Characterisation of porin genes from Mycobacterium fortuitum and their impact on growth
© Sharbati et al. 2009
Received: 01 April 2008
Accepted: 09 February 2009
Published: 09 February 2009
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© Sharbati et al. 2009
Received: 01 April 2008
Accepted: 09 February 2009
Published: 09 February 2009
Highly pathogenic mycobacteria like Mycobacterium tuberculosis are characterised by their slow growth and their ability to reside and multiply in the very hostile phagosomal environment and a correlation between the growth rate of mycobacteria and their pathogenicity has been hypothesised. Here, porin genes from M. fortuitum were cloned and characterised to address their impact on the growth rate of fast-growing and pathogenic mycobacteria.
Two genes encoding porins orthologous to MspA from M. smegmatis, porM1 and porM2, were cloned from M. fortuitum strains, which were originally isolated from human patients. Both porin genes were at least partially able to complement the mutations of a M. smegmatis mutant strain lacking the genes mspA and mspC with respect to the growth rate. PorM1 and porM2 were present in different strains of M. fortuitum including the type strain. Comparative expression analysis of porM genes revealed divergent porin expression among analysed M. fortuitum strains. Repression of the expression of porins by antisense technique decreased the growth rates of different M. fortuitum. The effects of over-expression of porM1 as well as porM2 varied depending on the strain and the concentration of antibiotic added to the medium and indicated that PorM1 and PorM2 enhance the growth of M. fortuitum strains, but also the diffusion of the antibiotic kanamycin into the cells.
This study demonstrates the important role of porin expression in growth as well as antibiotic susceptibility of the opportunistic bacterium M. fortuitum.
Mycobacterium is considered a diverse genus with highly pathogenic members like M. tuberculosis or M. leprae as well as less pathogenic, opportunistic and saprophytic species belonging to the so-called rapidly growing mycobacteria (RGM). The species of RGM able to cause human disease basically belong to the M. fortuitum group, the M. chelonae/abscessus group and the M. smegmatis group. Members of these groups are commonly seen in aquatic environments like municipal tap water, and health care-associated outbreaks are often associated with contact to tap water or water sources such as ice.
The M. fortuitum group includes three taxa: M. fortuitum, M. peregrinum and a third biovariant complex. The M. fortuitum group is involved in 60% of localised cutaneous infections in immunocompetent persons caused by RGM but is a rare cause of pulmonary disease. Most or all of the cases of community-acquired or health care-associated diseases caused by the M. fortuitum group are due to M. fortuitum. This species basically causes skin lesions, wound infections, postinjection abscesses, postsurgical wound infections or pulmonary disease in previously healthy hosts . Little is known about the virulence mechanisms and persistence of this human pathogen. However, Cirillo et al.  and Da Silva et al.  reported that M. fortuitum was capable to replicate in amoebae and murine monocytic cells, respectively.
In a previous study, we showed that the intracellular survival of M. smegmatis depended on the amount of porins in the mycobacterial outer membrane (OM). The mutant strain ML10 of M. smegmatis, which lacks the porins MspA and MspC , exhibited significantly enhanced intracellular survival compared to the parental strain SMR5 . MspA belongs to a novel class of mycobacterial OM proteins present in many RGM but apparently absent in slowly growing mycobacteria . The main porin of M. smegmatis, MspA, is an extremely stable octameric protein composed of 20 kDa monomers  and provides the uptake of hydrophilic nutrients across the extraordinarily restricting mycobacterial OM [7, 8]. By means of DNA hybridisations using a probe derived from the mspA sequence, Niederweis and colleagues  indicated that the genome of M. fortuitum contained orthologous porin genes.
Since the saprophytic bacterium M. smegmatis causes disease only in rare cases  and shows a very limited intracellular persistence , it is important to investigate the role of porins on virulence in pathogenic members of RGM, which are able to multiply intracellularly. M. fortuitum was suggested to be a suitable model Mycobacterium . Like M. tuberculosis, it resides intracellularly in vacuoles restricting interferon-γ-induced nitric oxide production and limits the maturation of phagosomes . Therefore, M. fortuitum was chosen to detect and characterise porins and to analyse their impact first on extracellular growth and in a later stage on intracellular growth. For this purpose, we used two different M. fortuitum strains (10851/03 and 10860/03) that originally were isolated from human patients. Comparative analysis was performed using also the type strain M. fortuitum DSM 46621.
In order to verify the taxonomic classification and to define the phylogenetic relationship between the strains analysed, complete sequences of the 16S rRNA genes were determined using the primers, which were described by Adekambi and Drancourt . The phylogenetic analysis of the 16S rRNA sequences confirmed the taxonomic classification of the M. fortuitum strains employed (data not shown).
Primers and probes used in this study.
