Complete mitochondrial genome sequences from five Eimeria species (Apicomplexa; Coccidia; Eimeriidae) infecting domestic turkeys
© Ogedengbe et al.; licensee BioMed Central Ltd. 2014
Received: 14 May 2014
Accepted: 11 July 2014
Published: 17 July 2014
Clinical and subclinical coccidiosis is cosmopolitan and inflicts significant losses to the poultry industry globally. Seven named Eimeria species are responsible for coccidiosis in turkeys: Eimeria dispersa; Eimeria meleagrimitis; Eimeria gallopavonis; Eimeria meleagridis; Eimeria adenoeides; Eimeria innocua; and, Eimeria subrotunda. Although attempts have been made to characterize these parasites molecularly at the nuclear 18S rDNA and ITS loci, the maternally-derived and mitotically replicating mitochondrial genome may be more suited for species level molecular work; however, only limited sequence data are available for Eimeria spp. infecting turkeys. The purpose of this study was to sequence and annotate the complete mitochondrial genomes from 5 Eimeria species that commonly infect the domestic turkey (Meleagris gallopavo).
Six single-oocyst derived cultures of five Eimeria species infecting turkeys were PCR-amplified and sequenced completely prior to detailed annotation. Resulting sequences were aligned and used in phylogenetic analyses (BI, ML, and MP) that included complete mitochondrial genomes from 16 Eimeria species or concatenated CDS sequences from each genome.
Complete mitochondrial genome sequences were obtained for Eimeria adenoeides Guelph, 6211 bp; Eimeria dispersa Briston, 6238 bp; Eimeria meleagridis USAR97-01, 6212 bp; Eimeria meleagrimitis USMN08-01, 6165 bp; Eimeria gallopavonis Weybridge, 6215 bp; and Eimeria gallopavonis USKS06-01, 6215 bp). The order, orientation and CDS lengths of the three protein coding genes (COI, COIII and CytB) as well as rDNA fragments encoding ribosomal large and small subunit rRNA were conserved among all sequences. Pairwise sequence identities between species ranged from 88.1% to 98.2%; sequence variability was concentrated within CDS or between rDNA fragments (where indels were common). No phylogenetic reconstruction supported monophyly of Eimeria species infecting turkeys; Eimeria dispersa may have arisen via host switching from another avian host. Phylogenetic analyses suggest E. necatrix and E. tenella are related distantly to other Eimeria of chickens.
Mitochondrial genomes of Eimeria species sequenced to date are highly conserved with regard to gene content and structure. Nonetheless, complete mitochondrial genome sequences and, particularly the three CDS, possess sufficient sequence variability for differentiating Eimeria species of poultry. The mitochondrial genome sequences are highly suited for molecular diagnostics and phylogenetics of coccidia and, potentially, genetic markers for molecular epidemiology.
KeywordsPoultry coccidiosis Evolution Mitochondrial DNA Parasitology Diagnosis
As many as seven Eimeria species, Eimeria dispersa, Eimeria meleagrimitis, Eimeria gallopavonis, Eimeria meleagridis, Eimeria adenoeides, Eimeria innocua and Eimeria subrotunda, can cause coccidiosis in the turkey, Meleagris gallopavo. Coccidiosis is widespread and pathogenic with considerable economic losses to the poultry industry[2, 3]. These parasites possess morphotypes of oocysts with overlapping biological features that make identification, characterization and diagnosis challenging[4, 2]. Delimiting individual species using morphological features, even when supplemented by 18S rDNA or internal transcribed spacer (ITS) sequence data, has been reported to be less than ideal for coccidia, especially for closely related parasites[5–10]. Sequences from the mitochondrial cytochrome c oxidase subunit I gene (mtCOI) have been shown to be reliable for delimiting closely related species and the mtCOI locus appears to lack paralog issues associated with rDNA of these parasites.
