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The phylogenetically related Mycoplasma capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony are two small-ruminant pathogens involved in contagious agalactia. Their respective contributions to clinical outbreaks are not well documented, because they are difficult to differentiate with the current diagnostic techniques. In order to identify DNA sequences specific to one taxon or the other, a suppression-subtractive hybridization approach was developed. DNA fragments resulting from the reciprocal subtraction of the type strains were used as probes on a panel of M. capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony strains to assess their intrataxon specificity. Due to a high intrataxon polymorphism and important cross-reactions between taxa, a single DNA fragment was shown to be specific for M. capricolum subsp. capricolum and to be present in all M. capricolum subsp. capricolum field isolates tested in this study. A PCR assay targeting the corresponding gene (simpA51) was designed that resulted in a 560-bp amplification only in M. capricolum subsp. capricolum and in M. capricolum subsp. capripneumoniae (the etiological agent of contagious caprine pleuropneumonia). simpA51 was further improved to generate a multiplex PCR (multA51) that allows the differentiation of M. capricolum subsp. capripneumoniae from M. capricolum subsp. capricolum. Both the simpA51 and multA51 assays accurately identify M. capricolum subsp. capricolum among other mycoplasmas, including all members of the M. mycoides cluster. simpA51 and multA51 PCRs are proposed as sensitive and robust tools for the specific identification of M. capricolum subsp. capricolum and M. capricolum subsp. capripneumoniae.
The Mycoplasma genus is composed of wall-less bacteria with small genomes (0.58 to 1.35 Mb) and includes several species known to cause important diseases in humans and animals (24). Most of these species can be grown under laboratory conditions, although they require complex, undefined media and several days to several weeks of incubation because of their limited biosynthetic capacities (24). So far, mycoplasma identification and diagnosis have been based mainly on serological assays after cultivation, but recent ongoing efforts have been directed toward replacing these assays with more rapid and accurate molecular approaches based on the detection of specific DNA sequences.
For the veterinary field, members of the so-called Mycoplasma mycoides cluster are of particular concern, because they are important ruminant pathogens that are responsible for economic losses worldwide (1, 28). This cluster includes six taxa, which are phylogenetically closely related based on their 16S rRNA gene sequences (21); present similar serological patterns associated with important intertaxon cross-reactivity (12); and, consequently, are difficult to differentiate. Four taxa contain pathogens for small ruminants, with three, namely, M. mycoides subsp. mycoides biotype Large Colony, M. mycoides subsp. capri, and M. capricolum subsp. capricolum (1, 4, 5), being responsible for contagious agalactia (CA) and one, M. capricolum subsp. capripneumoniae, being responsible for contagious caprine pleuropneumonia (CCPP) (11). Recently, it was suggested that M. mycoides subsp. mycoides biotype Large Colony and M. mycoides subsp. capri represent a single taxonomic entity and that they should be grouped in a single subspecies (26). The two other taxa of the M. mycoides cluster, namely, M. mycoides subsp. mycoides biotype Small Colony, the causative agent of contagious bovine peripneumonia, and Mycoplasma sp. bovine group 7, which induces pneumonia, mastitis, and arthritis, are bovine pathogens but occasionally are isolated from goats (1, 2, 9).
Direct PCR assays designed to assign a mycoplasma isolate to the M. mycoides cluster or to identify M. mycoides subsp. mycoides biotype Small Colony (20, 28) and M. capricolum subsp. capripneumoniae (27) are available, but the accurate identification of the remaining taxa of the M. mycoides cluster is more problematic because of intertaxon cross-reactivity and high intrataxon variability (12). Two direct PCR assays currently are proposed in the literature for the specific identification of M. capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony that both target a gene encoding the LppA lipoprotein, MCCPL PCR (16) and MMMLC PCR (17), respectively. However, they were both shown to be inappropriate for field isolates, with a relative intrataxon sensitivity of only 48 and 26% for M. capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony, respectively (12).
