http://orcid.org/0000-0002-5698-5713
Figures
Abstract
Mycoplasma anatis, M. anseris, M. cloacale and M. sp. 1220 colonise geese and ducks, and could be associated with infections of avian respiratory and nervous systems, cause mild to severe inflammation of cloaca and genital tracts, and embryo lethality. Co-occurrence of these Mycoplasma species in waterfowl is frequently detected and the identification of these mycoplasmas to the species level at a regular microbiology laboratory is difficult due to their similar morphological, cultural and biochemical properties. Moreover, species differentiation is only possible based on the sequence analysis of the product of a genus-specific PCR assay. Therefore, the aim of the current study was to develop an effective and robust method for the identification of these species in avian clinical specimens. Polymerase chain reaction (PCR) assays using species-specific primers, which target housekeeping genes in order to identify these species, were designed in the present study. The developed PCR assays can precisely identify these four mycoplasmas to the species level directly from DNA samples extracted from clinical specimens, and no cross-amplification was observed among these species and with other well-known avian mycoplasmas. The average sensitivity of the assays was 101−102 genomic equivalents per reaction. These conventional PCR assays can be run simultaneously at the same PCR cycling program, and the species can be differentiated directly (without sequence analysis) by gel electrophoresis due to the specific sizes of the amplicons. In conclusion, the presented species-specific assays were found to be suitable for routine use at regular veterinary diagnostic laboratories and promote the rapid, simple and cost-effective differentiation of these waterfowl Mycoplasma species.
Citation: Grózner D, Sulyok KM, Kreizinger Z, Rónai Z, Jánosi S, Turcsányi I, et al. (2019) Detection of Mycoplasma anatis, M. anseris, M. cloacale and Mycoplasma sp. 1220 in waterfowl using species-specific PCR assays. PLoS ONE 14(7): e0219071. https://doi.org/10.1371/journal.pone.0219071
Editor: Ruslan Kalendar, University of Helsinki, FINLAND
Received: December 17, 2018; Accepted: June 14, 2019; Published: July 11, 2019
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: The genes were selected for the primer design from the complete genomes of M. anatis, M. anseris and M. cloacale type strains (GenBank accession numbers CP030141, CP030140 and CP030103, respectively). The rpoB gene sequences of M. sp. 1220 type strain and field isolates can be found under GenBank accession numbers EU596576 and MH003302 – MH003317, respectively. The sequences obtained from the type strains, isolates/strains and clinical specimens provided in the S1 File were deposited in NCBI GenBank under accession numbers MK532897 – MK532910.
Funding: This work was funded by the Lendület (Momentum) program (LP2012-22) of the Hungarian Academy of Sciences (http://mta.hu/lendulet/) and the Élvonal KKP_19 129751 grant of the National Research, Development and Innovation Office (https://nkfih.gov.hu/palyazoknak/nkfi-alap/tamogatott-projektek-kkp-19). MG and ZK were supported by the Bolyai János Research Fellowship of the Hungarian Academy of Sciences (http://mta.hu/bolyai-osztondij/bolyaijanos-kutatasi-osztondij-105319). MG was supported by the Bolyai+ Fellowship (ÚNKP-18-4) of the New National Excellence Program of the Ministry of Human Capacities (http://www.kormany.hu/hu/emberi-eroforrasok-miniszteriuma/oktatasert-felelos-allamtitkarsag). The funders provided support in the form of salaries for authors DG, KMS, ZK, ÁBK and MG, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The TOLL 96 Kft. provided support in the form of salaries for MJK, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘authors contributions’ section.
