Background: Anaplasmosis, caused by Anaplasma species, poses significant threats to public health and livestock productivity. Understanding the distribution and genetic diversity of these pathogens in tick vectors across China is critical for risk assessment and disease control. Materials and Methods: From April to June 2023, 875 ticks were collected across three Chinese provinces: Jiangxi, Yunnan, and Shaanxi. The collected ticks comprised Rhipicephalus microplus (from Jiangxi and Yunnan) and Haemaphysalis longicornis (from Shaanxi). Pathogen detection was performed using PCR, followed by phylogenetic analysis of the obtained sequences to determine genetic relationships. Results: Anaplasma capra was detected predominantly in R. microplus from Yudu County, Jiangxi (4.95%), and in H. longicornis from Meixian County (3.16%), Long County (5.99%), and Zhenba County (0.83%) in Shaanxi, exhibiting regional genetic variations. The detection rate of Anaplasma marginale was 6.59% in Yudu County, Jiangxi; significantly higher rates were found in Yunnan province: 41.75% in Nanjian County, 40.38% in Weishan County, and 52.04% in Yongsheng County. Phylogenetic analysis revealed that A. marginale isolates from Lijiang (Yongsheng), Yunnan, were highly homologous (99.63%-100%) to those from Yudu County, Jiangxi, while isolates from Dali (Nanjian and Weishan), Yunnan, formed a distinct clade. Conclusion: The findings demonstrate the widespread distribution of A. capra and A. marginale in ticks across the surveyed regions of China, with notable variations in prevalence and genetic characteristics. These pathogens represent potential threats to local residents and livestock. Future research should expand the geographic sampling range to fully understand their distribution patterns and explore effective prevention and control strategies to safeguard public health and safety.
{"title":"Molecular Detection and Phylogenetic Analysis of <i>Anaplasma</i> Species in Ticks from Three Provinces of China.","authors":"Yuqing Cheng, Qinghong Yuan, Meng Yang, Junrong Liang, Zhongqiu Teng, Qingzhu Huang, Miao Lu, Tian Qin","doi":"10.1089/vbz.2024.0134","DOIUrl":"10.1089/vbz.2024.0134","url":null,"abstract":"<p><p><b><i>Background:</i></b> Anaplasmosis, caused by Anaplasma species, poses significant threats to public health and livestock productivity. Understanding the distribution and genetic diversity of these pathogens in tick vectors across China is critical for risk assessment and disease control. <b><i>Materials and Methods:</i></b> From April to June 2023, 875 ticks were collected across three Chinese provinces: Jiangxi, Yunnan, and Shaanxi. The collected ticks comprised Rhipicephalus microplus (from Jiangxi and Yunnan) and Haemaphysalis longicornis (from Shaanxi). Pathogen detection was performed using PCR, followed by phylogenetic analysis of the obtained sequences to determine genetic relationships. <b><i>Results:</i></b> Anaplasma capra was detected predominantly in R. microplus from Yudu County, Jiangxi (4.95%), and in H. longicornis from Meixian County (3.16%), Long County (5.99%), and Zhenba County (0.83%) in Shaanxi, exhibiting regional genetic variations. The detection rate of Anaplasma marginale was 6.59% in Yudu County, Jiangxi; significantly higher rates were found in Yunnan province: 41.75% in Nanjian County, 40.38% in Weishan County, and 52.04% in Yongsheng County. Phylogenetic analysis revealed that A. marginale isolates from Lijiang (Yongsheng), Yunnan, were highly homologous (99.63%-100%) to those from Yudu County, Jiangxi, while isolates from Dali (Nanjian and Weishan), Yunnan, formed a distinct clade. <b><i>Conclusion:</i></b> The findings demonstrate the widespread distribution of A. capra and A. marginale in ticks across the surveyed regions of China, with notable variations in prevalence and genetic characteristics. These pathogens represent potential threats to local residents and livestock. Future research should expand the geographic sampling range to fully understand their distribution patterns and explore effective prevention and control strategies to safeguard public health and safety.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"539-545"},"PeriodicalIF":2.1,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144555092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-06-19DOI: 10.1089/vbz.2025.0020
Ana Cláudia de Souza Andrade, Francieli Gesleine Capote Bonato, Isabela Carvalho Dos Santos, Lídia Kazue Iukava, Sarah Gabriella Delallo Charnovski, Bruna Pereira Bitencourt da Silva, Edilson Monteiro Suci Junior, Lucienne Garcia Pretto-Giordano, Ranulfo Piau Junior, Rodrigo Neca Ribeiro, Zilda Cristiani Gazim, Gabriela Catuzo Canonico Silva, Lidiane Nunes Barbosa, Daniela Dib Gonçalves
Introduction: Leptospirosis is a zoonotic disease caused by the bacterium Leptospira spp., which is divided into saprophytic and pathogenic. Transmission in zoos can occur due to infected urine in poorly sanitized environments, rodents, and animal accumulation. Aim: This study investigated the presence of antibodies and DNA of Leptospira spp. in nonhuman primates and wild felids from a zoo in western Paraná, Brazil. Materials and Methods: Samples were collected through chemical restraint and venipuncture. Antibody testing was performed by microscopic agglutination test and polymerase chain reaction (PCR). Results: Of the 24 samples analyzed (17 capuchin monkeys and 7 felines), 12.5% presented antibodies for the Butembo serovar, all in primates. No feline showed reaction or DNA amplification. Conclusion: The results highlight the importance of studies on leptospirosis in wild animals in captivity, considering factors such as biome and management of the zoo, which houses rescued species that cannot be reintroduced into the wild.
