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opencc-by-4.0Sep 2016View details →

Plasmodium falciparum infection in febrile Congolese children: prevalence of clinical malaria ten years after introduction of Artemisinin-combination therapies

<p>dataset used in the paper.</p>

Fig. 4 in Sexual differences in prevalence of a new species of trypanosome infecting túngara frogs

Fig. 4. Phylogeny of the aquatic clade, and PTP species delimitation results. Best maximum likelihood tree of the18S rRNA gene of member of the aquatic clade and selected outgroups. Numbers on the branches represent support values corresponding to ±70% bootstrap replicates (left) and ±0.9 Bayesian posterior probabilities (right). Subclades are highlighted with colored boxes to indicate host associations. Color of the branches indicate the PTP species delimitation results; monophyletic groups in red indicate members of a single species, blue terminal branches indicate that only one sample is included in such species. Names of the terminals indicate the GenBank accession numbers, scientific name, and sample or isolate code. Star indicates the position of T. tungarae n. sp. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)

Fig. 3 in Sexual differences in prevalence of a new species of trypanosome infecting túngara frogs

Fig. 3. Light microscopy of Trypanosoma tungarae n. sp. (Giemasa-staining). (a e) Trypomastigotes stained using Hemacolor ® Giemsa stain kit (Voigt Global Distribution Inc, USA); ‾ (f‾i) Trypomastigotes stained using Giemsa stain following Mohr (1981). Scale bars: 10 µm.

Fig. 1 in Sexual differences in prevalence of a new species of trypanosome infecting túngara frogs

Fig. 1. Photographs of túngara frogs (Engystomops pustulosus) and frog-biting midges (Corethrella spp). (a) Calling male túngara frog preyed upon by frog-biting midges; (b) female (bottom) in amplexus with a male (top) covered with biting midges; (c) female (bottom) with a biting midge on her nostril that was passed from the male during amplexus. Túngara frogs are about 30 mm long while the frog-biting midges are only about 1.5 mm. Photos taken by Alexander Baugh (a) and Ximena E Bernal (b,c).

Fig. 2 in Sexual differences in prevalence of a new species of trypanosome infecting túngara frogs

Fig. 2. Map of the Republic of Panaḿa indicating with a star the location of Gamboa, the type locality of Trypanosoma tungarae n. sp. Insert shows the location of Panamáin the New World.

opencc-by-4.0Dec 2022View details →

Figure 2 in Prevalence of cestodes infection among school children of urban parts of Lower Dir district, Pakistan

Figure 2. Tapeworm species eggs. (A) Taenia saginata; (B) Hymenolepis nana; (C) Hymenolepis diminuta.

opencc-by-4.0Aug 2016View details →

Fig. 1 in High Trypanosoma cruzi infection prevalence associated with minimal cardiac pathology among wild carnivores in central Texas

Fig. 1. Spatial occurrence and distribution of T. cruzi infected, hunter-harvested wildlife, 2014. Number of infected over total number of that species tested are shown by county.

opencc-by-4.0Dec 2016View details →

Fig. 3 in Haemosporidian parasite infections in grouse and ptarmigan: Prevalence and genetic diversity of blood parasites in resident Alaskan birds

Fig. 3. Bayesian phylogenetic tree of haemosporidian mtDNA cytochrome b haplotypes isolated from Alaskan grouse and ptarmigan species. Node tips are labeled with abbreviation for parasite genus (Haem = Haemoproteus, Leuc = Leucocytozoon, and Plas = Plasmodium), followed by the lineage name, GenBank accession number for each lineage, and avian (Phas = Phasianidae, Anat = Anatiade, Turd = Turdidae, Paru = Parulidae, Scol = Scolopacidae, Embe = Emberizidae, and Frin = Fringillidae) or invertebrate (Simu = Simuliidae) host family. All haplotypes identified in this study are highlighted in red and asterisks following tip labels indicate a lineage that was isolated from Alaskan bird hosts. Numbers on branches indicate posterior probabilities from our analysis. All reference sequences were obtained from the National Center for Biotechnology Information website or the MalAvi database. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

opencc-by-4.0Dec 2016View details →

Fig. 2. Minimum spanning network for haemosporidian mtDNA cytochrome b in Haemosporidian parasite infections in grouse and ptarmigan: Prevalence and genetic diversity of blood parasites in resident Alaskan birds

Fig. 2. Minimum spanning network for haemosporidian mtDNA cytochrome b haplotypes isolated from Alaskan grouse and ptarmigan species. Dark circles represent un-sampled nodes. All circles are proportional to the frequency at which the haplotypes were detected. Lines between nodes are drawn to scale based on the number of nucleotide mutations unless otherwise indicated by hash marks.

opencc-by-4.0Dec 2016View details →

Fig. 1 in Haemosporidian parasite infections in grouse and ptarmigan: Prevalence and genetic diversity of blood parasites in resident Alaskan birds

Fig. 1. Map of Alaskan sampling regions assembled from multiple game management units and sub-units. Regions were grouped for analysis of haemosporidian prevalence as follows: southcoastal (Kenai Peninsula and southeastern Alaska; GMUs 1C, 1D, 2, 7, 15A, 15B, and 15C), southcentral (Anchorage area and Matanuska-Susitna Valley; GMUs 13A, 13D, 14A, 14C, 16A, and 16B), southwestern (Bristol Bay, Alaska Peninsula, and eastern Aleutian islands; 9D, 9E, and 17C), southern interior (south side of Alaska Range; GMUs 12, 13B, and 13E), northern interior (north side of Alaska Range; GMUs 20A-20E and 25C), and Seward Peninsula (GMU 22C).

