International journal for parasitology最新文献

{"title":"Molecular characterisation of Australasian Ixodiphagus (Hymenoptera; Encyrtidae; Encyrtinae) reveals unexpected diversity and a potential novel host switch.","authors":"Madalene M Giannotta, Ina Smith, Michelle Michie, Kim Blasdell, Mike Dunn, James Nicholls, Allen C G Heath, Juanita Rodriguez, Alexander W Gofton","doi":"10.1016/j.ijpara.2024.09.001","DOIUrl":"10.1016/j.ijpara.2024.09.001","url":null,"abstract":"<p><p>Ticks are important medical and veterinary parasites that represent a substantial health threat to humans, companion animals, and livestock. Ixodiphagus wasps (Hymenoptera; Encyrtidae) are known endoparasitoids of ixodid (hard) and argasid (soft) ticks, with potential utility as natural biocontrol agents. Two species, Ixodiphagus brunneus and Ixodiphagus mysorensis, are previously recorded from Australia, however, the genus lacks formal revisionary work in Australia, and the validity and host ranges of these species remain uncertain. This work aimed to investigate the diversity of Ixodiphagus in Australasia and provide a molecular data resource for future work on these understudied endoparasitoids. We extracted DNA from archival Ixodiphagus specimens from Australian and New Zealand insect collections and performed high-throughput sequencing which resulted in complete or mostly complete mitochondrial genome sequences from 11 specimens, including I. brunneus, Ixodiphagus taiaroaensis, and a novel Ixodiphagus sp. reared from Rhipicephalus linnaei from Townsville, Australia. In addition, approximately 70% of the genome of the Wolbachia endosymbiont of I. brunneus was recovered. Finally, we screened 178 recently collected pooled tick samples from southern New South Wales, Australia, for Ixodiphagus spp. using 28S rRNA and cytochrome c oxidase subunit 1(COI) gene PCR, and recovered 14 positive samples. Phylogenetic analysis of Australasian Ixodiphagus spp. based on 28S rRNA and complete mitochondrial genome sequences determined that members of the Australasian fauna are distinct from Ixodiphagus hookeri (the only other Ixodiphagus species for which genetic data exists), and that at least two distinct species are present in Australia; I. brunneus identified from Ixodes holocyclus and Haemaphysalis bancrofti ticks, and an uncharacterised Ixodiphagus sp. found in Rhipicephalus linnaei ticks from northern Queensland. Furthermore, there was substantial genetic diversity at the 28S rRNA loci among I. brunneus samples, which may represent normal genetic variability or a secondary cryptic species. The molecular data generated here represents the first known for the genus Ixodiphagus in Australasia, doubling that of the world fauna, and provides the first known complete mitochondrial genomes for these important tick parasitoids.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":"743-753"},"PeriodicalIF":3.7,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142286308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Evidence for a constitutive cost of host resistance on body fat growth in ewe lambs from lines selected for resistance or susceptibility to experimental infections with Haemonchus contortus.","authors":"Frédéric Douhard, Xavier Matthey, Didier Marcon, Camille Coffre-Thomain, Lucie Estivalet, Delphine Serreau, Fabrice Guégnard, Guillaume Sallé, Papa Moussa Drame, Frédéric Elleboudt, François Lecompte, Hans Adriaensen","doi":"10.1016/j.ijpara.2024.09.004","DOIUrl":"10.1016/j.ijpara.2024.09.004","url":null,"abstract":"<p><p>Although benefits of selection for host resistance to gastro-intestinal nematodes have long been recognized, its costs on production traits remain unclear. A main difficulty when studying those costs is to disentangle genetic effects due to selection from plastic responses induced by infection. Putative costs of host resistance have been extensively investigated in growing sheep. However, while most of those studies have relied on live weight to assess body growth, more comprehensive assessments accounting for body composition are advocated to detect trade-offs. In this study we used 90 female lambs from lines divergently selected on resistance to Haemonchus contortus that we experimentally infected (n = 60) or not (n = 30) under controlled conditions. As those conditions were defined to enable uninfected lambs to fully express their growth potential, we sought to precisely identify the effects of selection for host resistance on health traits and on growth traits. We assessed muscular and fat growth based on repeated measurements with dorsal ultrasonography for all lambs on farm, and with whole-body computed tomography (CT) scans for a subgroup of 18 infected lambs. Lambs achieved a high growth rate, including infected ones despite their high worm burden (confirmed at necropsy in the subgroup). As expected, lambs from the resistant (R) line were less infected than those from the susceptible (S) line. However, the clear pathogenic effects observed on muscular growth and voluntary feed intake were similar between lines. In contrast, a line difference in body fat was supported both by dorsal and volumetric CT measurements. Specifically, lower fat in the R line compared with the S line was observed equally in infected and uninfected groups, thus providing evidence for a constitutive cost of host resistance. Although this cost is not necessarily disadvantageous in nutrient-rich environments exposing animals to excess fat deposition, its consequences in nutrient-scarce environments may be important to promote sustainable breeding strategies for host resistance.