{"title":"Presence of <i>Leptospira</i> spp. in Nonhuman Primates and Wild Felids from a Brazilian Zoo.","authors":"Ana Cláudia de Souza Andrade, Francieli Gesleine Capote Bonato, Isabela Carvalho Dos Santos, Lídia Kazue Iukava, Sarah Gabriella Delallo Charnovski, Bruna Pereira Bitencourt da Silva, Edilson Monteiro Suci Junior, Lucienne Garcia Pretto-Giordano, Ranulfo Piau Junior, Rodrigo Neca Ribeiro, Zilda Cristiani Gazim, Gabriela Catuzo Canonico Silva, Lidiane Nunes Barbosa, Daniela Dib Gonçalves","doi":"10.1089/vbz.2025.0020","DOIUrl":"10.1089/vbz.2025.0020","url":null,"abstract":"<p><p><b><i>Introduction:</i></b> Leptospirosis is a zoonotic disease caused by the bacterium <i>Leptospira</i> spp., which is divided into saprophytic and pathogenic. Transmission in zoos can occur due to infected urine in poorly sanitized environments, rodents, and animal accumulation. Aim: This study investigated the presence of antibodies and DNA of <i>Leptospira</i> spp. in nonhuman primates and wild felids from a zoo in western Paraná, Brazil. <b><i>Materials and Methods:</i></b> Samples were collected through chemical restraint and venipuncture. Antibody testing was performed by microscopic agglutination test and polymerase chain reaction (PCR). <b><i>Results:</i></b> Of the 24 samples analyzed (17 capuchin monkeys and 7 felines), 12.5% presented antibodies for the Butembo serovar, all in primates. No feline showed reaction or DNA amplification. <b><i>Conclusion:</i></b> The results highlight the importance of studies on leptospirosis in wild animals in captivity, considering factors such as biome and management of the zoo, which houses rescued species that cannot be reintroduced into the wild.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"553-557"},"PeriodicalIF":2.1,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144334005","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-06-26DOI: 10.1089/vbz.2024.0120
Linda A O Amoah, Evans P K Ameade, Benjamin Yeboah Ofori
Background: In Ghana, no research has recorded any positive cases of human babesiosis, despite the presence of Babesia reservoir hosts in many Ghanaian communities. Epidemiological studies have reported active infections in these hosts. Thus, this study explored possible cases of human babesiosis in selected major hospitals in the Greater Accra region and assessed the prevalence of Babesia infections in common reservoirs (dogs, cats, and rodents) from households and veterinary institutions. Methods: This cross-sectional study involved retrieving medical records from three major hospitals in urban (University of Ghana Hospital and Pentecost Hospital) and peri-urban (Shai-Osudoku District Hospital) areas that satisfied the eligibility criteria. Analysis of human babesiosis cases was conducted using appropriate search queries in Microsoft Excel. Genomic DNA was also isolated from 404 blood samples from Babesia reservoir hosts, and DNA analysis was performed using PIRO A1 and PIRO B primers targeting 18S rDNA. Results: These hospitals did not record cases of human babesiosis, although several cases of febrile illnesses and malaria were reported. The blood of 326 animals tested positive for Babesia DNA. Thus, the overall prevalence of Babesia infection in sampled animals was 80.69% (326/404), with infection prevalence varying among the targeted reservoir hosts: 53.07% (173/326) dogs, 3.99% (13/326) cats, and 42.9% (140/326) rodents. Conclusion: Although the hospitals documented no cases of human babesiosis, Babesia transmission was active among reservoir hosts. Therefore, clinicians and laboratory scientists in the Greater Accra region and Ghana should maintain a high index of suspicion of human babesiosis to avoid missing such cases.