Primers or probes
5'-CGG TCT CAG CGA CCG AAC-3'
5'-CCG GCG ATA CAG TTA GGG A-3'
5'-TCT CCA GGG GCT GCT TTT G-3'
5'-CGG GAC GCC AAC CAC ATA AC-3'
5'-CTG AAG CTT CAC CGA GCT GAG CAT CCT CAC-3'
5'-GAC ACT AGT CGT TGG CTA CAG AAC AAC ATT CC-3'
5'-ATG AAG GCA TTC AGT CGG G-3'
5'-TGC TCC TCA AAG GAG AAG CG-3'
5'-CGC TTC TCC TTT GAG GAG CA-3'
5'-TCC AGA CCC GCA TGA GAT ACG-3
5'-ACA AGC TTC AGC AAC GCT GTG AAC GCA-3'
5'-CAG TTA ACA CTA CGG GAC GCT CGT GTC C-3'
5'-CGC AAG CCT CTT CGT CGG C-3'
5'-CCA AGG TGC CCT CGA ACT CAT C-3'
5'-CGG ATC CTA GGG AGA ACA TGA AGG CAT TCA G-3'
5'-CGG ATC CTT GTC CAG ACC CGC ATG AGA T-3'
5'-ACA AGC TTG CTC TCA GCC GGT TTT CA-3'
5'-CAG TTA ACG AAC TGG GCG TTC ATG TGC-3'
5'-GCT GTT TAC GAG CAC GGG C-3'
5'-TTG CGG TCC AGG GGG AAC-3'
5'-CGT GCA GCA GTG GGA CAC CTT-3'
5'-CCA CGA TGT ACT TGG CGC GAC-3'
5'-FAM-TGG ACC GCA ACC GTC TTA CCC GTG AGT G-TAMRA-3'
5'-CGT TCA GCA GTG GGA CAC CTT-3'
5'-CCA CGG TGT ACT TGG CCC GGC-3'
5'-FAM-TGG ACC GCA ACC GGC TGA CCC GTG AGT G-TAMRA-3'
Nucleotide sequence similarity between porM1 and porM2 from members of the M. fortuitum-group and mspA.
Nucleotide similarity index
Accession-no. to the EMBL nucleotide sequence database
M. fortuitum DSM 46621
M. fortuitum 10851/03
M. fortuitum 10860/03
M. fortuitum 10851/03
M. fortuitum 10860/03
Besides the porin gene, two other complete ORFs and part of another ORF were detected. ORF1 was interrupted by one of the SacII sites and showed a high similarity to a molybdopterin biosynthesis protein of M. tuberculosis CDC 1551 (accession no.: AAK 45260). ORF2 turned out to be a mechanosensitive channel orthologous to the gene mscL from M. avium subsp. paratuberculosis str. 10 (accession no.: NP 959854). ORF3 was similar to the hypothetical protein Rv0990c from M. tuberculosis H37Rv (accession no.: NP 215505). The entire cloned genomic region was blasted against the M. tuberculosis genome from the Sanger Institute database http://www.sanger.ac.uk/cgi-bin/blast/submitblast/m_tuberculosis to examine if the whole region is conserved between M. fortuitum and M. tuberculosis. However, only ORF1 and ORF2 possessed nucleotide identities higher than 60% showing that the region is not conserved among these mycobacteria.
Next, the presence of porM1 in other M. fortuitum strains was analysed. For this purpose, the porM1-specific primers komf-3f and komf-4b (Figure 2A and Table 1) were chosen to amplify a fragment of approximately 1250 bp, comprising the porM1 gene and its flanking regions. PCRs using a polymerase-mix with proofreading activity generated a fragment of the expected size in all strains. Several PCRs were performed and both strands of the different fragments were sequenced. PorM1 was detected in all three M. fortuitum strains, and the nucleotide sequences were submitted to the EMBL nucleotide sequence database (Table 2). The nucleic acid subsequences such as the -10 signal of a promoter, the RBS, the signal peptide of 81 bp and the hairpin structure were also present and were conserved among all strains tested (data not shown). As already indicated in Table 2, the nucleotide sequences of the gene porM1 differed among different strains of M. fortuitum.
Since the southern blot experiments had indicated the existence of two genes orthologous to mspA in M. fortuitum, we also attempted to clone and characterise the second porin gene. This porin gene, termed porM2, was amplified by PCR and cloned as a 918 bp fragment into the mycobacterial vectors pMV306 and pMV261, as described in the section Methods. The corresponding recombinant plasmids were named pSRa104 and pSRb103, respectively. Positive clones were confirmed by sequencing. As shown in Figure 2B, the insert of the plasmids contained an ORF of 648 bp, which turned out to be paralogous to the gene porM1. The 648 bp ORF encodes a protein of 215 amino acids with an N-terminal signal sequence of 31 amino acids, which was predicted using the SignalP 3.0 Server at http://www.cbs.dtu.dk/services/SignalP/. The in silico analysis of the mature PorM2 showed a calculated molecular weight of the monomer of 19374 Da and a pI of 4.31, which were very similar to the calculated values of PorM1. A hypothetical -10 promoter sequence and a hypothetical RBS were located upstream of porM2. A hypothetical terminator sequence was, however, not detected (Figure 2B). The similarity between porM1 and porM2 from strains M. fortuitum 10851/03 and 10860/03 on nucleotide level amounted to 94.1% and 95.3%, respectively. The mspA gene revealed to be more similar to porM1 (87.4% to 88.4% similarity) than to porM2 (86.5% similarity). Sequence comparison revealed that porM2 encodes a protein mainly differing from porM1 within the signal sequence. PorM2 from M. fortuitum 10851/03 and 10860/03 exhibits an insertion of four amino acids and additional six amino acid exchanges within the signal peptide compared to PorM1 (Figure 4). Only one amino acid is replaced in the mature polypeptide [proline165 (PorM1) with alanine169 (PorM2)]. We sequenced a 1697 bp region comprising porM2, 500 bp of its upstream region as well as 549 bp downstream of porM2. The DNA sequences flanking the porM1 and porM2 genes revealed no similarity with exception of the 13 bp preceding the porM-coding sequences, which were identical in both regions. The 5' terminus of an ORF orthologous to a glycosyl transferase gene from M. tuberculosis CDC1551 (accession no.: AAK 48256) was detected upstream from porM2. An ORF orthologous to the gene for a pyridoxamine 5'-phosphate oxidase-related protein from M. vanbaalenii (accession no.: ZO 01208463) was present in the downstream region of porM2 (Figure 2B).