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":"767-777"},"PeriodicalIF":3.7,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142346128","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The invasive acanthocephalan parasite Pachysentis canicola is associated with a declining endemic island fox population on San Miguel Island.","authors":"O Alejandro Aleuy, Leslie W Woods, Benjamin J Padilla, Dennis Richardson, Juliann T Schamel, Stacy Baker, Martín García-Varela, Charlotte Hammond, Sarah P Lawson, Jasmine N Childress, Jason Rohr, Kevin D Lafferty","doi":"10.1016/j.ijpara.2024.09.003","DOIUrl":"10.1016/j.ijpara.2024.09.003","url":null,"abstract":"<p><p>In the late 1990s, the San Miguel Island fox (Urocyon littoralis littoralis) faced near-extinction. Fourteen of the 15 remaining foxes were placed into an island-based captive breeding program used to repopulate the island. Although the fox population in San Miguel reached pre-decline numbers by 2010, a second decline started around 2014, coincidental with a newly observed acanthocephalan parasite. To identify this introduced acanthocephalan species and determine the pathologic consequences of its infection on the health of foxes, we used an extensive record of island fox necropsies and associated parasite collections. In addition, we used detailed fox capture-recapture data to investigate population health and demographic trends of foxes before and after parasite emergence. We identify the parasite as Pachysentis canicola, a common acanthocephalan in mainland foxes in North America. The parasite was detected in 69% of the necropsied foxes from San Miguel Island and was not found in any of the other five Channel Island fox subspecies. Health impacts attributed to the acanthocephalan parasite, including erosive and ulcerative enteritis, transmural necrosis, and inflammation, were described in 47% of the foxes infected with the acanthocephalan. Despite infection with various other helminth parasite species, body condition remained good and the mortality rate low in San Miguel Island foxes until the arrival of the acanthocephalan. Body condition improved after 2018, perhaps due to increases in rainfall following a drought, but remained 27% lower than the pre-acanthocephalan period, which suggests that environmental conditions and parasitism jointly drive fox population dynamics.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":"723-732"},"PeriodicalIF":3.7,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142346130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The parasitic nematode Haemonchus contortus lacks molybdenum cofactor synthesis, leading to sulphite sensitivity and lethality in vitro.","authors":"Robert A Brinzer, Jennifer R McIntyre, Collette Britton, Roz Laing","doi":"10.1016/j.ijpara.2024.11.004","DOIUrl":"10.1016/j.ijpara.2024.11.004","url":null,"abstract":"<p><p>Sulphite oxidase has an essential role in detoxifying environmental and endogenously generated sulphite into sulphate and requires the molybdenum cofactor (Moco) to function. Until recently it was believed that the synthesis pathway for Moco was so important for survival that it was conserved in all multicellular animals. Here we report the use of comparative genomics to identify the absence of the first enzyme involved in Moco synthesis in Haemonchus contortus, a highly pathogenic and economically important helminth of livestock that, similar to many parasitic nematode species, has proved difficult to maintain in vitro. We show that Moco deficiency in Haemonchus leads to a high sensitivity to environmental sulphite and limits the ability to maintain the early parasitic larval stages in vitro. Analogous losses in Moco synthesis in other recently sequenced nematode species are also identified. These findings may lead to improved culture methods for parasitic nematodes and to novel approaches for their control.