{"title":"<i>Babesia</i> Infections in Reservoir Hosts and the Possibility of Human Babesiosis in Ghana.","authors":"Linda A O Amoah, Evans P K Ameade, Benjamin Yeboah Ofori","doi":"10.1089/vbz.2024.0120","DOIUrl":"10.1089/vbz.2024.0120","url":null,"abstract":"<p><p><b><i>Background:</i></b> In Ghana, no research has recorded any positive cases of human babesiosis, despite the presence of <i>Babesia</i> reservoir hosts in many Ghanaian communities. Epidemiological studies have reported active infections in these hosts. Thus, this study explored possible cases of human babesiosis in selected major hospitals in the Greater Accra region and assessed the prevalence of <i>Babesia</i> infections in common reservoirs (dogs, cats, and rodents) from households and veterinary institutions. <b><i>Methods:</i></b> This cross-sectional study involved retrieving medical records from three major hospitals in urban (University of Ghana Hospital and Pentecost Hospital) and peri-urban (Shai-Osudoku District Hospital) areas that satisfied the eligibility criteria. Analysis of human babesiosis cases was conducted using appropriate search queries in Microsoft Excel. Genomic DNA was also isolated from 404 blood samples from <i>Babesia</i> reservoir hosts, and DNA analysis was performed using PIRO A1 and PIRO B primers targeting 18S rDNA. <b><i>Results:</i></b> These hospitals did not record cases of human babesiosis, although several cases of febrile illnesses and malaria were reported. The blood of 326 animals tested positive for <i>Babesia</i> DNA. Thus, the overall prevalence of <i>Babesia</i> infection in sampled animals was 80.69% (326/404), with infection prevalence varying among the targeted reservoir hosts: 53.07% (173/326) dogs, 3.99% (13/326) cats, and 42.9% (140/326) rodents. <b><i>Conclusion:</i></b> Although the hospitals documented no cases of human babesiosis, <i>Babesia</i> transmission was active among reservoir hosts. Therefore, clinicians and laboratory scientists in the Greater Accra region and Ghana should maintain a high index of suspicion of human babesiosis to avoid missing such cases.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"546-552"},"PeriodicalIF":2.1,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144498184","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-07-11DOI: 10.1177/15303667251359822
Khalil Dachraoui, Raja Ben Osman, Sonia Ben Slama, Aida Sayadi, Yassine Maachach, Mounir Trifi, Imen Labidi, Jihene Lachheb, Chaima Badr, Imen Larbi, Elyes Zhioua
A total of 20 horses belonging to the Pasteur Institute of Tunis used for the production of therapeutic serum antiscorpion venom were tested for the presence of antibodies anti-West Nile virus (WNV) during the 2023 outbreak of West Nile disease that affected humans and horses in Tunisia. Of the 20 samples tested in November 2023 by enzyme-linked immuno-sorbent assay (ELISA), five were positive, leading to a seroprevalence of 25%. Since the number of horses is not substantial, all samples were tested also by virus microneutralization test (MNT) using the Tunisian strain of WNV lineage 1 isolated in 2014 from a pool of field-collected Culex pipiens from Central Tunisia. WNV-neutralizing antibodies were detected in two horses, yielding a seroprevalence of 10%. Of the five horses tested positive by ELISA, only two were positive by MNT. The follow-up of the serological analysis performed in December 2023 and January 2024 did not show any seroconversion in the remaining horses. No clinical cases were reported during the investigation. While molecular blood analysis failed to detect viral RNA, MNT-based seroprevalence provided strong evidence of the circulation of WNV during this outbreak. Taking into account that humans and horses share similar clinical symptoms and antibody responses following WNV infection, equid surveillance could provide an accurate and timely detection of WNV outbreaks.
{"title":"West Nile Virus Antibody Prevalence in Horses During the 2023 Outbreak in Tunisia, North Africa.","authors":"Khalil Dachraoui, Raja Ben Osman, Sonia Ben Slama, Aida Sayadi, Yassine Maachach, Mounir Trifi, Imen Labidi, Jihene Lachheb, Chaima Badr, Imen Larbi, Elyes Zhioua","doi":"10.1177/15303667251359822","DOIUrl":"10.1177/15303667251359822","url":null,"abstract":"<p><p>A total of 20 horses belonging to the Pasteur Institute of Tunis used for the production of therapeutic serum antiscorpion venom were tested for the presence of antibodies anti-West Nile virus (WNV) during the 2023 outbreak of West Nile disease that affected humans and horses in Tunisia. Of the 20 samples tested in November 2023 by enzyme-linked immuno-sorbent assay (ELISA), five were positive, leading to a seroprevalence of 25%. Since the number of horses is not substantial, all samples were tested also by virus microneutralization test (MNT) using the Tunisian strain of WNV lineage 1 isolated in 2014 from a pool of field-collected <i>Culex pipiens</i> from Central Tunisia. WNV-neutralizing antibodies were detected in two horses, yielding a seroprevalence of 10%. Of the five horses tested positive by ELISA, only two were positive by MNT. The follow-up of the serological analysis performed in December 2023 and January 2024 did not show any seroconversion in the remaining horses. No clinical cases were reported during the investigation. While molecular blood analysis failed to detect viral RNA, MNT-based seroprevalence provided strong evidence of the circulation of WNV during this outbreak. Taking into account that humans and horses share similar clinical symptoms and antibody responses following WNV infection, equid surveillance could provide an accurate and timely detection of WNV outbreaks.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"558-564"},"PeriodicalIF":2.1,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144620771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-07-11DOI: 10.1177/15303667251360262
Nunzia Esposito, Giulio Viceconte, Lidia Festa, Francesco Antimo Alfè, Canio Carriero, Alessio Vinicio Codella, Antonio Glielmo, Luigi Forgione, Antonio Riccardo Buonomo, Franco Carmine Muccio, Marcello Lamberti, Roberto Alfano, Maria Grazia Coppola, Angelo Salomone Megna, Ivan Gentile
Background: West Nile Virus (WNV) infection is endemic in Italy, but it has rarely reported in humans in Southern Italy. We report the first human outbreak of WNV infection in the Campania region, Italy. Results: Five confirmed and seven probable cases of WNV were identified from August to September 2024. Predominantly affecting elderly males with comorbidities, all but one patient developed West Nile neuroinvasive disease, presenting with fever and impaired consciousness. Remdesivir was administered off-label in four cases, potentially reducing hospitalization and improving outcomes. Mortality was limited to two cases, attributed to bacterial infections. Conclusions: The outbreak underscores the importance of heightened surveillance in Italy and raises the potential for remdesivir in WNV treatment.
