ABSTRACT
Physical impairments are widely assumed to reduce the viability of individual animals, but their impacts on individuals within natural populations of vertebrates are rarely quantified. By monitoring wild populations of white-footed mice over 26 years, we assessed whether missing or deformed limbs, tail or eyes influenced the survival, body mass, movement and ectoparasite burden of their bearers. Of the 27 244 individuals monitored, 543 (2%) had visible physical impairments. Persistence times (survival) were similar between mice with and without impairments. Mice with eye and tail impairments had 5% and 6% greater mass, respectively, than unimpaired mice. Mice with tail impairments had larger home ranges than did unimpaired mice. Burdens of black-legged ticks (Ixodes scapularis) were higher among mice with tail and limb impairments while burdens of bot fly larvae (Cuterebra) were higher among mice with cataracts compared to mice without impairments. Our findings do not support the presupposition that physical impairments reduce viability in their bearers and are inconsistent with the devaluation of impaired individuals that pervaded early thinking in evolutionary biology.
Subject(s)
Longevity , Peromyscus , Animals , Cataract/complications , Cataract/epidemiology , Diptera/physiology , Extremities/pathology , Homing Behavior , Ixodes/physiology , Limb Deformities, Congenital/complications , Limb Deformities, Congenital/epidemiology , Mice , Peromyscus/parasitology , Peromyscus/physiology , Survival Analysis , Tail/pathology , Tick Infestations/complications , Tick Infestations/epidemiologyABSTRACT
BACKGROUND: Anaplasma platys is a tick-borne bacterium which infects blood platelets of dogs, causing canine cyclic thrombocytopenia. The disease is distributed worldwide, particularly in the tropics and subtropics, but information on the epidemiology of A. platys infection in dogs is fragmentary in many countries, including Egypt. In this study, we investigated the prevalence and risk factors associated with A. platys infection in dogs from Egypt. METHODS: A conventional PCR targeting a fragment of the 16S rRNA gene of A. platys was used to screen 500 dogs from five North Egyptian governorates. DNA sequencing and phylogenetic analysis were performed for one of the positive samples. RESULTS: The overall prevalence of A. platys in the studied dogs was 6.4%. Females of the German shepherd breed without veterinary care had higher odds for A. platys positivity. High tick infestation and lack of anti-tick treatment were also identified as risk factors for A. platys infection. Phylogenetic analysis revealed that the sequence obtained herein was closely related to sequences from Egypt, South Africa and Uruguay. CONCLUSIONS: This is the first large-scale epidemiological study of A. platys in Egypt, where female German shepherd dogs without veterinary care, as well as dogs with high tick infestation and without anti-tick treatment are at a higher risk of infection.
Subject(s)
Anaplasma/genetics , Anaplasmosis/epidemiology , Dog Diseases/epidemiology , Phylogeny , Tick Infestations/veterinary , Anaplasma/classification , Animals , Dog Diseases/microbiology , Dogs , Egypt/epidemiology , Female , Male , Prevalence , RNA, Ribosomal, 16S/genetics , Risk Factors , Sequence Analysis, DNA , South Africa , Tick Infestations/complications , Tick Infestations/microbiology , UruguayABSTRACT
The aim of this study was to recognise the etiological factor of a disease with symptoms of lameness and cardiac failure, which occurred in one dog 4 weeks after invasion by ticks. A serological examination as well as molecular examination (PCR) was done. In the sample of the serum, the presence of antibodies specific to Borrelia burgdorferi were detected. Antibiotic therapy with doxycycline did not cause significant improvement, so the owners of the dog decided about its euthanasia. During the necroscopy, a dilated heart was recognised. In the heart samples, the genetic material of Borrelia was detected. The results of serological and molecular examinations showed that in the discussed case, an etiological factor of the disease was spirochetes. In light of the research, veterinary practitioners should keep in mind the presence of Lyme disease in dogs in Poland and include it in differential diagnoses for lameness and cardiological problems.
Subject(s)
Borrelia Infections , Dog Diseases , Myocarditis , Tick Infestations , Animals , Antibodies, Bacterial/blood , Borrelia Infections/complications , Borrelia Infections/diagnosis , Dog Diseases/diagnosis , Dog Diseases/etiology , Dog Diseases/microbiology , Dog Diseases/parasitology , Dogs , Euthanasia, Animal , Heart/parasitology , Myocarditis/diagnosis , Myocarditis/etiology , Poland , Tick Infestations/complications , Tick Infestations/microbiology , Tick Infestations/veterinarySubject(s)
Dermacentor , Scalp Dermatoses/diagnosis , Spotted Fever Group Rickettsiosis/diagnosis , Tick Infestations/diagnosis , Animals , Dermacentor/physiology , Female , Humans , Middle Aged , Neck/parasitology , Neck/pathology , Scalp/parasitology , Scalp/pathology , Scalp Dermatoses/etiology , Spotted Fever Group Rickettsiosis/pathology , Syndrome , Tick Infestations/complicationsABSTRACT
In 2017, a male elk (Cervus canadensis) was found dead in Pennsylvania, US. The elk was in poor nutritional condition and had alopecia and ulcerative dermatitis throughout the neck and dorsum region associated with severe Dermacentor albipictus infestations. Histologically, there was severe chronic-active dermatitis with hyperkeratosis and crust formation.