Competing interests: The TOLL 96 Kft. provided support in the form of salaries for MJK. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
Introduction
Mycoplasma anatis, M. anseris, M. cloacale and M. sp. 1220 are well-known waterfowl mycoplasmas. M. anatis, M. anseris, and M. cloacale are well-characterized, validly published species [1–3], while M. sp. 1220 has been isolated in 1983 in Hungary from a goose with clinical inflammation of the phallus [4] but not validly published yet as a novel species. However, biochemical, cultural, morphological and serological properties of M. sp. 1220 were comprehensively studied [4,5], which allowed for considering this microorganism as an independent Mycoplasma species, with a proposed name M. anserisalpingitis [6–8]. All these mycoplasmas could be a part of the normal microflora of geese and ducks, which do not demonstrate any clinical signs of mycoplasma infection (i.e., inapparent infections or carriers); however, these Mycoplasma species are also associated with some pathological conditions in waterfowl. Clinically manifested mycoplasmosis caused by these Mycoplasma species can occur in waterfowl during excessive stress, such as inadequate housing, crowding or extensive egg production [9–11], or due to inappropriate hygienic conditions and inadequate access of waterfowl to water. M. anatis could cause infection associated with neurological symptoms in ducks under stress conditions [12]. Airsacculitis, peritonitis and increased embryo lethality were also described in experimental infection studies in ducks infected with M. anatis [13]. However, M. anatis was also isolated from healthy geese [14]. M. anseris was associated with airsacculitis, peritonitis and embryo lethality in geese [11] and might have a role in the cloaca and phallus inflammation of ganders [7]. M. cloacale was associated with egg infertility in geese [10] but could be also isolated from healthy ducks, geese and other bird species [1,4,14,15]. Infections of geese with M. sp. 1220 cause the most significant production and economical losses in the goose farming business, especially in Central and Eastern European countries where the goose production is particularly popular [7,8,16,17]. Cloaca and phallus inflammation, salpingitis, airsacculitis, peritonitis and embryo lethality are the most frequent symptoms in the affected geese flocks [10,11,16,18,19]. All these four Mycoplasma species are well-known to be mainly vertically transmitted [7,11,20,21]. Co-occurrence (or co-infection) of M. anseris, M. cloacale and M. sp. 1220 in geese has been frequently observed [7,9]. Co-infections of waterfowl with these mycoplasmas together with other bacterial or viral pathogens may lead to more severe disease manifestations and their consequence [22,23].
The species pairs, M. anatis and M. sp. 1220, and M. anseris and M. cloacale have undistinguishable biochemical properties (phosphatase-positive glucose-utilizers and phosphatase-negative arginine-hydrolysers, respectively) and all isolates/strains of these species have typical “fried-egg” colony morphology on solid media. Practically, these species could be identified using serological testing via growth inhibition test (GIT) and immunofluorescent antibody test (IFA); however, these tests are time-consuming, require pure culture of isolates and the qualified reference antisera, which are not available at regular veterinary laboratories in most countries either due to absence of national veterinary mycoplasma reference centres or due to a limited use of animals for production of antibody reagents [4,9,14]. Therefore, the characterisation of the phenotypic features of these mycoplasmas is not sufficient for their routine identification to the species level [4,8]. However, their identification to the species level is essential for deeper understanding of their epidemiology and transmission, and for control and eradication of these infections in commercial waterfowl flocks, as well as for the development of experimental vaccines (e.g. against M. sp. 1220 in geese [24]) and assessment of their clinical efficacy.
The identification of these mycoplasmas to the species level is possible with the use of the Mycoplasma genus-specific PCR assay, which targets the 16S-23S rRNA intergenic transcribed spacer region (ITS) [25]; however, in this case the species identification is based on direct sequencing of obtained PCR amplicons that is not always feasible at regular veterinary laboratories, requires additional reagents and skills, and practically impossible for PCR products amplified from birds simultaneously co-infected with different mycoplasmas. To the best of our knowledge, no M. anatis-, M. anseris- or M. cloacale-specific PCR assays have been published, and only one study on the species-specific PCR detection and phylogenetic identification of M. sp. 1220 isolates in geese from the Russian Federation and Ukraine has been published [8]. The aim of the present study was to improve the detection of these mycoplasmas to the species level by developing species-specific PCR assays, which could be suitable for the robust detection of these mycoplasmas in clinical specimens obtained from waterfowl species.