Using the primer pairs porM2-fw-hind and porM2-bw-hpa or porM2-rna-fw and porM2-rna-bw (Table 1), porM2 was also detected in other strains analysed. No product was obtained using the plasmid pSSp107 carrying porM1 as template, demonstrating the specificity of this PCR approach for porM2.
Comparative expression analysis was also performed by means of quantitative reverse transcription polymerase chain reaction (qRT-PCR) using sequence-specific primers and probes (Table 1). The values were compared to porin expression in M. smegmatis. Because of the high degree of sequence conservation of the two paralogs porM1 and porM2, a qRT-PCR approach was established using primers and a dually labelled probe that hybridised to a region where both genes are identical (porM1 amplicon: nucleotide 132–232 and porM2 amplicon nucleotide 144–244, see also Table 1). This PCR approach enabled the quantification of the overall expression of the paralogs. As was already proven by the ELISA results, the highest porin mRNA expression was measured in M. smegmatis. It showed transcription rates about twice as high as the highest level among the M. fortuitum strains, which was detected in the type strain M. fortuitum DSM 46621. M. fortuitum 10851/03 exhibited the lowest transcription rate among all M. fortuitum strains (Figure 5C). The quantification of porM mRNA as well as the protein isolated from the various strains demonstrated consistence of transcriptional and translational levels and underlined the differential porin expression among the analysed M. fortuitum strains.
MspA was shown to be accessible on the cell surface of M. smegmatis by using pAK MspA#813 . Since the expression analysis showed a differing amount of porin in M. fortuitum strains, M. fortuitum DSM 46621 and M. fortuitum 10860/03 (the strains with the highest porin expressions) were employed for detection of porins at the surface of intact mycobacteria. Porins were accessible at the surface of intact cells of M. fortuitum and were detected by the porin-specific antibody. Significantly higher absorption at 450 nm (P < 0.001) was measured for M. fortuitum DSM 46621 as well as M. fortuitum 10860/03 when compared to the relative backgrounds (see Additional file 4).
Heterologous expression of porM1 as well as porM2 was performed in the porin mutant strain M. smegmatis ML10 (ΔmspA; ΔmspC) to prove the functionality of encoded porins. For this purpose, the plasmids pSRa102 and pSRa104 harbouring porM1 and porM2, respectively, were introduced to M. smegmatis ML10. The plasmid pSSa100  containing mspA was employed as a positive control.
The quantification of growth rates of the strains by cfu-counting confirmed these conclusions (Figure 6E). The strain complemented with mspA (containing pSSa100) had reached its final number of colonies after 72 hours. The transformant complemented with porM1 (containing pSRa102) also showed visible colonies after 72 hours, it had, however, not yet reached its final number of colonies after this time period. The strains containing pSRa104 (carrying porM2) and the empty vector pMV306 both showed visible colonies not until 96 hours, but ML10 (pSRa104) outnumbered ML10 (pMV306).
Knock-down of porin expression in M. fortuitum was performed by generating the plasmid pSRr106, which carries a porM antisense fragment (see Figure 2A) under the control of the hsp60 promoter. The employed antisense sequence was first tested for non-specific binding performing a blast search at http://blast.ncbi.nlm.nih.gov/Blast.cgi. The analysis ensured that the antisense fragment specifically binds to mspA class porins, such as porMs and did not show any hits to other sequences deposited in the database.
The efficiency of down-regulation via RNA antisense technique was proven by means of SYBR Green qRT-PCR using strain 10860/03. As shown in Additional file 5, the knock-down strain carrying the plasmid pSRr106 showed about four times lower porin expression compared to the control strain harbouring the vector pSHKLx1.
In order to over-express porM genes in M. fortuitum, the coding sequences of porM1 from strain M. fortuitum 10851/03 and of porM2 from strain 10860/03 were inserted downstream of the hsp60 promoter in the vector pMV261 to generate plasmids pSRb101 and pSRb103, respectively.
In recent studies, our research has concentrated on the impact of the cell wall permeability on growth and intracellular persistence of mycobacteria. We were able to show that the porin pathway affects the intracellular persistence of different species in different ways. The findings suggest that intracellular persistence of mycobacteria depends, inter alia, on the balance between "walling-off" towards the hostile environment and the uptake of required compounds in the nutrient-depleted phagosomal environment [5, 13, 14]. To further examine this hypothesis, we are searching for more appropriate models. Different views have been expressed among scientists about whether M. smegmatis could serve as an appropriate model to study aspects related to virulence of highly pathogenic mycobacteria. A notable number of M. tuberculosis genes that are related to virulence but also play a housekeeping role share closely related orthologs in M. smegmatis. In the case of common mycobacterial genes, M. smegmatis was suggested as an appropriate model organism [15, 16]. On the other hand, the physiological differences between M. smegmatis and M. tuberculosis were mentioned to narrow down the significance of direct comparisons . Mutagenesis of porin genes in M. smegmatis allows the investigation of the impact of cell wall permeability on persistence. However, more appropriate models for such studies must naturally be able to survive and multiply intracellularly. Additionally, they must possess a known class of porin. These conditions are fulfilled by M. fortuitum, which was recently suggested as a model Mycobacterium . This species is able to infect and grow in phagocytic cells [2, 3] and also possesses porins orthologous to MspA. We therefore decided to identify and characterise porin genes from M. fortuitum.
