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Author |
Traversa, D.; Giangaspero, A.; Galli, P.; Paoletti, B.; Otranto, D.; Gasser, R.B. |
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Title |
Specific identification of Habronema microstoma and Habronema muscae (Spirurida, Habronematidae) by PCR using markers in ribosomal DNA |
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Journal Article |
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Year |
2004 |
Publication |
Molecular and Cellular Probes |
Abbreviated Journal |
Mol Cell Probes |
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Volume |
18 |
Issue  |
4 |
Pages |
215-221 |
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Keywords |
Animals; Base Sequence; DNA, Ribosomal/blood/*genetics; Feces/parasitology; Genetic Markers; Horses/*parasitology; Molecular Sequence Data; Muscidae/*genetics; Polymerase Chain Reaction; Spirurida Infections/genetics; Spiruroidea/*genetics; Stomach/*parasitology |
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Abstract |
Gastric or cutaneous habronemosis caused by Habronema microstoma Creplin, 1849 and Habronema muscae Carter, 1865 is a parasitic disease of equids transmitted by muscid flies. There is a paucity of information on the epidemiology of this disease, which is mainly due to limitations with diagnosis in the live animal and with the identification of the parasites in the intermediate hosts. To overcome such limitations, a molecular approach, based on the use of genetic markers in the second internal transcribed spacer (ITS-2) of ribosomal DNA, was established for the two species of Habronema. Characterisation of the ITS-2 revealed sequence lengths and G+C contents of 296 bp and 29.5% for H. microstoma, and of 334 bp and 35.9% for H. muscae, respectively. Exploiting the sequence difference (approximately 40%) between the two species of nematode, primers were designed and tested by the polymerase chain reaction (PCR) for their specificity using a panel of control DNA samples from common equid endoparasites, and from host tissues, faeces or muscid flies. Effective amplification from each of the two species of Habronema was achieved from as little as 10 pg of genomic DNA. Hence, this molecular approach allows the specific identification and differentiation of the DNA from H. microstoma and H. muscae, and could thus provide a molecular tool for the specific detection of Habronema DNA (irrespective of developmental stage) from faeces, skin and muscid fly samples. The establishment of this tool has important implications for the specific diagnosis of clinical cases of gastric and cutaneous habronemosis in equids, and for studying the ecology and epidemiology of the two species of Habronema. |
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Department of Biomedical Comparative Sciences, Faculty of Veterinary Medicine, University of Teramo, Teramo, Italy |
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0890-8508 |
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PMID:15271381 |
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Call Number |
Equine Behaviour @ team @ |
Serial |
2634 |
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Author |
Lemasson, J.J.; Fontenille, D.; Lochouarn, L.; Dia, I.; Simard, F.; Ba, K.; Diop, A.; Diatta, M.; Molez, J.F. |
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Title |
Comparison of behavior and vector efficiency of Anopheles gambiae and An. arabiensis (Diptera:Culicidae) in Barkedji, a Sahelian area of Senegal |
Type |
Journal Article |
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Year |
1997 |
Publication |
Journal of Medical Entomology |
Abbreviated Journal |
J Med Entomol |
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Volume |
34 |
Issue |
4 |
Pages |
396-403 |
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Keywords |
Animals; Anopheles/*parasitology; *Behavior, Animal; Cattle; Desert Climate; Horses/parasitology; Humans; Insect Vectors/*parasitology; Longitudinal Studies; Malaria/*transmission; Malaria, Falciparum/transmission; Periodicity; Plasmodium malariae/isolation & purification; Protozoan Proteins/analysis; Rain; Seasons; Senegal; Sheep/parasitology; Species Specificity |
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Abstract |
The ecology, population dynamics, and malaria vector efficiency of Anopheles gambiae and An. arabiensis were studied for 2 yr in a Sahelian village of Senegal. Anophelines were captured at human bait and resting indoors by pyrethrum spray. Mosquitoes belonging to the An. gambiae complex were identified by polymerase chain reaction. Of 26,973 females, An. arabiensis represented 79% of the mosquitoes captured and remained in the study area longer than An. gambiae after the rains terminated. There were no differences in nocturnal biting cycles or endophagous rates between An. gambiae and An. arabiensis. Based on an enzyme-linked immunosorbent assay test of bloodmeals, the anthropophilic rate of these 2 vectors were both approximately 60%, when comparisons were made during the same period. Overall, 18% of the resting females had patent mixed bloodmeals, mainly human-bovine. The parity rates of An. gambiae and An. arabiensis varied temporally. Despite similar behavior, the Plasmodium falciparum circumsporozoite protein (CSP) rates were different between An. gambiae (4.1%) and An. arabiensis (1.3%). P. malariae and P. ovale only represented 4% of the total Plasmodium identified in mosquitoes. Transmission was seasonal, occurring mainly during 4 mo. The CSP entomological inoculation rates were 128 bites per human per year for the 1st yr and 100 for the 2nd yr. Because of the combination of a high human biting rate and a low CSP rate, An. arabiensis accounted for 63% of transmission. Possible origin of differences in CSP rate between An. gambiae and An. arabiensis is discussed in relation to the parity rate, blood feeding frequency, and the hypothesis of genetic factors. |
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Institut Francais de Recherche Scientifique pour le Developpement en cooperation (ORSTOM), Institut Pasteur, Dakar, Senegal |
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0022-2585 |
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Notes |
PMID:9220672 |
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Call Number |
Equine Behaviour @ team @ |