{"title":"Outbreak of Human Neuroinvasive West Nile Virus Infection in Campania, Italy, August-September 2024.","authors":"Nunzia Esposito, Giulio Viceconte, Lidia Festa, Francesco Antimo Alfè, Canio Carriero, Alessio Vinicio Codella, Antonio Glielmo, Luigi Forgione, Antonio Riccardo Buonomo, Franco Carmine Muccio, Marcello Lamberti, Roberto Alfano, Maria Grazia Coppola, Angelo Salomone Megna, Ivan Gentile","doi":"10.1177/15303667251360262","DOIUrl":"10.1177/15303667251360262","url":null,"abstract":"<p><p><b><i>Background:</i></b> West Nile Virus (WNV) infection is endemic in Italy, but it has rarely reported in humans in Southern Italy. We report the first human outbreak of WNV infection in the Campania region, Italy. <b><i>Results:</i></b> Five confirmed and seven probable cases of WNV were identified from August to September 2024. Predominantly affecting elderly males with comorbidities, all but one patient developed West Nile neuroinvasive disease, presenting with fever and impaired consciousness. Remdesivir was administered off-label in four cases, potentially reducing hospitalization and improving outcomes. Mortality was limited to two cases, attributed to bacterial infections. <b><i>Conclusions:</i></b> The outbreak underscores the importance of heightened surveillance in Italy and raises the potential for remdesivir in WNV treatment.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"565-567"},"PeriodicalIF":2.1,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144620770","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-06-05DOI: 10.1089/vbz.2025.0005
Aisha A Abd Al-Ghafar, Sherif A Marouf, Khaled A Abdel-Moein, Hala M Zaher, Ahmed Samir
Background: Although recent research has provided better insights into Helicobacter pylori, much remains unknown regarding non-H. pylori Helicobacter species in animals. Pet animals living close to humans may act as a potential reservoir for a diverse Helicobacter species. Hence, this study aimed to investigate Helicobacter spp.'s prevalence among pet animals suffering from gastroenteritis and their zoonotic relevance. Materials and methods: Eighty-seven fecal samples were collected from dogs (53) and cats (34) suffering from gastroenteritis. The DNA was extracted for the molecular detection of Helicobacter spp., H. canis, H. felis, and H. pylori through amplification of Helicobacter 16S rRNA as well as multiplex PCR targeting H. canis Hsp60, H. felis urease, and H. pylori urease C genes in all samples. Sequencing of some selected PCR amplicons and phylogenetic analysis were conducted. Results: The overall prevalence of Helicobacter spp. ws 34.5%, with the following rates: 37.7% and 29.4% among dogs and cats, respectively. H. canis had the highest occurrence rate (20.7%), whereas H. pylori was detected at 11.5%, followed by H. felis at 2.3%. Coinfection with more than one Helicobacter species has been documented. Furthermore, the phylogenetic analysis of three partial H. canis 16S rRNA sequences revealed a high genetic relatedness to strains derived from a diarrheic cat and human bacteremic patients with a history of pet exposure, indicating the public health implications of these sequences. Conclusion: The fecal carriage of diverse Helicobacter spp. among dogs and cats suffering from gastroenteritis, with a predominance of H. canis, highlights a potential risk of zoonotic transmission of such pathogens between pets and human contacts.