The results of this study show that different strains - including the type strain - of M. fortuitum possess orthologous porins of the MspA class. The amino acid sequences of PorM1 and PorM2 are highly conserved among the strains, whereas there is variability in their nucleotide sequence. PorM1 and PorM2 have the same apparent molecular mass as MspA and MspC, respectively. They are accessible at the surface of M. fortuitum. In detergent extracts of M. fortuitum mature oligomers of PorMs were detected, similar to M. smegmatis porin oligomers. As oligomer formation is necessary for channel activity , it can be concluded that M. fortuitum porins form functional pores in the OM. Mature PorM1 from M. fortuitum differs at only six amino acid positions from MspA. According to the studies of Faller et al.  and Mahfoud et al.  about the structure of MspA and its topology in the OM of M. smegmatis, it can be assumed that the amino acid replacements between PorM1 and MspA do not significantly affect the general porin structure. Remarkably, most of the exchanges are restricted to those residues, which are also variable within the Msp family. For example, the replacement of alanine138 with proline in the extracellular loop L9 between the β-sheets 9 and 10 supports the tight turn between the β-sheets and the change of direction. Interestingly, PorM2 does not feature the mentioned exchange of alanine with proline, which is the only amino acid exchange in the mature protein between PorM1 and PorM2. Faller et al.  proposed that the adjacent replacement of serine163 with lysine changes the antigenic properties of MspD compared to the other isomers. Although PorMs have the same exchange, they were readily detectable using a polyclonal antibody raised against MspA. The exchange of asparagine129 with glutamic acid within the periplasmatic loop L6 introduces a negative charge into the channel and may thus change the permeation properties slightly . The replacement of isoleucine76 with threonine within the β-sheet β3 should not affect the protein structure either, since both amino acids are C-beta branched amino acids and it is more favourable for them to lie between β-sheets .
The capacity of the encoded porins PorM1 and PorM2 to fulfil the function of a porin was tested in complementation experiments by introducing these genes into the double mutant strain M. smegmatis ML10 (ΔmspA; ΔmspC) and observing the growth rate. Interestingly, porM1 had a stronger complementation effect than porM2, which was indicated by faster appearance of colonies and larger colony sizes on plates after electroporation. This may be explained by the higher similarity of porM1 to mspA, which represents the main porin gene in M. smegmatis . The antiserum raised against MspA binds well to PorMs, and the growth defect of the mutant strain M. smegmatis ML10 is reduced after complementation with porM1 and porM2. All mentioned features indicate similar functions and characteristics of the porins from M. smegmatis and M. fortuitum.
As mentioned above, mature PorM2 only differs from the mature PorM1 in one amino acid. More remarkable differences occur in the signal peptide of the two porins. The calculated cleavage site (SHA-GL) of the signal peptides of PorM1, PorM2, MspA and MspC is identical. However, the length of the signal peptides differs. While PorM1 and MspA have signal peptides composed of 27 amino acids, PorM2 and MspC possess extended signal peptides consisting of 31 amino acids. The length and primary structure of the signal peptide could be important for the transport and integration of the particular porin to the mycobacterial OM. It will be very informative to analyse the different regulation mechanisms determining the importance of the two genes for growth under different environmental conditions.
It was interesting that the expression of porM genes both at the transcriptional level and at the translational level consistently differed among the analysed strains as shown by the three employed approaches (Western Blot, ELISA and qRT-PCR). The results of both quantitative assays show the lowest porin expression among M. fortuitum strains in 10851/03 followed by 10860/03 and the type strain. The use of a polyclonal antibody, which recognises different epitopes of the protein and the consistency among the results of three different approaches allows drawing the conclusion that the porin expression in M. fortuitum is lower compared to M. smegmatis and also varies between the different strains. The high sequence conservation of the two paralogs PorM1 and PorM2 does not allow their expressions to be distinguished. Therefore, we consider the expression rates as overall values of both paralogs. As shown by qRT-PCR and ELISA, the porin expression in different strains of M. fortuitum was significantly lower than that of M. smegmatis. It was shown that M. smegmatis possesses 1000 MspA-like pores per μm2 cell wall . Since the analysed strains of M. fortuitum exhibited a clearly lower porM expression both at the transcriptional and the translational level, the amount of pores in the cell wall of M. fortuitum must be distinctly lower than 1000 pores per μm2 cell wall. According to our results, the amount of MspA-like pores in the analysed strains of M. fortuitum varies between 600 in M. fortuitum DSM 46621 and less than 100 per μm2 cell wall in M. fortuitum 10851/03, which exhibits the lowest amount of porin at all. It is interesting that the strain exhibiting the lowest porin expression is identical with the strain showing the slowest growth rate. This finding supports the hypothesis that porins play an important part in determining the generation time of mycobacteria.