Serial |
2655 |
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Author |
Enileeva, N.K. |
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Title |
[Ecological characteristics of horse stomach botflies in Uzbekistan] |
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Journal Article |
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Year |
1987 |
Publication |
Parazitologiia |
Abbreviated Journal |
Parazitologiia |
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Volume |
21 |
Issue |
4 |
Pages |
577-579 |
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Keywords |
Animals; Diptera/*physiology; Ecology; Female; Flight, Animal; Horses/*parasitology; Larva/physiology; Male; Population Dynamics; Uzbekistan |
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Abstract |
The paper describes the flight periods and dynamics of abundance of horse botflies, life span of females and males, effect of environmental factors on the activity of flies and their behaviour, potential fecundity of different species of botflies, duration of embryonal development, preservation of viability of larvae in egg membranes, localization of different stages of botflies in the host, and methods of their control. |
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Russian |
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Original Title |
Ekologicheskie osobennosti zheludochnykh ovodov loshadei v Uzbekistane |
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0031-1847 |
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Notes |
PMID:2958767 |
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no |
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Call Number |
Equine Behaviour @ team @ |
Serial |
2680 |
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Author |
Gothe, R. |
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Title |
[Tapeworms, a problem in equine practice?] |
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Journal Article |
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Year |
1994 |
Publication |
Tierarztliche Praxis |
Abbreviated Journal |
Tierarztl Prax |
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22 |
Issue |
5 |
Pages |
466-470 |
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Keywords |
Animals; Cestode Infections/diagnosis/parasitology/therapy/*veterinary; *Horse Diseases/diagnosis/parasitology/therapy; Horses |
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This paper gives a survey on biology and ecology of equine tapeworms as well as on pathogenesis, clinics, diagnosis, therapy, and prophylaxis of tapeworm infections. |
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Institut fur Vergleichende Tropenmedizin und Parasitologie, Ludwig-Maximilians-Universitat Munchen |
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German |
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Bandwurmer, ein Problem in der Pferdepraxis? |
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0303-6286 |
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Notes |
PMID:7855855 |
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Call Number |
Equine Behaviour @ team @ |
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2663 |
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Author |
Mirzaeva, A.G. |
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[Age makeup of female Culicoides sinanoensis Tok. in the coniferous-broad-leaved forest zone of the southern Maritime Territory] |
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Journal Article |
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1974 |
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Parazitologiia |
Abbreviated Journal |
Parazitologiia |
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8 |
Issue |
6 |
Pages |
524-530 |
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Keywords |
Age Factors; Animals; *Ceratopogonidae/physiology; Corpus Luteum/physiology; Ecology; Female; Horses/parasitology; Humans; Ovulation; Pigments, Biological/physiology; Seasons; Siberia; Trees |
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Russian |
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Vozrastnoi sostav samok Culicoides sinanoensis Tok. v zone khvoino-shirokolistvennykh lesov Iuzhnogo Primor'ia |
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0031-1847 |
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PMID:4449654 |
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Equine Behaviour @ team @ |
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2707 |
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Author |
Barros, A.T. |
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Seasonality and relative abundance of Tabanidae (Diptera) captured on horses in the Pantanal, Brazil |
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Journal Article |
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Year |
2001 |
Publication |
Memorias do Instituto Oswaldo Cruz |
Abbreviated Journal |
Mem Inst Oswaldo Cruz |
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Volume |
96 |
Issue |
7 |
Pages |
917-923 |
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Keywords |
Animals; Brazil; Climate; Diptera/classification/*physiology; Ecology; Horses/*parasitology; Population Dynamics; Seasons; Species Specificity |
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Once a month, from June 1992 to May 1993, collections of tabanids on horse were conducted in the Nhecolandia, Pantanal State of Mato Grosso do Sul, Brazil. Tabanid catches using hand nets were conducted from sunrise to sunset at grassland and cerradao (dense savanna) habitats. A total of 3,442 tabanids from 21 species,12 genera, and 3 subfamilies were collected. Although species abundance varied seasonally depending on habitat, no habitat specificity was observed for the most abundant species. In the grassland, 1,625 (47.2%) tabanids belonging to 19 species were collected, while 1,817 (52.8%) tabanids from 17 species were caught in the cerradao. The number of tabanid species varied from 7 during winter (July/August) to 15 in the spring (October). Tabanus importunus (56%) was the most abundant species, followed by T. occidentalis (8.2%), and T. claripennis (8.1%). The tabanid peak, in October, coincided with the beginning of the rainy season. The population peak of most species, including those with higher vector potential, suggests that the rainy season can be considered as the period of potentially higher risk of mechanical transmission of pathogens by tabanids to horses in the region. |