Subject(s)
Alopecia/veterinary , Deer/parasitology , Dermacentor , Dermatitis/veterinary , Tick Infestations/veterinary , Alopecia/etiology , Animals , Dermatitis/etiology , Tick Infestations/complications , Tick Infestations/parasitologyABSTRACT
La enfermedad de Lyme es causada por la espiroqueta Borrelia Burgdoferi, que se transmite por la mordedura de la garrapata del género Ixodes. El diagnostico se realiza por ELISA y se confirma mediante Western blot o PCR. Una infección por Borrelia no solo desencadena una respuesta inmune humoral, sino que también activa la respuesta inmune celular medida por los linfocitos T, de allí la existencia del análisis Elispot-LTT, cual según la literatura científica tiene mayor especificidad y sensibilidad que incluso el Western blot. El presente caso de cuadro clínico atípico en un bombero con Enferemdad de Lyme y co-infección por Rickettsia conorii y Bartonella Heselae. Se declaró como enfermedad profesional dado que se adquirió en el ámbito laboral
Lyme disease is caused by the spirochete Borrelia Burgdoferi, which is transmitted by the bite of the tick of the genus Ixodes. The diagnosis is made by ELISA and confirmed by Western blot or PCR. A Borrelia infection not only triggers a humoral immune response, but also activates the cellular immune response measured by the T lymphocytes, hence the existence of the Elispot-LTT analysis, which according to the scientific literature has greater specificity and sensitivity than even the Western blot. The present case of an atypical clinical picture in a firefighter with Lyme disease and co-infection with Rickettsia conorii and Bartonella Heselae. It was declared as a occupational disease since it was acquired in the workplace
Subject(s)
Humans , Male , Adult , Lyme Disease/diagnosis , Occupational Diseases/diagnosis , Occupational Exposure/analysis , Erythema Chronicum Migrans/diagnosis , Tick Infestations/complications , Borrelia Infections/complications , Borrelia burgdorferi/isolation & purificationABSTRACT
BACKGROUND: Our study aimed to assess the diversity of the species of Anaplasmataceae in Senegal that infect animals and ticks in three areas: near Keur Momar Sarr (northern region), Dielmo and Diop (Sine Saloum, central region of Senegal), and in Casamance (southern region of Senegal). METHODS: A total of 204 ticks and 433 blood samples were collected from ruminants, horses, donkeys and dogs. Ticks were identified morphologically and by molecular characterization targeting the 12S rRNA gene. Molecular characterization of species of Anaplasmataceae infecting Senegalese ticks and animals was conducted using the 23S rRNA, 16S rRNA, rpoB and groEL genes. RESULTS: Ticks were identified as Rhipicephalus evertsi evertsi (84.3%), Hyalomma rufipes (8.3%), Hyalomma impeltatum (4.9%), R. bursa (1.5%) and R. muhsamae (0.9%). The overall prevalence of Anaplasmataceae infection in ticks was 0.9%, whereas 41.1% of the sampled animals were found infected by one of the species belonging to this family. We identified the pathogen Anaplasma ovis in 55.9% of sheep, A. marginale and A. centrale in 19.4% and 8.1%, respectively, of cattle, as well as a putative new species of Anaplasmataceae. Two Anaplasma species commonly infecting ruminants were identified. Anaplasma cf. platys, closely related to A. platys was identified in 19.8% of sheep, 27.7% of goats and 22.6% of cattle, whereas a putative new species, named here provisionally "Candidatus Anaplasma africae", was identified in 3.7% of sheep, 10.3% of goats and 8.1% of cattle. Ehrlichia canis and Anaplasma platys were identified only from dogs sampled in the Keur Momar Sarr area. Ehrlichia canis was identified in 18.8% of dogs and two R. e. evertsi ticks removed from the same sheep. Anaplasma platys was identified in 15.6% of dogs. Neither of the dogs sampled from Casamance region nor the horses and donkeys sampled from Keur Momar Sarr area were found infected by an Anaplasmataceae species. CONCLUSIONS: This study presents a summary of Anaplasmataceae species that infect animals and ticks in three areas from the northern, central and southern regions of Senegal. To our knowledge, our findings demonstrate for the first time the presence of multiple Anaplasmataceae species that infect ticks and domestic animals in Senegal. We recorded two potentially new species commonly infecting ruminants named here provisionally as Anaplasma cf. platys and "Candidatus Anaplasma africae". However, E. canis was the only species identified and amplified from ticks. None of the other Anaplasmataceae species identified in animals were identified in the tick species collected from animals.