Designing PCR assays that would accurately identify M. mycoides subsp. mycoides biotype Large Colony (or M. mycoides subsp. capri) and M. capricolum subsp. capricolum would be particularly valuable, as both mycoplasma species induce CA in goats; CA is a disease of economic importance with a worldwide distribution (1, 28). M. mycoides subsp. mycoides biotype Large Colony (or M. mycoides subsp. capri) and M. capricolum subsp. capricolum also can be isolated from asymptomatic animals (25), and in the absence of a reliable identification assay, the exact contribution of each taxon to CA has yet to be evaluated. Finally, M. mycoides subsp. mycoides biotype Large Colony (or M. mycoides subsp. capri) and M. capricolum subsp. capricolum both can occur in the same clinical specimen, but in culture the presence of M. capricolum subsp. capricolum often is masked by M. mycoides subsp. mycoides biotype Large Colony, which grows faster. Adequate, specific PCR assays would overcome this problem. Recently, the alignment of M. mycoides subsp. mycoides biotype Large Colony (strain GM12) genome draft sequence with the M. capricolum subsp. capricolum California Kid sequence (GenBank accession no. NC_007633) showed 91.5% nucleotide identity across 76% of the California Kid genome, underlying the important relatedness of the two taxa (10) and the difficulty in identifying DNA sequences that would be specific to each taxon while also being evenly distributed in field isolates.
In this study, DNA sequences that diverge between M. mycoides subsp. mycoides biotype Large Colony and M. capricolum subsp. capricolum strains were enriched using suppression subtractive hybridization (SSH), a method that previously has been successful in identifying sequences specific to two related mycoplasma species, Mycoplasma bovis and Mycoplasma agalactiae (14). Sequences specific to the type strain of M. capricolum subsp. capricolum, namely California Kid, and M. mycoides subsp. mycoides biotype Large Colony, namely Y-Goat, were further identified, and their distributions were assessed in a panel of field isolates belonging to the M. mycoides cluster. Based on these data, a PCR assay was developed that identifies M. capricolum subsp. capricolum among members of the M. mycoides cluster.
Escherichia coli strains DH5α (Invitrogen Ltd., Glasgow, United Kingdom) and XL1-blue MRF′ (Stratagene, La Jolla, CA) were used for DNA manipulations. They were both grown at 37°C in Luria-Bertani broth supplemented with ampicillin (100 μg/ml) and tetracycline (15 μg/ml) when required.
M. capricolum subsp. capricolum type strain California Kid (ATCC 27343) was purchased from the Pasteur Institute Collection (Paris, France). M. mycoides subsp. mycoides biotype Large Colony type strain Y-Goat was kindly provided by E. Vilei (University of Berne, Switzerland). These two strains were used as the driver and tester for SSH experiments. Mycoplasma field isolates were selected from the Agence Française de Sécurité Sanitaire des Aliments (AFSSA) collection (22). Mycoplasmas were grown in PPLO broth (Difco, Le Pont-De-Claix, France) at 37°C under 5% CO2 as previously described (23). Field isolates were cloned by filtering the isolates on a 0.22-μm filter, growing the filtrates onto 1% agar PPLO medium, and randomly selecting a single colony. This procedure was repeated twice.
The distribution of the DNA sequences identified in this study was assessed in three sets of mycoplasma isolates and clones. Set 1 is composed of (i) type strains (see below) that represent Mycoplasma species usually isolated from small ruminants in Europe and (ii) clones derived from field isolates of M. mycoides subsp. mycoides biotype Large Colony, M. capricolum subsp. capricolum, and Mycoplasma sp. bovine group 7 from various origins and clinical contexts (for details, see Table Table2).2). These clones were identified by the method of dot immunobinding on membrane filtration (MF-dot) with specific rabbit antisera (23), by the analysis of a segment of their 16S rRNA (8, 21), fusA (13), and rpoB (26) genes, and by the PCR assays performed as previously published (7, 16, 17, 20). The stability of the clones was tested by MF-dot and pulsed-field gel electrophoresis analyses after five successive subcultivation steps into liquid medium. The type strains of set 1 were PG1 (NCTC 10114) for M. mycoides subsp. mycoides biotype Small Colony, PG2 (NCTC 10123) for M. agalactiae, TS205 (ATCC 19852) for Mycoplasma sp. strain ovine/caprine group 11, KS1 (ATCC 15718) for Mycoplasma putrefaciens, TS1726 (ATCC 51348) for Mycoplasma auris, TS1874 (ATCC 51347) for Mycoplasma cottewii, TS1973 (ATCC 51346) for Mycoplasma yeatsii, PG3 (NCTC 10137) for M. mycoides subsp. capri, TS1399 (ATCC 27948) for Mycoplasma adleri, TS1581 (ATCC 25834) for Mycoplasma conjunctivae, TS2230 (ATCC 23838) for Mycoplasma arginini, and PG50 (NCTC 10114) for Mycoplasma sp. bovine group 7.