Materials and methods
Selection of species-specific regions
In order to design species-specific primers for detection of M. anatis, M. anseris, M. cloacale and M. sp. 1220, several housekeeping genes were randomly selected from the mycoplasma minimal genome set [26,27], which are presented in the genomes of the examined species. The sequences of the selected genes (listed below) were obtained from the recently published complete genomes of M. anatis, M. anseris and M. cloacale type strains [28]. The same genes of M. sp. 1220 type strain (ATCC BAA-2147) were obtained from the whole-genome sequence determined by de novo sequencing in our laboratory using the Illumina (Illumina Inc., San Diego, USA) next generation sequencing platform (unpublished data). Also, the rpoB gene sequences of M. sp. 1220 type strain and M. sp. 1220 field isolates were previously determined by our group and can be found under GenBank accession numbers EU596576 and MH003302—MH003317, respectively. The genome annotation for these species was performed using the RAST software [29]. The following 16 genes were selected for the analysis for the species-specific regions: the acetate/propionate family kinase (ackA), cytidine deaminase (cdd), DNA polymerase III subunit gamma/tau (dnaX), DNA-directed RNA polymerase subunit beta (rpoB), glucose-6-phosphate isomerase (pgi), ribulose-phosphate 3-epimerase (rpe), ATP-dependent DNA helicase (pcrA), and transcriptional regulator (mraZ) genes. Based on our genome analysis, these genes are presented in genomes of all these four Mycoplasma species. In addition, the genes that were found to be unique only for some studied Mycoplasma species were also included in this analysis. Thus, the 1-phosphofructokinase (pfkB), beta-phosphoglucomutase (pgmB), phosphoenolpyruvate-protein phosphotransferase (ptsP) and UTP-glucose-1-phosphate uridylyltransferase (gtaB) genes are presented only in the genomes of M. anatis and M. sp. 1220 type strains. The arginine deiminase (arcA) and 5'-methylthioadenosine nucleosidase (mtn) genes appeared only in the genomes of M. anseris and M. cloacale type strains. The thymidylate synthase (thyA) and deoxycytidylate deaminase (comEB) genes were only found in genomes of M. anatis and M. anseris type strains, respectively. Based on the genome analysis, all these genes are presented as a single copy in the genomes of these four mycoplasmas.
Primer design
The sequences of the selected genes were aligned and analysed using the Geneious software [30]. The genes were manually analysed and the primer pairs were designed according to the following three main acceptance criteria: (i) the gene of interest should have at least two regions (20–30 bp) containing as many species-specific nucleotide substitutions as possible, and these short sequence regions should be suitable for design of species-specific primers, i.e., to have similar melting temperatures, and do not form hairpin, or self- and cross-dimers, (ii) the distance between the primers’ regions should be approx. 500–1000 bp, and (iii) the selected species-specific primers should be able to amplify the target gene from all tested isolates/strains of the same species but not from others. Primer design was performed using the NetPrimer software (http://www.premierbiosoft.com/netprimer). The specificity of the primers was analysed in silico using BLAST NT algorithm (https://blast.ncbi.nlm.nih.gov/Blast.cgi), as well as in vitro to demonstrate a possibility for any cross-amplification among the tested species and with other Mycoplasma/Acholeplasma species that could be found in avian clinical specimens (Table 1).
Development of species-specific PCR assays
To evaluate the PCR assays designed in this study, a total of 57 Mycoplasma isolates/strains were used (Table 1). The type strains were obtained from the reference collections (ATCC and NCTC), and field isolates were previously obtained by the authors during routine diagnostic examinations of clinical specimens from domestic geese, ducks and chickens and from wild ducks. In addition, 28 clinical specimens, including cloaca swabs, follicule tissue, trachea tissue, phallus lymph, and sperm, were also examined in this study (Table 2). These samples were collected during routine clinical examinations or at necropsies of geese and ducks. No ethical approval was required for these sample collections. The tested Mycoplasma field isolates and the avian clinical specimens were collected mainly in Hungary between 2003 and 2018 (Table 1). DNA was extracted from the isolates/strains and the clinical specimens using the QIAamp DNA Mini Kit (Qiagen Inc., Hilden, Germany) according to the manufacturers’ instructions. The primary screening and identification of the 57 Mycoplasma isolates/strains were performed by the genus-specific PCR assay [25] followed by direct sequencing of the produced amplicons on ABI Prism 3100 automated DNA sequencer (Applied Biosystems, Foster City, USA), and by nucleotide sequence analysis in BLAST database. The 28 clinical specimens were also primary screened for the presence of Mycoplasma DNA using the genus-specific PCR [25], and then these samples were further investigated using the species-specific PCRs developed in this study.
