Pub Date : 2024-10-02DOI: 10.1017/S0031182024000982
Abid Ali, Mehran Khan, Muhammad Numan, Abdulaziz Alouffi, Mashal M Almutairi, Ronel Pienaar, Minique H de Castro, Lidia Chitimia-Dobler, Sebastián Muñoz-Leal, Ben J Mans
The genus Ornithodoros is notably diverse within the family Argasidae, comprising approximately 134 species distributed among 4 subgenera, 1 of which is the subgenus Pavlovskyella. In an earlier study, we identified distinct soft ticks as Ornithodoros (Pavlovskyella) sp., which were collected from animal shelters in Khyber Pakhtunkhwa, Pakistan. Providing additional collections from that same locality and a comprehensive analysis involving detailed morphological and mitogenome-based comparisons with closely related species, this study formally designates a novel species for these specimens. Adults and late-instar nymphs of the new species display a dorsoventral groove, small cheeks not covering the capitulum, 5 small even humps on tarsus I and a transverse postanal groove intersecting the median postanal groove perpendicularly. It also lacks a tuft of setae on the ventral surface of the hood which separates the novel species from Ornithodoros papillipes. Ventral chaetotaxy of tarsus IV indicates 4–7 setal pairs in nymphs and 5–7 pairs in adults that separate the new species from Ornithodoros tholozani sensu stricto and Ornithodoros crossi, 2 morphologically closely related species that occur in geographical proximity. Phylogenetic analyses of the full-length mitochondrial genome and the 18S and 28S ribosomal RNA genes, combined with pairwise nucleotide comparisons of cox1, cox2, atp8, atp6, cox3, nad3, nad5, nad4, nad4L, nad6, cytb, nad1, nad2, 12S rDNA, 16S rDNA, 18S rDNA and 28S rDNA further support that the new species belongs to the Pavlovskyella subgenus, clustering with O. tholozani, Ornithodoros verrucosus and Ornithodoros tartakovskyi.
{"title":"Description of a new <i>Ornithodoros</i> (<i>Pavlovskyella</i>) (Ixodida: Argasidae) tick species from Pakistan.","authors":"Abid Ali, Mehran Khan, Muhammad Numan, Abdulaziz Alouffi, Mashal M Almutairi, Ronel Pienaar, Minique H de Castro, Lidia Chitimia-Dobler, Sebastián Muñoz-Leal, Ben J Mans","doi":"10.1017/S0031182024000982","DOIUrl":"https://doi.org/10.1017/S0031182024000982","url":null,"abstract":"<p><p>The genus <i>Ornithodoros</i> is notably diverse within the family Argasidae, comprising approximately 134 species distributed among 4 subgenera, 1 of which is the subgenus <i>Pavlovskyella</i>. In an earlier study, we identified distinct soft ticks as <i>Ornithodoros</i> (<i>Pavlovskyella</i>) sp., which were collected from animal shelters in Khyber Pakhtunkhwa, Pakistan. Providing additional collections from that same locality and a comprehensive analysis involving detailed morphological and mitogenome-based comparisons with closely related species, this study formally designates a novel species for these specimens. Adults and late-instar nymphs of the new species display a dorsoventral groove, small cheeks not covering the capitulum, 5 small even humps on tarsus I and a transverse postanal groove intersecting the median postanal groove perpendicularly. It also lacks a tuft of setae on the ventral surface of the hood which separates the novel species from <i>Ornithodoros papillipes</i>. Ventral chaetotaxy of tarsus IV indicates 4–7 setal pairs in nymphs and 5–7 pairs in adults that separate the new species from <i>Ornithodoros tholozani</i> sensu stricto and <i>Ornithodoros crossi</i>, 2 morphologically closely related species that occur in geographical proximity. Phylogenetic analyses of the full-length mitochondrial genome and the 18S and 28S ribosomal RNA genes, combined with pairwise nucleotide comparisons of <i>cox1</i>, <i>cox2</i>, <i>atp8</i>, <i>atp6</i>, <i>cox3</i>, <i>nad3</i>, <i>nad5</i>, <i>nad4</i>, <i>nad4L</i>, <i>nad6</i>, <i>cytb</i>, <i>nad1</i>, <i>nad2</i>, 12S rDNA, 16S rDNA, 18S rDNA and 28S rDNA further support that the new species belongs to the <i>Pavlovskyella</i> subgenus, clustering with <i>O. tholozani</i>, <i>Ornithodoros verrucosus</i> and <i>Ornithodoros tartakovskyi</i>.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-14"},"PeriodicalIF":2.1,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142361900","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The genus Tanqua Blanchard, 1904, infests reptiles, particularly those inhabiting aquatic environments. This study examined a population of rainbow water snakes, Enhydris enhydris (Schneider, 1799), collected from southern Thailand. Adult nematodes consistent with Tanqua were found in the stomach. Various morphometric, meristic and qualitative morphological variables, including size, ratios, distances, cephalic appearance, the number of caudal papillae and other features, serve to distinguish the specimens from other species within the genus. In particular, Tanqua anomala and Tanqua diadema, which closely resemble our Tanqua specimens, can be differentiated by key