Set 2 included 66 clones derived from field isolates that either (i) belong to the M. mycoides cluster (15 M. mycoides subsp. mycoides biotype Large Colony/M. mycoides subsp. capri isolates, 8 M. mycoides subsp. mycoides biotype Small Colony isolates, 3 Mycoplasma sp. bovine group 7 isolates, and 10 M. capricolum subsp. capricolum isolates); (ii) are closely related to this cluster (five M. putrefaciens isolates and four M. yeatsii isolates); or (iii) are from different phylogenetic clades (eight M. agalactiae isolates, seven M. bovis isolates, and six M. arginini isolates). All clones of set 2 were identified by MF-dot and fusA sequence analyses, which were shown to be efficient for species identification within the M. mycoides cluster and less expensive than 16S rRNA gene analysis (which requires the assembly of five individual sequences).
Set 3 included 28 noncloned isolates of M. capricolum subsp. capricolum obtained from bulk cultures of clinical specimens (from udder, joints, respiratory tract, etc.) and were identified only by MF-dot analysis.
Additionally, eight Mycoplasma sp. bovine group 7 and three M. capricolum subsp. capripneumoniae strains (including the F38 M. capricolum subsp. capripneumoniae type strain), kindly provided by F. Thiaucourt (CIRAD [French Agricultural Research Centre Working for International Development], Montpellier, France), were used in the course of PCR assay validation.
SSH was performed as previously described using the RN48 (5′-AGCACTCTCCAGCCTCTCACCGAGAGGCAACTGTGCTATCCGAGGGAG) and RJ48 (5′-AGCACTCTCCAGCCTCTCACCGAGACCGACGTCGACTATCCATGAACG) adapters (15).
Genomic DNA of M. capricolum subsp. capricolum California Kid was used as the tester against M. mycoides subsp. mycoides biotype Large Colony Y-Goat, which was the driver (SSH-A), and then roles of driver and tester were reversed (SSH-B). Before ligation with the adapters, genomic DNAs were digested with the Sau3A restriction endonuclease. Hybridization was performed at 45°C for SSH-B and 55°C for SSH-A. Tester-specific sequences were amplified by PCR and cloned into Escherichia coli (either the chemically competent DH5α or electrocompetent XL1-blue MRF′ strain) using the pGEM-T Easy plasmid (Promega, Lyon, France).
The presence in E. coli libraries of cloned DNA sequences was assessed by PCR directly on individual colonies, using the N24 and J24 primers that correspond to specific parts of the adapters (Table (Table1).1). Plasmids from clones yielding a single amplicon with an estimated size of >100 bp were purified and sent to Cogenics (Grenoble, France) for the sequence analysis of the inserted DNA using cloning vector primers (T7).
Genomic DNA was extracted from mycoplasmas grown in liquid medium using the DNeasy tissue kit (Qiagen, Courtaboeuf, France). Plasmids were purified from E. coli using a QIAprep spin miniprep kit (Qiagen).
PCR assays were performed with an iCycler thermocycler (Bio-Rad, Marnes La Coquette, France) using recombinant Taq polymerases and reaction buffer from Qiagen (Taq PCR core kit) or Promega (GoTaq DNA polymerase). The PCR conditions and oligonucleotides used are listed in Table Table11.
Before sequence analysis, the fusA, rpoB, and 16S rRNA gene PCR amplicons were purified using the QIAquick PCR purification kit (Qiagen).
For the M. capricolum subsp. capricolum-specific PCR assay developed in this study, PCR primers were designed using e-primer3 (http://bioweb.pasteur.fr/seqanal/interfaces/eprimer3.html). Amplifications for both simplex (simpA51) and multiplex (multA51) assays were performed in a final volume of 25 μl containing 1 to 10 ng of DNA template, 8 pmol of each primer, 2 U Taq DNA polymerase, 200 μM of each deoxynucleoside triphosphate, and 1.5 mM MgCl2. PCR comprised an initial denaturation for 2 min at 94°C and then 35 cycles of 94°C for 30 s, 48°C for 15 s, and 72°C for 15 s, followed by a final extension for 5 min at 72°C.