Subject(s)
Anaplasmataceae Infections/veterinary , Anaplasmataceae/classification , Anaplasmataceae/genetics , Animals, Domestic/microbiology , Ticks/microbiology , Anaplasmataceae Infections/microbiology , Animals , Animals, Domestic/parasitology , Cattle , Chaperonin 60/genetics , DNA, Ribosomal/blood , DNA, Ribosomal/chemistry , DNA, Ribosomal/isolation & purification , DNA-Directed RNA Polymerases/genetics , Dog Diseases/microbiology , Dog Diseases/parasitology , Dogs , Equidae/microbiology , Equidae/parasitology , Female , Genetic Variation , Goats , Horse Diseases/microbiology , Horse Diseases/parasitology , Horses , Male , Phylogeny , RNA, Ribosomal/genetics , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 23S/genetics , Ruminants/microbiology , Ruminants/parasitology , Senegal , Sequence Alignment/veterinary , Sheep , Tick Infestations/complications , Tick Infestations/veterinaryABSTRACT
Canine babesiosis (CB) is a significant tick-borne disease caused by intra-erytrocytic protozoa of the genus Babesia (Apicomplexa: Piroplasmida) and is currently emerging or re-emerging in many European countries. Despite the increasing incidence of clinical CB, little is known of the epidemiology of this disease in Romania. Therefore, the present study was conducted to provide epidemiological data on CB in the coastal area of the Black Sea (Dobrogea), southeastern Romania. For this, 306 owned dogs presented during 2016-2018 at a veterinary clinic in the area and clinically suspected for CB were tested for the presence of intra-erytrocytic piroplasms using Giemsa-stained thin blood smears. Overall, 27.8% (95% CI: 22.83-33.16) of dogs were positive for large piroplasms. The Babesia spp.-positive dogs were 51 males and 34 females aged from 3 mo to 13 yr (mean 4.2 yr; SD = 3.6). A higher rate of infection was registered in Bichon Maltese (n = 13) and mixed-breed (n = 28) dogs. Most cases (76/85; 89.4%) were diagnosed from March to June, with only a few cases registered in November and December (1 case each). Infected dogs displayed different clinical presentations, varying from mild (38.8%) to moderate (29.4%) and severe disease (29.4%). Based on clinical- pathological changes, 38 (44.7%), 34 (40.0%), and 13 (15.3%) dogs were diagnosed with uncomplicated babesiosis, complicated babesiosis with a single organ dysfunction, and complicated babesiosis with multiple-organ-dysfunction syndrome (MODS), respectively. The recovery rate (81.6%, 70.1%, and 38.4%, respectively) was significantly different in these groups. The age of dogs appeared to be a risk factor for both severe disease (mean age of 5.8 yr) and MODS (mean age 6.8 yr). These findings document the common occurrence of CB in Dobrogea, southeastern Romania, and suggest that appropriate control measures need to be taken.
Subject(s)
Babesiosis/epidemiology , Dog Diseases/epidemiology , Dog Diseases/parasitology , Age Distribution , Age Factors , Animals , Antiprotozoal Agents/therapeutic use , Babesia/isolation & purification , Babesiosis/drug therapy , Babesiosis/etiology , Babesiosis/parasitology , Black Sea/epidemiology , Dog Diseases/drug therapy , Dog Diseases/mortality , Dogs , Erythrocytes/parasitology , Female , Imidocarb/analogs & derivatives , Imidocarb/therapeutic use , Male , Risk Factors , Romania/epidemiology , Seasons , Sex Distribution , Tick Infestations/complications , Tick Infestations/epidemiology , Tick Infestations/veterinaryABSTRACT
An epidemic of Rocky Mountain spotted fever (RMSF) is ongoing in Mexicali, México. We visited 100 neighborhoods with diagnosed human cases and 100 control neighborhoods to evaluate knowledge of the epidemic; obtain data on the spatial distribution of dogs, canine seroprevalence and active infection, tick infestations, and presence of rickettsial DNA in ticks; and evaluate risk factors for human cases, seropositivity, and tick infestation within an unbiased study design. The majority (80%) of residents had heard of RMSF, but only 48% used acaricides in the home or on dogs. Case neighborhoods and those with high canine seroprevalence tended to be on the city periphery or in the agricultural valley. No dogs were polymerase chain reaction (PCR) positive for Rickettsia rickettsii, and the overall seroprevalence was 65% (titers from 64 to 1,024). PCR prevalence in ticks was 0.70%, confirmed by DNA sequencing as R. rickettsii; neighborhood prevalence ranged from 0.7% to 6.1%. Twelve percent of dogs had high tick burdens, and all ticks were Rhipicephalus sanguineus. Epidemiologically significant risk factors were ground covering for a neighborhood having a human case; dogs having poor body condition and weighing < 10 kg for canine seropositivity; dogs living at the home for the number of ticks in the environment; and being near canals, having trash on the patio, and a dog being thin for tick burdens on dogs. A One Health approach is crucial to understanding RMSF and brown dog ticks.