To investigate the impact of the porins PorM1 and PorM2 on the growth rate of M. fortuitum, we generated strains over-expressing porM1 or porM2. Additionally, M. fortuitum knock-down strains were generated by antisense technique. This technique has contributed to the clarification of the function of many mycobacterial genes. Advantages are the possibility to analyse essential genes whose mutagenesis would be lethal and to repress genes present in several copies. Some examples of the application of the antisense technique in mycobacteria are the repression of ahpC from M. bovis , dnaA from M. smegmatis , FAP-P from M. avium subsp. paratuberculosis , pknF from M. tuberculosis  or MDP1 from M. bovis BCG . A further advantage of knocking-down genes by antisense technique can be the possibility to repress paralogous genes in the same bacterium. As described in Dryselius et al. , the most effective region for antisense inhibition is the region covering the Shine-Dalgarno Sequence and the start codon. The authors furthermore show, that antisense RNAs of only 10–12 bases exhibit strong inhibitory effects on gene expression. The antisense fragment used in this study is identical to the corresponding region of porM1. While it displays a homology of 71.4% to porM2, the antisense fragment and porM2 still exhibit long stretches of identical nucleic acid sequences. Of particular importance is the similarity in the beginning of the antisense fragment covering the Shine-Dalgarno Sequence and the start codon (40 bp, 95% identity). We therefore are convinced that a down-regulation of both, porM1 as well as porM2, may be achieved using the strategy described in this study. Deletion- or insertion mutagenesis of either porM1 or porM2 might result in complementation of the deleted porin gene by the remaining one. Such an effect has been observed in M. smegmatis, where the deletion of the mspA gene caused the activation of the transcription of mspB and/or mspD . Mutagenesis of both porin genes in the same derivative, on the other hand, would probably restrain the diffusion across the OM to an extent compromising cellular functions.
The effects of an over-expression of porin in our M. fortuitum strains depended on characteristics of the strains as well as the amount of kanamycin added to the medium. The over-expression of porM1 and porM2 showed the most considerable influence on growth rate in strain 10851/03. Among the tested strains, 10851/03 has the slowest growth rate and produces least porin. Therefore, this strain probably benefits most from a better nutrient supply caused by porin over-production. Otherwise, the adverse effect of kanamycin on the growth rate was most pronounced in strain DSM 46621, which expresses the highest amount of porin among the analysed strains. Disposing of a relatively high amount of porin, this strain probably takes less advantage of an ameliorated nutrient supply and instead suffers most from more kanamycin diffusion into the cells. When the kanamycin concentration in the plates was reduced to 25 μg ml-1, the over-expressing DSM 46621 derivatives did not show any growth inhibition compared to the control strain and even had a slight growth advantage. It seems that at this kanamycin concentration the beneficial effects of better nutrient influx slightly exceed the adverse effects of better antibiotic influx. The changes in growth behaviour in 10851/03 as well as in DSM 46621 were more pronounced upon over-expression of porM2 compared to over-expression of porM1. The down-regulation of the expression of PorM1 together with PorM2 by antisense-technology reduced the growth of both M. fortuitum strains to a similar and very low level suggesting that lack of porins in the knock-down strains strongly impairs the nutrient supply.
Our observations point to a passage of kanamycin through the PorM porins. Studies performed with M. smegmatis gave rise to contrarious conclusions [29, 30]. Stephan et al.  observed no reduction of kanamycin resistance in a mspA mutant compared to the M. smegmatis wild type strain and Danilchanka and colleagues  had postulated using structural models that due to its size kanamycin cannot diffuse through the MspA porin. These differing results may in part be explained by the use of different experimental systems. Stephan et al.  employed a mutant strain, while we observed differential effects of kanamycin only in over-expressing strains. Furthermore, Stephan et al.  performed their studies with M. smegmatis and we observed strong strain-dependent variations even among different isolates within the same species. The amino acid exchanges occurring between MspA on the one hand and PorM1 and PorM2 on the other hand may be responsible for differences in channel properties of these porins and influence their permeability for kanamycin.
As we discussed earlier, the growth rate of mycobacteria may contribute to their pathogenicity . Hence, it can be suggested that the low porin expression in M. fortuitum strains isolated from human patients compared to saprophytic species of RGM like M. smegmatis contributes to higher pathogenicity caused by an enhanced ability to multiply intracellularly. Interestingly, it was shown that the mspA expression in M. smegmatis is specifically downregulated at acidic pH . Moreover, the M. tuberculosis porin OmpATB, which belongs to the OmpA class of porins has been shown to be necessary for the persistence in the acidic milieu enabling M. tuberculosis to respond to reduced environmental pH [32, 33]. Although the MspA like porins do not belong to the OmpA class of porins, the results of these studies underline the role of porins concerning the intracellular persistence of mycobacteria.
An interesting result from various genome-sequencing projects of mycobacteria is that genome sizes of RGM and the pathogenic slow-growing mycobacteria largely differ. Highly pathogenic species like M. tuberculosis and M. leprae have genome sizes of about 4.4 Mb and 3.27 Mb, respectively. On the other hand, M. smegmatis has a genome size of about 7 Mb, which is similar to that of the related actinomycete Streptomyces coelicolor. Brosch et al.  reviewed different data such as 16S rRNA sequences or genome sizes and suggested that the branch of slow-growing mycobacteria represents the part of the genus that has evolved most recently. They proposed that the loss of genes rather than gain of genetic material by horizontal transfer contributed both to the pathogenicity of slow-growing mycobacteria and to the fine-tuning of their virulence. Loss of efficient porins of the MspA class or a decreased density of porins in the OM plays an important role to "wall-off" toward the hostile phagosomal environment and thus is of particular importance for the evolution of a successful intracellular pathogen. The presence of several copies of porin genes and, in turn, a high density of efficient porins in the OM of M. smegmatis would provide a selective advantage for saprophytes. A decreased amount of efficient porins in the OM of pathogenic RGM like M. fortuitum may represent an evolutionary intermediate stage between saprophytic mycobacteria like M. smegmatis and the highly pathogenic slow-growing mycobacteria.