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142768446","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Bat microfilariae in the cityscape: a transmission tale between bats, mites, and bat flies.","authors":"Román Espinal-Palomino, Ana Celia Montes de Oca-Aguilar, Martha Pilar Ibarra-López, Víctor M Vidal-Martínez, Carlos N Ibarra-Cerdeña","doi":"10.1016/j.ijpara.2024.11.001","DOIUrl":"10.1016/j.ijpara.2024.11.001","url":null,"abstract":"<p><p>Litomosoides includes filarial nematodes capable of infecting various vertebrate species. While Litomosoides has been extensively studied in rodents, research on its association with bats remains limited. The transmission dynamics of this parasite are complex, involving moving between different invertebrate hosts before reaching the final host. Most investigations concerning microfilariae have concentrated on their morphological characteristics, with scant attention paid to ecological aspects, particularly in human-altered landscapes. This study represents the first known documentation of Litomosoides in bats within an urban environment. It investigates their response to urbanization in their interaction with the synanthropic bat Artibeus jamaicensis and its ectoparasites. The objective was to explore the influence of urban landscapes on Litomosoides prevalence in synanthropic hosts. Blood samples were collected along urban-rural gradients, and parasite presence was confirmed through direct observation in blood smears and PCR. Phylogenetic analysis based on the mitochondrial cytochrome c oxidase subunit 1 gene (COX1), which exhibited robust support values, indicates that the microfilaria found in A. jamaicensis is closely related to Litomosoides chandleri. However, it also suggests the possibility of an unidentified, and therefore potentially new, species within the genus Litomosoides. Additionally, Litomosoides DNA was detected in Periglischrus iheringi (Acari: Spinturnicidae) and in the bat fly Trichobius intermedius collected from the bat. The parasite sequences obtained from these three interacting species exhibited a genetic distance as low as 0.002. The highest prevalences were recorded in forested areas (28.6%) compared with urban areas (21.2%). However, within the urban landscape, prevalence varied from 3.8% to 21.2%, being highest in densely built-up areas. Analysis of the urban landscape suggested that the prevalence of Litomosoides in A. jamaicensis is the result of a multifactorial and synergistic process involving ectoparasite load, host abundance, and the extent of impervious surfaces (NDBI).</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Dense aquatic vegetation can reduce parasite transmission to amphibians.","authors":"Marin Milotic, Dino Milotic, Janet Koprivnikar","doi":"10.1016/j.ijpara.2024.11.003","DOIUrl":"10.1016/j.ijpara.2024.11.003","url":null,"abstract":"<p><p>Submerged aquatic vegetation (macrophytes) can provide prey with refuges from predators and may perform a similar role for interactions with other natural enemies such as parasites. This could occur by interfering with the ability of free-swimming infectious parasite stages to locate or move towards hosts, reducing infections. Alternatively, infections may increase if macrophytes reduce host anti-parasite behaviours such as detection or evasion. Both scenarios could be affected by macrophyte density and structural complexity. Here we investigated whether experimental infection of tadpoles (Rana sylvatica and Rana pipiens) by parasitic flatworms (the trematodes Ribeiroia ondatrae and Echinostoma spp. was affected by the presence of artificial vegetation with varying density and complexity (simple versus branching), as well as tadpole activity under these conditions. Macrophyte presence significantly reduced tadpole infection loads only in the highest density treatment, but there was no effect of structural complexity. Related to this, tadpoles spent significantly more time near aquatic vegetation when it was dense but showed no preference for either structural type. Our results indicate that aquatic vegetation can reduce parasite transmission in certain scenarios, with further studies needed to explore how structural complexity in natural systems can affect host-parasite interactions, considering the massive physical alterations possible through eutrophication and the introduction of invasive plant species.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619800","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Mitogenomic analysis of the position of the Azygiidae and constituent genera, with a new species of Azygia.","authors":"Danimar López-Hernández, Florian B Reyda, Wenxiang Li, Hudson A Pinto, Sean A Locke","doi":"10.1016/j.ijpara.2024.11.002","DOIUrl":"10.1016/j.ijpara.2024.11.002","url":null,"abstract":"<p><p>The Azygiidae Looss, 1899 is a family of digeneans with a Holarctic distribution in which members of some genera mature in marine elasmobranchs while others occur only in freshwater teleosts. Some have questioned whether the marine genus Otodistomum Stafford, 1904 indeed belongs to the same family as the freshwater azygiid genera, namely Azygia Looss, 1899, Proterometra Horsfall, 1933, and Leuceruthrus Marshall and Gilbert, 1905. We present phylogenetic analyses