A single, complete mitochondrial (mt) genome copy for parasites within the Apicomplexa is about 6 KB long[11, 12]. Genome organisation varies considerably among eukaryotes in general and also within the Apicomplexa[13, 14]. Among apicomplexan parasites, genome structures that have been reported include linear concatemers[15, 16], linear genomes with terminal inverted telomeric repeats[17, 18] and circular genomes[12, 19]. Regardless of overall genome structure, all apicomplexan mt genomes examined to date possess three genes encoding cytochrome c oxidase subunit I (COI), cytochrome c oxidase subunit III (COIII) and cytochrome b (CytB), as well as numerous fragments of discontinuous and scrambled small subunits (SSU) and large subunit (LSU) rDNA. The specific LSU and SSU rDNA fragments found in the mt genome of apicomplexan parasites differ among distantly related parasites. Unlike many eukaryotic mt genomes, apicomplexan mt genomes do not encode 5S rRNA or tRNAs[20–24].
In the present study we report six new PCR generated, complete mt genome sequences from single oocyst derived lines of five Eimeria species infecting turkeys: Eimeria dispersa Briston strain, Eimeria meleagrimitis USMN08-01 strain, Eimeria gallopavonis Weybridge strain, Eimeria gallopavonis USKS06-01 strain, Eimeria meleagridis USAR97-01 strain and Eimeria adenoeides Guelph strain.
Six single oocyst-derived lines of five Eimeria species were used in this study. A description of the origins of the original isolates from which each line was derived is provided by El Sherry et al.. The resulting lines used were as follows: 1) Eimeria adenoeides Guelph strain in submission, for biological features of the line), 2) Eimeria dispersa Briston strain; 3) E. meleagrimitis USMN08-01 strain see[27, 28] for biological features); 4) E. meleagridis USAR97-01 strain see, for biological features); 5) E. gallopavonis Weybridge strain see for biological features); and 6) E. gallopavonis USKS06-01 strain. All lines were derived from parent isolates using the method of Remmler and McGregor with the modification that agar plugs carrying a single oocyst were given within gelatin capsules orally to specific-parasite free poults. All animal experimentation was conducted in SPF birds at the Campus Animal Facility, (University of Guelph, Guelph ON, Canada); all experimental procedures were reviewed and approved by the University of Guelph’s Animal Care Committee and complied with the Canadian Council on Animal Care’s Guide to the Care and Use of Experimental Animals (2nd edition).
DNA extraction and long PCR amplification
Purification of oocysts and genomic DNA extraction was carried out as previously described by Ogedengbe et al.[9, 24]. Mitochondrial whole genome amplification for all five Eimeria species was initiated using two sets of specific primers that generated overlapping PCR fragments: 1) Cocci_MT-WG-F (5′-TACACCTAGCCAACACGAT-3′) and Cocci_MT-WG-R (5′-GCAGCTGTAGATGGATGCTT-3′); and, 2) Inv_COI_262R (5′-AAWGCGGCATCRTAGAATTG-3′) and Inv_COI_461F (5′-CTAGCYATGGGATGTATTACTG-3′). Primers were designed from highly conserved regions within publically available mitochondrial genome sequences for Eimeria species infecting chickens (see Ogedengbe et al. 2013 for the species used in the primer design). The primer pairs Inv_COI_461F and Inv_COI_262R annealed 148 bp apart at bp 2069-2090 and bp 1920-1901 respectively, and the primer pairs Cocci_MT-WG-F and Cocci_MT-WG-R annealed 97 bp apart at bp 6322-6340 and bp 6224-6205, respectively, on the published mitochondrial genome sequence of Eimeria mitis [GenBank: KF501573]. Each pair of primers was used independently in a 50 μl reaction. PCR reactions using QIAGEN LongRange PCR kit (QIAGEN, Valencia, CA, USA) protocol according to the manufacturer’s instructions with the modification that an additional 1.5 mM MgCl2 was added to the PCR buffer provided by the manufacturer. For each Eimeria species, long PCR reactions consisted of ~200 ng genomic DNA template (when using the Inv_COI_461F/Inv_COI_262R primers), and 25 ng genomic DNA template (when using primers Cocci_MT-WG-F and Cocci_MT-WG-R), 1× LongRange PCR buffer, 4 mM MgCl2, 500 μM of each dNTP, 2U LongRange PCR enzyme mix and 0.4 μM of each primer. The PCR reaction profile consisted of denaturing at 93°C for 3 min followed by 35 cycles of 93°C for 15 s, 50°C for 30 s, 68°C for 6 min with a final extension cycle of 68°C for 10 min in an MJ mini thermal cycler (Bio Rad, CA, USA). PCR products were electrophoresed at 50 V through a 0.8% agarose gel prepared with 1 × TAE buffer containing ethidium bromide. DNA bands were viewed using UV transillumination (Spectronics Corporation, New York, USA) and their sizes were compared to a 100 bp to 10 kb DNA ladder (Bio Basic Inc., Mississauga ON, Canada). DNA bands were excised from the gel and purified using a QIA quick gel extraction and purification kit (Qiagen, Toronto ON, Canada) according to the manufacturer’s instruction.