Our study provides detailed information about porin genes of the mspA class in M. fortuitum and their importance for the growth rate and susceptibility to antibiotics. Our future studies will concentrate on the elucidation of the role of PorM1 and PorM2 in survival and replication of phagocytosed M. fortuitum.
Mycobacterial strains used in this work.
M. smegmatis SMR5
M. smegmatis mc2155 derivative, SMR
M. smegmatis ML10
SMR5 derivative, ΔmspA and ΔmspC
M. fortuitum DSM 46621
Type strain; HYGR
M. fortuitum 10851/03
Human patient isolate
M. fortuitum 10860/03
Human patient isolate; HYGR
M. bovis BCG Copenhagen
To compare the growth rates of M. fortuitum strains, Middlebrook 7H9/DC medium was inoculated with preparatory cultures to obtain an initial OD600 of 0.02. During 16 days, the optical densities of the cultures were measured daily. Growth of the strains was monitored by quantification of the ATP content of the cultures with the luminescence-based kit BacTiter-Glo™ Microbial Cell Viability Assay (Promega). The luminescence was reported as relative light units (RLU) with the microplate luminometer LB96V (EG&G Berthold) .
Common molecular biology techniques were carried out according to standard protocols  or according to the recommendations of the manufacturers of kits and enzymes. Transformation of E. coli was performed according to the method of Hanahan . PCR reactions were performed with the following kits: Taq DNA Polymerase (MBI Fermentas, St. Leon-Roth, Germany), BC Advantage GC Polymerase Mix (Takara Bio Europe S.A., Gennevilliers, France), BIO-X-ACT Short Mix and BIOTAQ DNA Polymerase (Bioline GmbH, Luckenwalde, Germany). Sequencing reactions were performed by using the Prism Big Dye™ FS Terminator Cycle Sequencing Ready Reaction Kit from PE Applied Biosystems (Darmstadt, Germany).
Protein and nucleotide sequence analysis such as identification of DNA subsequences (e.g. promoters and terminators) was performed using the software packages MacVector™ 7.2.3 (Accelrys, Cambridge, UK) and Lasergene (DNASTAR, Inc., Madison, WI, USA). Signal peptides were predicted using the SignalP 3.0 Server at http://www.cbs.dtu.dk/services/SignalP/.
Phylogenetic relationships among the RGM were analysed using the program ClustalW in the MacVector™ 7.2.3 package. Before analysing the phylogenetic relationships, sequences were trimmed in order to start and finish at the same nucleotide position for all employed strains. Phylograms were obtained from nucleotide sequences using the neighbour-joining method with Kimura 2-Parameter distance correction .
In order to clone porin genes, genomic DNA from M. fortuitum was digested to completion with the restriction enzyme SacII and separated by agarose gel electrophoresis. The DNA was then transferred to the Hybond+ membrane (GE Healthcare, Munich, Germany) as described by Sambrook and Russell . Porin genes were detected by means of Fluorescein-labelled probes using the primer pairs hpor and npor or mf-4IV-fw and mf-4-bw (Table 1) and the PCR Fluorescein Labelling Kit (Roche, Mannheim, Germany) according to the manufacturer's instructions. The region around 3000 bp that was shown to hybridise to the probe was isolated out of the gel and was ligated into the unique SacII site of the plasmid pIV2 . After transformation of E. coli DH5α, clones were screened by Dot Blot analysis. Inserts of two positive recombinant plasmids, pSSp107 and pSSp108, were sequenced. The inserts contained mspA-related sequences referred to as porM1. Identification of orthologous genes among other members of M. fortuitum was performed by PCR using the primers komf-3f and komf-4b (Table 1), which were derived from the cloned genomic region of porM1.
For the cloning of porM2, genomic DNA from M. fortuitum 10851/03 DNA was digested with the restriction enzyme SmaI and a 4200 bp SmaI fragment that had shown to hybridise to the Fluorescein-labelled probe before was eluted from the agarose gel and ligated into the SmaI site of pLITMUS38 (New England Biolabs, Frankfurt, Germany) and clones were screened as mentioned above. The insert of the only positive clone was sequenced. A 181 bp sequence similar to the 3' terminus of the coding sequence of porM1 was identified, while the following 256 bp of the 3' flanking region showed no similarity to the porM1 flank. A PCR primer within the porM2 flanking region (porM2-51-bw) and another primer hybridising to the first 19 bp of the porM1 coding sequence (porM2-51-fw) were used to amplify porM2 sequences (Table 1). After sequencing the PCR product, a reverse PCR approach was adapted to discover the 5' flanking region of porM2 including its start. Therefore, genomic DNA of M. fortuitum 10851/03 was digested with NcoI. The DNA fragments were circularised by ligation. Then a PCR was performed using the reverse primers porM2-rev-1 and porM2-rev-2 (Table 1) and the product was sequenced to obtain a complete sequence of porM2 and its flanking regions. The primers porM2-fw-hind (located 268 bp upstream of the porM2 coding sequence [CDS]) and porM2-bw-hpa (located directly downstream of the porM2 cds) (Table 1) were derived from the sequence mentioned and were chosen to amplify and clone porM2 and its regulatory sequences. The 918 bp product was cloned into the HindIII/HpaI restriction sites of the integrative mycobacterial vector pMV306  and the shuttle vector pMV261  to generate the recombinant plasmids pSRa104 and pSRb103, respectively. Positive clones were verified by sequencing. PorM2 was detected in other strains using the primer pairs porM2-fw-hind and porM2-bw-hpa or porM2-rna-fw and porM2-rna-bw (Table 1).
