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Forcipomyia Meigen, 1818, is the second-largest genus of the family Ceratopogonidae, having medico veterinary and agricultural importance. A few mitogenomes of Ceratopogonidae have previously been available. Here, we aimed to characterize the whole mitogenome of Forcipomyia pulchrithorax Edwards, 1924, collected from Central Anatolia Region of the Türkiye using NGS to contribute to the genetic diversity within this family. The mitogenome of F. pulchrithorax (OR666457) consisted of a circular DNA molecule spanning 15,930 bp and containing 72.7% AT content. It includes 13 proteincoding genes (PCGs), 22 transfer RNA (tRNA) genes, 2 ribosomal RNA (rRNA) genes, and 1 control region. All PCGs exhibited typical ATN start codons and followed the conventional TAN stop codons, except COX1, COX2, COX3, ND1, and ND5, which ended with incomplete codons. The 22 tRNA genes demonstrated the ability to form a cloverleaf structure, except tRNA-Ser1, which lacked DHU arm, similar to most insect mitogenomes. The ML phylogenetic analyses clearly delineated the species of Culicomorpha into well supported monophyletic clades. Forcipomyia pulchrithorax was clustered with the Ceratopogonidae species constituting an outer taxon among the Culicomorpha. The comprehensive mitogenome of F. pulchrithorax will be valuable for future studies focused on the phylogenetic characterization and diversity of Ceratopogonidae within the Culicomorpha. [ABSTRACT FROM AUTHOR]

As a reference mitogenome, the complete mitochondrial genome of the white-breasted hedgehog, Erinaceus concolor , was firstly presented in this study by employing Long-Range PCR and Next-Generation Sequencing. The total lengths of the mitogenomes were 17.451 bp and 17.455 bp. A total of 37 genes, namely two ribosomal RNAs (rRNAs), 22 transfer RNAs (tRNAs), 13 protein-coding genes (PCGs), and a non-coding D-loop were encoded in the mitogenome, compatible with the previously reported mitogenomes belonging to representatives of the family Erinaceidae (Mammalia: Eulipotyphla). Maximum Likelihood and Bayesian Inference phylogenetic analyses of Eulipotyphla and Erinaceidae based on the complete mitogenomes revealed a conventional relationship for the relevant organism's groups. Divergence time analyses based on complete mitogenome data revealed that evolutionary divergence events within Erinaceidae began about 58.87 Myr ago corresponding to the early Eocene, and the basal split of Erinaceus dates back to approximately 11.01 Myr ago in the late Miocene. Single cytochrome b -based analyses can be considered weaker, as they produce phylogenies that are relatively inconsistent with the natural classification of Eulipotyphla and put the onset of evolutionary divergence events earlier. The genetic information obtained as a result of this study can be used as a genetic resource for conservation biology studies; it will also undoubtedly contribute to the understanding of molecular evolution of E. concolor and closely related taxa. [ABSTRACT FROM AUTHOR]

Purpose: Leishmania subgenus Leishmania causes leishmaniosis, which is a chronic systemic disease in humans and animals, in which the skin and visceral organs can be affected. The disease generally consists of three different clinical types in humans: visceral (kala-azar, VL), cutaneous (CL) and mucocutaneous leishmaniosis (MCL). According to the World Health Organization (WHO), leishmaniosis is still one of the world's most neglected diseases. It has been nearly 13–14 years since the completion of the first complete genome sequence of a Leishmania parasite. However, much information about these parasites remains to be elucidated, such as the causes of differences in tissue tropism. The aim of this study is to perform the whole-genome sequencing of Leishmania infantum causing cutaneous leishmaniosis from a Turkish isolate with next-generation sequencing technology. Methods: Genomic sequencing was performed on the Illumina HiSeq 2500 platform. The TruSeq Nano DNA Low Throughput Library Prep Kit, compatible with the Illumina HiSeq 2500 platform, was used to generate the library. Synthesis sequencing (SBS) was performed with a HiSeq Rapid SBS Kit v2 to generate single-fragment reads (2 × 150 bp; PE) with two fragment end-to-end assemblies. Bioinformatics analyses were performed on the Geneious 11.0.5. (www.genius.com) platform. Results: In our study, a high-quality whole-genome sequence (WGS) of L. infantum was successfully generated, and a total of 32,009,137 base pairs of genomic DNA from 36 chromosomes were obtained. The resulting genomic DNA sequence was submitted to the US National Center for Biotechnology Information (NCBI) GenBank (www.ncbi.nlm.nih.gov) database and registered under the name Leishmania infantum_TR01 (Lin_TR01). The following accession numbers were assigned by NCBI to the 36 chromosomes of the Lin_TR01 genome: CP027807, CP027810, CP027808, CP027811, CP027809, CP027812, CP027813, CP027814, CP027817, CP027818, CP027819, CP027815, CP027821, CP027816, CP027823, CP027820, CP027822, CP027824, CP027825, CP027826, CP027827, CP027828, CP027829, CP027830, CP027831, CP027832, CP027833, CP027834, CP027835, CP027836, CP027837, CP027838, CP027839, CP027840, CP027841, CP027842. As a result of the annotation of the Lin_TR01 genome, 3153 polymorphisms, 8324 genes, 8199 CDSs, 8109 mRNAs, 67 tRNAs, 11 rRNAs and 58 ncRNA were identified. Among the 8199 CDS obtained, 5278 encode hypothetical proteins. Conclusion: In this study, a high-quality WGS of Leishmania infantum was successfully obtained for the first time in Turkey. According to a review of WGS studies on this subject, the Lin_TR01 strain is the first strain to be isolated from cutaneous leishmaniosis. The reference genome of L. infantum JPCM5 (Peacock et al., 2007) was obtained from a visceral leishmaniosis case, in accordance with the classical tissue and organ tropism of the species. Lin_TR01 is the second whole-genome-sequenced strain in the world after the JPCM5 strain. The Lin_TR01 genome is the only L. infantum whole-genome sequence that is completed assembly level from 36 chromosomes among the genomes obtained thus far (https://www.ncbi.nlm.nih.gov/genome/genomes/249). [ABSTRACT FROM AUTHOR]