Subject(s)
Dog Diseases/microbiology , Rhipicephalus sanguineus/physiology , Rickettsia rickettsii/isolation & purification , Rocky Mountain Spotted Fever/veterinary , Tick Infestations/veterinary , Animals , Arachnid Vectors/microbiology , Dog Diseases/epidemiology , Dogs , Humans , Mexico/epidemiology , Rhipicephalus sanguineus/microbiology , Risk Factors , Rocky Mountain Spotted Fever/epidemiology , Seroepidemiologic Studies , Tick Infestations/complications , Tick Infestations/epidemiologyABSTRACT
BACKGROUND: The interplay of speed of activity of acaricidal products and tick-borne pathogen transmission time is the major driver for disease prevention. This study aimed to investigate the time required for transmission of Anaplasma phagocytophilum by adult Ixodes ricinus ticks in vivo on dogs, and to confirm the time required for transmission observed in vivo, in vitro. METHODS: Nymphs of I. ricinus were experimentally infected with an A. phagocytophilum strain of canine origin. Dogs were allocated to 6 groups of 3 dogs each. Groups 1-5 were infested with 50 A. phagocytophilum-infected female adult ticks on Day 0. Ticks were removed post-infestation at 3, 6, 12, 24 and 48 h. Dogs in Group 6 were infested with 60 A. phagocytophilum-infected female adult ticks (left on dogs until engorged). Dogs were observed daily for general health and clinically examined on Day 0, and weekly from Day 14. Blood was collected for qPCR and serological analysis on Day 0 (pre-challenge) and weekly thereafter. In the in vitro study each artificial feeding chamber was seeded with 10 adult ticks (5 male/5 female), attachment assessed, and blood pools sampled for qPCR at 6 h intervals up to 72 h after first tick attachment. RESULTS: Anaplasma phagocytophilum specific antibodies and DNA were detected in all 3 dogs in Group 6. No A. phagocytophilum-specific antibodies or DNA were detected in any dogs in Groups 1-5. All dogs remained healthy. Female tick attachment in 60 artificial feeding chambers over 72 h ranged between 20-60%. Anaplasma phagocytophilum DNA was detected in the blood collected from 5% of chambers sampled at 6 h, with the highest number of positive samples (16.3%) observed at 36 h. CONCLUSIONS: Transmission of A. phagocytophilum by I. ricinus ticks starts within a few hours after attachment but establishment of infections in dogs is apparently dependent on a minimum inoculation dose that was only observed when ticks attached for greater than 48 h. These findings highlight the need for acaricidal products to exert a repellent and/or rapid killing effect on ticks to forestall transmission and subsequent disease.
Subject(s)
Anaplasma phagocytophilum , Dog Diseases/microbiology , Ehrlichiosis/transmission , Ixodes/microbiology , Tick Infestations/veterinary , Tick-Borne Diseases/transmission , Animals , Dog Diseases/transmission , Dogs , Ehrlichiosis/parasitology , Female , Male , Membranes, Artificial , Tick Infestations/complications , Time FactorsABSTRACT
BACKGROUND: Elucidating which wildlife species significantly contribute to the maintenance of Ixodes ricinus populations and the enzootic cycles of the pathogens they transmit is imperative in understanding the driving forces behind the emergence of tick-borne diseases. Here, we aimed to quantify the relative contribution of four mustelid species in the life-cycles of I. ricinus and Borrelia burgdorferi (sensu lato) in forested areas and to investigate their role in the transmission of other tick-borne pathogens. Road-killed badgers, pine martens, stone martens and polecats were collected in Belgium and the Netherlands. Their organs and feeding ticks were tested for the presence of tick-borne pathogens. RESULTS: Ixodes hexagonus and I. ricinus were found on half of the screened animals (n = 637). Pine martens had the highest I. ricinus burden, whereas polecats had the highest I. hexagonus burden. We detected DNA from B. burgdorferi (s.l.) and Anaplasma phagocytophilum in organs of all four mustelid species (n = 789), and Neoehrlichia mikurensis DNA was detected in all species, except badgers. DNA from B. miyamotoi was not detected in any of the investigated mustelids. From the 15 larvae of I. ricinus feeding on pine martens (n = 44), only one was positive for B. miyamotoi DNA, and all tested negative for B. burgdorferi (s.l.), N. mikurensis and A. phagocytophilum. The two feeding larvae from the investigated polecats (n = 364) and stone martens (n = 39) were negative for all four pathogens. The infection rate of N. mikurensis was higher in feeding nymphs collected from mustelids compared to questing nymphs, but not for B. burgdorferi (s.l.), B. miyamotoi or A. phagocytophilum. CONCLUSIONS: Although all stages of I. ricinus can be found on badgers, polecats, pine and stone martens, their relative contribution to the life-cycle of I. ricinus in forested areas is less than 1%. Consequently, the relative contribution of mustelids to the enzootic cycles of I. ricinus-borne pathogens is negligible, despite the presence of these pathogens in organs and feeding ticks. Interestingly, all four mustelid species carried all stages of I. hexagonus, potentially maintaining enzootic cycles of this tick species apart from the cycle involving hedgehogs as main host species.