Purified PCR products were sequenced in both directions using a primer-walking strategy to generate near–complete mitochondrial genomes essentially as described by Ogedengbe et al.. Sequencing was carried out using the ABI PRISM 7000 Sequence Detection System (Applied Biosystem Inc., Foster City, CA, USA) at the Laboratory services Division, University of Guelph (Guelph, ON, Canada).
Sequence data assembly and analysis
The de novo sequence assembler within Geneious bioinformatics software (Version 6.1 and later versions, available from http://www.geneious.com) was used to trim and assemble Sanger sequencing chromatograms into high quality contigs for the primary PCR product from each species. To complete each mt genome, PCR products were generated using a reverse primer downstream of the original forward primer (i.e. Cocci_MT-WG-F or Inv_COI_461F) and a forward primer upstream of the original reverse primer (i.e. Cocci_MT-WG-R or Inv_COI_262R, respectively); primers were designed such that a minimum of 100 bp of the resulting fragment overlapped the original long PCR product at each end. Each resulting PCR product was sequenced in both directions and the resulting consensus sequence was used to fill in the region between the two original long PCR amplification primers. The coding genes and rDNA fragments were first mapped by comparison with other Eimeria mt genomes (i.e. E. tenella AB564272, annotated by Hikosaka et al., and E. mitis KF501573, annotated by Ogedengbe et al.. Additional putative rDNA fragments were identified by comparing well conserved unannotated regions found in all of the aligned Eimeria sp. genomes to the mt genome of Plasmodium falciparum (M76611). Sequence identity between such conserved regions and rDNA fragments from P. falciparum greater than 60% were mapped as putative rDNA fragments. Putative start and stop codon positions for each of the coding DNA sequences (CDS) were identified following methods previously described by Ogedengbe et al.. Translations using the mold/protozoan mitochondrial codon translation (i.e. translation_table_4) were searched using Blastp against the non redundant sequence database to confim the identity of the translation product produced by each CDS. Base compositions and nucleotide changes within the CDS among the six mt genome sequences were analysed from within the Geneious software package.
The six newly generated, PCR–based mt genome sequences of Eimeria spp infecting turkey: Eimeria dispersa Briston strain; E. meleagrimitis USMN08-01 strain; E. meleagridis USAR97-01 strain; E. adenoeides Guelph strain and E. gallopavonis Weybridge strain; E. gallopavonis USKS06-01 strain were aligned with the 10 publically available complete mt genome sequences from seven Eimeria spp. infecting chickens and Eimeria magna that infects rabbits (i.e. all available apicomplexan taxa that had the same genome structure). Three sequences of Eimeria mitis (KCE409029; KC409030 and KC409031) generated from clones were not included in the phylogenetic analysis because of the likelihood of PCR artifacts in these sequences as documented by Ogedengbe et al.. GenBank sequence accession numbers are indicated on the trees.
To permit whole genome alignments, all mt genome sequences were linearized at the same position, 85-87 nt upstream of the small subunit rDNA fragment SSU/A corresponding to the binding site of the Cocci_MT-WG-F primer. Linearized sequences were aligned based on the primary structure using the multiple sequence alignment algorithm implemented from within Geneious 6.1; indels downstream of the Cocci_MT-WG-R primer binding site made unambiguous alignment in that region unlikely so the short sequences downstream of this primer binding region (44 to 97 bp depending on the Eimeria sp.) were not included in subsequent phylogenetic analyses using whole genome sequences.