Williams's jerboa (Scarturus williamsi), a medium-sized jerboa distributed in Anatolia and its adjacent regions, is a member of the four- and five-toed jerboas found mostly in Asia. Disagreements about the taxonomy of this taxon at the genus/species level continue to exist. Here, we report the first effort to sequence and assemble the mitochondrial genome of Williams's jerboa from Turkey. The mitochondrial genome of S. williamsi was 16,653 bp in total length and contained 13 protein-coding genes (PCGs), 22 transfer RNAs (tRNAs), two ribosomal RNAs (rRNAs), and two non-coding regions (the D-loop and OL region) with intergenic spacer. All of the genes, except ND6 and eight tRNAs, were encoded on the heavy chain strand, similar to the features of mitogenomes of other rodents. When compared with all available rodent mitochondrial genomes, Williams's jerboa showed (1) a serine deletion at the 3'-end of the ATP8 gene, (2) the ND5 gene terminated with a TAG codon and (3) a tandem repeat cluster (273 bp in length) in the control region. Williams's jerboa and Siberian jerboa grouped as sister taxa despite the high genetic distance (17.6%) between them, belonging to Allactaginae. This result is consistent with the latest pre-revision, which suggests that Williams's jerboa and the Siberian jerboa may belong to separate genera, as Scarturus and Orientallactaga, respectively. The present study provides a reference mitochondrial genome for Williams's jerboa for further molecular studies of other species of Dipodoidea and Rodentia. [ABSTRACT FROM AUTHOR]

Diversity of ecological conditions in Anatolia enables many species to adapt to different environments. Thus Turkey is inhabited by various strains of A.m. mellifera Linnaeus, 1978; A.m. mellifera carnica, A.m. mellifera anatoliaca, A.m. mellifera caucasica, A.m. mellifera syriaca, and A.m. mellifera meda. Analysis of mtDNA variants is a widely used tool to determine the phylogenetic relationships at the species and subspecies levels. In this study sequencing results of tRNAleu-COX2 and ND5 gene segments of mtDNA were presented in comparison with some previously published mitochondrial haplotypes. According to the UPGMA dendogram and estimates of evolutionary distances, divergence among the subspecies and ecotypes were not verified strongly. Reproductive isolation barriers could be uneffective and lead to the exchange of the genetic materials between the populations. Intensive care should be taken while managing the colonies of different subspecies in bee yards. Degradation of biodiversity of honey bee subspecies through hybridization was also reported at wider geographic areas rather than small breeding units in some studies. Broad ranges of isolated colonies of subspecies should be established with proper selection studies to reduce the hazards of migratory beekeeping activities. Succesful management practices are needed through better beekeeping technologies and beekeeper training programmes to prevent the homogenization of the genetic structure of different subspecies and to conserve honey bee diversity. [ABSTRACT FROM AUTHOR]

Using high-throughput sequencing technology, the complete mitochondrial genome of Awassi-Jo breed (Ovis aries) was decoded. Mitochondrial genome was 16,617 bp in length. The genome contained 37 genes (13 protein-coding, 22 tRNA, and 2 rRNA) and a control region (D-loop region). The genes were encoded on the H-strand, except for the ND6 gene and 8 tRNA genes, which were encoded on the L-strand. The GC content is 38.9%. Phylogenetic analysis was performed to compare Awassi-Jo with other sheep breeds. The phylogenetic tree showed that Awassi-Jo diverged earlier than related breeds (Turkey, Italy, Germany, and Netherland) with a common ancestor in haplogroup HB. The results revealed the importance of mitochondrial data in studying sheep evolution and domestication. [ABSTRACT FROM AUTHOR]

Apis mellifera anatoliaca had a mitochondrial genome that was 16,256 bp long, with 13 protein-coding genes, 22 tRNA genes, two rRNA genes, and an AT-rich control region. The phylogenetic tree showed that A. m. anatoliaca was closely related to other subspecies found in Turkey, A. m. caucasica and A. m. meda. [ABSTRACT FROM AUTHOR]