diagnostic characteristics such as a retractable head, the distance from the anterior end to the cervical sac, the relative positions of caudal papillae and excretory pore, and the length of the uterus. Molecular analysis (COI and 18s rRNA genes) confirmed its status as a species of Tanqua, genetically distinct from Tanqua tiara, and matching the genetic sequence found in larvae of Tanqua sp. from a snakehead fish species from Bangladesh. Tanqua siamensis sp. nov. is described, supported by morphological traits, microscopic illustrations and genetic information. This study reports the first evidence of a caudal papillary pair in females. This species causes significant lesions on the stomach wall of the snake host, raising possible issues for snakes held in captivity regarding food hygiene and parasite protection.
{"title":"A new nematode species, <i>Tanqua siamensis</i> sp. nov. (Nematoda: Gnathostomatidae) in the rainbow water snake, <i>Enhydris enhydris</i>, from Thailand.","authors":"Vachirapong Charoennitiwat, Urusa Thaenkham, Supakit Tongpon, Kittipong Chaisiri, Panithi Laoungbua, Tanapong Tawan, Tapanee Kanjanapruthipong, Sumate Ampawong, Abigail Hui En Chan, Napat Ratnarathorn","doi":"10.1017/S0031182024000908","DOIUrl":"10.1017/S0031182024000908","url":null,"abstract":"<p><p>The genus <i>Tanqua</i> Blanchard, 1904, infests reptiles, particularly those inhabiting aquatic environments. This study examined a population of rainbow water snakes, <i>Enhydris enhydris</i> (Schneider, 1799), collected from southern Thailand. Adult nematodes consistent with <i>Tanqua</i> were found in the stomach. Various morphometric, meristic and qualitative morphological variables, including size, ratios, distances, cephalic appearance, the number of caudal papillae and other features, serve to distinguish the specimens from other species within the genus. In particular, <i>Tanqua anomala</i> and <i>Tanqua diadema</i>, which closely resemble our <i>Tanqua</i> specimens, can be differentiated by key diagnostic characteristics such as a retractable head, the distance from the anterior end to the cervical sac, the relative positions of caudal papillae and excretory pore, and the length of the uterus. Molecular analysis (<i>COI</i> and 18s rRNA genes) confirmed its status as a species of <i>Tanqua</i>, genetically distinct from <i>Tanqua tiara</i>, and matching the genetic sequence found in larvae of <i>Tanqua</i> sp. from a snakehead fish species from Bangladesh. <i>Tanqua siamensis</i> sp. nov. is described, supported by morphological traits, microscopic illustrations and genetic information. This study reports the first evidence of a caudal papillary pair in females. This species causes significant lesions on the stomach wall of the snake host, raising possible issues for snakes held in captivity regarding food hygiene and parasite protection.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"821-831"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11579038/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142293104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-10-08DOI: 10.1017/S0031182024000969
Boris R Krasnov, Irina S Khokhlova, Natalya P Korallo-Vinarskaya, Anne Laudisoit, M Fernanda López Berrizbeitia, Sonja Matthee, Julliana P Sanchez, Michal Stanko, Luther van der Mesht, Maxim V Vinarski
We applied a novel framework based on network theory and a concept of modularity that estimates congruence between trait-based ( = functional) co-occurrence networks, thus allowing the inference of co-occurrence patterns and the determination of the predominant mechanism of community assembly. The aim was to investigate the relationships between species co-occurrence and trait similarity in flea communities at various scales (compound communities: across regions within a biogeographic realm or across sampling sites within a geographic region; component communities: across sampling sites within a geographic region; and infracommunities: within a sampling site). We found that compound communities within biogeographic realms were assembled via environmental or host-associated filtering. In contrast, functional and spatial/host-associated co-occurrence networks, at the scale of regional compound communities, mostly indicated either stochastic processes or the lack of dominance of any deterministic process. Analyses of congruence between functional and either spatial (for component communities) or host-associated (for infracommunities) co-occurrence networks demonstrated that assembly rules in these communities varied among host species. In component communities, stochastic processes prevailed, whereas environmental filtering was indicated in 4 and limiting similarity/competition in 9 of 31 communities. Limiting similarity/competition processes dominated in infracommunities, followed by stochastic mechanisms. We conclude that assembly processes in parasite communities are scale-dependent, with different mechanisms acting at different scales.