Regions between rDNA fragments contained frequent indels that made unambiguous alignment of these regions difficult and the CDS for the three genes contained the majority of the genetic diversity found within the mt genomes. For these reasons, we chose to use concatenated CDS for CytB, COI and COIII (or their corresponding amino acid sequences) as datasets for phylogenetic analyses. The sequence data was thus partitioned into 3 datasets as follow: 1) a global nucleotide sequence data set for all 16 whole genome sequences (after removal of the short regions downstream of the Cocci_MT-WG-R primer); 2) concatenated DNA sequences for the 3 CDS; 3) concatenated amino acid (aa) translations of the 3 CDS.
Phylogenetic analyses were performed on all 3 data sets using three tree building methods, Bayesian analysis (BI) performed using MrBayes (Version 3.2.), Maximum Parsimony (MP) using PAUP 4.0 and Maximum Likelihood (ML) using PhyML, executed from within the Geneious bioinformatics software package (Version 6.1 and later versions).
Data set one, consisting of whole mt genome nucleotide sequences (excluding the short regions downstream of the Cocci_MT-WG-R primer), for all 16 whole genome sequences and data set two, consisting of concatenated CDS were analysed using all three tree-building methods (BI, ML or MP). Selection of the best fit evolutionary model for the BI and ML analyses was evaluated in both MrModeltest v2.3 (Nylander J. A. A. 2004. MrModeltest v2. Program; distributed by the author, Evolutionary Biology Centre, Uppsala University) and MEGA. For the Bayesian analyses, Markov Chain Monte Carlo was performed for 1,000,000 generations with four chains and heated chain temperature of 0.2. The burn-in length was set at 400,000 and subsample frequency of 1000[32, 36]. For the ML analyses, 500 bootstrap replicates were calculated to estimate node support. In the MP analyses, characters were unordered and given equal weight; trees were searched using the branch and bound search algorithm.
Data set three, consisting of concatenated amino acid (aa) translations of the 3 CDS was analysed with the same three tree-building methods. The empirical Jones-Taylor-Thornton (JTT) model of amino acid substitution with gamma distribution frequency (G + F) for all sites by Jones et al. was selected for the ML and BI analyses. Substitution models were assessed in MEGA. Where outgroup rooting was appropriate, the Eimeria magna mitochondrial genome sequence [GenBank: KF419217] was used as the functional outgroup.
Although sequences were truncated to remove the short indel-rich region downstream of the reverse primer for the phylogenetic analyses, complete genome sequence alignments were used within Geneious for calculating the pairwise genetic distances and number of nucleotide differences among the six newly sequenced genome sequences.
Six mt genomes from five Eimeria species infecting turkeys
Base composition of whole mitochondrial genomes from five Eimeria species infecting turkeys
Eimeria adenoeides Guelph [GenBank: KJ608415]
Eimeria dispersa Briston [GenBank: KJ608416]
Eimeria gallopavonis USKS06-01 [GenBank: KJ608417]
Eimeria gallopavonis Weybridge [GenBank: KJ608413]
Eimeria meleagridis USAR97-01 [GenBank: KJ608418]
Eimeria meleagrimitis USMN08-01 [GenBank: KJ608414]
Percent pairwise sequence identities (lower values) and number of nucleotide differences (upper values) for six mitochondrial genomes from five Eimeria species that infect turkeys
Eimeria dispersa Briston [GenBank: KJ608416]
Eimeria meleagrimitis USMN08-01 [GenBank: KJ608414]
Eimeria adenoeides Guelph [GenBank: KJ608415]
Eimeria meleagridis USAR97-01 [GenBank: KJ608418]
Eimeria gallopavonis Weybridge [GenBank: KJ608413]
Eimeria gallopavonis USKS06-01 [GenBank: KJ608417]
Eimeria dispersa Briston
Eimeria meleagrimitis USMN08-01
Eimeria adenoeides Guelph
[GenBank: KJ608415 ]
Eimeria meleagridis USAR97-01
Eimeria gallopavonis Weybridge
Eimeria gallopavonis USKS06-01
