Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2025.100253
Radouane Ouali, Sabrina Bousbata
Rhodnius prolixus Stål (Hemiptera: Reduviidae: Triatominae) a hematophagous model organism and vector of Chagas disease, relies on a complex repertoire of digestive enzymes to process its blood meals. Among these, aspartic proteases from the A1 peptidase family play a crucial role in nutrient breakdown. This study aims to refine the gene annotation of the A1 peptidase family in this organism through proteogenomics. A comprehensive analysis of aspartic protease gene sequences and protein isoforms, identified by proteomics, revealed discrepancies in existing gene annotations, including the identification of novel open reading frames and the consolidation of previously separated gene sequences. Our efforts led to the correction of seven gene annotations, reducing the total count of A1 peptidase genes from 19 to 15. Notably, 11 of these genes were confirmed at the protein level, while two were supported by transcriptomic data. Furthermore, our findings highlight instances of alternative splicing, as seen in RPRC015076, where proteoforms T1IFK7 and R4G5J6 are expressed through intron retention. This study not only provides a more accurate and comprehensive genomic framework for the A1 peptidase family but also offers new insights into the functional complexity and regulation of digestive enzymes in R. prolixus. These findings pave the way for future studies on insect digestive biology and their potential applications in vector control strategies.
{"title":"Refining the annotation of Rhodnius prolixus aspartic proteases A1 family genes through proteogenomics","authors":"Radouane Ouali, Sabrina Bousbata","doi":"10.1016/j.crpvbd.2025.100253","DOIUrl":"10.1016/j.crpvbd.2025.100253","url":null,"abstract":"<div><div><em>Rhodnius prolixus</em> Stål (Hemiptera: Reduviidae: Triatominae) a hematophagous model organism and vector of Chagas disease, relies on a complex repertoire of digestive enzymes to process its blood meals. Among these, aspartic proteases from the A1 peptidase family play a crucial role in nutrient breakdown. This study aims to refine the gene annotation of the A1 peptidase family in this organism through proteogenomics. A comprehensive analysis of aspartic protease gene sequences and protein isoforms, identified by proteomics, revealed discrepancies in existing gene annotations, including the identification of novel open reading frames and the consolidation of previously separated gene sequences. Our efforts led to the correction of seven gene annotations, reducing the total count of A1 peptidase genes from 19 to 15. Notably, 11 of these genes were confirmed at the protein level, while two were supported by transcriptomic data. Furthermore, our findings highlight instances of alternative splicing, as seen in RPRC015076, where proteoforms T1IFK7 and R4G5J6 are expressed through intron retention. This study not only provides a more accurate and comprehensive genomic framework for the A1 peptidase family but also offers new insights into the functional complexity and regulation of digestive enzymes in <em>R. prolixus</em>. These findings pave the way for future studies on insect digestive biology and their potential applications in vector control strategies.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"7 ","pages":"Article 100253"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143684031","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2025.100295
Ceri Edwards , Frank Katzer , Paul M. Bartley , Janet Roden , Hannah J. Shaw
Cryptosporidium spp., particularly Cryptosporidium parvum, pose a significant threat to raw water quality and public health. Cryptosporidiosis, a gastrointestinal zoonotic disease, causes diarrhoea in dairy and beef production systems worldwide. Infected calves shed Cryptosporidium spp. oocysts in faeces, posing risks of contaminating surface water sources. Understanding the dynamics of Cryptosporidium contamination is crucial for effective water quality management. This study investigated Cryptosporidium spp. prevalence in neonatal calves and its potential impact on water quality before abstraction and treatment. The study analysed faecal samples from 1–3-week-old calves on two English dairy farms upstream of a water abstraction point. Initial screening used C. parvum immune chromatographic assays (ICT) on 47 faecal samples. This was followed by DNA extraction and species identification, with gp60 subtyping. Raw and treated water quality data were analysed to determine Cryptosporidium oocyst counts. Cryptosporidium parvum was the predominant species in calves at both farms, with gp60 subtype IIaA17G2R1 being the only subtype detected. Some calf samples revealed mixed infections with C. parvum and C. ryanae. Raw-water samples (n = 214) revealed a 50.00% positivity rate for Cryptosporidium oocysts, with 22.43% (24/107) containing C. parvum/C. hominis and the remainder 77.57% (83/107) C. andersoni. Water treatment significantly reduced oocyst counts (P < 0.001); however, due to the increase in popularity of bathing in rivers, oocysts present in raw river water may still prove a public health risk.