The species-specific PCR assays were carried out in 25 μl total volume, containing 2 μl target DNA sample, 5 μl 5X Green GoTaq Flexi Buffer (Promega Inc., Madison, WI), 2 μl MgCl2 (25mM), 0.5 μl dNTP (10 mM, Qiagen Inc., Hilden, Germany), 2 μl of each primer (10 pmol/μl) and 0.25 μl GoTaq DNA polymerase (5 U/μl). The final primer set was selected based on specificity and sensitivity criteria detailed in section “Assessment of specificity and sensitivity of the developed assays”. The sequences of the designed primers and the sizes of the species-specific amplicons are provided in Table 3 (Fig 1). The actual sequences of the species-specific amplicons are provided in the S1 File. Thermocycling parameters were 95°C for 5 min, followed by 40 cycles at 95°C for 1 min, 61°C for 1 min and 72°C for 1 min and a final elongation step was performed at 72°C for 5 min. Detection of PCR products with the expected molecular weights were confirmed by electrophoresis in 1% TBE-agarose gel stained with ECO Safe Nucleic Acid Staining Solution (Pacific Image Electronics Co., Ltd, New Taipei City, Taiwan) followed by UV visualization. Ultrapure water was used as a negative control matrix in parallel to monitor for cross-contamination. The amplification quality of extracted mycoplasma DNA was tested using the genus-specific PCR primers [25].
Abbreviations: m—molecular weight marker (GeneRuler 100 bp Plus DNA Ladder, Thermo Fisher Scientific, Waltham, USA); Mana—product from the M. anatis-specific assay; Mans—product from the M. anseris-specific assay; Mclo—product from the M. cloacale-specific assay; M1220—product from the M. sp. 1220-specific assay; nc—negative control.
Assessment of specificity and sensitivity of the developed assays
The specificity of the PCR assays was analysed by DNA testing of the following avian Mycoplasma and Acholeplasma type strains: M. anatis (NCTC 10156), M. anseris (ATCC 49234), M. cloacale (NCTC 10199), M. columbinasale (ATCC 33549), M. columborale (ATCC 29258), M. gallinaceum (ATCC 33550), M. gallinarum (ATCC 19708), M. gallisepticum (ATCC 19610), M. gallopavonis (ATCC 33551), M. iners (ATCC 19705), M. iowae (ATCC 33552), M. meleagridis (NCTC 10153), M. pullorum (ATCC 33553), M. sp. 1220 (ATCC BAA-2147), M. synoviae (NCTC 10124) and Acholeplasma laidlawii (NCTC 10116).
In order to test the sensitivity of the PCR assays, all designed primer pairs were tested with the corresponding DNA of the M. anatis (NCTC 10156), M. anseris (ATCC 49234), M. cloacale (NCTC 10199) and M. sp. 1220 (ATCC BAA-2147) type strains 10-fold serially diluted (106−100) in nuclease-free water. Template copy numbers (corresponding to genomic equivalents or GE in the current study) per reaction for these strains were calculated based on the used DNA concentrations using an online dsDNA copy number calculator (https://cels.uri.edu/gsc/cndna.html) and the following genome size information: 956,093 bp for M. anatis (GenBank accession number CP030141), 750,010 bp for M. anseris (CP030140), 659,552 bp for M. cloacale (CP030103) and 908,787 bp for M. sp. 1220.
During the selection of the final primer set, primers which demonstrated cross-amplification between the tested Mycoplasma/Acholeplasma strains were excluded from further study. The sensitivity of the PCR assays using different primer pairs for the detection of a certain waterfowl Mycoplasma species were compared visually during gel electrophoresis. Primer pairs showing the highest sensitivity and specificity were chosen for the final study.
In order to evaluate the performance of the designed assays in mixed infections, the DNA of the waterfowl Mycoplasma type strains (containing 106 GE) were mixed in a ratio of 1:1:1:1 and tested. Also, DNA mixes were created with one DNA sample containing 103 GE and the other three are represented with 106 GE in a ratio of 1:1:1:1, and submitted to the corresponding waterfowl Mycoplasma-specific assay (i.e. DNA mix of 103 GE M. anatis, 106 GE M. anseris, 106 GE M. cloacale and 106 GE M. sp. 1220 in the M. anatis-specific PCR assay).