{"title":"The Fecal Carriage of <i>Helicobacter</i> Species Among Pet Animals Suffering from Gastroenteritis: A Potential Public Health Concern.","authors":"Aisha A Abd Al-Ghafar, Sherif A Marouf, Khaled A Abdel-Moein, Hala M Zaher, Ahmed Samir","doi":"10.1089/vbz.2025.0005","DOIUrl":"10.1089/vbz.2025.0005","url":null,"abstract":"<p><p><b><i>Background:</i></b> Although recent research has provided better insights into <i>Helicobacter pylori</i>, much remains unknown regarding non-<i>H. pylori Helicobacter</i> species in animals. Pet animals living close to humans may act as a potential reservoir for a diverse <i>Helicobacter</i> species. Hence, this study aimed to investigate <i>Helicobacter</i> spp.'s prevalence among pet animals suffering from gastroenteritis and their zoonotic relevance. <b><i>Materials and methods:</i></b> Eighty-seven fecal samples were collected from dogs (53) and cats (34) suffering from gastroenteritis. The DNA was extracted for the molecular detection of <i>Helicobacter</i> spp., <i>H. canis</i>, <i>H. felis</i>, and <i>H. pylori</i> through amplification of <i>Helicobacter</i> 16S rRNA as well as multiplex PCR targeting <i>H. canis</i> Hsp60, <i>H. felis</i> urease, and <i>H. pylori</i> urease C genes in all samples. Sequencing of some selected PCR amplicons and phylogenetic analysis were conducted. <b><i>Results:</i></b> The overall prevalence of <i>Helicobacter</i> spp. ws 34.5%, with the following rates: 37.7% and 29.4% among dogs and cats, respectively. <i>H. canis</i> had the highest occurrence rate (20.7%), whereas <i>H. pylori</i> was detected at 11.5%, followed by <i>H. felis</i> at 2.3%. Coinfection with more than one <i>Helicobacter</i> species has been documented. Furthermore, the phylogenetic analysis of three partial <i>H. canis</i> 16S rRNA sequences revealed a high genetic relatedness to strains derived from a diarrheic cat and human bacteremic patients with a history of pet exposure, indicating the public health implications of these sequences. <b><i>Conclusion:</i></b> The fecal carriage of diverse <i>Helicobacter</i> spp. among dogs and cats suffering from gastroenteritis, with a predominance of <i>H. canis</i>, highlights a potential risk of zoonotic transmission of such pathogens between pets and human contacts.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"504-510"},"PeriodicalIF":2.1,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144226821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-06-13DOI: 10.1089/vbz.2025.0037
Eveliina Ekström, Katariina Kaansalo, Phuoc T Truong Nguyen, Maija T Suvanto, Olli Vapalahti, Hannimari Kallio-Kokko, Essi Korhonen, Hanna Vauhkonen, Teemu Smura, Eili Huhtamo, Anne J Jääskeläinen
Background: Strains of Sindbis virus (SINV) are rarely detected and isolated from human blood samples as the viremia is low and short in Pogosta disease patients. Materials and Methods: To optimize SINV RNA detection in patient samples, a sensitive and specific SINV-RT-qPCR method was developed and validated. Results: The new SINV-RT-qPCR method was determined to be more sensitive than a previously used method. The assay was used to screen 882 serum samples from 846 patients suspected of Pogosta disease in Finland in 2023-2024. One sample was detected to be SINV-RNA-positive and was further subjected to virus isolation with whole genome sequencing. The sequence analysis suggested the strain to be closely related to those detected in Finland in 2005 and 2018, Germany in 2012 and 2016, and Sweden in 2009. Conclusions: The new optimized SINV RNA detection method is a useful tool for the detection of viremic samples for further studies.
{"title":"Optimized Sindbis Virus RNA Detection Using Novel RT-qPCR: Isolation and Characterization of Sindbis Virus from a Patient Sample.","authors":"Eveliina Ekström, Katariina Kaansalo, Phuoc T Truong Nguyen, Maija T Suvanto, Olli Vapalahti, Hannimari Kallio-Kokko, Essi Korhonen, Hanna Vauhkonen, Teemu Smura, Eili Huhtamo, Anne J Jääskeläinen","doi":"10.1089/vbz.2025.0037","DOIUrl":"10.1089/vbz.2025.0037","url":null,"abstract":"<p><p><b><i>Background:</i></b> Strains of Sindbis virus (SINV) are rarely detected and isolated from human blood samples as the viremia is low and short in Pogosta disease patients. <b><i>Materials and Methods:</i></b> To optimize SINV RNA detection in patient samples, a sensitive and specific SINV-RT-qPCR method was developed and validated. <b><i>Results:</i></b> The new SINV-RT-qPCR method was determined to be more sensitive than a previously used method. The assay was used to screen 882 serum samples from 846 patients suspected of Pogosta disease in Finland in 2023-2024. One sample was detected to be SINV-RNA-positive and was further subjected to virus isolation with whole genome sequencing. The sequence analysis suggested the strain to be closely related to those detected in Finland in 2005 and 2018, Germany in 2012 and 2016, and Sweden in 2009. <b><i>Conclusions:</i></b> The new optimized SINV RNA detection method is a useful tool for the detection of viremic samples for further studies.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"523-525"},"PeriodicalIF":2.1,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144286624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Intracellular bacteria such as Rickettsia spp., Borrelia spp., Coxiella spp., and Bartonella spp. cause febrile illnesses similar to malaria and arboviruses, leading to under-reporting in sub-Saharan Africa. Methods: Following Preferred Reporting Items for Systematic Review and Meta-Analyses guidelines, we included studies on these bacteria in humans, animals, and vectors in West Africa (2000-2023). Case reports, editorials, studies on other pathogens, and coinfections were excluded. Data was retrieved from African Journals Online, Google Scholar, and PubMed (last search: December 31, 2023). The risk of bias was assessed using an adapted Cochrane RoB 2.0 tool. Data were analyzed using Excel 2016 and QGIS. A random-effects model estimated prevalence, with subgroup analysis based on country, detection method, period, and host type. Heterogeneity was measured via the I2 index (>50% indicating moderate heterogeneity). Publication bias was assessed by stratifying studies by risk of bias. Results: Out of 27 articles included, 10 covered studies on Rickettsia spp., 5 Borrelia spp., 6 Coxiella spp., 3 Bartonella spp., and 3 both Rickettsia spp. and Coxiella spp. Among them, 10 studies focused on vectors, 5 on animals, 5 on humans, and 7 on One Health. The prevalence of Rickettsia spp. was the highest in humans, 19.46%, 95% confidence interval: [19.42-19.50]. Bartonella spp. had the highest prevalence in animals, 82.57%, 95% CI: [82.46-82.69], and vectors 37.62%, 95% CI: [37.53-37.71]. Prevalence increased significantly post 2010 (81.4%). PCR-based detection showed a higher prevalence (63%). In the risk-of-bias analysis, the quality of the studies, which were included, did not affect the results and overall validity of findings. Conclusion: Intracellular bacteria spread widely among humans, animals, and vectors. One Health approach is essential for managing zoonotic bacterial diseases in Africa. Variation in prevalence underlines the need for methodological standardization and future research should focus on harmonizing methods by integrating molecular methods.