The detection limit of the simpA51 and multA51 PCRs was assessed directly on crude DNA extracts prepared from mycoplasma liquid cultures of M. capricolum subsp. capricolum California Kid alone or mixed with 10-fold-concentrated M. mycoides subsp. mycoides biotype Large Colony Y-Goat. Briefly, 1.5 ml of pelleted cultures were incubated in 50 μl of proteinase K lysis buffer (0.1 M Tris-HCl, pH 8.5; 0.05% Tween 20; 0.25 mg/ml proteinase K) for 1 h at 37°C. Proteinase K then was inactivated for 10 min at 95°C. Serial 10-fold dilutions of this lysate were made. Each dilution was further diluted to 1/30, and 1 μl was used as the template in the PCR assays. The number of CFU in liquid broth was estimated by plating serial dilutions of the original culture onto 1% PPLO agar medium. The robustness of the multiplex PCR for diagnosis purposes was assessed by performing PCR on bulk bacterial extracts (pelleted cultures heated for 5 min at 100°C) or directly on colonies picked from plated liquid cultures incubated for 2 days.
For dot blotting, 400 ng of genomic DNA from subtracted strains was denaturated at 100°C and spotted onto a Hybond N+ membrane with a 40-min passive transfer on Whatman paper saturated with 0.4 M NaOH. For Southern blotting, 1 μg of EcoRI-digested DNA was transferred onto a Hybond N+ membrane after electrophoresis. Membranes were hybridized with DNA probes corresponding to PCR products labeled with the enhanced chemiluminescence direct nucleic acid labeler. Hybridization signals were revealed using detection systems (GE Healthcare, Chalfont St. Giles, United Kingdom) according to the manufacturer's instructions. Briefly, membranes were incubated overnight at 42°C with 10 ng/ml of heat-denatured probe in hybridization buffer (0.5 M NaCl and a 5% concentration of the blocking agent in the buffer provided by the supplier). Membranes then were washed three times for 10 min in washing buffer (6 M Urea, 0.4% sodium dodecyl sulfate, 0.5× SSC [1× SSC is 0.15 M NaCl plus 0.015 M sodium citrate]) and were washed twice for 5 min in 2× SSC. The detection of hybridized probes was performed with a 1-min incubation in detection reagents and exposure (5 min for dot blots and 30 min for Southern blots) to Hyperfilm ECL.
Nucleotide sequence comparisons with databanks were performed with BLASTN (without a filter) through the National Center for Biotechnology Information (NCBI) resource (http://www.ncbi.nlm.nih.gov). Alignments and phylogenetic trees were realized with SeaView and Phylo_Win programs at the PBIL website (http://pbil.univ-lyon1.fr). The redundancy of subtracted libraries was checked using the CAP3 sequence assembly program (http://pbil.univ-lyon1.fr/cap3.php). We checked that the A51 target sequence was present in a single copy in the M. capricolum subsp. capricolum California Kid genome by in silico analysis using the Molligen website (http://cbi.labri.fr/outils/molligen/home.php). The genome sequence of California Kid also is available at http://www.ncbi.nlm.nih.gov (GenBank accession no. NC_007633).
To assess the specificity and the distribution of M. capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony sequences identified in this study, clones derived from a representative panel of field goat isolates belonging to the M. mycoides cluster were selected on the basis of their reactivity with taxon-specific antisera using the previously described MF-dot assay (see Materials and Methods). The set of clones is described in Table Table22 and includes (i) 10 isolates of M. capricolum subsp. capricolum, of which 2 (no. 10276 and no. 14141) also gave positive results with Mycoplasma sp. bovine group 7-specific serum; (ii) 12 M. mycoides subsp. mycoides biotype Large Colony isolates, (iii) 4 Mycoplasma sp. bovine group 7 isolates, and (iv) one clone (no. 4234) that could not be clearly identified.