{"title":"Congruence between co-occurrence and trait-based networks is scale-dependent: a case study with flea parasites of small mammalian hosts.","authors":"Boris R Krasnov, Irina S Khokhlova, Natalya P Korallo-Vinarskaya, Anne Laudisoit, M Fernanda López Berrizbeitia, Sonja Matthee, Julliana P Sanchez, Michal Stanko, Luther van der Mesht, Maxim V Vinarski","doi":"10.1017/S0031182024000969","DOIUrl":"10.1017/S0031182024000969","url":null,"abstract":"<p><p>We applied a novel framework based on network theory and a concept of modularity that estimates congruence between trait-based ( = functional) co-occurrence networks, thus allowing the inference of co-occurrence patterns and the determination of the predominant mechanism of community assembly. The aim was to investigate the relationships between species co-occurrence and trait similarity in flea communities at various scales (compound communities: across regions within a biogeographic realm or across sampling sites within a geographic region; component communities: across sampling sites within a geographic region; and infracommunities: within a sampling site). We found that compound communities within biogeographic realms were assembled <i>via</i> environmental or host-associated filtering. In contrast, functional and spatial/host-associated co-occurrence networks, at the scale of regional compound communities, mostly indicated either stochastic processes or the lack of dominance of any deterministic process. Analyses of congruence between functional and either spatial (for component communities) or host-associated (for infracommunities) co-occurrence networks demonstrated that assembly rules in these communities varied among host species. In component communities, stochastic processes prevailed, whereas environmental filtering was indicated in 4 and limiting similarity/competition in 9 of 31 communities. Limiting similarity/competition processes dominated in infracommunities, followed by stochastic mechanisms. We conclude that assembly processes in parasite communities are scale-dependent, with different mechanisms acting at different scales.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"853-863"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578890/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142392416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-10-02DOI: 10.1017/S003118202400091X
Adriano José Silva Félix, Luiz Felipe Ferreira Trindade, Gabriel Lima Rebêlo, Jorge Kevin Silva Neves, Ana Nunes Santos, Arnaldo Maldonado Júnior, Carlos Eduardo Costa-Campos, Jeannie Nascimento Santos, Francisco Tiago Vasconcelos Melo
Schrankiana are gastrointestinal parasites of anurans, distributed throughout Central and South America. Schrankiana formosula and Schrankiana inconspicata are some of the most commonly reported species parasitising anurans from Brazil, and the morphological differences between them are unclear. In the present study, we redescribed S. formosula based on a re-examination of type series and newly collected material from the frog Leptodactylus pentadactylus in the state of Amapá, Brazil. Additionally, we re-examined the type series of S. inconspicata, and propose it as a junior synonym of S. formosula. We provide detailed morphological and morphometric data with intraspecific variation analyses and new molecular data for S. formosula. In the present phylogeny, S. formosula formed a well-supported clade with Raillietnema sp. and Labeonema synodontisi. Based on molecular phylogenetic analyses and some morphological similarities, our findings support the hypothesis that Schrankiana is a member of the family Cosmocercidae, not Atractidae. Additionally, we provide the first ultrastructural descriptions of S. formosula, and establish the species' phylogenetic position from the Cosmocercidae.
