Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters










Database
Publication year range
1.
Infect Genet Evol ; 51: 104-107, 2017 07.
Article in English | MEDLINE | ID: mdl-28323069

ABSTRACT

The taxon Trypanosoma cruzi, causative agent of Chagas disease, is composed of several discrete typing units (DTUs) named TcI-TcVI, and Tcbat. The history of the taxon T. cruzi is known, even though several controversial aspects remain as the relationships between TcIII and TcIV. We analyzed cloned T. cruzi stocks pertaining to the seven DTUs by filter hybridization tests of PCR amplicons from minicircle variable regions and kinetoplast DNA probes. Minicircle DNA blots from the cloned stocks and filter hybridization with one TcI, one TcII, one TcV, one TcVI, three TcIII, one TcIV from North America and one TcIV kinetoplast DNA probes from South America revealed minicircle variable region cross-reaction in some T. cruzi DTUs probed. TcIII was heterogeneous in minicircle class composition, even though two TcIII probes revealed that a small fraction of minicircles cross-hybridized with the minicircles from the TcIII, TcV and TcVI DTUs. The minicircles of TcIV from North America cross-reacted only with TcIV from North America but not with TcIV stocks from Brazil and Bolivia. The results on minicircle cross-hybridizations are discussed in the context of RNA editing, mitochondrial function in T. cruzi DTUs.


Subject(s)
DNA, Kinetoplast/genetics , Genetic Variation , Genotype , RNA, Protozoan/genetics , Trypanosoma cruzi/genetics , Animals , Chagas Disease/parasitology , Cloning, Molecular , DNA, Kinetoplast/classification , Humans , Molecular Typing , North America , Nucleic Acid Hybridization/methods , Polymerase Chain Reaction , South America , Trypanosoma cruzi/classification , Trypanosoma cruzi/isolation & purification
2.
PLoS One ; 10(7): e0132493, 2015.
Article in English | MEDLINE | ID: mdl-26177101

ABSTRACT

In 2008 and 2009, an outbreak of desert-subtype zoonotic visceral leishmaniasis occurred in Jiashi county, Xinjiang, China. So far, no animal reservoir has been identified for this type of visceral leishmaniasis. Therefore, we surveyed the most common mammals (wild and domestic) for Leishmania infections during the outbreak in 2008 and 2009 in order to identify the source of the visceral leishmaniasis in this region. Spleen, liver, bone marrow and blood samples collected from 86 wood mice (Apodemus sylvaticus), 61midday jirds (Meriones meridianus) and 27 Yarkand hares (Lepus yarkandensis) were tested for the presence of Leishmania by microscopy, culture and PCR. All of the animals were found to be negative for Leishmania infections; On the other hand, Leishmania DNA was detected in blood samples collected from livestock reared in the outbreak area: 30.36% (17/56) of sheep, 21.57% (11/51) of goats, 17.78% (8/45) of cattle, and 21.62 (8/37) of donkeys were positive for Leishmania DNA by PCR. The amplified kDNA sequences from the livestock samples matched Leishmania DNA sequences isolated from patients with visceral leishmaniasis in the study area. We suggest that these domestic mammals are a possible reservoir host for Leishmania infantum in the outbreak area.


Subject(s)
Disease Outbreaks , Leishmania infantum/physiology , Leishmaniasis, Visceral/parasitology , Zoonoses/parasitology , Animals , Cattle , China/epidemiology , DNA, Kinetoplast/classification , DNA, Kinetoplast/genetics , DNA, Protozoan/classification , DNA, Protozoan/genetics , Desert Climate , Equidae , Geography , Gerbillinae , Goats , Hares , Host-Parasite Interactions , Humans , Leishmania infantum/classification , Leishmania infantum/genetics , Leishmaniasis, Visceral/epidemiology , Liver/metabolism , Liver/parasitology , Murinae , Phylogeny , Polymerase Chain Reaction , Sheep , Species Specificity , Spleen/metabolism , Spleen/parasitology , Zoonoses/epidemiology
3.
PLoS One ; 8(7): e67463, 2013.
Article in English | MEDLINE | ID: mdl-23861767