{"title":"Cryptosporidium prevalence in calves and its effect on local water quality prior to abstraction and treatment","authors":"Ceri Edwards , Frank Katzer , Paul M. Bartley , Janet Roden , Hannah J. Shaw","doi":"10.1016/j.crpvbd.2025.100295","DOIUrl":"10.1016/j.crpvbd.2025.100295","url":null,"abstract":"<div><div><em>Cryptosporidium</em> spp., particularly <em>Cryptosporidium parvum</em>, pose a significant threat to raw water quality and public health. Cryptosporidiosis, a gastrointestinal zoonotic disease, causes diarrhoea in dairy and beef production systems worldwide. Infected calves shed <em>Cryptosporidium</em> spp. oocysts in faeces, posing risks of contaminating surface water sources. Understanding the dynamics of <em>Cryptosporidium</em> contamination is crucial for effective water quality management. This study investigated <em>Cryptosporidium</em> spp. prevalence in neonatal calves and its potential impact on water quality before abstraction and treatment. The study analysed faecal samples from 1–3-week-old calves on two English dairy farms upstream of a water abstraction point. Initial screening used <em>C. parvum</em> immune chromatographic assays (ICT) on 47 faecal samples. This was followed by DNA extraction and species identification, with <em>gp60</em> subtyping. Raw and treated water quality data were analysed to determine <em>Cryptosporidium</em> oocyst counts. <em>Cryptosporidium parvum</em> was the predominant species in calves at both farms, with <em>gp60</em> subtype IIaA17G2R1 being the only subtype detected. Some calf samples revealed mixed infections with <em>C. parvum</em> and <em>C. ryanae</em>. Raw-water samples (<em>n</em> = 214) revealed a 50.00% positivity rate for <em>Cryptosporidium</em> oocysts, with 22.43% (24/107) containing <em>C. parvum/C. hominis</em> and the remainder 77.57% (83/107) <em>C. andersoni</em>. Water treatment significantly reduced oocyst counts (<em>P</em> < 0.001); however, due to the increase in popularity of bathing in rivers, oocysts present in raw river water may still prove a public health risk.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"8 ","pages":"Article 100295"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144654635","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2025.100329
Erica Burkman , Lucienne Tritten , Christopher C. Evans , Guilherme G. Verocai , Caroline Sobotyk , Timothy G. Geary , Andrew R. Moorhead
Host specificity is a critical feature of the survival and proliferation of parasites. In the context of interactions with the host, numerous mechanisms have been identified, particularly in parasitic helminths, that enable manipulation of the host immune system to enhance their own survival. The evolutionary history of these interactions often results in hosts becoming disease-tolerant or asymptomatic, even when burdened with a high number of worms, until a disruption in the host’s immune system can trigger a disease state. However, the molecular mechanisms underlying host specificity and the ways in which parasites alter the host’s immune system remain largely unexplored. Research conducted on parasite-derived microRNAs (miRNAs) suggests they may play a role in remodeling the host to improve parasite survival and growth, possibly through directed pathology. To further explore this host-parasite relationship, we analyzed plasma of four cats experimentally infected with the filarial nematode Brugia malayi, each with varying levels of microfilaremia, six months post-infection. Out of approximately 32 million sequencing reads, we detected 185 mature miRNA candidates potentially originating from B. malayi, with 26 miRNAs present in 10 or more copies. We also identified seven immunity-related host genes (Ptgs1, Irf4, Irf5, Numbl, Tnfsf15, Stat3, and Txlnb) that are predicted to be targets of parasite-derived miRNAs. Additional investigation is warranted to elucidate the role of these miRNAs in the host-parasite interaction. These data offer promising targets for further exploration, and potentially the discovery of novel therapeutics that disrupt parasite immune evasion and pathological alterations to the host.