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Embrapa Pantanal, 79320-900 Corumba, MS, Brasil. thadeu@cpap.embrapa.br |
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0074-0276 |
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PMID:11685255 |
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Equine Behaviour @ team @ |
Serial |
2644 |
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Author |
Polley, L. |
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Title |
Strongylid parasites of horses: experimental ecology of the free-living stages on the Canadian prairie |
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Journal Article |
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Year |
1986 |
Publication |
American Journal of Veterinary Research |
Abbreviated Journal |
Am J Vet Res |
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47 |
Issue |
8 |
Pages |
1686-1693 |
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Keywords |
Animals; Canada; Ecology; Feces; Female; Horse Diseases/*epidemiology/parasitology; Horses; Larva; Ovum/cytology; Seasons; Strongyloides/isolation & purification; Strongyloidiasis/epidemiology/*veterinary |
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Each month for a 1-year period (October through September), equine fecal masses containing eggs of strongylid nematodes were placed outdoors on small grass plots in Saskatchewan, Canada. Thereafter, feces and grass from the plots were sampled after intervals of 1 week or longer, and the strongylid eggs and larvae recovered were counted. These observations were made over a 2-year period. Development of eggs to infective larvae occurred in all experiments, except those established in October, December, and January. Infective larvae from experiments set up in April through September survived that winter. During the summer, there was a gradual build up of infective larvae in the fecal masses, which reached a peak in August and September and then decreased into the winter. These results are discussed in the context of the control of strongylid parasites of horses on the Canadian prairie and in other areas of the world with a similar climate and similar horse management practices. |
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0002-9645 |
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Notes |
PMID:3752676 |
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Call Number |
Equine Behaviour @ team @ |
Serial |
2682 |
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Author |
Traversa, D.; Giangaspero, A.; Iorio, R.; Otranto, D.; Paoletti, B.; Gasser, R.B. |
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Title |
Semi-nested PCR for the specific detection of Habronema microstoma or Habronema muscae DNA in horse faeces |
Type |
Journal Article |
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Year |
2004 |
Publication |
Parasitology |
Abbreviated Journal |
Parasitology |
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Volume |
129 |
Issue |
Pt 6 |
Pages |
733-739 |
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Keywords |
Animals; DNA, Helminth/*analysis; DNA, Ribosomal Spacer/*chemistry; Feces/*chemistry; Female; Horse Diseases/*diagnosis/parasitology; Horses; Male; Polymerase Chain Reaction/*methods; Species Specificity; Spirurida Infections/diagnosis/*veterinary; Spiruroidea/*genetics |
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Abstract |
Habronema microstoma and Habronema muscae (Spirurida: Habronematidae) are parasitic nematodes which infect the stomach and/or skin of equids. The accurate diagnosis of gastric habronemosis is central to studying its epidemiology, but data on its distribution and prevalence are lacking, mainly due to the limitations of clinical and coprological diagnosis in live horses. To overcome this constraint, a two-step, semi-nested PCR-based assay was validated (utilizing genetic markers in the nuclear ribosomal DNA) for the specific amplification of H. microstoma or H. muscae DNA from the faeces from horses (n = 46) whose gastrointestinal parasite status had been determined at autopsy and whose faeces were examined previously using a conventional parasitological approach. Of these horses examined at autopsy, some harboured adults of either H. microstoma (n= 19) or H. muscae (n =4), and others (n = 7) harboured both species. Most of them were also infected with other parasites, including strongylid nematodes (subfamilies Cyathostominae and Strongylinae), bots and/or cestodes; there was no evidence of metazoan parasites in 2 horses. Larvated spirurid eggs were detected in the faeces of 1 of the 30 horses (3.3 %) shown to be infected with Habronema at autopsy. For this set of 46 samples, the PCR assay achieved a diagnostic specificity of 100 % and a sensitivity of approximately 97 % (being able to specifically detect as little as approximately 0.02 fg of Habronema DNA). The specificity of the assay was also tested using a panel of control DNA samples representing horse, the gastric spirurid Draschia megastoma and 26 other species of parasites from the alimentary tract of the horse. H. microstoma, H. muscae and D. megastoma could be readily differentiated from one another based on the sizes of their specific amplicons in the PCR. The results of this study showed that the performance of the PCR for the diagnosis of gastric habronemosis was similar to that of autopsy but substantially better than the traditional coprological examination procedure used. The ability to specifically diagnose gastric habronemosis in equids should have important implications for investigating the epidemiology and ecology of H. microstoma and H. muscae. |
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Department of Biomedical Comparative Sciences, Faculty of Veterinary Medicine, University of Teramo, Teramo, Italy. traversa@unite.it |
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0031-1820 |
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Notes |
PMID:15648696 |
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Call Number |
Equine Behaviour @ team @ |
Serial |
2631 |
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