{"title":"Epidemiology of Intracellular Bacterial Pathogens <i>Rickettsia</i> spp., <i>Borrelia</i> spp., <i>Coxiella</i> spp., and <i>Bartonella</i> spp. in West Africa from 2000 to 2023: A Systematic Review.","authors":"Merci Muhigwa, Nina Gouba, Etienne Bilgo, Aboubakar Soma, Fernand Michodigni, Yaya Sozanga Sanou, Abdoulaye Diabate, Abdoul-Salam Ouedraogo","doi":"10.1089/vbz.2025.0011","DOIUrl":"10.1089/vbz.2025.0011","url":null,"abstract":"<p><p><b><i>Background:</i></b> Intracellular bacteria such as <i>Rickettsia</i> spp., <i>Borrelia</i> spp., <i>Coxiella</i> spp., and <i>Bartonella</i> spp. cause febrile illnesses similar to malaria and arboviruses, leading to under-reporting in sub-Saharan Africa. <b><i>Methods:</i></b> Following Preferred Reporting Items for Systematic Review and Meta-Analyses guidelines, we included studies on these bacteria in humans, animals, and vectors in West Africa (2000-2023). Case reports, editorials, studies on other pathogens, and coinfections were excluded. Data was retrieved from African Journals Online, Google Scholar, and PubMed (last search: December 31, 2023). The risk of bias was assessed using an adapted Cochrane RoB 2.0 tool. Data were analyzed using Excel 2016 and QGIS. A random-effects model estimated prevalence, with subgroup analysis based on country, detection method, period, and host type. Heterogeneity was measured via the <i>I</i><sup>2</sup> index (>50% indicating moderate heterogeneity). Publication bias was assessed by stratifying studies by risk of bias. <b><i>Results:</i></b> Out of 27 articles included, 10 covered studies on <i>Rickettsia</i> spp., 5 <i>Borrelia</i> spp., 6 <i>Coxiella</i> spp., 3 <i>Bartonella</i> spp., and 3 both <i>Rickettsia</i> spp. and <i>Coxiella</i> spp. Among them, 10 studies focused on vectors, 5 on animals, 5 on humans, and 7 on One Health. The prevalence of <i>Rickettsia</i> spp. was the highest in humans, 19.46%, 95% confidence interval: [19.42-19.50]. <i>Bartonella</i> spp. had the highest prevalence in animals, 82.57%, 95% CI: [82.46-82.69], and vectors 37.62%, 95% CI: [37.53-37.71]. Prevalence increased significantly post 2010 (81.4%). PCR-based detection showed a higher prevalence (63%). In the risk-of-bias analysis, the quality of the studies, which were included, did not affect the results and overall validity of findings. <b><i>Conclusion:</i></b> Intracellular bacteria spread widely among humans, animals, and vectors. One Health approach is essential for managing zoonotic bacterial diseases in Africa. Variation in prevalence underlines the need for methodological standardization and future research should focus on harmonizing methods by integrating molecular methods.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"491-503"},"PeriodicalIF":2.1,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143987461","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Backgrounds: Leishmaniasis is one of the neglected tropical diseases, distributed across 89 countries in both the Old and New Worlds. Among the 54 identified Leishmania species, 21 are known to be pathogenic to humans. Cutaneous leishmaniasis (CL) is primarily caused by L. major and L. tropica, while visceral leishmaniasis (VL) in Iran is caused by L. infantum. Accurate detection and species identification of Leishmania spp. are crucial for more effective treatment, epidemiology, and control strategies for the disease. Among the molecular targets recently used for detecting Leishmania species, the heat-shock protein 70 (Hsp70) gene has proven to be highly suitable. Methods: This study aimed to establish and evaluate a SYBR Green real-time PCR targeting the Hsp70 gene to identify and differentiate three Leishmania species: L. major, L. tropica, and L. infantum in clinical specimens. A total of 219 microscopic smears, consisting of both positive and negative leishmaniasis cases diagnosed by microscopy, were subjected to DNA extraction and the Hsp70 real-time PCR assay designed in this study. Results: Based on the analysis of the melting temperature (Tm) of the amplified Hsp70 target, 115 microscopy-positive smears were identified, comprising 70.4% L. major, 23.5% L. tropica, and 6.1% L. infantum. All results were confirmed using a commercial diagnostic kit. Sanger sequencing of selected positive amplicons unequivocally confirmed the accuracy of this method in identifying and distinguishing the three Leishmania species. Conclusions: The Hsp70 real-time PCR can be considered an effective method for detecting and identifying Leishmania species from microscopic slides prepared from CL and VL cases in different regions of Iran.