Subject(s)
Borrelia burgdorferi/isolation & purification , Ixodes/microbiology , Mustelidae/parasitology , Tick Infestations/veterinary , Tick-Borne Diseases/veterinary , Anaplasma phagocytophilum/genetics , Anaplasma phagocytophilum/isolation & purification , Anaplasma phagocytophilum/pathogenicity , Anaplasmataceae/genetics , Anaplasmataceae/isolation & purification , Anaplasmataceae/pathogenicity , Animals , Animals, Wild , Belgium/epidemiology , Borrelia Infections/transmission , Borrelia Infections/veterinary , Borrelia burgdorferi/genetics , Borrelia burgdorferi/pathogenicity , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Bacterial/isolation & purification , Ehrlichiosis/complications , Ehrlichiosis/epidemiology , Ehrlichiosis/transmission , Ehrlichiosis/veterinary , Ferrets/microbiology , Hedgehogs/parasitology , Life Cycle Stages , Lyme Disease/epidemiology , Lyme Disease/microbiology , Lyme Disease/transmission , Lyme Disease/veterinary , Netherlands/epidemiology , Nymph/microbiology , Rickettsia/genetics , Rickettsia/isolation & purification , Rickettsia/pathogenicity , Tick Infestations/complications , Tick Infestations/epidemiology , Tick-Borne Diseases/microbiology , Tick-Borne Diseases/transmissionABSTRACT
Oriental theileriosis caused by Theileria orientalis is an economically significant disease in cattle farming. The lack of laboratory animal models and in vitro culture systems is a major obstacle in the drive to better understand the biology of this parasite. Notably, research on the sporozoite stage of T. orientalis has rarely been undertaken, although such investigations are of paramount importance for vaccine development based on blocking sporozoite invasion of its host animals. In the present study, we established a mouse-tick infection model for propagating T. orientalis in mice and for producing the sporozoite stage in tick salivary glands. Splenectomized severe combined immunodeficient mice transfused with bovine erythrocytes were infected with T. orientalis. The larval ticks of Haemaphysalis longicornis were then fed on the T. orientalis-infected mice. The piroplasm and sporozoite stages were microscopically observed in the mouse blood and nymphal salivary glands, respectively. The transcriptomics data generated from the piroplasm and sporozoite stages revealed a stage-specific expression pattern for the parasite genes. The mouse-tick infection model and the transcriptomics data it has provided will contribute to a better understanding of T. orientalis biology and will also provide much needed information for the design of effective control measures targeting oriental theileriosis.
Subject(s)
Gene Expression Profiling , Host-Pathogen Interactions , Sporozoites/growth & development , Theileria/growth & development , Theileriasis/pathology , Tick Infestations/complications , Animals , Blood/parasitology , Disease Models, Animal , Ixodidae/growth & development , Mice , Mice, SCID , Saliva/parasitology , Sporozoites/genetics , Theileria/genetics , Theileriasis/parasitologyABSTRACT
This study describes experimental infection of guinea pigs (Cavia porcellus) infested with naturally infected Amblyomma ovale nymphs with Rickettsia sp. (Atlantic rainforest strain), and the capacity of A. ovale nymphs to transmit this bacterium. Twenty-six guinea pigs were divided into the following groups: G1, 10 animals infested with uninfected A. ovale nymphs; G2, 10 animals infested with nymphs infected with Rickettsia sp. (Atlantic rainforest strain); and G3, 6 animals without tick infestation. Blood samples were taken 7, 14, 21, and 28 days post-infestation for serological and hematological tests. For histopathological analysis and rickettsial DNA detection, fragments of the spleen, lung, brain, and liver were harvested after euthanasia. The average feeding period for nymphs was 6.6 days for G1 and 6 days for G2. Hemolymph and PCR assays, performed to detect the causative agent in ticks, indicated that in G1, all ticks were negative, and in G2, all nymphs were positive by PCR and 80% (8/10) was positive by hemolymph tests. The only clinical change was skin scarring at the tick attachment site. Hematological parameters indicated leukopenia and total plasma protein (TPP) increased with decreased platelets in G1. In G2, leukocytosis, neutrophilia, monocytosis, an increase in platelets, and reduced TPP were observed. Only G2 guinea pigs were seroconverted (80%; 8/10). Histopathology tests indicated mild, diffuse hemosiderosis and mild, multifocal, follicular hyperplasia in the spleen. Molecular analysis did not detect Rickettsia sp. DNA in C. porcellus tissues. We demonstrated the capacity of A. ovale nymphs to transmit Rickettsia sp. (Atlantic rainforest strain) to guinea pigs.