based on mitochondrial genomes, rDNA operons, and partial cytochrome c oxidase I (Cox1) sequences from North American and Asian species that support the monophyly of Azygiidae, and placement of Azygioidea in the suborder Hemiurata, in contrast to recently published mitochondrial genome phylogenies. All phylogenies indicate that Azygia includes Leuceruthrus, which we therefore propose to be a junior synonym, together with suppression of the Leuceruthrinae. The status of Proterometra was equivocal, with support in some but not all analyses of 28S, but not in other markers. We describe a new species of Azygia from northeastern North America. Our results confirm the morphological variability of adults in Azygia, with worm size positively correlated with host size in Azygia angusticauda. Phylogenies suggest a marine origin for the Azygiidae, and a Palearctic origin for freshwater azygiids, with a single trans-Atlantic radiation to the Nearctic.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619801","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A footworm in the door: revising Onchocerca phylogeny with previously unknown cryptic species in wild North American ungulates.","authors":"Matthew R Kulpa, Emilie Lefoulon, Kimberlee B Beckmen, Samantha E Allen, Jennifer Malmberg, John A Crouse, Daniel P Thompson, Bridgett M Benedict, Dayna A Goldsmith, Sara McCarthy, Lee C Jones, Michael J Yabsley, James M Crum, Susan J Kutz, Guilherme G Verocai","doi":"10.1016/j.ijpara.2024.10.006","DOIUrl":"10.1016/j.ijpara.2024.10.006","url":null,"abstract":"<p><p>Onchocerca is an important genus of vector-borne filarial nematodes that infect both humans and animals worldwide. Many Onchocerca spp., most of medical and veterinary health relevance, are the focus of a variety of diagnostic and molecular research. However, despite the importance of these parasites, there is growing evidence of previously unexplored genetic diversity of these nematodes, particularly among wild ungulate hosts in North America. These understudied parasites prevent us from comprehending the evolutionary history of the genus Onchocerca, monitoring potential One Health threats, and improving our filarioid diagnostic capabilities. In order to fill these knowledge gaps, we identified five uncharacterized Onchocerca lineages and compared them with other well-known filarioid species using single and concatenated gene regions (i.e., nd5, cox1, 12S, 18S, 28S, hsp70, MyoHC, rbp1). Phylogenetic analyses revealed that the novel Onchocerca lineages of wild North American ungulates segregate into two clades. One clade comprised Onchocerca lineages II, IV, and V and other species found mainly in domestic animals and humans, and the second comprised Onchocerca lineages I and III and other species from a variety of hosts including cervids, bovids, and equids. The formation of two clearly separate clades supports the idea of at least two independent expansion events of ancestral Onchocerca spp. into the North American continent via the Bering land bridge. Cophylogenetic analysis shows evidence of ancestral Onchocerca spp. of Bovidae host-switching to wild Cervidae and giving rise to the novel Onchocerca spp. Lastly, pairwise analysis confirms informative molecular markers of diagnostic relevance in both mitochondrial and nuclear gene regions of filarioid nematodes. The overall information provides greater context to the genus Onchocerca and emphasizes the need to discover, characterize, and monitor neglected parasites, especially those of wildlife origin.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619798","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The microRNAome of Strongylus vulgaris larvae and their excretory/secretory products with identification of parasite-derived microRNAs in horse arterial tissue.","authors":"Katrine Toft, Marie Louise Honoré, Nichol E Ripley, Martin K Nielsen, Bastian Fromm, Maibritt Mardahl, Lise N Nielsen, Peter Nejsum, Stig Milan Thamsborg, Susanna Cirera, Tina Holberg Pihl","doi":"10.1016/j.ijpara.2024.10.005","DOIUrl":"10.1016/j.ijpara.2024.10.005","url":null,"abstract":"<p><p>The equine bloodworm, Strongylus vulgaris, is a highly pathogenic parasite causing potentially fatal vascular and intestinal damage. Parasites express and release microRNAs (miRNAs) for internal regulation and to modulate host immunity. The complete set of miRNAs expressed by S. vulgaris (the S. vulgaris miRNAome) remains unannotated and the aim of this study was to annotate the miRNAome of L4 and L5 stages of S. vulgaris, and to examine differences in miRNA abundance between larval stages and sexes. Furthermore, we aimed to determine if miRNAs were detectable in excretory/secretory products (ESPs) from larvae and in arterial tissue from their predilection site, the cranial mesenteric artery (CMA). Larvae were collected from naturally infected foals, and categorized by sex and stage. A subset of larvae was