背景:利什曼病是一种被忽视的热带病,分布在新旧世界的89个国家。在已查明的54种利什曼原虫中,已知21种对人类具有致病性。皮肤利什曼病(CL)主要由大利什曼原虫和热带利什曼原虫引起,而伊朗内脏利什曼病(VL)由婴儿利什曼原虫引起。利什曼原虫的准确检测和物种鉴定对该病的更有效治疗、流行病学和控制策略至关重要。在最近用于检测利什曼原虫的分子靶标中,热休克蛋白70 (Hsp70)基因已被证明是非常合适的。方法:本研究旨在建立针对Hsp70基因的SYBR Green实时荧光定量PCR,用于临床标本中利什曼原虫(L. major, L. tropica, L. infumtum)的鉴定和区分。对镜检确诊的利什曼病阳性和阴性病例共219例镜检涂片进行DNA提取和本研究设计的Hsp70实时PCR检测。结果:通过对扩增Hsp70靶细胞的熔融温度(Tm)分析,共检出115个显微镜阳性涂片,其中主要L.占70.4%,热带L.占23.5%,婴儿L.占6.1%。所有结果均使用商用诊断试剂盒进行确认。所选阳性扩增子的Sanger测序明确证实了该方法在鉴定和区分三种利什曼原虫时的准确性。结论:Hsp70实时荧光定量PCR可作为检测和鉴定伊朗不同地区CL和VL病例显微载玻片中利什曼原虫种类的有效方法。
{"title":"Sensitive and Specific Detection/Identification of <i>Leishmania major</i>, <i>Leishmania tropica</i>, and <i>Leishmania infantum</i> by a Single Real Time PCR Targeting <i>Hsp70</i>.","authors":"Reza Mohammadi Manesh, Parisa Mousavi, Mahshid Shakibapour, Mehdi Mohebali, Behrooz Ataei, Hossein Mirhendi","doi":"10.1089/vbz.2024.0087","DOIUrl":"10.1089/vbz.2024.0087","url":null,"abstract":"<p><p><b><i>Backgrounds:</i></b> Leishmaniasis is one of the neglected tropical diseases, distributed across 89 countries in both the Old and New Worlds. Among the 54 identified <i>Leishmania</i> species, 21 are known to be pathogenic to humans. Cutaneous leishmaniasis (CL) is primarily caused by <i>L. major</i> and <i>L. tropica</i>, while visceral leishmaniasis (VL) in Iran is caused by <i>L. infantum</i>. Accurate detection and species identification of <i>Leishmania</i> spp. are crucial for more effective treatment, epidemiology, and control strategies for the disease. Among the molecular targets recently used for detecting <i>Leishmania</i> species, the heat-shock protein 70 (<i>Hsp70</i>) gene has proven to be highly suitable. <b><i>Methods:</i></b> This study aimed to establish and evaluate a SYBR Green real-time PCR targeting the <i>Hsp70</i> gene to identify and differentiate three <i>Leishmania</i> species: <i>L. major</i>, <i>L. tropica</i>, and <i>L. infantum</i> in clinical specimens. A total of 219 microscopic smears, consisting of both positive and negative leishmaniasis cases diagnosed by microscopy, were subjected to DNA extraction and the <i>Hsp70</i> real-time PCR assay designed in this study. <b><i>Results:</i></b> Based on the analysis of the melting temperature (T<sub>m</sub>) of the amplified <i>Hsp70</i> target, 115 microscopy-positive smears were identified, comprising 70.4% <i>L. major</i>, 23.5% <i>L. tropica</i>, and 6.1% <i>L. infantum</i>. All results were confirmed using a commercial diagnostic kit. Sanger sequencing of selected positive amplicons unequivocally confirmed the accuracy of this method in identifying and distinguishing the three <i>Leishmania</i> species. <b><i>Conclusions:</i></b> The <i>Hsp70</i> real-time PCR can be considered an effective method for detecting and identifying <i>Leishmania</i> species from microscopic slides prepared from CL and VL cases in different regions of Iran.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"511-516"},"PeriodicalIF":2.1,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144217101","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-05-22DOI: 10.1089/vbz.2025.0019
Mabatho M Nkoko, Ndivhuwo Shivambu, Tinyiko C Shivambu, Takalani Nelufule, Nozipho Khumalo, Nimmi Seoraj-Pillai, Tshifhiwa C Nangammbi