These 27 cloned isolates were further characterized by PCR assays described as specific (i) for the M. mycoides cluster (20) and (ii) for each of the Mycoplasma sp. bovine group 7, M. capricolum subsp. capricolum, and M. mycoides subsp. mycoides biotype Large Colony taxa (7, 16, 17). The PCR results confirmed that all isolates belonged to the M. mycoides cluster and that the discrimination between M. capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony was problematic, as only 6/10 M. capricolum subsp. capricolum clones and 4/12 M. mycoides subsp. mycoides biotype Large Colony clones gave an unequivocal amplification. For the Mycoplasma sp. bovine group 7-specific PCR assay (7), the four Mycoplasma sp. bovine group 7 isolates gave the expected amplicon, but two isolates (no. 5475 and no. 10277) that were MF-dot positive for M. mycoides subsp. mycoides biotype Large Colony and one isolate (no. 4234) that was not clearly identified by MF-dot analysis also were positive. Finally, the three species-specific PCRs also gave doubtful or atypical amplifications (i.e., multiple PCR products or amplicons of a different size than expected) with isolates not targeted by the primers (Table (Table22).
To resolve the discrepancies observed between MF-dot and PCR results, three housekeeping genes known or proposed to be good markers of the M. mycoides cluster phylogeny were partially sequenced. These genes were (i) the 16S rRNA gene (8); (ii) rpoB, which encodes the DNA-directed β subunit of the RNA polymerase (26); and (iii) fusA, which encodes an elongation factor (13). Phylogenic trees constructed with 16S rRNA gene sequences failed to discriminate M. capricolum subsp. capricolum from Mycoplasma sp. bovine group 7. The rpoB- and fusA-based phylogenic trees gave more stringent subclusterization of these two taxa and were in agreement with the MF-dot results. Interestingly, the rpoB phylogenetic tree revealed four subgroups among the M. mycoides subsp. mycoides biotype Large Colony isolates (see isolates 1 to 4 in Table Table2).2). Finally, trees constructed with rpoB, fusA, and 16S rRNA gene concatenated sequences showed the highest bootstrap values and were the most accurate in assigning a clone to a subcluster. The three clones identified as M. mycoides subsp. mycoides biotype Large Colony or atypical by MF-dot analysis but as Mycoplasma sp. bovine group 7 by PCR assays turned out to be M. mycoides subsp. mycoides biotype Large Colony by phylogeny analysis and were considered as such (Table (Table22).
DNA sequences present in M. capricolum subsp. capricolum California Kid and absent from M. mycoides subsp. mycoides biotype Large Colony Y-Goat were enriched by SSH (SSH-A and SSH-B) and cloned into E. coli. After detailed analyses, 80 and 79 recombinant clones obtained from SSH-A and SSH-B, respectively, were selected that had a single DNA insert ranging from 100 to 1,000 bp. PCR products corresponding to each of these cloned, subtracted DNA fragments then were labeled and used as probes on a dot blot nylon membrane carrying the denaturated tester and driver DNA. Hybridization results revealed that 27/80 probes (from SSH-A) and 40/79 probes (from SSH-B) reacted specifically with M. capricolum subsp. capricolum California Kid DNA or M. mycoides subsp. mycoides biotype Large Colony Y-Goat DNA, respectively, while the remaining probes recognized both species (Fig. (Fig.1A).1A). These results were confirmed by Southern blot analysis as illustrated in Fig. Fig.1B.1B. Southern blot hybridization data further indicated that most California Kid-specific sequences occur as single copies in the genome. When two hybridizing fragments were observed, they were further shown to correspond after sequencing (see below) to (i) the presence of an EcoRI site within the hybridizing fragment, (ii) the presence of two paralogs (MCAP_0442 and MCAP_0561) in the California kid genome, and (iii) a concatenation during the cloning of two sequences nonadjacent on the chromosome.
The 27 and 40 DNA fragments described above that specifically hybridized with M. capricolum subsp. capricolum California Kid or M. mycoides subsp. mycoides biotype Large Colony Y-Goat genomic DNA, respectively, were sequenced. Sequences with an internal Sau3A site suspected to correspond to a concatenation of nonadjacent chromosomal fragments were excluded from the study. In total, 23 and 35 unique sequences corresponding to SSH-A and SSH-B, respectively, were used to search nonredundant databases using BLASTN algorithms. BLAST results indicated that 16 DNA sequences cloned from California Kid and 18 DNA sequences cloned from Y-Goat presented no or little identity with other mycoplasma sequences available in the databases and were, therefore, tester specific. To assess whether these sequences are good target candidates for diagnosis, their specificity and distribution were tested using a panel of cloned clinical isolates and type strains representing mycoplasma species usually isolated from small ruminants (Table (Table2).2). This was performed by dot blot hybridization using each tester-specific sequence as a probe. Results showed that only one (A51) out of the 16 probes specific for the California Kid strain reacted exclusively with all M. capricolum subsp. capricolum strains (Fig. (Fig.2).2). Of the remaining, 10 recognized some M. capricolum subsp. capricolum field strains, but not all, and 5 reacted with all M. capricolum subsp. capricolum field strains but also with other field isolates belonging to different mycoplasma species (four probes also recognized Mycoplasma sp. bovine group 7; one probe recognized the M. mycoides subsp. mycoides biotype Small Colony type strain PG1) (data not shown). In contrast, only 1 out of 18 Y-Goat-specific sequences hybridized with all M. mycoides subsp. mycoides biotype Large Colony isolates; however, it also cross-reacted with all M. capricolum subsp. capricolum and Mycoplasma sp. bovine group 7 field strains as well as with the M. cottewii and M. mycoides subsp. capri type strains.