Objective: To determine tandem repeat polymorphism and heteroplasmy in three sturgeon species (A. stellatus, A. gueldenstaedtii and H. huso) from the Turkish coast of Black Sea. Methods: tRNApro and D-loop segment of mtDNA from three sturgeon species were amplified via PCR and sequenced. For each species, homoplasmic individuals with different product lengths, repeat motifs and regions were determined and the repeat numbers and frequencies were calculated. The variation in mtDNA size present in the overall sample of sturgeon from Turkish waters was apportioned into hierarchical components. Also, the statistical approach described by other researchers was used for the calculation of interspecies and intra-species genetic variation. Results: The results showed that all three species reveal 2-6 copies of different mtDNA length variants attributable to varying copy numbers of an 82-84bp repeat sequences. A total of 9.9% of the sturgeons were heteroplasmic, bearing three to five repeat variants. The highest number of observed repeat units rate was 45.8% in 3 repeats morph in A. gueldenstaedtii. The mean genetic diversity within individuals (Kb) was higher in A. gueldenstaedtii and A. stellatus than in H. huso (0.625, 0.620, and 0.500, respectively). Conclusion: The repeat region, responsible for length variations and heteroplasmy, is located near the end of the D-loop and control region separated by only a few nucleotides from the tRNApro gene. [ABSTRACT FROM AUTHOR]

• In this study, it is obtained the whole genome sequence of Toxoplasma gondii with "Next Generation Sequencing Technology succesfully. • In this study, whole genome of T. gondii study was conducted for the first time in Turkey. • Toxoplasma gondii Turkısh ısolate genome data were submitted to the National Center for Biotechnology Information, USA, (NCBI) GenBank (www.ncbi.nlm.nih.gov) database under the name Toxoplasma gondii TR01 (TG_TR01). • The accession numbers of 14 chromosomes belonging to the genome sequences of Toxoplasma gondii TR01 (TG_TR01) are CM019722.1, CM019723.1, CM019724.1, CM019725.1, CM019726.1, CM019727.1, CM019728.1, CM019729.1, CM019728.1, CM019729.1, CM019730.1, CM019731.1, CM019732.1, CM019733.1, CM019734.1, CM019735.1. Toxoplasma gondii is an intracellular parasite that can affect all vertebrae and is the causative agent of toxoplasmosis. At present, the United States CDC (Centers for Disease Control and Prevention) recognizes this infection as a neglected disease. Toxoplasma gondii infection profiles exhibit differences because of the different regional and climatic responses to these parasites in Turkey, and these protozoan infections are notably common in this country. In this study, we attempted to obtain the whole-genome sequence of T. gondii using next-generation sequencing technology. Toxoplasma gondii isolates were isolated from an infant with congenital toxoplasmosis by Ekmen et al. (1974) in Ankara, Turkey. Whole-genome sequencing (WGS) was performed using the Illumina HiSeq 2500 and HiSeq SBS Kit v2. A T. gondii library was created on this device in the initial stage. After the completion of the library phase, sequence analysis was begun with a next-generation sequencing device. The resulting fragments were combined using paired-end (PE) reading and converted into a single DNA fragment. Bioinformatic analysis was performed using the Geneious 2.1. program. In our study, WGS was successfully performed on T. gondii. The T. gondii whole-genome sequence has a coverage value of 50x, a size of 61,5763 Mb and a GC ratio of 52.6%. Data from this sequence were submitted to the National Center for Biotechnology Information (NCBI) GenBank (www.ncbi.nlm.nih.gov) database under the name Toxoplasma gondii TR01 (TG_TR01). The accession number of the genome obtained in this study is WOEV00000000.1. The biological sample access number is SAMN13338796. The genome of the T. gondii strain obtained in this study was compared with the reference genome, and 8312 CDSs (coding sequences), 183 tRNAs, 294 rRNAs and 8789 genes were identified. Among the 8312 CDSs, 4284 encoded hypothetical proteins (hypothetical protein CDSs/proteins of unknown function). The entire genome sequence of T gondii TR01 was compared with that of Toxoplasma gondii ME49. The results of this comparison demonstrate that the analyzed genome was 99,98% similar to the reference genome. The accession numbers of 14 chromosomes belonging to the genome sequences of T. gondii TR01 (TG_TR01) are CM019722.1, CM019723.1, CM019724.1, CM019725.1, CM019726.1, CM019727.1, CM019728.1, CM019729.1, CM019730.1, CM019731.1, CM019732.1, CM019733.1, CM019734.1, and CM019735.1. In this study, a whole-genome sequences of T. gondii was conducted for the first time in Turkey. The analyzed strain was named T. gondii TR01. The data obtained from this study may contribute to a better understanding of T. gondii. T. gondii is an important pathogen with an unusual population structure. Although T. gondii is highly zoonotic and has a complicated life cycle, some strains of this parasite have exhibited high genetic sequence similarity, and our study supports this knowlegde. The characterization of this strain may be very useful for the scientific community of our country and may help to establish a foundation for further research investigating the genome of T. gondii. [ABSTRACT FROM AUTHOR]