Rodents are associated with the spread of deadly zoonotic and emerging infectious diseases. Their widespread distribution is strongly linked to their ability to thrive in human-altered environments with access to food and shelter. Thus, humans are exposed to zoonotic agents that can spread and infect them directly and indirectly. We sourced published literature on ectoparasites associated with Rattus rattus, R. norvegicus, and Mus musculus from various academic databases such as Google Scholar, PubMed, Web of Science, and Scopus. The relevant literature was screened and selected in R statistical software using the packages ''metagear'' and ''revtool.'' We reviewed and analyzed a total of 53 articles published between 1994 and 2024. The literature review covered studies from 29 countries, represented by six continents, namely, Africa, Asia, Europe, North America, Oceania, and South America, with the majority of the studies from Asia. R. rattus had the most published studies. Our literature review identified 87 species of zoonotic ectoparasites, with Xenopsylla cheopis, Polyplax spinulosa, and Laelaps echidninus being the most reported across all host species. Mites were the most reported ectoparasites (40.83%), followed by fleas (25%), ticks (20%), and lice (14.17%). Most of these ectoparasites were reported from R. rattus, with the highest number of documented ectoparasites. Investigating the prevalence, distribution, and potential risks of alien invasive rodents and their ectoparasites is paramount for public health and improving integrated pest management control strategies.
啮齿动物与致命的人畜共患疾病和新出现的传染病的传播有关。它们的广泛分布与它们在人类改变的环境中茁壮成长并获得食物和住所的能力密切相关。因此,人类暴露于可以直接或间接传播和感染他们的人畜共患病原体。我们从谷歌Scholar、PubMed、Web of Science和Scopus等不同的学术数据库中获取了与Rattus Rattus、褐家鼠和小家鼠相关的体外寄生虫的已发表文献。在R统计软件中使用“metagear”和“revtool”软件包筛选和选择相关文献。“我们审查并分析了1994年至2024年间发表的53篇文章。文献综述涵盖了来自非洲、亚洲、欧洲、北美、大洋洲和南美洲六大洲29个国家的研究,其中大部分研究来自亚洲。家鼠发表的研究最多。文献综述共鉴定出87种人畜共患体外寄生虫,其中报道最多的是棘外蚤、棘多蚤和针鼹。报告的体外寄生虫以螨类最多(40.83%),其次是蚤(25%)、蜱(20%)和虱(14.17%)。这些外寄生虫大多来自大鼠,记录的外寄生虫数量最多。调查外来入侵啮齿动物及其外寄生虫的流行、分布和潜在风险对公共卫生和改进害虫综合防治策略至关重要。
{"title":"Zoonotic Ectoparasites Infesting Commensal Invasive Murid Rodents.","authors":"Mabatho M Nkoko, Ndivhuwo Shivambu, Tinyiko C Shivambu, Takalani Nelufule, Nozipho Khumalo, Nimmi Seoraj-Pillai, Tshifhiwa C Nangammbi","doi":"10.1089/vbz.2025.0019","DOIUrl":"10.1089/vbz.2025.0019","url":null,"abstract":"<p><p>Rodents are associated with the spread of deadly zoonotic and emerging infectious diseases. Their widespread distribution is strongly linked to their ability to thrive in human-altered environments with access to food and shelter. Thus, humans are exposed to zoonotic agents that can spread and infect them directly and indirectly. We sourced published literature on ectoparasites associated with <i>Rattus rattus</i>, <i>R. norvegicus</i>, and <i>Mus musculus</i> from various academic databases such as Google Scholar, PubMed, Web of Science, and Scopus. The relevant literature was screened and selected in R statistical software using the packages ''metagear'' and ''revtool.'' We reviewed and analyzed a total of 53 articles published between 1994 and 2024. The literature review covered studies from 29 countries, represented by six continents, namely, Africa, Asia, Europe, North America, Oceania, and South America, with the majority of the studies from Asia. <i>R. rattus</i> had the most published studies. Our literature review identified 87 species of zoonotic ectoparasites, with <i>Xenopsylla cheopis</i>, <i>Polyplax spinulosa</i>, and <i>Laelaps echidninus</i> being the most reported across all host species. Mites were the most reported ectoparasites (40.83%), followed by fleas (25%), ticks (20%), and lice (14.17%). Most of these ectoparasites were reported from <i>R. rattus</i>, with the highest number of documented ectoparasites. Investigating the prevalence, distribution, and potential risks of alien invasive rodents and their ectoparasites is paramount for public health and improving integrated pest management control strategies.</p>","PeriodicalId":23683,"journal":{"name":"Vector borne and zoonotic diseases","volume":" ","pages":"481-490"},"PeriodicalIF":2.1,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144120974","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}