Searching conserved regions along the aligned mt genomes in the present study against the annotated P. falciparum mt genome identified three additional regions that are putative rDNA. The first two regions had high sequence identity to a single rDNA of P. falciparum encoding RNA14 (SSU/1) that appears to have been further fragmented on the Eimeria sp. mt genomes; the two resulting smaller fragments were found to map to two widely separated regions on these genomes. The first 29 bp of RNA14 from the P. falciparum mt genome (bp 5576-5548 of M76611) has high pairwise sequence identity (~79%) to a region designated RNA14a on the mt genomes of all Eimeria spp. The following 41 bp of RNA14 from the P. falciparum mt genome (bp 5547–5508 of M76611) has high pairwise sequence identity (75.6%) to a region designated RNA14b on the six mt genomes reported in the present study. The newly annotated rDNA fragment RNA14a (SSU/1a) was found in reverse orientation starting at bp 5141-5110 (varies in each Eimeria sp. mt genome) and RNA14b (SSU/1b) was found in forward orientation starting at bp 3104–3111 (varies in each Eimeria sp. mt genome). The remaining conserved region for which high sequence identity was discovered with the mt genome of P. falciparum corresponded to RNA5 (SSU/9) annotated by Feagin et al.. This putative rDNA fragment was found in reverse orientation starting at bp 6130-6199 (varies in each Eimeria sp. mt genome) and corresponded to bp 4724-4802 on the P. falciparum mt genome. Although the pairwise sequence identity between the complete RNA5 (SSU/9) regions on the Eimeria spp. and P. falciparum mt genomes was only 63.2%, both the 5′ and 3′ ends of these regions were highly conserved (i.e. 80-85% sequence identity in the 20 bp at each end of the region).
The COIII CDS was most divergent (76.3% identical sites across the six mt genome sequences). The COI and CytB CDS showed 81.2% and 81.8% identical sites, respectively. Of the 272 sites demonstrating variation among the 6 COI CDS examined, 239 were synonymous (KS) changes and 33 were non-synonymous (KA) changes. The COIII CDS had 179 sites with variation (74 KS and 40 KA) and the CytB CDS had 197 variable sites (167 KS and 30 KA changes). The CDS were more divergent than the rDNA fragments (80.2% sequence identity over the 3279 bp of the genomes identified as CDS versus 95.9% sequence identity over the 1880 bp identified as rDNA regions). Nucleotide differences and indels were observed within some fragmented rDNA regions but were most commonly observed within intergenic regions (i.e. between regions annotated as CDS or rDNA).
Start codon determinations for COI, COIII and CytB
Start codon assignments were made by comparison with 13 publically available complete mt genomes from various Eimeria species and subsequent confirmation of appropriate open-reading frames. In the six mt genomes obtained in this study, an ATG start codon for the CytB CDS beginning 214 or 215 bp downstream of the start of the Cocci_MT-WG-F primer binding site was shared among all Eimeria spp. for which complete mitochondrial sequences have been obtained. Preceding the ATG start codon was a poly–T-rich ‘GTTTATGTTTA’ motif that was conserved in all Eimeria spp. of turkeys with the exception of Eimeria meleagrimitis USMN08-01. The latter sequence had a single substitution of ‘T’ with a ‘C’ producing a slightly different motif ‘GTTTATGTTCA’. A single stop codon, TAA, terminated the CDS for CytB, COI and COIII in all six mt genome sequences. Potential start codons for the COI CDS identified upstream of the highly conserved ‘Asn–His–Lys’ motif associated with the start of the heme–copper oxidase subunit I core region of COI were numerous for most of the new genome sequences except for E. meleagrimitis that had only 2 ORF’s that start upstream of that functionally conserved region c.f.. Of these two potential start codons for COI in the E. meleagrimitis sequence, only one potential start codon was shared among all Eimeria species; this ATD (ATG or ATA or ATT) start codon is located 27 bp upstream of the ‘Asn–His–Lys’ site in all Eimeria species sequenced to date. The start codon for the COIII CDS was determined to be a TTA codon located 14-20 bp downstream of the LSU/1 (LSUA) region. Use of this conserved start codon produces a COIII product of 252 aa. In all Eimeria species studied thus far there is a poly-A- and poly-T-rich region located upstream of both the COI and COIII start codons.