Sequence alignments revealed that the entire A51 probe (394 bp) was identical to the 3′-terminal region of the MCAP0862 gene of California Kid and showed no significant identity with any other sequences from GenBank. The MCAP0862 gene is 2,253 bp long and codes a putative membrane protein with one transmembrane segment in the N-terminal region and four leucine zipper motifs. The MCAP0862 product belongs to a cluster of orthologous groups of ATPases involved in DNA repair (L-COG0419), but its exact function has not been explored so far.
Two primers were designed to specifically amplify a 570-bp DNA fragment from MCAP0862 with one primer, A51-R, located within the A51 fragment (Fig. (Fig.3).3). Using the Molligen database, we confirmed that the target sequence was present as a single copy in M. capricolum subsp. capricolum California Kid and was absent from other sequenced mollicutes. The PCR assay was performed using clones from set 1 as the DNA template and an additional eight Mycoplasma sp. bovine group 7 isolates in order to reflect the phylogenetic relatedness existing between M. capricolum subsp. capricolum and Mycoplasma sp. bovine group 7. Results were negative for all M. mycoides subsp. mycoides biotype Large Colony and Mycoplasma sp. bovine group 7 strains and for non-M. capricolum subsp. capricolum type strains of set 1 (data not shown).
In addition, the A51 PCR assay was performed using three Mycoplasma capricolum subsp. capripneumoniae strains. This taxon previously had not been used in our study, because it does not normally require differential diagnosis in countries currently free of CCPP (i.e., most of the world outside of Africa and the Middle East). Results showed that the three strains also gave an amplicon of ca. 570 bp, suggesting the presence in these strains of sequences similar to that of the amplified A51 region. Indeed, the sequencing of a PCR product obtained with primers flanking the A51 pair (VarA51 primers) revealed that the M. capricolum subsp. capripneumoniae sequences matched those of the M. capricolum subsp. capricolum MCAP0862 gene with 90% nucleotide identity. We therefore shortened the A51-F and A51-R primers (21-nucleotide primers designated ShA51-F and ShA51-R) to combine our PCR assay (simpA51) with that designed by Woubit et al. (27). As illustrated in Fig. Fig.4,4, the resulting multiplex PCR assay (multA51) yields a 560-bp amplicon with both M. capricolum subsp. capricolum and M. capricolum subsp. capripneumoniae strains with an additional fragment of 316 bp specific for M. capricolum subsp. capripneumoniae strains.
Both simpA51 and multA51 PCR assays, run as described in Table Table1,1, were validated using strains from set 1 with some additional Mycoplasma sp. bovine group 7 and M. capricolum subsp. capripneumoniae strains as mentioned above. The specificity of both simpA51 and multA51 PCRs also was assessed on a second set of cloned field strains from different species belonging or related to the M. mycoides cluster (set 2). As expected, no amplification was observed for all species tested, except for the M. capricolum subsp. capricolum strains (a single band at 560 bp) and M. capricolum subsp. capripneumoniae (one band of 560 bp in simplex conditions, or two bands, one of 560 bp and the other of 316 bp, in multiplex conditions) (Fig. (Fig.4).4). We checked that the 560-bp amplicon corresponded to the multA51 target sequence by hybridizing our PCR products with the labeled A51 probe (data not shown).