Schrankiana 是无尾类的胃肠道寄生虫,分布于中美洲和南美洲。Schrankiana formosula 和 Schrankiana inconspicata 是巴西最常报道的寄生于无尾类的物种,它们之间的形态差异尚不清楚。在本研究中,我们根据对模式系列的重新研究以及从巴西阿马帕州的五爪蛙中新采集的材料,对 S. formosula 进行了重新描述。此外,我们还重新研究了 S. inconspicata 的模式系列,并提议将其作为 S. formosula 的初级异名。我们为 S. formosula 提供了详细的形态学和形态计量学数据以及种内变异分析和新的分子数据。在目前的系统发育中,S. formosula与Raillietnema sp.和Labeonema synodontisi形成了一个支持良好的支系。基于分子系统进化分析和一些形态上的相似性,我们的研究结果支持 Schrankiana 是 Cosmocercidae 而非 Atractidae 科成员的假设。此外,我们还首次对 S. formosula 进行了超微结构描述,并确定了该物种与 Cosmocercidae 的系统发育位置。
{"title":"Two names, one species: redescription and phylogenetic position of <i>Schrankiana formosula</i> Freitas, 1959 provides new insights into the evolutionary history of the Cosmocercidae.","authors":"Adriano José Silva Félix, Luiz Felipe Ferreira Trindade, Gabriel Lima Rebêlo, Jorge Kevin Silva Neves, Ana Nunes Santos, Arnaldo Maldonado Júnior, Carlos Eduardo Costa-Campos, Jeannie Nascimento Santos, Francisco Tiago Vasconcelos Melo","doi":"10.1017/S003118202400091X","DOIUrl":"10.1017/S003118202400091X","url":null,"abstract":"<p><p><i>Schrankiana</i> are gastrointestinal parasites of anurans, distributed throughout Central and South America. <i>Schrankiana formosula</i> and <i>Schrankiana inconspicata</i> are some of the most commonly reported species parasitising anurans from Brazil, and the morphological differences between them are unclear. In the present study, we redescribed <i>S. formosula</i> based on a re-examination of type series and newly collected material from the frog <i>Leptodactylus pentadactylus</i> in the state of Amapá, Brazil. Additionally, we re-examined the type series of <i>S. inconspicata</i>, and propose it as a junior synonym of <i>S. formosula</i>. We provide detailed morphological and morphometric data with intraspecific variation analyses and new molecular data for <i>S. formosula</i>. In the present phylogeny, <i>S. formosula</i> formed a well-supported clade with <i>Raillietnema</i> sp. and <i>Labeonema synodontisi</i>. Based on molecular phylogenetic analyses and some morphological similarities, our findings support the hypothesis that <i>Schrankiana</i> is a member of the family Cosmocercidae, not Atractidae. Additionally, we provide the first ultrastructural descriptions of <i>S. formosula</i>, and establish the species' phylogenetic position from the Cosmocercidae.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"832-847"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11579040/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142361909","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-10-21DOI: 10.1017/S0031182024001021
William Jones, P Navaneeth Krishna Menon, Anna Qvarnström
Sex biases in prevalence of disease are often attributed to intrinsic factors, such as physiological differences while a proximate role of extrinsic factors such as behavioural or ecological differences may be more difficult to establish. We combined large-scale screening for the presence and lineage identity of avian malaria (haemosporidian) parasites, in 1234 collared flycatchers (Ficedula albicollis) with life-history information from each bird to establish the location and timing of infection. We found an overall infection rate of 36.2% ± 0.03 (95% CI) with 25 distinct malaria lineages. Interestingly, first-year breeding males and females had similar infection prevalence while females accrued a significantly higher infection rate than males later in life. The sex difference in infection rate was driven by the most abundant Haemoproteus, lineage, hPHSIB1, while the infection rate of Plasmodium lineages was similar in males and females. Furthermore, when infections were assigned to an apparent transmission location, we found that the sex difference in infection rate trend was driven by lineages transmitted in Europe, more specifically by one lineage (the hPHSIB1), while no similar pattern was found in African lineages. We deduce that the observed infection patterns are likely to be caused by differences in breeding behaviour, with incubating females (and nestling individuals of both sexes) being easy targets for the biting insects that are the vectors of avian malaria parasites. Overall, our results are most consistent with ecological factors rather than intrinsic factors underlying the observed sex-biased infection rate of avian malaria in collared flycatchers.