M. smegmatis MspA as well as porins from M. fortuitum were extracted in PBS buffer supplemented with 0.5% (w/v) n-octylpolyoxyethylene (nOPOE, Bachem, Heidelberg) and 0.2% EDTA (POP05), slightly modifying the method of Heinz and Niederweis . Mycobacteria were grown to an OD600 of up to 1. Subsequently, about 150 mg of mycobacteria (wet weight) were washed twice in PBS buffer supplemented with 0.2% EDTA. Pellets were resuspended in POP05 using a ratio of 200 μl POP05 per 100 mg mycobacteria and were incubated at 100°C for 30 min. Afterwards, cell debris was sedimented by centrifugation at 27,000 × g and 4°C and the supernatant was transferred to a new tube. Quantification of protein samples was carried out using the BCA Protein Assay Reagent Kit (Pierce, Rockford, IL, USA). Western Blot analysis was performed using the antiserum pAK MspA#813 as described previously . For 2D-analysis, about 75 μg of protein was precipitated by acetone and pellets were washed with 70% acetone to desalt the sample. Afterwards pellets were resuspended in 200 μl Rehydration solution (8 M Urea, 0.5% CHAPS, 0.2% DTT, 0.5% Pharmalyte, 0.002% Bromphenol blue), incubated for 5 h at room temperature and loaded on IPG strips pH 3–5.6 NL, 11 cm (GE Healthcare). The strips were focused on an Ettan pIGphorII unit and the second dimension was run on vertical 10% SDS-PAGE gels using the Ettan Daltsix electrophoresis unit (GE Healthcare) according to the manufacturer's instructions. The gels were silver-stained using Roti-Black P (Carl Roth GmbH, Karlsruhe, Germany). The porin was detected by Western Blotting as mentioned above.
Expression of porin genes in the different strains was determined by means of qRT-PCR using the Mx3000P™ Real-time PCR System (Stratagene, La Jolla, CA, USA) or the StepOnePlus™ Real-Time PCR-System (Applied Biosystems). Mycobacteria were grown to an OD600 of 0.8 and RNA was extracted according to the method of Bashyam and Tyagi . 1 or 5 μg of the RNA was treated prior to qRT-PCR with RNase-Free DNase (Fermentas GmbH, St. Leon-Roth, Germany). Reverse transcription of mycobacterial RNA was carried out using the RevertAid™ M-MuLV Reverse Transcriptase (Fermentas GmbH) and hexamers or the Access RT-PCR System (Promega, Mannheim, Germany) according to the manufacturer's protocols. The porin cDNA from M. smegmatis SMR5  and M. fortuitum was quantified either by amplifying a fragment of about 100 bp using the primers (mspATaqfw, mspATaqbw, mfpqPCRfw and mfpqPCRrev) as well as TaqMan-probes (mspATaqProbe and mfpqPCRprobe) or the primers porM1-51-sybr-fw and bw based on SYBR Green detection chemistry (Table 1). The qPCR reactions were performed using the SensiMix DNA Kit (Quantace Ltd., Berlin, Germany) or the Access RT-PCR System (Promega) according to the manufacturer's protocol. TaqMan quantification was carried out by running a first step at 95°C for 10 min followed by 40 cycles with 30 s at 95°C and 1 min at 58°C. SYBR Green quantification was performed by initial 10 min at 95°C followed by 40 cycles with 15 s at 95°C, 10 s at 58°C and 20 s at 72°C. Afterwards, the amplicon's melting temperature was determined ramping the temperature from 60°C to 90°C by 0.5°C steps and acquiring the fluorescence signal. cDNA amounts were determined by three measurements for each sample using a calibration curve established with known amounts of linearised pSSa100  in case of M. smegmatis or pSSp107 in case of M. fortuitum. DNase treated and non-reverse-transcribed controls were performed with the same samples to guarantee the absence of contaminating genomic DNA.