Subject(s)
Ixodidae/microbiology , Rickettsia Infections/veterinary , Tick Infestations/veterinary , Animals , Guinea Pigs , Nymph , Polymerase Chain Reaction , Rainforest , Rickettsia/genetics , Rickettsia Infections/microbiology , Rickettsia Infections/transmission , Tick Infestations/complicationsABSTRACT
Piroplasmosis is one of the most important diseases of livestock, constraining optimal production and leading to economic loss. This study was carried out to detect Theileria annulata by using 2 different molecular techniques: recombinase polymerase amplification (RPA) and conventional polymerase chain reaction (PCR). Blood samples were collected from 274 ticks infesting asymptomatic cattle from several counties in the Chakwal, Faisalabad, and Jhang districts of Punjab Province in Pakistan by using FTA cards. After extraction of genomic DNA, each sample was subjected to RPA optimized to amplify a 281-bp fragment of the Enolase gene for T. annulata. The specificity of the test was confirmed using positive DNA samples of related piroplasm species, whereas the analytical sensitivity was calculated using different serial dilutions of a long fragment of the same gene. The RPA results were positive for 48 (17.51%) of 274 samples. All 274 samples were screened using conventional PCR, and 21 (7.66%) samples were positive for T. annulata. All the samples that were RPA positive but PCR negative were sequenced, which confirmed the results of RPA. The highest positive rate was found in Chakwal district, followed by Faisalabad and Jhang districts. This study demonstrates the application of highly sensitive and specific rapid diagnostic methods for T. annulata to a regional screening program. This is the first report of tick-borne disease from Pakistan by using RPA.
Subject(s)
Theileria annulata/isolation & purification , Theileriasis/diagnosis , Tick Infestations/veterinary , Animals , Cattle , Cattle Diseases/diagnosis , Cattle Diseases/epidemiology , Cattle Diseases/parasitology , Pakistan/epidemiology , Polymerase Chain Reaction/veterinary , Prevalence , Recombinases/metabolism , Sensitivity and Specificity , Sequence Alignment/veterinary , Theileria annulata/genetics , Theileriasis/epidemiology , Theileriasis/parasitology , Tick Infestations/blood , Tick Infestations/complicationsABSTRACT
Anaplasma phagocytophilum and Borrelia burgdorferi are both transmitted by Ixodes spp. and are associated with clinical illness in some infected dogs. This study evaluated canine antibody responses to the A. phagocytophilum p44 peptides APH-1 and APH-4 as well as the B. burgdorferi C6 peptide before and after doxycycline treatment. A total of eight dogs were infested with wild-caught I. scapularis for 1 week. Blood was collected prior to tick attachment and from Days 3-77 to 218-302 with doxycycline treatment beginning on Day 218. Blood was assayed for A. phagocytophilum DNA by PCR assay. Sera was assessed for antibodies by immunofluorescent antibody (IFA) test and ELISA. Anaplasma phagocytophilum DNA was amplified from blood of all dogs by Day 7. Antibodies to APH-4 were detected in serum as early as 14days after tick exposure and six dogs had APH-4 antibodies detected 3-7 days before antibodies against APH-1. All dogs were seropositive for A. phagocytophilum from Days 218 to 302. Antibodies to B. burgdorferi were detected in 6/8 dogs beginning 21days after I. scapularis infestation. Among the five dogs that remained seropositive at Day 218, C6 antibody levels declined on average 81% within 84days of initiating treatment. The results suggest that the APH-4 peptide may be more useful than APH-1 for detecting antibodies earlier in the course of an A. phagocytophilum infection. After doxycycline administration, C6 antibody levels but not APH-1 or APH-4 antibody levels decreased, suggesting a treatment effect on C6 antibody production.
Subject(s)
Anaplasma phagocytophilum/immunology , Borrelia burgdorferi/immunology , Dog Diseases/parasitology , Ehrlichiosis/veterinary , Ixodes , Lyme Disease/veterinary , Tick Infestations/veterinary , Animals , Anti-Bacterial Agents/therapeutic use , Antibodies, Bacterial/blood , Bacterial Proteins/immunology , Dog Diseases/immunology , Dogs , Doxycycline/therapeutic use , Ehrlichiosis/drug therapy , Ehrlichiosis/immunology , Ehrlichiosis/transmission , Female , Lyme Disease/drug therapy , Lyme Disease/immunology , Lyme Disease/transmission , Male , Peptides/immunology , Real-Time Polymerase Chain Reaction/veterinary , Tick Infestations/complications , Tick Infestations/immunologyABSTRACT
The objectives of our research on equine piroplasmosis were to clarify the prevalence of the piroplasms Babesia caballi and Theileria equi among reintroduced Przewalski's horses (takhi, Equus ferus przewalskii) in comparison with horses (Equus caballus) of nomads from around Hustai National Park in Mongolia and to determine the mortality among takhi during 2012 to 2015. The prevalence of T. equi was high in 2014 at 80% among nomadic horses and 84% among takhi. We found no evidence of B. caballi infection among takhi. A homology comparison of the 18S rRNA base sequence of T. equi showed the same sequence in both domestic horses and takhi. According to the national park records, piroplasmosis is a cause of high mortality in young takhi (19%). The results suggested that takhi were infected with T. equi in this park, and the infection is an important issue when reintroducing the takhi into the wild and increasing the numbers of the animals in nature. Continuous monitoring and vector control were noted as important issues in future conservation programs.