{"title":"Brugia malayi miRNAs and potential targets within the feline host (Felis catus)","authors":"Erica Burkman , Lucienne Tritten , Christopher C. Evans , Guilherme G. Verocai , Caroline Sobotyk , Timothy G. Geary , Andrew R. Moorhead","doi":"10.1016/j.crpvbd.2025.100329","DOIUrl":"10.1016/j.crpvbd.2025.100329","url":null,"abstract":"<div><div>Host specificity is a critical feature of the survival and proliferation of parasites. In the context of interactions with the host, numerous mechanisms have been identified, particularly in parasitic helminths, that enable manipulation of the host immune system to enhance their own survival. The evolutionary history of these interactions often results in hosts becoming disease-tolerant or asymptomatic, even when burdened with a high number of worms, until a disruption in the host’s immune system can trigger a disease state. However, the molecular mechanisms underlying host specificity and the ways in which parasites alter the host’s immune system remain largely unexplored. Research conducted on parasite-derived microRNAs (miRNAs) suggests they may play a role in remodeling the host to improve parasite survival and growth, possibly through directed pathology. To further explore this host-parasite relationship, we analyzed plasma of four cats experimentally infected with the filarial nematode <em>Brugia malayi</em>, each with varying levels of microfilaremia, six months post-infection. Out of approximately 32 million sequencing reads, we detected 185 mature miRNA candidates potentially originating from <em>B. malayi</em>, with 26 miRNAs present in 10 or more copies. We also identified seven immunity-related host genes (<em>Ptgs1</em>, <em>Irf4</em>, <em>Irf5</em>, <em>Numbl</em>, <em>Tnfsf15</em>, <em>Stat3</em>, and <em>Txlnb</em>) that are predicted to be targets of parasite-derived miRNAs. Additional investigation is warranted to elucidate the role of these miRNAs in the host-parasite interaction. These data offer promising targets for further exploration, and potentially the discovery of novel therapeutics that disrupt parasite immune evasion and pathological alterations to the host.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"8 ","pages":"Article 100329"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145361535","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2024.100240
Bronislava Víchová , Michal Stanko , Martina Miterpáková , Zuzana Hurníková , Yaroslav Syrota , Patrícia Schmer-Jakšová , Petronela Komorová , Lucia Vargová , Veronika Blažeková , Dana Zubriková , Klaudia Mária Švirlochová , Gabriela Chovancová
Rodents and insectivores are significant reservoirs of many zoonotic pathogens, contributing to the transmission of diseases affecting human and animal health. This study investigated the prevalence and diversity of vector-borne pathogens in small mammals within the High Tatras region of Slovakia, an area with substantial recreational activity and protected zones. A total of 156 small mammals, comprising ten species, were screened for pathogens such as Bartonella spp., Borrelia spp., Anaplasma phagocytophilum, and Babesia spp. The prevalence of vector-borne pathogens in the studied animals reached 74.35%, with Bartonella spp. being the most common, identified in 57.7% of the animals, particularly in Apodemus flavicollis and Clethrionomys glareolus. Borrelia burgdorferi (sensu lato) was detected in 11.5% of the rodents, with Borrelia afzelii identified as the predominant species. Babesia microti was found in A. flavicollis and Mus musculus, with a total prevalence of 3.2%. The lowest was the prevalence of A. phagocytophilum reaching 1.9%. This study provides evidence of the significant role of rodents as reservoirs of vector-borne pathogens in protected areas of the High Tatras region and Tatra National Park.