snap-frozen, while those remaining were incubated and the (ESPs) collected. Arterial tissue samples were collected from the CMA. Small RNA sequencing, followed by a custom bioinformatic pipeline, was used for annotation. We identified 142 S. vulgaris miRNAs in larvae and 136 in ESPs. Significant differences in miRNA abundance were observed between larvae and ESPs, and between L5 females (L5Fs) and L5 males (L5Ms), L4s and L5Fs, and L4s and L5Ms. No differences were found between L4s and L5s overall. In ESPs, several miRNAs were differentially abundant across all groups. Validation through quantitative real-time PCR (qPCR) detected selected miRNAs and their differential abundance in larvae and ESPs. One parasite-derived miRNA was detected in some of the horse arterial tissue samples but at very low levels. This study provided the first annotation of the S. vulgaris miRNAome. Most of the annotated larval miRNAs were also detectable in ESPs, and differences in miRNA abundance between sexes were found for larvae, and between sexes and stages for ESPs. Parasite-derived miRNAs were, however, not consistently detectable in the surrounding host arterial tissue.</p>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":" ","pages":""},"PeriodicalIF":3.7,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142604442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Genomic and metagenomic analyses of the domestic mite Tyrophagus putrescentiae identify it as a widespread environmental contaminant and a host of a basal, mite-specific Wolbachia lineage (supergroup Q)","authors":"Pavel B. Klimov ,&nbsp;Jan Hubert ,&nbsp;Tomas Erban ,&nbsp;M. Alejandra Perotti ,&nbsp;Henk R. Braig ,&nbsp;Alex Flynt ,&nbsp;Qixin He ,&nbsp;Yubao Cui","doi":"10.1016/j.ijpara.2024.07.001","DOIUrl":"10.1016/j.ijpara.2024.07.001","url":null,"abstract":"<div><div><em>Tyrophagus putrescentiae</em> (mould mite) is a global, microscopic trophic generalist that commonly occurs in various human-created habitats, causing allergies and damaging stored food. Its ubiquity and extraordinary ability to penetrate research samples or cultures through air currents or by active walking through tights spaces (such as treads of screw caps) may lead to sample contamination and introduction of its DNA to research materials in the laboratory. This prompts a thorough investigation into potential sequence contamination in public genomic databases. The trophic success of <em>T. putrescentiae</em> is primarily attributed to the symbiotic bacteria housed in specialized internal mite structures, facilitating adaptation to varied nutritional niches. However, recent work suggests that horizontal transfer of bacterial/fungal genes related to nutritional functionality may also contribute to the mite’s trophic versatility. This aspect requires independent confirmation. Additionally, <em>T. putrescentiae</em> harbors an uncharacterized and genetically divergent bacterium, <em>Wolbachia</em>, displaying blocking and microbiome-modifying effects. The phylogenomic position and supergroup assignment of this bacterium are unknown. Here, we sequenced and assembled the <em>T. putrescentiae</em> genome, analyzed its microbiome, and performed detailed phylogenomic analyses of the mite-specific <em>Wolbachia</em>. We show that <em>T. putrescentiae</em> DNA is a substantial source of contamination of research samples. Its DNA may inadvertently be co-extracted with the DNA of the target organism, eventually leading to sequence contamination in public databases. We identified a diversity of bacterial species associated with <em>T. putrescentiae</em>, including those capable of rapidly developing antibiotic resistance, such as <em>Escherichia coli</em>. Despite the presence of diverse bacterial communities in <em>T. putrescentiae</em>, we did not detect any recent horizontal gene transfers in this mite species and/or in astigmatid (domestic) mites in general. Our phylogenomic analysis of <em>Wolbachia</em> recovered a basal, mite-specific lineage (supergroup Q) represented by two <em>Wolbachia</em> spp. from the mould mite and a gall-inducing plant mite. Fluorescence in situ hybridization confirmed the presence of <em>Wolbachia</em> inside the mould mite<em>.</em> The discovery of an early derivative <em>Wolbachia</em> lineage (supergroup Q) in two phylogenetically unrelated and ecologically dissimilar mites suggests that this endosymbiotic bacterial lineage formed a long-term association with mites. This finding provides a unique insight into the early evolution and host associations of <em>Wolbachia</em>. Further discoveries of <em>Wolbachia</em> diversity in acariform mites are anticipated.</div></div>","PeriodicalId":13725,"journal":{"name":"International journal for parasitology","volume":"54 13","pages":"Pages 661-674"},"PeriodicalIF":3.7,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141590232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}