Confirmation of the assays’ specificity by PCR amplicon sequencing
In order to demonstrate that the obtained PCR products were species-specifically amplified we performed direct DNA sequencing of all amplicons from the type strains and amplicons generated from some selected isolates/strains and clinical specimens. All PCR products amplified from goose specimens using the M. anatis-specific PCR assay (i.e., MYCAV 314 and 317 isolates and clinical specimens No. 2, 3, 5, 7) were also sequenced to confirm their species identity because the presence of M. anatis in geese is not commonly reported. Randomly selected amplicons were also sequenced from the M. anseris- and M. cloacale-specific PCRs to verify their species identity (clinical specimens No. 1 and 6, respectively). In the case of the M. sp. 1220-specific PCR, product of the MYCAV 47 isolate originating from a duck, and a randomly selected amplicon (clinical specimen No. 21) were sequenced to confirm their species identity. The Mycoplasma genus-specific PCR products of clinical specimens No. 1, 13, 25 and 28, which according to the results of the developed species-specific PCR assays represented mixed mycoplasma DNA samples due to natural mycoplasma co-infections in geese, were also sequenced in order to analyse their DNA sequence chromatograms for the presence of mixed sequences. All analysed amplicons were purified using the QIAquick PCR Purification Kit (Qiagen Inc., Hilden, Germany) and directly sequenced with the same primers used for their PCR amplification. The sequences obtained from the type strains, isolates/strains and clinical specimens are deposited in GenBank under accession numbers MK532897 –MK532910.
Results
Sixteen mycoplasma housekeeping genes were analysed in the study, out of which eight genes were found suitable for the design of species-specific primers based on the above-mentioned acceptance criteria. Therefore, the species-specific primers were designed for the following genes: the dnaX, pgmB, ptsP and thyA genes to detect M. anatis; the dnaX, pcrA and mtn genes to detect M. anseris; the dnaX and mtn genes to detect M. cloacale; and the rpoB, pfkB and pgmB genes to detect M. sp. 1220. These primary PCR assays based on these designed primers showed species-specificity in silico; however, in vitro analyses revealed cross-amplification among the species in one case (between M. anatis and M. anseris, primer sequences 5’ TCAAATTCAAAAATTGTTCCTTGC 3’ and 5’ ATGTGTTCTAATTGAAGCCATTTTAAT 3’ specific for dnaX gene), which was excluded from further examinations. The rest of the omitted primers showed one- to two-fold lower sensitivity in the species-specific PCR amplification based on UV visualization, hence, they were excluded from further analyses. According to the combined results on the primers specificity and sensitivity performed by testing the DNA samples of the mycoplasma type strains, PCR assays, which did not demonstrate any cross-amplification with other tested Mycoplasma/Acholeplasma strains and showed superior sensitivity, were selected as the final assays. The dnaX gene-based PCR assays were the most suitable for precise species identification of M. anatis and M. cloacale (sensitivity of these assays was 102 GE per reaction), the pcrA gene-based PCR assay was accepted for species identification of M. anseris (sensitivity of 101 GE per reaction), and the rpoB gene-based PCR assay was suitable for precise identification of M. sp. 1220 (sensitivity of 102 GE per reaction). As end-point PCR systems were designed in the study, the yield of a PCR product does not provide quantity result after UV visualization. However, the visual detection of the PCR products in the sensitivity tests means that the minimum GEs detectable in the samples are 101 in the case of M. anseris-specific PCR and 102 in the cases of M. anatis-, M. cloacale- and M. sp. 1220-specific assays. The similarity between the dnaX gene of M. anatis and M. cloacale is 51.32% and the highest similarity among the bonding sites of the M. anatis- and M. cloacale-specific primer pairs is 54.55%; therefore, cross-amplification among the two species in the specific PCR assays is unlikely. Species identification was successful in all cases during the tests of the M. anatis, M. anseris, M. cloacale and M. sp. 1220 type strain DNA mixes, the presence of the other waterfowl pathogen mycoplasmas did not have any effect on the assays’ performance.
The result of the species-specific PCRs obtained with the testing of 28 clinical specimens is provided in Table 2. Among the 28 clinical specimens 5 were negative in all PCR assays, 4 specimens were positive for one Mycoplasma species, 9 specimens for two species, other 9 specimens for three species and one specimen was positive for all tested Mycoplasma species. Sequences of the amplicons obtained from these species-specific assays on the clinical specimens and isolates/strains showed their 97.7–100% identity with the corresponding sequences of the type strains (Tables 2 and 3, and the S1 File), confirming that the assays were able to amplify the gene regions specific to the given species.