{"title":"Location and timing of infection drives a sex-bias in <i>Haemoproteus</i> prevalence in a hole-nesting bird.","authors":"William Jones, P Navaneeth Krishna Menon, Anna Qvarnström","doi":"10.1017/S0031182024001021","DOIUrl":"10.1017/S0031182024001021","url":null,"abstract":"<p><p>Sex biases in prevalence of disease are often attributed to intrinsic factors, such as physiological differences while a proximate role of extrinsic factors such as behavioural or ecological differences may be more difficult to establish. We combined large-scale screening for the presence and lineage identity of avian malaria (haemosporidian) parasites, in 1234 collared flycatchers (<i>Ficedula albicollis</i>) with life-history information from each bird to establish the location and timing of infection. We found an overall infection rate of 36.2% ± 0.03 (95% CI) with 25 distinct malaria lineages. Interestingly, first-year breeding males and females had similar infection prevalence while females accrued a significantly higher infection rate than males later in life. The sex difference in infection rate was driven by the most abundant <i>Haemoproteus,</i> lineage, hPHSIB1, while the infection rate of <i>Plasmodium</i> lineages was similar in males and females. Furthermore, when infections were assigned to an apparent transmission location, we found that the sex difference in infection rate trend was driven by lineages transmitted in Europe, more specifically by one lineage (the hPHSIB1), while no similar pattern was found in African lineages. We deduce that the observed infection patterns are likely to be caused by differences in breeding behaviour, with incubating females (and nestling individuals of both sexes) being easy targets for the biting insects that are the vectors of avian malaria parasites. Overall, our results are most consistent with ecological factors rather than intrinsic factors underlying the observed sex-biased infection rate of avian malaria in collared flycatchers.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"875-883"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578888/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142472250","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Toxocara vitulorum is one of the deadliest parasite of buffalo calves in Bangladesh. This study was conducted to explore genetic variability within and among the T. vitulorum populations in buffalo calves of Bangladesh. Genomic DNA was extracted, ITS2, COX1 and NAD1 gene were amplified and sequenced. Distinct 29 ITS2, 21 unique NAD1 and 24 COX1 genotypes were detected among the T. vitulorum of different geographic regions. These three gene genotypes similarities ranged from 97 to 99%, when these were compared to best hit scoring T. vitulorum sequences retrieved from GenBank. A total of 12 and 6 unique haplotypes were detected for COX1 and NAD1 gene sequences. The average nucleotide and haplotype diversity for COX1 and NAD1 were 0.0931 & 0.89493 and 0.00658 & 0.77895 respectively and the recorded values were more dispersed than previously published values. The pairwise Nst values ranged from −0.050 to 0.602 and Fst from −0.050 to 0.600 between all the T. vitulorum genotypes indicated huge genetic differentiation which were reportedly higher than other published reports Fst values. This is the first report of T. vitulorum on the basis of COX1 gene in Bangladesh. The study findings will be helpful for further extensive epidemiological studies regarding anthelmintic resistance, control and prevention of T. vitulorum infection in buffalo calves.
{"title":"Molecular characterization and genetic variability of <i>Toxocara vitulorum</i> from naturally infected buffalo calves for the first time in Bangladesh.","authors":"Hiranmoy Biswas, Nurnabi Ahmed, Babul Chandra Roy, Mohammad Manjurul Hasan, Md Khalilur Rahman, Md Hasanuzzaman Talukder","doi":"10.1017/S0031182024000842","DOIUrl":"10.1017/S0031182024000842","url":null,"abstract":"<p><p><i>Toxocara vitulorum</i> is one of the deadliest parasite of buffalo calves in Bangladesh. This study was conducted to explore genetic variability within and among the <i>T. vitulorum</i> populations in buffalo calves of Bangladesh. Genomic DNA was extracted, <i>ITS2, COX1</i> and <i>NAD1</i> gene were amplified and sequenced. Distinct 29 <i>ITS2</i>, 21 unique <i>NAD1</i> and 24 <i>COX1</i> genotypes were detected among the <i>T. vitulorum</i> of different geographic regions. These three gene genotypes similarities ranged from 97 to 99%, when these were compared to best hit scoring <i>T. vitulorum</i> sequences retrieved from GenBank. A total of 12 and 6 unique haplotypes were detected for <i>COX1</i> and <i>NAD1</i> gene sequences. The average nucleotide and haplotype diversity for <i>COX1</i> and <i>NAD1</i> were 0.0931 & 0.89493 and 0.00658 & 0.77895 respectively and the recorded values were more dispersed than previously published values. The pairwise Nst values ranged from −0.050 to 0.602 and Fst from −0.050 to 0.600 between all the <i>T. vitulorum</i> genotypes indicated huge genetic differentiation which were reportedly higher than other published reports Fst values. This is the first report of <i>T. vitulorum</i> on the basis of <i>COX1</i> gene in Bangladesh. The study findings will be helpful for further extensive epidemiological studies regarding anthelmintic resistance, control and prevention of <i>T. vitulorum</i> infection in buffalo calves.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"795-807"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11579036/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142472252","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-09-25DOI: 10.1017/S0031182024000891
Jerzy M Behnke, Joseph A Jackson, Francis Gilbert, Eman M E Mohallal, Anna Bajer
