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Thekisoe OM Inoue N Kuboki N Tuntasuvan D Bunnoy W Borisutsuwan S Igarashi I Sugimoto C 《Veterinary parasitology》2005,130(3-4):327-330
Six surra negative piglets (6-week-old) were infected with Trypanosoma evansi and two uninfected piglets were used as negative controls. Detection performances of various diagnostic tests (LAMP, PCR and parasitological tests) were compared by analysing blood samples collected weekly over a period of 11 weeks. With a two by two analysis without a gold standard, all methods were 100% specific. MI had the highest sensitivity of 65%, while LAMP, PCR, MHCT and TBS had sensitivities of 45, 33, 38 and 24%, respectively. However, when the analysis was done using MI as a gold standard, the sensitivity of MHCT was the highest at 53% followed by LAMP, PCR and TBS at 49, 44 and 35%, respectively. All methods gave high specificity above 60%. This study validates LAMP as an alternative method for the diagnosis of surra. 相似文献
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Terkawi MA Thekisoe OM Katsande C Latif AA Mans BJ Matthee O Mkize N Mabogoane N Marais F Yokoyama N Xuan X Igarashi I 《Veterinary parasitology》2011,182(2-4):337-342
A total of 719 serum samples collected from clinically healthy cattle from eight provinces located in different districts of South Africa were examined by the indirect enzyme-linked immunosorbent assay (ELISA) and the standard indirect fluorescent antibody test (IFAT) to determine the serological prevalence of Babesia bovis and Babesia bigemina. The results showed that 35.3% and 39.7% of cattle were positive for B. bovis and 30% and 36.5% were positive for B. bigemina antibodies on ELISA and IFAT, respectively. Mixed infections were detected in 18.2% and 26.3% of the samples using ELISA and IFAT, respectively. Consequently, the ELISAs with recombinant B. bovis spherical body protein-4 (BbSBP-4) and B. bigemina C-terminal rhoptry-associated protein-1 (BbigRAP-1/CT) were proven to be highly reliable in the serological diagnoses of bovine babesiosis in South African cattle, as evidenced by the significant concordance rates when the results were compared to those of IFAT. Moreover, the serological prevalence was significantly different among the tested provinces, in which the ranges exhibited between 15% and 73% for B. bovis infection and between 13% and 54% for B. bigemina infection. High sero-positive rates were present in Mpumalanga and KwaZulu-Natal provinces, while the lowest rate was in the North West province. Our data provide important information regarding the current seroprevalence of bovine babesiosis in South Africa, which might be beneficial in developing rational strategies for disease control and management. 相似文献
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Thu-Thuy NGUYEN Mono Sophie MOTSIRI Moeti Oriel TAIOE Moses Sibusiso MTSHALI Yasuyuki GOTO Shin-Ichiro KAWAZU Oriel Matlhahane Molifi THEKISOE Noboru INOUE 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2015,77(2):217-220
A total of 231 serum samples were collected from sheep (n=9), goats (n=99) and cattle (n=123) in northeastern KwaZulu-Natal, South Africa. Trypanosome infection was detected using Trypanosoma brucei brucei crude antigen (TbbCA) and T. congolense crude antigen (TcoCA) ELISA assays. Recombinant antigen (T. evansi GM6 which consisted of 4 repeat domains, TeGM6-4r) ELISA and immunochromatographic test (ICT) were also used. Crude antigen ELISA, TeGM6-4r-ELISA and ICT detected 27.3%, 29% and 19.9% of trypanosome seropositive samples, respectively. Trypanosome infection prevalence in cattle and goats was 35.8–46.3% and 0–9.1%, respectively. Out of 9 sheep serum samples, 2–4 sera (22.2–44.4%) were positive. The detection performance of crude and recombinant antigen ELISAs was relatively similar (K=0.6–0.7); both are recommended for reference diagnosis and large scale epidemiological surveys. There is potential application for ICT in
on-site diagnosis, but its sensitivity should be improved. 相似文献
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Development of loop-mediated isothermal amplification (LAMP) method for diagnosis of equine piroplasmosis 总被引：1，自引：0，他引：1
Alhassan A Thekisoe OM Yokoyama N Inoue N Motloang MY Mbati PA Yin H Katayama Y Anzai T Sugimoto C Igarashi I 《Veterinary parasitology》2007,143(2):155-160