{"title":"Small mammals as hosts of vector-borne pathogens in the High Tatra Mountains region in Slovakia, Central Europe","authors":"Bronislava Víchová , Michal Stanko , Martina Miterpáková , Zuzana Hurníková , Yaroslav Syrota , Patrícia Schmer-Jakšová , Petronela Komorová , Lucia Vargová , Veronika Blažeková , Dana Zubriková , Klaudia Mária Švirlochová , Gabriela Chovancová","doi":"10.1016/j.crpvbd.2024.100240","DOIUrl":"10.1016/j.crpvbd.2024.100240","url":null,"abstract":"<div><div>Rodents and insectivores are significant reservoirs of many zoonotic pathogens, contributing to the transmission of diseases affecting human and animal health. This study investigated the prevalence and diversity of vector-borne pathogens in small mammals within the High Tatras region of Slovakia, an area with substantial recreational activity and protected zones. A total of 156 small mammals, comprising ten species, were screened for pathogens such as <em>Bartonella</em> spp., <em>Borrelia</em> spp., <em>Anaplasma phagocytophilum</em>, and <em>Babesia</em> spp. The prevalence of vector-borne pathogens in the studied animals reached 74.35%, with <em>Bartonella</em> spp. being the most common, identified in 57.7% of the animals, particularly in <em>Apodemus flavicollis</em> and <em>Clethrionomys glareolus</em>. <em>Borrelia burgdorferi</em> (<em>sensu lato</em>) was detected in 11.5% of the rodents, with <em>Borrelia afzelii</em> identified as the predominant species. <em>Babesia microti</em> was found in <em>A. flavicollis</em> and <em>Mus musculus</em>, with a total prevalence of 3.2%. The lowest was the prevalence of <em>A. phagocytophilum</em> reaching 1.9%. This study provides evidence of the significant role of rodents as reservoirs of vector-borne pathogens in protected areas of the High Tatras region and Tatra National Park.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"7 ","pages":"Article 100240"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11751563/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143026256","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The evolutionary origin of coronaviruses is related to bats (order Chiroptera), and their association with pathologies in animals and humans is expected. Anthropic threats reduce bat diversity and expose humans to extraordinary transmission and spread of associated viruses, putting health and food security at risk owing to the multiple ecological roles that bats play. This study aimed to determine the presence of coronaviruses in bats in the Department of Córdoba, Colombia. Between 2022 and 2023, 11 municipalities were selected using non-probabilistic sampling methods. A total of 262 bats belonging to 16 species of five families were captured and identified. Serological tests were performed to detect SARS-CoV-2, and nested polymerase chain reaction (PCR) was performed to detect the coronavirus RdRp gene. RdRp-positive samples were sequenced using Sanger sequencing. Five specimens (2.7%) had antibodies against the coronavirus N protein, and the RdRp gene was detected in 55 specimens (21.0%), all belonging to the family Phyllostomidae. Phylogenetic analysis of the RdRp gene revealed that the newly generated sequences represented alphacoronaviruses. Bats tested in ecoregions with greater anthropogenic intervention were shown to be carriers of coronaviruses, unlike bats from conserved ecoregions. Coronavirus surveillance in bats has revealed previous infections through serology and circulating infections in natural populations of different ecoregions of the Department of Córdoba, where inter-species jumps could be generated by contact between bats and domestic/wild animals, or humans.
{"title":"Bats from an area of the Colombian Caribbean reveal the circulation of Alphacoronavirus","authors":"Caty Martínez , Daniel Echeverri , Alfonso Calderón , Eliana Hurtado , Bertha Gastelbondo , Yésica López , Jairo Martínez , Yeimy López , Yesica Botero , Camilo Guzmán , Ketty Galeano , Valeria Bertel , Yonairo Herrera , Germán Arrieta , Joao Pessoa Araujo , Salim Mattar","doi":"10.1016/j.crpvbd.2025.100261","DOIUrl":"10.1016/j.crpvbd.2025.100261","url":null,"abstract":"<div><div>The evolutionary origin of coronaviruses is related to bats (order Chiroptera), and their association with pathologies in animals and humans is expected. Anthropic threats reduce bat diversity and expose humans to extraordinary transmission and spread of associated viruses, putting health and food security at risk owing to the multiple ecological roles that bats play. This study aimed to determine the presence of coronaviruses in bats in the Department of Córdoba, Colombia. Between 2022 and 2023, 11 municipalities were selected using non-probabilistic sampling methods. A total of 262 bats belonging to 16 species of five families were captured and identified. Serological tests were performed to detect SARS-CoV-2, and nested polymerase chain reaction (PCR) was performed to detect the coronavirus RdRp gene. RdRp-positive samples were sequenced using Sanger sequencing. Five specimens (2.7%) had antibodies against the coronavirus N protein, and the RdRp gene was detected in 55 specimens (21.0%), all belonging to the family Phyllostomidae. Phylogenetic analysis of the RdRp gene revealed that the newly generated sequences represented alphacoronaviruses. Bats tested in ecoregions with greater anthropogenic intervention were shown to be carriers of coronaviruses, unlike bats from conserved ecoregions. Coronavirus surveillance in bats has revealed previous infections through serology and circulating infections in natural populations of different ecoregions of the Department of Córdoba, where inter-species jumps could be generated by contact between bats and domestic/wild animals, or humans.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"7 ","pages":"Article 100261"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143942773","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2025.100256