Subject(s)
Babesiosis/prevention & control , DNA, Protozoan/chemistry , Horse Diseases/prevention & control , Theileria/genetics , Theileriasis/prevention & control , Animals , Animals, Domestic , Animals, Wild , Babesiosis/epidemiology , DNA, Protozoan/blood , DNA, Protozoan/isolation & purification , Endangered Species , Horse Diseases/epidemiology , Horse Diseases/parasitology , Horses , Phylogeny , Polymerase Chain Reaction/veterinary , Prevalence , Theileria/classification , Theileriasis/epidemiology , Tick Infestations/complications , Tick Infestations/epidemiology , Tick Infestations/veterinaryABSTRACT
There are only few reports on Lyme borreliosis (LB) in cats. The reasons might be a different tick infestation in cats compared to dogs, a low susceptibility for tick-borne infections or a low awareness of veterinarians for tick-borne diseases in feline patients. The aim of this study was to determine the proportion of antibodies against Borrelia burgdorferi sensu lato (Bbsl) in feline sera, to compare the significance of feline versus canine LB, as well as to evaluate possible implications on disease occurrence. Specific antibodies against the C6-peptide of Bbsl in cats were detected by a rapid test based on enzyme immunoassay technique. The serum samples were sent to a diagnostic laboratory by veterinarians from Germany and other European countries with request for Borrelia serology in the years 2009-2011. Veterinarians were asked for information regarding the cats' location, age, gender, clinical signs, treatment and follow-up. In six of 271 (2.2%; 95% CI: 0.8-4.8%) cat sera, antibodies against the C6-peptide of Bbsl were detected. Proportion of Borrelia antibody-positive cat sera was significantly lower than the one determined for dogs during the same time period. All positive cats lived in countries endemic for LB (Germany, Sweden and Belgium), and all C6-antibody positive cats with the exception of one cat showed clinical signs. Possible implications on disease occurrence are discussed. Data presented here demonstrate a lower prevalence of Borrelia specific C6-antibodies in European cats when compared to dogs residing in the same regions. The absence of antibodies against Bbsl in 97.8% (95% CI: 95.2-99.2%) of the submitted samples indicate that diagnosis "feline LB"is rare in cats. Nevertheless, LB should be considered in cats with compatible clinical signs (e.g. shifting leg lameness, to less extent neurological signs) when other differential diagnoses are ruled out.
Subject(s)
Antibodies, Bacterial/blood , Borrelia burgdorferi Group/immunology , Cat Diseases/epidemiology , Lyme Disease/veterinary , Tick Infestations/veterinary , Animals , Belgium/epidemiology , Cat Diseases/parasitology , Cats , Cohort Studies , Diagnosis, Differential , Dog Diseases/epidemiology , Dog Diseases/parasitology , Dogs , Female , Germany/epidemiology , Lyme Disease/epidemiology , Lyme Disease/parasitology , Male , Seroepidemiologic Studies , Sweden/epidemiology , Tick Infestations/complications , Tick Infestations/parasitologyABSTRACT
A cross-sectional study combining different serological and molecular techniques for the detection of Ehrlichia species in dogs and their ticks was carried out with data from all regions of Costa Rica. A seroprevalence of 32.1% (131/408), and infection with E. canis of 3.2% (13/407) was found, whereas 6.9% (9/130) of ticks attached to the dogs were PCR positive to E. canis. Higher prevalences were found outside the Greater Metropolitan Area (GMA). Risk factors associated with E. canis seropositivity were age, between 2 and 7 years (RR: 1.6, 95% CI: 1.2-2.2) and 8-15 years (RR: 1.8, 95% CI: 1.2-3.0), number of dogs/total of households [Dogs per Household Ratio (DHR) ≥3.1 (RR: 2.0; 95% CI: 1.4-3.0)], number of dogs infested with at least one tick/total of dogs sampled [Tick Infestation Prevalence (TIP)≥31% (RR: 2.1; 95% CI:1.3-3.3)] and living outside the GMA (RR: 1.7; 95% CI: 1.2-2.4) and being a mixed-breed dog (RR: 1.5; 95% CI: 1.1-2.1). Risk factors for E. canis PCR positive dogs were a depressive attitude (OR: 11.2; 95% CI: 1.1-115.9), fever (OR:4.8; 95% CI:1.2-19.3), DHR≥3.1 (OR: 5.7; 95% CI:1.7-19.2)], number of ticks/total of dogs sampled [Tick Distribution Ratio (TDR) ≥2.1 (OR: 6.5; 95% CI: 1.3-31.8)], and TIP≥40% (OR: 5.7; 95% CI: 1.7-19.2). This paper describes E. canis seroprevalence, PCR prevalence and tick analysis in dogs from Costa Rica, with associated clinical signs and owner perceptions. In summary, most of the E. canis infections in dogs in our country seemed to pass unnoticed by owners. Since most of the seropositive dogs (97.7%, 131/134) were negative for E. canis DNA in their blood, it is important to determine in future studies if these dogs recovered from the E. canis infection without any medication, or are persistently infected, and will develop chronic disease.