In the BI and ML trees, for global complete mitochondrial nucleotide sequences and the concatenated CDS, all Eimeria species causing ‘cecal coccidiosis’ in turkeys (i.e. E. meleagridis, E. gallopavonis and E. adenoeides) formed a monophyletic clade that was the sister group to E. meleagrimitis; the latter species infects the intestinal tract of turkeys excluding the ceca. The Eimeria species causing ‘cecal coccidiosis’ in chickens (i.e. E. tenella and E. necatrix) formed a monophyletic clade that was the sister clade to these four Eimeria species infecting turkeys. In the MP trees based on the same DNA sequences (complete genome or concatenated CDS), Eimeria meleagrimitis was the sister taxon to a monophyletic clade consisting of species causing ‘cecal coccidiosis’ in chickens and turkeys. In none of the analyses did all Eimeria species infecting turkeys form a monophyletic group; in all phylogenetic analyses E. dispersa branched near the base of the tree and was the sister taxon to all other Eimeria species within the functional ingroup. The Eimeria spp infecting chickens, excluding E. tenella and E. necatrix, formed a monophyletic clade in all analyses and all datasets (DNA and AA-based); however, the branching order within this monophyletic clade varied among analyses. All of these parasites (i.e. E. acervulina, E. brunetti, E. mitis, E. praecox and E. maxima) infect the intestinal tract of chickens outside of the cecal pouches.
The six newly reported mt genome sequences obtained in this study varied modestly in genome lengths (6165-6238 bp) and were comparable to the lengths (6148 bp to 6408 bp) of the mt genomes of Eimeria spp infecting chickens[22–24, 39] and rabbits. Genome organization of all mt genome sequences is highly conserved among eimeriid coccidia; however, eimeriid mt genome organization differs markedly from that of other apicomplexan mt genomes e.g.[12, 17, 20]. No sequence differences (100% sequence identity) were recorded between the two strains of Eimeria gallopavonis (i.e. Weybridge strain and USKS06-01 strain) analysed in this study despite being isolated from different geographical regions. The two E. tenella sequences isolated from two geographical areas (Japan and China) also did not differ in their sequences[22, 23], respectively). In comparison, the two E. mitis isolates from the US and China showed sequence differences at 32 positions; perhaps the longer domestication of the chicken host has permitted greater genetic variation in its parasites compared to the domesticated turkey.
The number, direction and lengths of the three CDS were identical in all six mt genome sequences obtained in the present work. Although the COI, COIII and CytB CDS have been annotated inconsistently in the publically available mt genome sequences, alignment of all 16 complete mt genomes from 13 Eimeria species demonstrated conserved CDS using the start codons identified by Ogedengbe et al. for E. mitis USDA50. An assessment of the three CDS across all six genome sequences yielded large numbers of nucleotide substitutions scattered within each gene.
Fragmented rDNA (from 16 to 188 bp in length) annotated in the present study were more highly conserved than the CDS, possibly due to functional constraints in the former. A single rDNA fragment (SSUA (SSU/4) was found upstream of the CytB and COI genes, fifteen rRNA fragments were located between the COI and COIII genes and the ten remaining rRNA fragments were found between the COIII and the end of the mt genome. In addition to rDNA fragments identified in P. falciparum that had been previously annotated as putative homologs on Eimeria sp. mt genomes see,, three regions of each Eimeria sp. mt genome had high sequence identities with rDNA fragments encoding RNA14 (SSU/1) or RNA5 (SSU/9) in P. falciparum see,. A nearly complete rDNA encoding RNA5 (SSU/9) was located near the 3′ end of each genome and includes the binding site for the Cocci_MT-WG-R primer. The remaining two regions had high sequence identities to two portions of the rDNA encoding RNA14 (SSU/1) in P. falciparum see,. However, this rDNA fragment appeared to have been further fragmented on the Eimeria sp. mt genomes and the two resulting smaller fragments (29 bp and 41 bp) were found to map to two widely separated regions on these genomes that we annotated as RNA14a (SSU/1a) and RNA14b (SSU/1b), respectively, on all six mt genomes reported in the present study.
