al. Comparative evaluation of low-molecular-mass proteins from Mycobacterium tuberculosis identifies members of the ESAT-6 family as immunodominant T-cell antigens. Infect Immun. 2000;68:214–220. [PMC free article] [PubMed]
37. Cole ST, Brosch R, Parkhill J, Garnier T, Churcher C, et al. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature. 1998;393:537–544. [PubMed]
38. Gey van Pittius NC, Sampson SL, Lee H, Kim Y, van Helden PD, et al. Evolution and expansion of the Mycobacterium tuberculosis PE and PPE multigene families and their association with the duplication of the ESAT-6 (esx) gene cluster regions. BMC Evol Biol. 2006;6:95. [PMC free article] [PubMed]
39. Fortune SM, Jaeger A, Sarracino DA, Chase MR, Sassetti CM, et al. Mutually dependent secretion of proteins required for mycobacterial virulence. Proc Natl Acad Sci U S A. 2005;102:10676–10681. [PMC free article] [PubMed]
40. MacGurn JA, Raghavan S, Stanley SA, Cox JS. A non-RD1 gene cluster is required for Snm secretion in Mycobacterium tuberculosis. Mol Microbiol. 2005;57:1653–1663. [PubMed]
41. Raghavan S, Manzanillo P, Chan K, Dovey C, Cox J. Secreted transcription factor controls Mycobacterium tuberculosis virulence. Nature. 2008;454:717–721. [PMC free article] [PubMed]
42. Cole ST, Eiglmeier K, Parkhill J, James KD, Thomson NR, et al. Massive gene decay in the leprosy bacillus. Nature. 2001;409:1007–1011. [PubMed]
43. Gao LY, Guo S, McLaughlin B, Morisaki H, Engel JN, et al. A mycobacterial virulence gene cluster extending RD1 is required for cytolysis, bacterial spreading and ESAT-6 secretion. Mol Microbiol. 2004;53:1677–1693. [PubMed]
44. Tan T, Lee WL, Alexander DC, Grinstein S, Liu J. The ESAT-6/CFP-10 secretion system of Mycobacterium marinum modulates phagosome maturation. Cell Microbiol. 2006;8:1417–1429. [PubMed]
45. Xu J, Laine O, Masciocchi M, Manoranjan J, Smith J, et al. A unique Mycobacterium ESX-1 protein co-secretes with CFP-10/ESAT-6 and is necessary for inhibiting phagosome maturation. Mol Microbiol. 2007;66:787–800. [PubMed]
46. McLaughlin B, Chon JS, MacGurn JA, Carlsson F, Cheng TL, et al. A mycobacterium ESX-1-secreted virulence factor with unique requirements for export. PLoS Pathog. 2007;3:e105. doi: 10.1371/journal.ppat.0030105. [PMC free article] [PubMed]
47. Davis JM, Ramakrishnan L. The role of the granuloma in expansion and dissemination of early tuberculous infection. Cell. 2009;136:37–49. [PMC free article] [PubMed]
48. Stinear TP, Seemann T, Harrison PF, Jenkin GA, Davies JK, et al. Insights from the complete genome sequence of Mycobacterium marinum on the evolution of Mycobacterium tuberculosis. Genome Res. 2008;18:729–741. [PMC free article] [PubMed]
49. Flint JL, Kowalski JC, Karnati PK, Derbyshire KM. The RD1 virulence locus of Mycobacterium tuberculosis regulates DNA transfer in Mycobacterium smegmatis. Proc Natl Acad Sci U S A. 2004;101:12598–12603. [PMC free article] [PubMed]
50. Converse SE, Cox JS. A protein secretion pathway critical for Mycobacterium tuberculosis virulence is conserved and functional in Mycobacterium smegmatis. J Bacteriol. 2005;187:1238–1245. [PMC free article] [PubMed]
51. Coros A, Callahan B, Battaglioli E, Derbyshire KM. The specialized secretory apparatus ESX-1 is essential for DNA transfer in Mycobacterium smegmatis. Mol Microbiol. 2008;69:794–808. [PMC free article] [PubMed]
52. Abdallah AM, Verboom T, Hannes F, Safi M, Strong M, et al. A specific secretion system mediates PPE41 transport in pathogenic mycobacteria. Mol Microbiol. 2006;62:667–679. [PubMed]
53. Abdallah AM, Savage ND, van Zon M, Wilson L, Vandenbroucke-Grauls CM, et al. The ESX-5 secretion system of Mycobacterium marinum modulates the macrophage response. J Immunol. 2008;181:7166–7175. [PubMed]
54. Rodriguez GM, Voskuil MI, Gold B, Schoolnik GK, Smith I. ideR, An essential gene in Mycobacterium tuberculosis: role of IdeR in iron-dependent gene expression, iron metabolism, and oxidative stress response. Infect Immun. 2002;70:3371–3381. [PMC free article] [PubMed]
55. Maciag A, Dainese E, Rodriguez GM, Milano A, Provvedi R, et al. Global analysis of the Mycobacterium tuberculosis Zur (FurB) regulon. J Bacteriol. 2007;189:730–740. [PMC free article] [PubMed]
56. Sassetti CM, Boyd DH, Rubin EJ. Genes required for mycobacterial growth defined by high density mutagenesis. Mol Microbiol. 2003;48:77–84. [PubMed]
57. Burts ML, Williams WA, Debord K, Missiakas DM. EsxA and EsxB are secreted by an ESAT-6-like system that is required for the pathogenesis of Staphylococcus aureus infections. Proc Natl Acad Sci U S A. 2005;102:1169–1174. [PMC free article] [PubMed]
58. Garufi G, Butler E, Missiakas D. ESAT-6-like protein secretion in Bacillus anthracis. J Bacteriol. 2008;190:7004–7011. [PMC free article] [PubMed]
59. Brown GD, Dave JA, Gey van Pittius NC, Stevens L, Ehlers MR, et al. The mycosins of Mycobacterium tuberculosis H37Rv: a family of subtilisin-like serine proteases. Gene. 2000;254:147–155. [PubMed]
60. Jones DT. Improving the accuracy of transmembrane protein topology prediction using evolutionary information. Bioinformatics. 2007;23:538–544. [PubMed]

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