In addition to the qRT-PCR experiments, the amount of porin in isolates of M. fortuitum and M. smegmatis was determined by Enzyme-Linked Immunosorbent Assay (ELISA). Protein was isolated from mycobacteria using the detergent nOPOE as described above. The isolated protein (15 μl corresponding approximately to 25 μg) was diluted in 50 mM NaHCO3, pH 9.6 to yield a protein concentration of 1 μg/100 μl. Aliquots (100 μl) of the sample and dilutions thereof were loaded to wells of a Nunc-Immuno Maxisorp Module (Nalgene Nunc International, NY, USA). After incubating the samples at 4°C overnight, wells were washed twice with TBS-T (50 mM Tris-HCl, pH 7.8, 150 mM NaCl, 1 mM MgCl2 and 0.05% Tween 80). The surface was blocked with 3% powdered skim milk in TBS for 1.5 h at room temperature followed by three steps of washing with TBS-T. Samples were then treated with the primary antibody for 1.5 h at room temperature, using a 1:1500 dilution of the antiserum pAK MspA#813  in TBS. The wells were washed five times with TBS-T and were incubated for 1 h at room temperature with a 1:7500 dilution of Peroxidase-conjugated AffiniPure F (ab') 2 Fragment Goat Anti-Rabbit IgG (H+L) (Jackson Immuno Research, Soham, UK) in TBS. After five steps of washing, the reaction was performed using the SureBlue™ TMB Microwell Peroxidase Substrate (KPL, Gaithersburg, MD, USA) according to the instructions of the manufacturer. Absorption at 450 nm was measured with the microplate reader SPECTRA Fluor (TECAN, Crailsheim, Germany).
40 ml of mycobacterial culture was harvested at OD600 of 0.8, washed with PBS-T and the pellet was resuspended in 1 ml PBS-T. 200 μl aliquots were then incubated for 30 min on ice with 1 μl of antiserum (pAK MspA#813); for detection of background pre-immune serum was given to the samples. Afterwards 1 ml PBS-T was given to each sample; mycobacteria were harvested by centrifugation and washed once with PBS-T. Pellets were resuspended in 100 μl of PBS-T, 1 μl of the secondary Peroxidase-conjugated AffiniPure F (ab') 2 Fragment Goat Anti-Rabbit IgG (H+L) (Jackson Immuno Research) was added to each sample and bacilli were incubated on ice for 30 min. After addition of 1 ml PBS-T, mycobacteria were pelleted by centrifugation and were washed once with PBS-T. Pellets were then resuspended in 500 μl of PBS-T, and 100 μl of dilutions thereof were transferred to wells of a Nunc-Immuno Polysorp Module (Nalgene Nunc International). After addition of 100 μl SureBlue™ TMB Microwell Peroxidase Substrate (KPL) and stopping the reaction by addition of 50 μl 1 M HCl, the reaction was detected by the reader SPECTRAFluor (TECAN).
Plasmids used in this work.
cloning vector with an origin of replication functional in Enterobacteriacea and a kanamycin resistance gene
cloning vector with the origin of replication from pUC, an ampicillin resitance gene and the lacZ' gene for blue/white selection
New England Biolabs
cloning vector replicating in E. coli with the kanamycin resistance gene aph from transposon Tn903 and the gene for the integrase and the attP site of phage L5 for integration into the mycobacterial genome
Mycobacterium/E. coli shuttle vector with the kanamycin resistance gene aph from transposon Tn903 and the promoter from the hsp60 gene from M. tuberculosis
Mycobacterium/E. coli shuttle vector with a kanamycin resistance gene from Tn5, a hygromycin resistance gene and the promoter from the hsp60 gene from M. tuberculosis
pMV306 with a 3429 bp genomic DNA fragment from M. smegmatis SMR5 carrying mspA
pIV2 with a 2895 bp genomic DNA fragment from M. fortuitum 10860/03 carrying the porM1 gene
pMV261 carrying the porM1 gene from M. fortuitum 10860/03
pMV261 carrying the porM2 gene from M. fortuitum 10851/03
pMV306 carrying the porM1 gene from M. fortuitum 10860/03
pMV306 carrying the porM2 gene from M. fortuitum 10851/03
pSHKLx1 carrying a 100 bp genomic DNA fragment from M. fortuitum 10860/03 containing the beginning of the porM1 gene with the SD-sequence in antisense-orientation with respect to the hsp60 promoter
In order to accomplish a simultanous knock-down of porM1 and porM2, we generated a plasmid containing a transcriptional fusion of the hsp60 promoter with the 5' region of porM genes. The primers porM1-as-1 and porM1-as-2 were used to amplify a 100 bp PCR amplicon covering the 5' region of porM1 including the Shine-Dalgarno Sequence. The PCR product was cloned into the BamHI site of pSHKLx1 , and recombinant plasmids containing the insert in antisense orientation with respect to the hsp60 promoter were identified by sequencing. Afterwards, the selected recombinant plasmid pSRr106 was introduced into M. fortuitum by electroporation. The knock-down efficiency of the introduced antisense RNA was analysed at transcriptional level. For this purpose, RNA was isolated from M. fortuitum strains containing either pSRr106 or pSHKLx1, and porin expression was measured by SYBR Green qRT-PCR as described above.
Over-expression of porM1 or porM2, was achieved by introducing plasmids pSRb101 or pSRb103, respectively, into M. fortuitum.
We would like to thank Prof. Dr. Michael Niederweis (University of Alabama, Birmingham, AL) for providing the antiserum and the M. smegmatis strain ML10. We also thank Dr. Rüsch-Gerdes (Nationales Referenzzentrum für Mykobakterien, Borstel) for providing the M. fortuitum strains 10851/03 and 10860/03. Furthermore, we thank Prof. Dr. Robertson (Imperial College, London) and Prof. Dr. Jacobs (Howard Hughes Medical Institute, New York) for providing plasmids pSHKLx1 and pMV261, respectively. We are grateful to Elisabeth Kamal for excellent technical assistance. Kira Schramm was supported by a European Union Equal Project grant.
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