ABSTRACT

Little is known on the role played by Neotropical wild carnivores in the Trypanosoma cruzi transmission cycles. We investigated T. cruzi infection in wild carnivores from three sites in Brazil through parasitological and serological tests. The seven carnivore species examined were infected by T. cruzi, but high parasitemias detectable by hemoculture were found only in two Procyonidae species. Genotyping by Mini-exon gene, PCR-RFLP (1f8/Akw21I) and kDNA genomic targets revealed that the raccoon (Procyon cancrivorus) harbored TcI and the coatis (Nasua nasua) harbored TcI, TcII, TcIII-IV and Trypanosoma rangeli, in single and mixed infections, besides four T. cruzi isolates that displayed odd band patterns in the Mini-exon assay. These findings corroborate the coati can be a bioaccumulator of T. cruzi Discrete Typing Units (DTU) and may act as a transmission hub, a connection point joining sylvatic transmission cycles within terrestrial and arboreal mammals and vectors. Also, the odd band patterns observed in coatis' isolates reinforce that T. cruzi diversity might be much higher than currently acknowledged. Additionally, we assembled our data with T. cruzi infection on Neotropical carnivores' literature records to provide a comprehensive analysis of the infection patterns among distinct carnivore species, especially considering their ecological traits and phylogeny. Altogether, fifteen Neotropical carnivore species were found naturally infected by T. cruzi. Species diet was associated with T. cruzi infection rates, supporting the hypothesis that predator-prey links are important mechanisms for T. cruzi maintenance and dispersion in the wild. Distinct T. cruzi infection patterns across carnivore species and study sites were notable. Musteloidea species consistently exhibit high parasitemias in different studies which indicate their high infectivity potential. Mesocarnivores that feed on both invertebrates and mammals, including the coati, a host that can be bioaccumulator of T. cruzi DTU's, seem to take place at the top of the T. cruzi transmission chain.


Subject(s)
Chagas Disease/transmission , Chagas Disease/veterinary , DNA, Kinetoplast/classification , Procyonidae/parasitology , Trypanosoma cruzi/classification , Trypanosoma cruzi/genetics , Animals , Brazil/epidemiology , Chagas Disease/epidemiology , Chagas Disease/parasitology , DNA Fingerprinting , DNA, Kinetoplast/genetics , Disease Reservoirs , Exons , Food Chain , Genotype , Phylogeny , Tropical Climate , Trypanosoma cruzi/isolation & purification
5.
Parazitologiia ; 34(3): 169-82, 2000.
Article in Russian | MEDLINE | ID: mdl-10920838

ABSTRACT

The results of comparative analysis of two phylogenetic trees of the trypanosomatids based on morphological and molecular characters are discussed. The morphological dendrogram was based on 33 ultrastructural characters, 6 light microscope characteristics and 8 biological characters. Molecular UPGMA dendrogram depicting differences (Dice distance) between examined trypanosomatids is based on the universally primed PCR polymorphisms. The general topology of both dendrograms are similar, with the Trypanosoma at the base. The genus Wallaceina appears to be monophyletic. In a contrary, the genera Leptomonas, Crithidia and Herpetomonas look like artificial groups according to both methods used. The cyst-forming homoxenous trypanosomatids from insects represent a monophyletic clade, which seems to be a separate genus. Two species of within genus Wallaceina are arranged as a separate subgenus.


Subject(s)
Phylogeny , Trypanosomatina/classification , Animals , DNA, Kinetoplast/classification , DNA, Kinetoplast/ultrastructure , Insecta/parasitology , Polymerase Chain Reaction , Russia , Software , Trypanosomatina/genetics , Trypanosomatina/ultrastructure
6.
Trop Med Int Health ; 4(6): 448-53, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10444321

ABSTRACT

Kala azar or visceral leishmaniasis, a parasitic disease caused by Leishmania donovani, is presently causing an epidemic in the eastern region of India. Diagnosis of kala azar is often complicated. We developed a pair of oligonucleotides suitable as primers from the variable region of a predominant sequence class of minicircles of L. donovani. These primers were used in a nonisotopic polymerase chain reaction and found to be highly specific for the parasites of L. donovani complex. Using these primers, amplification of L. donovani kinetoplast DNA minicircle from the peripheral blood of kala azar patients results in a product of 204 bp. The patient group was comprised of individuals from a highly endemic region of India. We feel that PCR could assess the efficacy of new leishmanicidal drugs under investigation in these patients. PCR could also predict response to therapy which would be useful for both clinical and research applications.


Subject(s)
Amphotericin B/therapeutic use , Antiprotozoal Agents/therapeutic use , DNA, Kinetoplast/analysis , Leishmania donovani/genetics , Leishmaniasis, Visceral/diagnosis , Polymerase Chain Reaction/methods , Adolescent , Adult , Amphotericin B/administration & dosage , Animals , Antiprotozoal Agents/administration & dosage , Child , Child, Preschool , DNA Primers , DNA, Kinetoplast/blood , DNA, Kinetoplast/classification , Drug Administration Schedule , Female , Humans , Leishmaniasis, Visceral/drug therapy , Leishmaniasis, Visceral/parasitology , Male , Middle Aged , Sequence Analysis, DNA , Treatment Outcome
SELECTION OF CITATIONS
SEARCH DETAIL
...