The Mycoplasma genus-specific PCR [25] amplified PCR products of approx. 460 bp from M. anatis and M. sp. 1220, and smaller products of approx. 370 bp from M. anseris and M. cloacale. This assay revealed two amplicons at the corresponding molecular weights when M. anatis / M. sp. 1220 and M. anseris / M. cloacale co-occurred in the samples, with the exception of three samples. In these three cases (No. 1, 13 and 28) a single amplicon was amplified by the genus-specific PCR assay, while the species-specific PCR assays were able to detect mixed infections of M. sp. 1220, along with M. anseris and/or M. cloacale in these geese (Table 2). Moreover, both M. anseris and M. cloacale were detected in a clinical specimen (No. 25) by the developed assays, which showed the same amplicon size by the genus-specific PCR assay. The DNA sequence chromatogram analysis performed on the genus-specific PCR amplicons from the clinical samples No. 1 and 25 revealed major sequences of M. sp. 1220 and M. anseris, respectively, with evidence of well-visible secondary peaks indicating a mixed DNA sequence due to the natural co-infections. However, the DNA sequence chromatogram analysis performed on the genus-specific PCR amplicons from the clinical samples No. 13 and 28 also revealed major sequences of M. sp. 1220 and M. anseris, respectively, but did not demonstrate any detectable mixed sequences (S2 File). This discrepancy between the results of the Mycoplasma genus-specific PCR and the developed species-specific PCR assays could be associated with a substantial difference of these assays in term of their detection specificity and/or sensitivity for different Mycoplasma species, especially if the analysed mycoplasma sample presents a mixed DNA sample (see discussion below).
Discussion
M. anatis, M. anseris, M. cloacale and M. sp. 1220 can cause infections in waterfowl clinically manifested with respiratory and neurological symptoms, inflammation of cloaca and genital tracts, and embryo lethality, which eventually result in significant economic and poultry production losses. Co-infection of waterfowl with these Mycoplasma species that share similar phenotypic characteristics is frequent, and therefore the isolation of pure culture and the precise identification of these species by biochemical and serological tests are challenging issues in routine veterinary laboratories. The species-specific PCR assays developed in the present study enable the species-specific identification of these waterfowl Mycoplasma species and expedite laboratory diagnosis of these infections (including mixed infections), providing valuable support for the selection and the use of adequate control and/or feasible treatment of affected birds [31,32].
The nucleotide sequences of the 16S rRNA genes of M. anatis and M. sp. 1220 demonstrate significant similarity (90.5% according to Sprygin et al., 99.1% based on our observation) and therefore cannot be used for the unambiguous differentiation between these two species [8]. Also, the high percentage of similarity of the 16S rRNA genes and the 16S-23S rRNA ITS sequences between M. anseris and M. cloacale (98.3% and 87.3%, respectively) [33] makes these genetic markers less suitable for precise identification of these species. The previously published PCR assays targeting these genetic regions for the detection of mycoplasmas [25,34–36] demonstrated low reliability in the identification of waterfowl Mycoplasma species. Moreover, these methods almost always require the direct sequencing of amplicons for the species confirmation, which can be difficult or impossible in cases of co-infections with different Mycoplasma species, as well as in laboratories in which DNA sequencing technologies are not available.
The Mycoplasma genus-specific PCR assay [25] provides different amplicon sizes for certain Mycoplasma species (e.g. 90bp difference between amplicon sizes of M. anatis / M. sp. 1220 and M. anseris / M. cloacale) due to the length variation of the 16S-23S rRNA ITS among the species [33]. Therefore, amplicons at different molecule weights already indicate co-occurrence of mycoplasma species. However, the detection of only one amplicon does not necessarily mean the presence of only one species, and in certain cases even the analysis of the chromatograms could not indicate the presence of co-occurring species. In the current study, comparison of the results of the primary screening of clinical samples using the genus-specific PCR assay with the results of the developed species-specific PCR assays revealed discrepancies in certain cases. The observed differences could be the consequences in the ratio between the mixed DNAs presented in the clinical samples, which can influence their equally efficient detectability [37]. The presented results confirm that the 16S-23S ITS-based PCR assay is well suitable for primary detection or screening of clinical specimens for the presence of mycoplasma DNA; however, it is unsuitable for the detection and identification of all presented species in samples from mixed mycoplasma infection cases, which could be common. This observation highlights the importance of the utilisation of other genetic targets to avoid potential false identifications and incorrect diagnostic results for mycoplasma detection in clinical specimens.