To analyze the robustness of the multA51 PCR assay, the amplification reaction also was performed directly on bulk bacterial extracts (see Material and Methods) and on colonies using 28 noncloned field isolates of M. capricolum subsp. capricolum (set 3). For each assay, M. capricolum subsp. capricolum California Kid was used as a positive control, and a field strain of M. mycoides subsp. mycoides biotype Large Colony was used as a negative control. The 560-bp amplicon was obtained systematically and exclusively with M. capricolum subsp. capricolum strains regardless of the nature of the sample tested (bacterial extract or colony), as shown in Fig. Fig.5A5A.
The limits of detection of the multA51 and simpA51 PCRs were analyzed using 10-fold dilutions of crude DNA extracts from 4 × 109 CFU/ml M. capricolum subsp. capricolum liquid cultures left untreated or spiked with nontargeted mycoplasmas (M. mycoides subsp. mycoides biotype Large Colony) as the template. For both PCR assays, the amplification reaction was not affected by the presence of M. mycoides subsp. mycoides biotype Large Colony (data not shown), and a PCR product was obtained up to a dilution of 10−6, which corresponded to a limit of detection of 4 CFU per reaction (Fig. (Fig.5B5B).
The small-ruminant pathogens M. capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony are two members of the M. mycoides cluster, and both are involved in CA. Because of the economic importance of CA, control strategies have been developed that are based mainly on the eradication of the infection by an accurate detection of the CA causative agents. This goal can be achieved by two recently developed PCRs, one specific for M. agalactiae (14) and the other one globally targeting the members of the M. mycoides cluster (28). However, the identification of an isolate to the taxon level is important in order to survey the individual prevalence of taxa and the emergence of new molecular types (18). So far, PCR assays developed to distinguish M. capricolum subsp. capricolum from M. mycoides subsp. mycoides biotype Large Colony in a culture-independent manner were shown to be poorly specific (12). In this study, we applied an SSH approach to detect molecular differences existing between M. capricolum subsp. capricolum and M. mycoides subsp. mycoides biotype Large Colony type strains, with the ultimate goal of identifying candidate sequences for the design of taxon-specific PCR assays. The high relatedness of the subtracted strains and their very low %G+C content (24% for California Kid and an estimated 24% for Y-Goat ) were limiting factors for efficient SSH, and indeed only 34% (27/80) and 50% (40/79) of the subtracted fragments were shown to be specific for M. capricolum subsp. capricolum California Kid (SSH-A) and M. mycoides subsp. mycoides biotype Large Colony Y-Goat (SSH-B), respectively. Although only a part of the subtracted fragments was analyzed here, several fragments were found to overlap or to locate in the same genes, suggesting that they were representative of the overall genomic differences existing between Y-Goat and California Kid.
Subtracted sequences that were specific to the M. mycoides subsp. mycoides biotype Large Colony type strain Y-Goat were not found in some M. mycoides subsp. mycoides biotype Large Colony field isolates or cross-reacted with other members of the M. mycoides cluster. This result indicates that fragments obtained by SSH represent sequences that are highly variable not only between taxa but also within one taxon, such as insertion sequences (IS). This is in agreement with recent data obtained from the M. mycoides subsp. mycoides biotype Large Colony GM12 genomic draft sequence, which shows 91.5% identity with 76% of the M. capricolum subsp. capricolum California Kid genome, while the remaining 24% of the genome is composed mainly of IS (10). Thus, M. mycoides subsp. mycoides biotype Large Colony GM12, an isolate found in the United States that is considered to be serologically and biochemically equivalent to M. mycoides subsp. mycoides biotype Large Colony Y-Goat (6), and M. capricolum subsp. capricolum California Kid are not only highly related but also differ mainly in mobile, repeated elements, such as IS. In contrast, the overall specific genetic content of the Y-Goat type strain that was isolated in 1956 in Australia and that of current field strains from France may have diverged from a common ancestor. Indeed, hybridization patterns obtained in this study with SSH-B-subtracted fragments tend to indicate that the recent M. mycoides subsp. mycoides biotype Large Colony field isolates are not very similar to the Y-Goat type strain, since only 1 probe out of 18 reacted with all M. mycoides subsp. mycoides biotype Large Colony field strains while 10 probes reacted with Mycoplasma sp. bovine group 7 or M. capricolum subsp. capricolum. This observation is in agreement with the evolution of the clinical signs observed over time. In 1983, Cottew proposed a clear distinction of the body sites affected by M. mycoides subsp. mycoides biotype Large Colony (respiratory tract) and M. capricolum subsp. capricolum (joints and udder) (4), while in 1996 DaMassa was less definite (5) and reported the isolation of both M. mycoides subsp. mycoides biotype Large Colony and M. capricolum subsp. capricolum from the mouth, udder, joints, respiratory tract, and external ear; M. mycoides subsp. mycoides biotype Large Colony was isolated from the eyes as well. Although these differences might reflect an improvement in isolation and identification methods, they also may reflect the evolution of these organisms over the past 10 years. In this context, the genome description of the currently sequenced M. mycoides subsp. mycoides biotype Large Colony strain, a field strain isolated in France in 1995 (and the subject of an ongoing sequencing project by V. Barbe [Genoscope] and F. Thiaucourt [CIRAD]), will be very informative.