All putative ribosomal fragments (fragmented LSU and SSU rDNA) were highly conserved among all Eimeria spp[22–24, 39, 40]; present study. These putative rDNA fragments showed high sequence identity (from 62% to 93.8% pairwise identity) to functionally annotated rRNA fragments of P. falciparum M76611. Occurrence of fragmented and incomplete rRNA genes is not an uncommon phenomenon in apicomplexan parasites; similar fragmented rRNA genes have been reported in all other apicomplexan mt genomes examined to date e.g.[12, 17, 19, 22, 23]. Although three additional conserved regions were annotated as putative rDNA fragments in the present study, other highly conserved regions in the six genome sequences remain unannotated but these comparatively conserved regions may represent as yet uncharacterized rDNA fragments.
Phylogenetic analyses under Bayesian, Maximum likelihood and Maximum parsimony evolutionary models using complete mt sequences or concatenated sequences from the three CDS from each mt genome did not support the conclusion that all Eimeria species infecting turkeys evolved from a common ancestor. Instead, although many turkey coccidia apparently share a common ancestor, at least one, E. dispersa was found branching as the sister taxon to all other Eimeria spp in the functional ingroup. It is possible that E. dispersa may not have evolved within turkeys but rather arrived in that host via a host switch from some other avian host. Eimeria dispersa has been shown to infect both Bobwhite quail (Colinus virginianus) and turkeys, and perhaps other hosts as well. In addition, the mt genome sequences suggest that the cecal coccidia of chickens (E. tenella and E. necatrix) are distantly related to the other Eimeria of chickens and are more closely related to some of the Eimeria spp that infect turkeys; this had been previously suggested on biological and molecular grounds. Analyses of the mt genome sequence data support the suggestion that Eimeria spp in chickens represent two distinct ancestral colonisations of the intestine. In one, E. tenella and E. necatrix, that appear closely related to a number of coccidia infecting turkeys, invaded the ceca of chickens; the remaining five Eimeria spp. infecting chickens are closely related using nu 18S rDNA[24, 43, 44], partial mt COI sequences[24, 44] or complete mt genome sequences (current study) and all of these species colonize regions of the intestine excluding the cecum.
Complete mt genome sequences could easily differentiate closely related parasites. For example, the pairwise genetic distance of E. adenoeides and E. meleagridis of turkeys and E. tenella and E. necatrix of chickens was 98.2% and 98.4%, respectively. Interestingly, the COI partial sequences for E. adenoeides (KCH strain) and E. adenoeides (KR strain), are 100% identical to the COI CDS of E. adenoeides (Guelph strain) and E. meleagridis (USAR97-01 strain), respectively, suggesting that the KCH and KR strains of E. adenoeides of Poplstein and Vrba are distinct species rather than strains of a single species.
The mt genomes of Eimeria species infecting turkeys are similar with respect to genome size, organisation, start codon positions and overall base composition with all other Eimeria species. Complete mitochondrial genome sequences possess sufficient sequence variability for differentiating Eimeria species infecting turkeys or chickens and, in the three cases where more than one complete mt genome is available from a single species (i.e. E. mitis, E. tenella and E. gallopavonis), the intraspecific variation between mt genomes was much smaller (0–0.5%) than the genetic distance between that species and the most closely related Eimeria species (1.6 –3.2%). Genetic variability is concentrated within the three CDS encoding COI, COIII and CytB. This makes these mt genes of Eimeria spp. suitable (either as individual genes or as concatenated sequences) for species delimitation studies and phylogenetic analyses without the confounding presence of paralogous genome copies encountered with nu rDNA sequences e.g.[24, 45]. The nature of the mt genome sequences, and particularly the CDS regions, of Eimeria spp. make the mt genome highly suited for development of diagnostic assays as well as, potentially, genetic markers for molecular epidemiology and phylogenetics of coccidia.
We thank Dr. H. D. Chapman (University of Arkansas, Fayetteville, Arkansas, USA) for providing parent stocks of five Eimeria sp. isolates used in this study from which single oocyst derived lines were obtained. This work was supported by scholarship support to MEO from the Ontario Veterinary College. Research was funded through a Discovery Grant from the Natural Sciences and Engineering Research Council of Canada (NSERC #400566) and the Ontario Ministry of Agriculture and Food (OMAF Project #200331) to JRB.
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