M. sp. 1220 represents a serious threat to the geese industry, especially in Central and Eastern Europe, therefore the detection of this agent is required for a comprehensive laboratory diagnostic analysis of goose clinical specimens. Previous attempts have been made to design primers for the detection and specific identification of this species based on the sequences of the rpoB, DNA polymerase III subunit alpha (dnaE), elongation factor (fusA), and the pyruvate kinase (pyk) genes [8]; however, those primers were not analysed for the detection sensitivity of M. sp. 1220 in avian clinical samples. The primers for the M. sp. 1220-specific PCR assay described in this study also target the rpoB gene but the sensitivity of the assay was established to ensure its applicability for the diagnostic use.
The PCR assays developed in this study were able to identify these Mycoplasma species in new or rarely-observed waterfowl hosts. According to the available literature M. sp. 1220 has been previously isolated only from geese [7]; however, in this study this species was also identified in a domestic duck using the Mycoplasma genus-specific PCR [25] and this result was confirmed by the newly designed species-specific PCR assay, as well as, by the DNA sequence analysis of the PCR amplicons. Fibrin deposition on the visceral serous membranes of the duck in this case was also consistent with the pathological evidences observed in M. sp. 1220-infected geese [19]. To our best knowledge this is the first official isolation of M. sp. 1220 (isolate MYCAV 47) from an avian species other than goose. The partial rpoB gene (1997 bp long) was also sequenced for this M. sp. 1220 isolate (MYCAV 47; GenBank accession number MH003302) using primers and conditions described previously [33], and the nucleotide sequencing analysis demonstrated its 99% identity to the rpoB gene of the type strain of M. sp. 1220.
M. anatis normally colonises ducks and it was rarely detected in geese [7,14]. In the present study, eight M. anatis isolates were identified in the tested specimens out of which two isolates originated from geese (MYCAV 314 and 317). The observed pathological changes such as the fibrinous peritonitis and lymphohistiocytic infiltration in the lungs of these geese were similar to the pathological evidences reported for M. anatis-infected ducks [12]. Moreover, 15% (n = 4/26) of the examined clinical specimens from geese were found to be positive for M. anatis according to our results generated using the newly designed species-specific PCR assays. DNA sequence analysis of the dnaX amplicons from the two isolates and the four clinical specimens revealed their 97.7–97.9% sequence identity to the same gene of M. anatis type strain (S1 File). This high level of nucleotide identity is sufficient for the identification to the species level and demonstrates the adequate detection specificity of the M. anatis-based PCR assay. In addition, the partial rpoB gene (1994 bp long) was also sequenced for these two M. anatis isolates originated from geese (MYCAV 314 and 317; GenBank accession numbers MH003311 and MH003313, respectively) using primers and conditions as mentioned above, and the corresponding sequencing result demonstrated their 99% identity to the rpoB gene of the type strain of M. anatis. Thus, the species identity of M. sp. 1220 isolate from a duck and M. anatis isolates from geese was clearly demonstrated in both cases.
The developed assays clearly discriminated the targeted waterfowl pathogen Mycoplasma species in the examined samples, isolates and type strains; however, as the majority of the samples originated from a restricted geographic region, further examinations on a wider selection of samples would enable the determination of the robustness of the assays.
Finally, the species-specific PCR assays developed in the current study showed high sensitivity and specificity, enabling rapid, precise and reliable identification of these four Mycoplasma species in waterfowl specimens, and therefore proved to be suitable and cost-effective method for the identification of these mycoplasmas in routine veterinary laboratory diagnostics. In addition, these assays can be run simultaneously using the same thermal cycling PCR conditions on conventional PCR equipment.
Supporting information
S1 File. Comparison of nucleotide sequences of the amplicons generated for the type strains, field isolates and mycoplasma amplicons detected in clinical specimens using the designed species-specific PCR assays.
Primers (grey) and single nucleotide polymorphisms (black) are highlighted in the sequences.
https://doi.org/10.1371/journal.pone.0219071.s001
(PDF)
S2 File. Comparison of DNA sequence chromatograms from samples with natural co-infections generated by the Mycoplasma genus-specific PCR assay.
https://doi.org/10.1371/journal.pone.0219071.s002
(PDF)
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