Six of the subtracted sequences isolated following SSH-A and specific for the California Kid type strain recognized all M. capricolum subsp. capricolum field strains that were included in set 1. This suggests that the California Kid type strain is more representative of the M. capricolum subsp. capricolum field isolates than is Y-Goat for M. mycoides subsp. mycoides biotype Large Colony field isolates. One fragment, A51, which specifically reacted with all M. capricolum subsp. capricolum strains used in this study, was further used to design a PCR assay, simpA51, for the identification of M. capricolum subsp. capricolum within the M. mycoides cluster. The validation of the specificity of the simpA51 assay was addressed using strains from the M. mycoides cluster with a greater emphasis on M. mycoides subsp. mycoides biotype Large Colony, which is the Mycoplasma taxon most frequently recovered from small-ruminant clinical samples in France (25), and Mycoplasma sp. bovine group 7, the closest phylogenetic relative of M. capricolum subsp. capricolum, which often gives cross-serological reactivity with M. capricolum subsp. capricolum in diagnoses derived from MF-dot analyses (12). The simpA51 PCR assay, performed with 133 representative strains and isolates of M. mycoides (48 M. capricolum subsp. capricolum strains and 85 non-M. capricolum subsp. capricolum strains), gave no ambiguous results. This contrasts with the previously developed PCR assay that targeted the lppA gene (16), which previously was shown to be of poor specificity on field isolates (12) and which, in our hands, gave false-negative results 40% of the time (Table (Table2).2). One drawback of the A51 PCR assay is that it does not discriminate the two M. capricolum subspecies, namely M. capricolum subsp. capricolum and M. capricolum subsp. capripneumoniae. In the alignment of the specific sequence targeted by A51 PCR from M. capricolum subsp. capricolum and M. capricolum subsp. capripneumoniae type strains, 90% identity was obtained, underlining the high genetic relatedness of the two subspecies. We solved this problem by multiplexing the A51 PCR with the PCR described by Woubit et al. (27) to exclude any non-M. capricolum subsp. capricolum isolates. Initially we did not include M. capricolum subsp. capripneumoniae strains in the set of strains used for the A51 PCR validation, since CCPP is regarded as an exotic pathology raging in some regions of Africa and the Middle East. However, a recent short communication showed that CCPP was getting closer to European frontiers, with recent outbreaks in Thrace, in the western part of Turkey (19). Therefore, the choice of using simpA51 or multA51 PCR for diagnosis will be determined by the local epidemiology.
Very recently, we became aware that an ortholog to the M. capricolum subsp. capricolum MCAP0862 gene that contains the A51 sequence is present in an M. mycoides subsp. mycoides biotype Large Colony strain currently being sequenced (F. Thiaucourt, personal communication). With an overall identity between the two genes of 65%, the sequence divergence between the two orthologs still opens the way for the design and validation of taxon-specific PCR assays. This finding not only allows us to confirm the high specificity of the A51 PCR but also illustrates the efficiency of the SSH approach to amplify specific chromosomic fragments despite the high genetic relatedness of subtracted strains.
We thank P. Cuchet and C. Bovo for their technical assistance in MF-dot experiments as well as L. Manso-Silvan, F. Thiaucourt (CIRAD, Montpellier, France), and P. Sirand-Pugnet (INRA and University of Bordeaux 2) for helpful discussions and for sharing data on mollicute genomes prior to publication. We also are very grateful to F. Thiaucourt's team for supplying DNA from M. capricolum subsp. capripneumoniae strains and Mycoplasma sp. bovine group 7 isolates and to P. Mercier (AFSSA, Niort, France) for supplying clinical isolates from goats.
Published ahead of print on 30 January 2008.