Fig. 3 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 3. Single nucleotide polymorphisms in the ND2 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Speciesspecific SNPs are shown in bold.

Fig. 1 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 1. Single nucleotide polymorphisms in the Cox1 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Italicized numbers represent the position number from a previously published partial sequence of the B. columnaris Cox1 gene (Franssen et al., 2013). Species-specific SNPs are shown in bold.

Fig. 2 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 2. Single nucleotide polymorphisms in the Cox2 gene of B. columnaris, compared to B. procyonis. Nucleotide position numbers are shown at the top of the figure. Italicized numbers represent the position number from a previously published partial sequence of the B. columnaris Cox2 gene (Franssen et al., 2013).

Fig. 4 in Partial molecular characterization of the mitochondrial genome of Baylisascaris columnaris and prevalence of infection in a wild population of Striped skunks

Fig. 4. Single nucleotide polymorphisms in several tRNA genes of B. columnaris, compared to B. procyonis, B. transfuga and B. schroederi. Nucleotide position numbers are shown at the top of the figure. SNPs which distinguish B. columnaris from other Baylisascaris species are shown in bold.

opencc-by-4.0Apr 2019View details →

Fig. 3. A in Wild horse populations in south-east Australia have a high prevalence of Strongylus vulgaris and may act as a reservoir of infection for domestic horses

Fig. 3. A box and whisker plot (with individual data points) of the total strongyle egg counts across the different populations, showing the highest FECs were from samples from Bogong High Plains and Tin Mines, both alpine heathland habitats. Overall 89% of samples had FECs> 500 EPG, classed as 'high level shedders'.

opencc-by-4.0Apr 2019View details →

Fig. 1 in Prevalence and co-infection with tick-borne Anaplasma phagocytophilum and Babesia spp. in red deer (Cervus elaphus) and roe deer (Capreolus capreolus) in Southern Norway

Fig. 1. Phylogenetic tree of Babesia isolates and samples of this study (●), based on fragments of 18S rRNA, generated using the Maximum-Likelihood clustering method in MEGA 6 software (1000 replicates; bootstrap values indicated at the nodes). Abbreviations: AU - Austria, BE - Belgium, CA - Canada, DE - Germany, FR - France, HU - Hungary, IT - Italy, JP - Japan, LT - Lithuania, NO - Norway, PL - Poland, RU - Russia, SK - Slovakia, SP - Spain, TU - Turkey, US - United States.

opencc-by-4.0Apr 2019View details →

Fig. 2 in Wild horse populations in south-east Australia have a high prevalence of Strongylus vulgaris and may act as a reservoir of infection for domestic horses

Fig. 2. Microscopic view of the different eggs. A = Anoplocephala spp. eggs, S <90 = strongyle eggs <90 μm length, S> 90 = strongyle eggs ≥90 μm length, P = Parascaris spp. eggs.

opencc-by-4.0Aug 2018View details →

Fig. 1 in Variable changes in nematode infection prevalence and intensity after Rabbit Haemorrhagic Disease Virus emerged in wild rabbits in Scotland and New Zealand

Fig. 1. Differences in mean intensity of nematode parasite infection in rabbits sampled seasonally from New Zealand and Scotland before the spread of RHDV (a), rabbits sampled seasonally from Sotland before and after RHDV (b), and rabbits sampled in autumn season from New Zealand and Scotland before and after RHDV (c). Nematode parasites included T. retortaeformis (i) G. strigosum (ii) and P. ambiguus (iii) found in rabbits sampled in spring (Spr), summer (Sum), autumn (Aut) and winter (Win).

opencc-by-4.0Aug 2022View details →

Fig. 3 in Prevalence of fish-borne zoonotic trematode infection in Jilin Province, China

Fig. 3. The phylogenetic tree of FZTs obtained in this study with other trematodes based on ITS sequences. ITS sequences of C. sinensis, M. orientalis and E. japonicus from fish were obtained and compared. They had the same similarity and were deposited into NCBI (No. MW828640, MW828729 and MW828605). The phylogenetic relationship between the FZTs obtained in this study and other trematodes based on ITS sequences was analyzed via MP, NJ and ML using A. chongqingens as the outgroup. The scale bar indicates an evolutionary distance of 0.10 substitutions per site in the sequence. The ITS sequences of C. sinensis, M. orientalis and E. japonicus obtained in this study (marked with *) was 100% consistent with the sequences of C. sinensis (MF319654), M. orientalis (MK482055) and E. japonicus (KT873314) deposited in NCBI GenBank.