The dominant helminths infecting spiny mice (Acomys dimidiatus) in the montane wadis of the Sinai Peninsula of Egypt are spirurid nematodes, notably Protospirura muricola and Mastophorus muris. Both are relatively large robust stomach worms that accumulate in hosts resulting in high worm burdens. To ascertain whether the presence of spirurid worms or their burdens alters the host's likelihood of infection with other helminth species, we analysed a database containing quantitative data on helminth parasites of these mice (n = 431). This comprised of worm burdens recorded during 4 surveys, conducted at 4-year intervals, in 4 wadis, during late summer of each year. The presence of spirurid worms did not significantly alter species richness with other helminth species nor the likelihood of mice carrying other nematode species. However, there was a significant association, particularly of P. muricola, with the presence of intestinal stages of cestodes, and with the acanthocephalan Moniliformis acomysi. After controlling for intrinsic and extrinsic factors, mice harbouring spirurid worms had greater worm burdens of other helminths compared with mice without spirurids. Moreover, spirurid worm burdens showed a significant positive covariation with similarly adjusted species richness of other helminths, non-spirurid helminths, non-spirurid nematodes, oxyuroid nematodes and intestinal stage cestode worm burdens. We interpret these results as an indication that the key driver for co-occurrence of spirurids with other helminths is likely to be transmission via common arthropod hosts (for cestodes and acanthocephalans), but also that mice carrying the heavier spirurid worm burdens become more susceptible to directly transmitted nematodes such as the Oxyuroidea.
{"title":"Large-bodied gastric spirurids (Nematoda, Spirurida) predict structure in the downstream gastrointestinal helminth community of wild spiny mice (<i>Acomys dimidiatus</i>).","authors":"Jerzy M Behnke, Joseph A Jackson, Francis Gilbert, Eman M E Mohallal, Anna Bajer","doi":"10.1017/S0031182024000891","DOIUrl":"10.1017/S0031182024000891","url":null,"abstract":"<p><p>The dominant helminths infecting spiny mice (<i>Acomys dimidiatus</i>) in the montane wadis of the Sinai Peninsula of Egypt are spirurid nematodes, notably <i>Protospirura muricola</i> and <i>Mastophorus muris</i>. Both are relatively large robust stomach worms that accumulate in hosts resulting in high worm burdens. To ascertain whether the presence of spirurid worms or their burdens alters the host's likelihood of infection with other helminth species, we analysed a database containing quantitative data on helminth parasites of these mice (<i>n</i> = 431). This comprised of worm burdens recorded during 4 surveys, conducted at 4-year intervals, in 4 wadis, during late summer of each year. The presence of spirurid worms did not significantly alter species richness with other helminth species nor the likelihood of mice carrying other nematode species. However, there was a significant association, particularly of <i>P. muricola</i>, with the presence of intestinal stages of cestodes, and with the acanthocephalan <i>Moniliformis acomysi</i>. After controlling for intrinsic and extrinsic factors, mice harbouring spirurid worms had greater worm burdens of other helminths compared with mice without spirurids. Moreover, spirurid worm burdens showed a significant positive covariation with similarly adjusted species richness of other helminths, non-spirurid helminths, non-spirurid nematodes, oxyuroid nematodes and intestinal stage cestode worm burdens. We interpret these results as an indication that the key driver for co-occurrence of spirurids with other helminths is likely to be transmission <i>via</i> common arthropod hosts (for cestodes and acanthocephalans), but also that mice carrying the heavier spirurid worm burdens become more susceptible to directly transmitted nematodes such as the Oxyuroidea.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"808-820"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11579037/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142351809","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-10-23DOI: 10.1017/S0031182024000714
Alyssa J Little, Conrad A Matthee, Eddie A Ueckermann, Ivan G Horak, Cang Hui, Sonja Matthee
Mastomys natalensis and M. coucha are commensal rodent species endemic to Africa. A recent taxonomic revision within Mastomys leaves the parasite–host list of M. natalensis questionable and that of M. coucha incomplete. The current study aimed to develop a better understanding of the ectoparasite diversity associated with the 2 distinct but closely related rodent species and to explore the influence of host and habitat type on ectoparasite infestations. Between 2014 and 2020, 590 rodents were trapped in 3 habitat types (village, agriculture and natural) across a wildlife-human/domestic animal interface. In total 48 epifaunistic species (45 ectoparasitic and 3 predatory) represented by 29 genera from 4 taxonomic groups (fleas, lice, mites and ticks) were recorded. Only 50% of the epifauna were shared between the 2 rodent species, with mites the most speciose taxon in both host species. The abundance of epifaunistic individuals, and also those of mites and fleas, were significantly higher on male M. natalensis, while ticks were significantly higher on reproductively active M. natalensis. For both rodent species, infestations by most epifaunistic taxa (on M. natalensis) and some taxa (on M. coucha) were significantly lower in the village as opposed to the less disturbed agricultural and natural habitat types. The study highlights the importance of host life history, even in closely related rodent species, in shaping parasite profiles and a loss of parasite diversity in more extreme anthropogenic habitats.