Pichet Ruenchit
Many antiparasitic drugs have become obsolete and ineffective in treating parasitic diseases. This ineffectiveness arises from parasite drug resistance, high toxicity, and low drug efficacy. Thus, the discovery of novel agents is urgently needed to control parasitic diseases. Various strategies are employed in drug discovery, design, and development. This review highlights the paradigm of searching for bioactive molecules produced during inter- and intraspecific competition among organisms, particularly between microbes and parasites, as a strategy for de novo antiparasitic drug discovery. Competitive interactions occur when individuals of the same or different species coexist in overlapping niches and compete for space and resources. These interactions are well recognized. Therefore, bioactive molecules released during these interactions are promising targets for novel drug discovery. Compelling data indicate that microbes remain a potential source for the discovery of novel antiparasitic drugs because of their diversity. Many antimicrobial producers in nature have yet to be isolated and investigated. This body of evidence underscores the success of numerous therapeutic drugs, including penicillin, β-lactams, and tetracyclines, which have been successfully discovered and developed for treating infectious diseases. This review comprehensively covers these concepts, with a particular focus on inter- and intraspecific competition in the discovery of novel antiparasitic agents. This approach will pave the way for identifying alternative strategies to control and eradicate parasitic diseases that continue to threaten human health. Additionally, this review discusses current antiparasitic drugs and their mechanisms of action, limitations, and existing gaps. This discussion emphasizes the ongoing need to explore novel antiparasitic drugs.
{"title":"Exploring bioactive molecules released during inter- and intraspecific competition: A paradigm for novel antiparasitic drug discovery and design for human use","authors":"Pichet Ruenchit","doi":"10.1016/j.crpvbd.2025.100256","DOIUrl":"10.1016/j.crpvbd.2025.100256","url":null,"abstract":"<div><div>Many antiparasitic drugs have become obsolete and ineffective in treating parasitic diseases. This ineffectiveness arises from parasite drug resistance, high toxicity, and low drug efficacy. Thus, the discovery of novel agents is urgently needed to control parasitic diseases. Various strategies are employed in drug discovery, design, and development. This review highlights the paradigm of searching for bioactive molecules produced during inter- and intraspecific competition among organisms, particularly between microbes and parasites, as a strategy for <em>de novo</em> antiparasitic drug discovery. Competitive interactions occur when individuals of the same or different species coexist in overlapping niches and compete for space and resources. These interactions are well recognized. Therefore, bioactive molecules released during these interactions are promising targets for novel drug discovery. Compelling data indicate that microbes remain a potential source for the discovery of novel antiparasitic drugs because of their diversity. Many antimicrobial producers in nature have yet to be isolated and investigated. This body of evidence underscores the success of numerous therapeutic drugs, including penicillin, β-lactams, and tetracyclines, which have been successfully discovered and developed for treating infectious diseases. This review comprehensively covers these concepts, with a particular focus on inter- and intraspecific competition in the discovery of novel antiparasitic agents. This approach will pave the way for identifying alternative strategies to control and eradicate parasitic diseases that continue to threaten human health. Additionally, this review discusses current antiparasitic drugs and their mechanisms of action, limitations, and existing gaps. This discussion emphasizes the ongoing need to explore novel antiparasitic drugs.