Subject(s)
Dog Diseases/microbiology , Ehrlichiosis/veterinary , Tick Infestations/veterinary , Aging , Animals , Costa Rica/epidemiology , Dog Diseases/epidemiology , Dogs , Ehrlichia canis , Ehrlichiosis/epidemiology , Ehrlichiosis/microbiology , Risk Factors , Serologic Tests , Tick Infestations/complications , Tick Infestations/epidemiologyABSTRACT
BACKGROUND: The ability of the topical spot-on Advantix(®) (50 % permethrin/10 % imidacloprid) to prevent transmission of Ehrlichia canis by infected Rhipicephalus sanguineus ticks to dogs has previously been reported. The recent market introduction of chewable tablets containing the novel compounds, afoxolaner (NexGard™) and fluralaner (Bravecto™) enabled us to conduct a comparative efficacy study with respect to the ability of these three products to block transmission of E. canis by ticks to dogs. The speed of kill, immediate drop-off rate and anti-attachment efficacy of the respective products were also studied. METHODS: The study was a blinded parallel group design, wherein 32 dogs were randomised into four different groups of eight dogs. Group 1 served as negative placebo control, group 2 and 3 were treated on Days 0, 28 and 56 with NexGard™ and Advantix(®), respectively. Group 4 was dosed once on Day 0 with Bravecto™. For tick efficacy assessments 50 non-infected ticks were placed onto the dogs on Days 30, 35, 42, 49, 56, 63, 70, 77 and 84 and on animal tick counts were performed at 3 h, 6 h and 12 h after infestation. To evaluate the ability to block transmission of E. canis, each dog was challenged by releasing 80 adult E. canis-infected R. sanguineus ticks into their sleeping kennels on Days 31, 38, 45 and 52. The animals were monitored for clinical signs of monocytic ehrlichiosis (pyrexia and thrombocytopenia) and were tested for E. canis DNA by PCR and for specific antibodies using IFA. A dog was considered infected with E. canis if both PCR and IFA yielded positive test results up to Day 84. RESULTS: Mean arithmetic tick counts on dogs treated with the Advantix(®) spot-on were significantly (P < 0.0005) lower throughout the study as compared with the negative controls and was, with respect to the speed of kill and resulting onset of acaricidal efficacy, superior over NexGard™ and Bravecto™ at all time points in the 12 h period observed (3 h, 6 h and 12 h). None of the dogs treated with the Advantix(®) spot-on became infected with E. canis, whereas six out of eight untreated control dogs acquired the infection. Furthermore, E. canis infection was diagnosed in four out of eight dogs treated with NexGard™ and in two out of eight dogs treated with Bravecto™. CONCLUSIONS: The speed of kill of the two recently registered systemic compounds against R. sanguineus was not sufficiently fast to prevent transmission of E. canis and resulted in only low partial blocking and protection capacity while Advantix(®) effectively blocked transmission of E. canis to dogs in the challenge period and thus provided adequate protection for dogs against monocytic ehrlichiosis.
Subject(s)
Dog Diseases/prevention & control , Ehrlichiosis/veterinary , Imidazoles/pharmacology , Isoxazoles/pharmacology , Naphthalenes/pharmacology , Nitro Compounds/pharmacology , Permethrin/pharmacology , Acaricides/administration & dosage , Acaricides/pharmacology , Administration, Oral , Administration, Topical , Animals , Arachnid Vectors/microbiology , Dog Diseases/parasitology , Dogs , Drug Combinations , Drug Therapy, Combination , Ehrlichia canis/drug effects , Ehrlichia canis/physiology , Ehrlichiosis/prevention & control , Ehrlichiosis/transmission , Imidazoles/administration & dosage , Insecticides/administration & dosage , Insecticides/pharmacology , Isoxazoles/administration & dosage , Naphthalenes/administration & dosage , Neonicotinoids , Nitro Compounds/administration & dosage , Permethrin/administration & dosage , Rhipicephalus sanguineus/microbiology , Tick Infestations/complications , Tick Infestations/veterinaryABSTRACT
Small rodents serve as reservoir hosts for tick-borne pathogens, such as the spirochetes causing Lyme disease. Whether natural coinfections with other macroparasites alter the success of tick feeding, antitick immunity, and the host's reservoir competence for tick-borne pathogens remains to be determined. In a parasitological survey of wild mice in Berlin, Germany, approximately 40% of Ixodes ricinus-infested animals simultaneously harbored a nematode of the genus Heligmosomoides We therefore aimed to analyze the immunological impact of the nematode/tick coinfection as well as its effect on the tick-borne pathogen Borrelia afzelii Hosts experimentally coinfected with Heligmosomoides polygyrus and larval/nymphal I. ricinus ticks developed substantially stronger systemic type 2 T helper cell (Th2) responses, on the basis of the levels of GATA-3 and interleukin-13 expression, than mice infected with a single pathogen. During repeated larval infestations, however, anti-tick Th2 reactivity and an observed partial immunity to tick feeding were unaffected by concurrent nematode infections. Importantly, the strong systemic Th2 immune response in coinfected mice did not affect susceptibility to tick-borne B. afzelii An observed trend for decreased local and systemic Th1 reactivity against B. afzelii in coinfected mice did not result in a higher spirochete burden, nor did it facilitate bacterial dissemination or induce signs of immunopathology. Hence, this study indicates that strong systemic Th2 responses in nematode/tick-coinfected house mice do not affect the success of tick feeding and the control of the causative agent of Lyme disease.