{"title":"Host and habitat shape ectoparasite diversity on <i>Mastomys natalensis</i> and <i>Mastomys coucha</i> (Muridae).","authors":"Alyssa J Little, Conrad A Matthee, Eddie A Ueckermann, Ivan G Horak, Cang Hui, Sonja Matthee","doi":"10.1017/S0031182024000714","DOIUrl":"10.1017/S0031182024000714","url":null,"abstract":"<p><p><i>Mastomys natalensis</i> and <i>M. coucha</i> are commensal rodent species endemic to Africa. A recent taxonomic revision within <i>Mastomys</i> leaves the parasite–host list of <i>M. natalensis</i> questionable and that of <i>M. coucha</i> incomplete. The current study aimed to develop a better understanding of the ectoparasite diversity associated with the 2 distinct but closely related rodent species and to explore the influence of host and habitat type on ectoparasite infestations. Between 2014 and 2020, 590 rodents were trapped in 3 habitat types (village, agriculture and natural) across a wildlife-human/domestic animal interface. In total 48 epifaunistic species (45 ectoparasitic and 3 predatory) represented by 29 genera from 4 taxonomic groups (fleas, lice, mites and ticks) were recorded. Only 50% of the epifauna were shared between the 2 rodent species, with mites the most speciose taxon in both host species. The abundance of epifaunistic individuals, and also those of mites and fleas, were significantly higher on male <i>M. natalensis</i>, while ticks were significantly higher on reproductively active <i>M. natalensis</i>. For both rodent species, infestations by most epifaunistic taxa (on <i>M. natalensis</i>) and some taxa (on <i>M. coucha</i>) were significantly lower in the village as opposed to the less disturbed agricultural and natural habitat types. The study highlights the importance of host life history, even in closely related rodent species, in shaping parasite profiles and a loss of parasite diversity in more extreme anthropogenic habitats.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"769-783"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11579041/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142505756","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-10-15DOI: 10.1017/S0031182024001008
Megan Porter, Diane P Barton, Joel Williams, Jo Randall, Otso Ovaskainen, David A Crook, Shokoofeh Shamsi
The functioning and richness of marine systems (and biological interactions such as parasitism) are continuously influenced by a changing environment. Using hierarchical modelling of species communities (HMSC), the presence and abundance of multiple parasite species of the black-spotted croaker, Protonibea diacanthus (Sciaenidae), was modelled against environmental measures reflecting seasonal change. Protonibea diacanthus were collected in three seasons across 2019–2021 from four locations within the waters of the Northern Territory, Australia. The length of P. diacanthus proved to have a strong positive effect on the abundance of parasite taxa and overall parasitic assemblage of the sciaenid host. This finding introduces potential implications for parasitism in the future as fish body size responds to fishing pressure and climate changes. Of the various environmental factors measured during the tropical seasons of northern Australia, water temperature and salinity changes were shown as potential causal factors for the variance in parasite presence and abundance, with changes most influential on external parasitic organisms. As environmental factors like ocean temperature and salinity directly affect parasite–host relationships, this study suggests that parasite assemblages and the ecological functions that they perform are likely to change considerably over the coming decades in response to climate change and its proceeding effects.