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"7 ","pages":"Article 100256"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143826358","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Burmese fighting chickens (Gallus gallus) raised in Nakhon Ratchasima Province, eastern Thailand, were investigated for filarioids and co-infection with other haemoparasites. Microscopy and molecular diagnostic targeting the cox1 gene revealed that 2 out of 12 chickens tested positive for onchocercid filarioids. One chicken carried a single infection (Onchocercidae sp. CH09), characterized by unsheathed microfilariae with a cross-striated cuticle, a blunt anterior end, a short cephalic space, and a hook-like tail tip. Another chicken exhibited a mixed filarioid infection, necessitating the subcloning of two distinct isolates (Onchocercidae sp. CH07-S1 and CH07-S2). This chicken had two distinct microfilarial forms: (i) unsheathed microfilariae resembling Onchocercidae sp. CH09 and (ii) sheathed microfilariae with a short cephalic space and paired nuclei at both extremities. Genetic analyses of cox1 sequences demonstrated that these forms belong to two distinct species. Isolates CH09 and CH07-S1 closely resembled Onchocercidae sp. (Eufilaria sp.) ROE14 (GenBank: PQ564658) derived from a chicken in eastern Thailand. They constituted a clade phylogenetically distinct from other species of Eufilaria and Filarioidea in passerine birds and Culex mosquitoes, suggesting they may represent a potentially novel onchocercid or a distant Eufilaria species. CH07-S2 exhibited the closest genetic affinity to Onchocercidae sp. KLS08 (GenBank: PQ564657) derived from a chicken in eastern Thailand. Interestingly, they established a distinct clade from the other reported filarial genera that parasitize avian hosts, perhaps being a novel onchocercid species or genus within galliforms. Plasmodium juxtanucleare was identified in 6 out of 12 chickens, including one case of co-infection with onchocercids. Our study highlights the significance of molecular approaches in revealing filarial diversity and genetic relationships, while underscoring emerging hotspots of avian filariasis in Thailand and beyond.
{"title":"Discovery of potentially novel species of the Onchocercidae (Nematoda: Filarioidea) in Burmese fighting chickens (Gallus gallus): Genetic insights into avian filariasis and co-infection with Plasmodium juxtanucleare","authors":"Duriyang Narapakdeesakul , Witchuta Junsiri , Rittidet Kongtawee , Kajornsak Lattisarapunt , Piyanan Taweethavonsawat","doi":"10.1016/j.crpvbd.2025.100303","DOIUrl":"10.1016/j.crpvbd.2025.100303","url":null,"abstract":"<div><div>Burmese fighting chickens (<em>Gallus gallus</em>) raised in Nakhon Ratchasima Province, eastern Thailand, were investigated for filarioids and co-infection with other haemoparasites. Microscopy and molecular diagnostic targeting the <em>cox</em>1 gene revealed that 2 out of 12 chickens tested positive for onchocercid filarioids. One chicken carried a single infection (Onchocercidae sp. CH09), characterized by unsheathed microfilariae with a cross-striated cuticle, a blunt anterior end, a short cephalic space, and a hook-like tail tip. Another chicken exhibited a mixed filarioid infection, necessitating the subcloning of two distinct isolates (Onchocercidae sp. CH07-S1 and CH07-S2). This chicken had two distinct microfilarial forms: (i) unsheathed microfilariae resembling Onchocercidae sp. CH09 and (ii) sheathed microfilariae with a short cephalic space and paired nuclei at both extremities. Genetic analyses of <em>cox</em>1 sequences demonstrated that these forms belong to two distinct species. Isolates CH09 and CH07-S1 closely resembled Onchocercidae sp. (<em>Eufilaria</em> sp.) ROE14 (GenBank: PQ564658) derived from a chicken in eastern Thailand. They constituted a clade phylogenetically distinct from other species of <em>Eufilaria</em> and Filarioidea in passerine birds and <em>Culex</em> mosquitoes, suggesting they may represent a potentially novel onchocercid or a distant <em>Eufilaria</em> species. CH07-S2 exhibited the closest genetic affinity to Onchocercidae sp. KLS08 (GenBank: PQ564657) derived from a chicken in eastern Thailand. Interestingly, they established a distinct clade from the other reported filarial genera that parasitize avian hosts, perhaps being a novel onchocercid species or genus within galliforms. <em>Plasmodium juxtanucleare</em> was identified in 6 out of 12 chickens, including one case of co-infection with onchocercids. Our study highlights the significance of molecular approaches in revealing filarial diversity and genetic relationships, while underscoring emerging hotspots of avian filariasis in Thailand and beyond.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"8 ","pages":"Article 100303"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144865458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2025.100309
Andrea Springer , Christin Krüger , Christina Strube , Dirk Steinhauer
Infections with facultatively parasitic Halicephalobus spp. nematodes are usually fatal in animals and humans. Here, transplacental transmission of a species of Halicephalobus is described for the first time, causing reproductive failure of a mare during two consecutive gestations. In both cases, histology showed adult and larval nematodes in the placenta and various foetal organs, without signs of generalized halicephalobosis in the mare. An identical 18S rRNA-ITS1-5.8S rRNA-ITS2 sequence generated from both placentas showed considerable divergence from a previously sequenced equine isolate, suggesting cryptic diversity among Halicephalobus isolates in vertebrates. This ubiquitous nematode may be a cause of equine abortion associated with considerable economic loss. Future research should aim at exploring effective treatment options and clarifying the true taxonomic diversity within the genus Halicephalobus.