Loop-mediated isothermal amplification (LAMP) is a novel nucleic acid method whereby DNA is amplified with high specificity, efficiency, and rapidity under isothermal conditions using a set of four specifically designed primers and a DNA polymerase with strand displacement activity. In this study, we used LAMP primer sets designed from EMA-1 and Bc 48 genes for detection of Theileria equi and Babesia caballi infections, respectively. These primer sets specifically amplified DNA of the respective parasites. Both primer sets amplified T. equi and B. caballi up to 10(-6) dilution of 10-fold serially diluted samples. Furthermore, DNA extracted from blood collected from a horse experimentally infected with T. equi was amplified by a T. equi LAMP primer set from days 2 to 35 post-infection, demonstrating the high sensitivity of these primers. Of 55 samples collected from China, 81.8% and 56.3% were positively detected by LAMP for T. equi and B. caballi infections, respectively. In contrast, 91.8% and 45.9% of the 37 samples collected from South Africa were LAMP positive for T. equi and B. caballi, respectively. These results suggest that LAMP could be a potential diagnostic tool for epidemiological studies of equine piroplasmosis. 相似文献
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Khethiwe MTSHALI Zamantungwa T. H. KHUMALO Ryo NAKAO Dennis J. GRAB Chihiro SUGIMOTO Oriel M. M. THEKISOE 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2015,77(12):1573-1579
Ticks carry and transmit a remarkable array of pathogens including bacteria, protozoa and
viruses, which may be of veterinary and/or of medical significance. With little to no
information regarding the presence of tick-borne zoonotic pathogens or their known vectors
in southern Africa, the aim of our study was to screen for Anaplasma
phagocytophilum, Borrelia burgdorferi, Coxiella
burnetii, Rickettsia species and Ehrlichia
ruminantium in ticks collected and identified from ruminants in the Eastern
Cape, Free State, KwaZulu-Natal and Mpumalanga Provinces of South Africa. The most
abundant tick species identified in this study were Rhipicephalus evertsi
evertsi (40%), Rhipicephalus species (35%), Amblyomma
hebraeum (10%) and Rhipicephalus decoloratus (14%). A total of
1634 ticks were collected. DNA was extracted, and samples were subjected to PCR
amplification and sequencing. The overall infection rates of ticks with the target
pathogens in the four Provinces were as follows: A. phagocytophilum, 7%;
C. burnetii, 7%; E. ruminantium, 28%; and
Rickettsia spp., 27%. The presence of B. burgdorferi
could not be confirmed. The findings of this study show that zoonotic pathogens are
present in ticks in the studied South African provinces. This information will aid in the
epidemiology of tick-borne zoonotic diseases in the country as well as in raising
awareness about such diseases in the veterinary, medical and tourism sectors, as they may
be the most affected. 相似文献
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Bakheit MA Torra D Palomino LA Thekisoe OM Mbati PA Ongerth J Karanis P 《Veterinary parasitology》2008,158(1-2):11-22
Three LAMP (loop-mediated isothermal DNA amplification) assays were applied to detect Cryptosporidium species DNA in a total number of 270 fecal samples originating from cattle, sheep and horses in South Africa. DNA was extracted from 0.5 g of fecal material. Results of LAMP detection were compared to those obtained by nested PCR targeting the Cryptosporidium 18 small subunit rRNA (18S) gene. All samples were negative by nested PCR, while up to one-third of samples were positive by LAMP assays. The SAM-1 LAMP assay, shown to detect C. parvum, C. hominis and C. meleagridis, amplified Cryptosporidium DNA in 36 of 107 cattle (33.64%), in 26 of 85 sheep (30.5%) and in 17 of 78 horses (21.79%). The HSP LAMP specific to C. muris and C. andersoni, amplified Cryptosporidium DNA in one cow (0.9%), five sheep (5.8%) and seven horses (8.9%). The gp60 LAMP assay, shown to detect C. parvum produced no amplified Cryptosporidium DNA, likely due to low sample DNA concentrations. The specificity of LAMP assays was confirmed by sequencing of the LAMP products generated in positive samples. Sequence products from the three LAMP assays showed high identity to the target gene sequences confirming the specificity of LAMP. In this study, the LAMP procedure was clearly superior to nested PCR in the detection of Cryptosporidium species DNA. Use of LAMP is proposed as an efficient and effective tool for epidemiologic survey studies including screening of healthy animals in which Cryptosporidium oocyst shedding is characteristically low and likely below the detection limit of PCR in conventional sample concentrates. 相似文献
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Mphahlele Morutse Tsotetsi-Khambule Ana M. Moerane Rebone Mashiloane Majela L. Thekisoe Oriel M. M. 《Tropical animal health and production》2019,51(3):555-563
Tropical Animal Health and Production - Anthelmintic treatment is the most common way of controlling nematode infections in ruminants even though several countries have reported anthelmintic... 相似文献
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