{"title":"Influence of body size and environmental conditions on parasite assemblages of the black-spotted croaker (<i>Protonibea diacanthus</i>) (Teleostei: Sciaenidae) in northern Australia.","authors":"Megan Porter, Diane P Barton, Joel Williams, Jo Randall, Otso Ovaskainen, David A Crook, Shokoofeh Shamsi","doi":"10.1017/S0031182024001008","DOIUrl":"10.1017/S0031182024001008","url":null,"abstract":"<p><p>The functioning and richness of marine systems (and biological interactions such as parasitism) are continuously influenced by a changing environment. Using hierarchical modelling of species communities (HMSC), the presence and abundance of multiple parasite species of the black-spotted croaker, <i>Protonibea diacanthus</i> (Sciaenidae), was modelled against environmental measures reflecting seasonal change. <i>Protonibea diacanthus</i> were collected in three seasons across 2019–2021 from four locations within the waters of the Northern Territory, Australia. The length of <i>P. diacanthus</i> proved to have a strong positive effect on the abundance of parasite taxa and overall parasitic assemblage of the sciaenid host. This finding introduces potential implications for parasitism in the future as fish body size responds to fishing pressure and climate changes. Of the various environmental factors measured during the tropical seasons of northern Australia, water temperature and salinity changes were shown as potential causal factors for the variance in parasite presence and abundance, with changes most influential on external parasitic organisms. As environmental factors like ocean temperature and salinity directly affect parasite–host relationships, this study suggests that parasite assemblages and the ecological functions that they perform are likely to change considerably over the coming decades in response to climate change and its proceeding effects.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"864-874"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578883/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142472249","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In recent years, air sac parasitic helminths have been reported to cause severe disease in birds. In addition, various species appear to be expanding and infecting new avian hosts in various regions worldwide. In this context, an air sac nematode was initially detected in 2014 infecting the Eurasian scops owl, hospitalized in the local wildlife hospital in Mallorca (Balearic Islands, Spain). Years later, the parasite was detected in 2 other owl species. Air sac nematodes had never been reported in the Mallorcan Strigiformes before. A comprehensive molecular and morphological characterization analysis, including scanning electron microscopy, was required for species confirmation. The species was identified as Lissonema sicki, a parasite infrequently reported in South American owls. Since its first introduction to Mallorca, it has dramatically increased in prevalence in hospitalized birds, being highly prevalent in the Eurasian scops owl (41%), in the long-eared owl (11%) and in the barn owl (4%). The introduction pathway of this parasite to Europe remains unknown. This discovery underscores the expanding range and impact of L. sicki, emphasizing the importance of ongoing surveillance and research to comprehend and manage the implications of its emergence in new territories.
{"title":"<i>Lissonema sicki</i>, an emerging air sac nematode of European owls: introduction, host switching and rapid establishment on a Mediterranean island.","authors":"Sebastià Jaume-Ramis, Sofía Delgado-Serra, Jordi Miquel, Nieves Negre, Ugo Mameli, Carles Feliu, Claudia Paredes-Esquivel","doi":"10.1017/S0031182024000805","DOIUrl":"10.1017/S0031182024000805","url":null,"abstract":"<p><p>In recent years, air sac parasitic helminths have been reported to cause severe disease in birds. In addition, various species appear to be expanding and infecting new avian hosts in various regions worldwide. In this context, an air sac nematode was initially detected in 2014 infecting the Eurasian scops owl, hospitalized in the local wildlife hospital in Mallorca (Balearic Islands, Spain). Years later, the parasite was detected in 2 other owl species. Air sac nematodes had never been reported in the Mallorcan Strigiformes before. A comprehensive molecular and morphological characterization analysis, including scanning electron microscopy, was required for species confirmation. The species was identified as <i>Lissonema sicki</i>, a parasite infrequently reported in South American owls. Since its first introduction to Mallorca, it has dramatically increased in prevalence in hospitalized birds, being highly prevalent in the Eurasian scops owl (41%), in the long-eared owl (11%) and in the barn owl (4%). The introduction pathway of this parasite to Europe remains unknown. This discovery underscores the expanding range and impact of <i>L. sicki</i>, emphasizing the importance of ongoing surveillance and research to comprehend and manage the implications of its emergence in new territories.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"784-794"},"PeriodicalIF":2.1,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11579039/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142351808","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}