{"title":"Worms and reproductive failure: First evidence of transplacental Halicephalobus transmission leading to repeated equine abortion","authors":"Andrea Springer , Christin Krüger , Christina Strube , Dirk Steinhauer","doi":"10.1016/j.crpvbd.2025.100309","DOIUrl":"10.1016/j.crpvbd.2025.100309","url":null,"abstract":"<div><div>Infections with facultatively parasitic <em>Halicephalobus</em> spp. nematodes are usually fatal in animals and humans. Here, transplacental transmission of a species of <em>Halicephalobus</em> is described for the first time, causing reproductive failure of a mare during two consecutive gestations. In both cases, histology showed adult and larval nematodes in the placenta and various foetal organs, without signs of generalized halicephalobosis in the mare. An identical 18S rRNA-ITS1-5.8S rRNA-ITS2 sequence generated from both placentas showed considerable divergence from a previously sequenced equine isolate, suggesting cryptic diversity among <em>Halicephalobus</em> isolates in vertebrates. This ubiquitous nematode may be a cause of equine abortion associated with considerable economic loss. Future research should aim at exploring effective treatment options and clarifying the true taxonomic diversity within the genus <em>Halicephalobus</em>.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"8 ","pages":"Article 100309"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144923056","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2025.100270
Dana Zubriková , Lucia Vargová , Júlia Halapy , Branislav Lukáč , Veronika Blažeková , Klaudia Mária Švirlochová , Eva Čisovská Bazsalovicsová , Ján Čurlík , Ivana Heglasová , Bronislava Víchová
Some piroplasmids and haemotropic mycoplasmas are important pathogens affecting domestic and wild animals, leading to various clinical symptoms and economic losses. This study aimed to determine, for the first time, the prevalence of haemotropic mycoplasmas and Babesia/Theileria species in domestic and wild ruminants in Slovakia, Central Europe. Blood samples from cattle, goats, and sheep (n = 549) and liver samples from red deer (n = 43) were collected across Slovakia between 2008 and 2024. DNA was extracted and screened by PCR and sequencing for haemotropic mycoplasmas and piroplasmids. The overall prevalence of haemotropic mycoplasmas was highest in cattle at 53.3% (124/232) and in sheep at 60% (90/150), whereas the prevalence in goats was substantially lower (4.2%; 7/167). Specifically, Mycoplasma wenyonii and “Candidatus Mycoplasma haematobovis” were detected in cattle, while Mycoplasma ovis-like microorganisms were identified in sheep and goats. For Babesia/Theileria species, a prevalence of 1.8% was recorded in goats, with no detections in sheep, and a prevalence of 65.1% was confirmed in red deer, where sequencing confirmed the presence of Theileria capreoli. This study presents the first report on the prevalence of haemotropic mycoplasmas in ruminants in Slovakia, highlighting the need for further research into transmission dynamics and potential zoonotic risks.
{"title":"Prevalence of haemotropic mycoplasmas and blood piroplasmids in domestic and wild ruminants in Slovakia, Central Europe","authors":"Dana Zubriková , Lucia Vargová , Júlia Halapy , Branislav Lukáč , Veronika Blažeková , Klaudia Mária Švirlochová , Eva Čisovská Bazsalovicsová , Ján Čurlík , Ivana Heglasová , Bronislava Víchová","doi":"10.1016/j.crpvbd.2025.100270","DOIUrl":"10.1016/j.crpvbd.2025.100270","url":null,"abstract":"<div><div>Some piroplasmids and haemotropic mycoplasmas are important pathogens affecting domestic and wild animals, leading to various clinical symptoms and economic losses. This study aimed to determine, for the first time, the prevalence of haemotropic mycoplasmas and <em>Babesia</em>/<em>Theileria</em> species in domestic and wild ruminants in Slovakia, Central Europe. Blood samples from cattle, goats, and sheep (<em>n</em> = 549) and liver samples from red deer (<em>n</em> = 43) were collected across Slovakia between 2008 and 2024. DNA was extracted and screened by PCR and sequencing for haemotropic mycoplasmas and piroplasmids. The overall prevalence of haemotropic mycoplasmas was highest in cattle at 53.3% (124/232) and in sheep at 60% (90/150), whereas the prevalence in goats was substantially lower (4.2%; 7/167). Specifically, <em>Mycoplasma wenyonii</em> and “<em>Candidatus</em> Mycoplasma haematobovis” were detected in cattle, while <em>Mycoplasma ovis</em>-like microorganisms were identified in sheep and goats. For <em>Babesia</em>/<em>Theileria</em> species, a prevalence of 1.8% was recorded in goats, with no detections in sheep, and a prevalence of 65.1% was confirmed in red deer, where sequencing confirmed the presence of <em>Theileria capreoli</em>. This study presents the first report on the prevalence of haemotropic mycoplasmas in ruminants in Slovakia, highlighting the need for further research into transmission dynamics and potential zoonotic risks.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"8 ","pages":"Article 100270"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144480458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crpvbd.2025.100280
Samantha Gunasekera , Jessica C. Kissinger
Parasites of the genus Cryptosporidium have evolved to have a highly compact genome of ∼9.1 Mb. The mechanisms that regulate gene expression in Cryptosporidium spp. remain incompletely understood at all levels, including chromatin accessibility, transcription factor activation and repression and RNA processing. This review discusses possible mechanisms of gene regulation in Cryptosporidium spp., including histone modifications, cis regulatory elements, transcription factors and non-coding RNAs. Cryptosporidium spp. are among the most basal branching apicomplexans and existing evidence suggests that they diverge from other members of their phylum via retention of the E2F/DP1 transcription factor family, and the recent discovery that C. parvum produces polycistronic transcripts. Most of what we know about gene regulation in the genus Cryptosporidium is based on sequence conservation and homology with other members of the phylum Apicomplexa, and in some cases, more distant eukaryotes. Very few putative gene regulatory components identified in Cryptosporidium spp. are supported by experimental confirmation. This review summarizes what we know about gene regulation in Cryptosporidium spp. and identifies gaps in our current understanding.
{"title":"Gene regulation in Cryptosporidium: New insights and unanswered questions","authors":"Samantha Gunasekera , Jessica C. Kissinger","doi":"10.1016/j.crpvbd.2025.100280","DOIUrl":"10.1016/j.crpvbd.2025.100280","url":null,"abstract":"<div><div>Parasites of the genus <em>Cryptosporidium</em> have evolved to have a highly compact genome of ∼9.1 Mb. The mechanisms that regulate gene expression in <em>Cryptosporidium</em> spp. remain incompletely understood at all levels, including chromatin accessibility, transcription factor activation and repression and RNA processing. This review discusses possible mechanisms of gene regulation in <em>Cryptosporidium</em> spp., including histone modifications, <em>cis</em> regulatory elements, transcription factors and non-coding RNAs. <em>Cryptosporidium</em> spp. are among the most basal branching apicomplexans and existing evidence suggests that they diverge from other members of their phylum <em>via</em> retention of the E2F/DP1 transcription factor family, and the recent discovery that <em>C. parvum</em> produces polycistronic transcripts. Most of what we know about gene regulation in the genus <em>Cryptosporidium</em> is based on sequence conservation and homology with other members of the phylum Apicomplexa, and in some cases, more distant eukaryotes. Very few putative gene regulatory components identified in <em>Cryptosporidium</em> spp. are supported by experimental confirmation. This review summarizes what we know about gene regulation in <em>Cryptosporidium</em> spp. and identifies gaps in our current understanding.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"8 ","pages":"Article 100280"},"PeriodicalIF":1.7,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144480459","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}