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1.
J Clin Microbiol ; 50(10): 3293-300, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22855512

ABSTRACT

In this study, we introduce a multilocus sequence typing (MLST) scheme, comprised of seven single-copy housekeeping genes, to genetically characterize Trichomonas vaginalis. Sixty-eight historical and recent isolates of T. vaginalis were sampled from the American Type Culture Collection and female patients at area health care facilities, respectively, to assess the usefulness of this typing method. Forty-three polymorphic nucleotide sites, 51 different alleles, and 60 sequence types were distinguished among the 68 isolates, revealing a diverse T. vaginalis population. Moreover, this discriminatory MLST scheme retains the ability to identify epidemiologically linked isolates such as those collected from sexual partners. Population genetic and phylogenetic analyses determined that T. vaginalis population structure is strongly influenced by recombination and is composed of two separate populations that may be nonclonal. MLST is useful for investigating the epidemiology, genetic diversity, and population structure of T. vaginalis.


Subject(s)
Multilocus Sequence Typing/methods , Parasitology/methods , Trichomonas Infections/parasitology , Trichomonas vaginalis/classification , Trichomonas vaginalis/genetics , DNA, Protozoan/chemistry , DNA, Protozoan/genetics , Female , Humans , Molecular Epidemiology/methods , Molecular Sequence Data , Polymorphism, Genetic , Sequence Analysis, DNA , Trichomonas Infections/epidemiology , Trichomonas vaginalis/isolation & purification
2.
Am J Trop Med Hyg ; 83(6): 1283-6, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21118935

ABSTRACT

We have determined the metronidazole susceptibility status of 20 Trichomonas vaginalis isolates from American Type Culture Collection (ATCC) and assessed the level of genetic relatedness in these isolates using 32 additional T. vaginalis clinical isolates for comparison. These ATCC isolates are commonly used as reference strains in T. vaginalis research and this information provides a rational basis for selection of reference strains for use in comparative studies of T. vaginalis phenotypic and clinical characteristics.


Subject(s)
Genetic Variation , Trichomonas vaginalis/genetics , Antiprotozoal Agents/pharmacology , Drug Resistance/genetics , Humans , Metronidazole/pharmacology , Microbial Sensitivity Tests , Phylogeny , Trichomonas Infections/parasitology , Trichomonas vaginalis/drug effects
3.
Am J Trop Med Hyg ; 80(2): 245-51, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19190222

ABSTRACT

Restriction fragment length polymorphism (RFLP) analysis using a multilocus heat-inducible cytoplasmic heat-shock protein 70 (Hsp70) hybridization probe with EcoRI-digested genomic DNA was used in molecular typing of 129 Trichomonas vaginalis isolates. Results indicate that Trichomonas organisms exhibit considerable polymorphism in their Hsp70 RFLP patterns. Analysis of seven American Type Culture Collection reference strains and 122 clinical isolates, including 84 isolates from Jackson, Mississippi, 18 isolates from Atlanta, Georgia, and 20 isolates from throughout the United States, showed 105 distinct Hsp70 RFLP pattern subtypes for Trichomonas. Phylogenetic analysis of the Hsp70 RFLP data showed that the T. vaginalis isolates were organized into two clonal lineages. These results illustrate the substantial genomic diversity present in T. vaginalis and indicate that a large number of genetically distinct Trichomonas isolates may be responsible for human trichomoniasis in the United States.


Subject(s)
Genetic Variation , HSP70 Heat-Shock Proteins/genetics , Trichomonas Vaginitis/parasitology , Trichomonas vaginalis/classification , Trichomonas vaginalis/genetics , Animals , Bacterial Typing Techniques , Deoxyribonuclease EcoRI/metabolism , Female , Humans , Male , Phylogeny , Polymorphism, Restriction Fragment Length , Trichomonas vaginalis/isolation & purification
4.
Am J Med Sci ; 333(6): 340-5, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17570986

ABSTRACT

BACKGROUND: Intestinal parasites are difficult to eradicate in tropical climates where poor sanitation exists. In addition, pharmaceutical stability is poor making traditional three day dosing for the treatment of A. lumricoides challenging. METHODS: Single 100 mg doses of mebendazole were administered to persons living along Amazon tributaries in Northeastern Peru. Directly-observed treatment was repeated at 3-month intervals over a 2-year period in a single treatment village. Treatment was repeated at 12-month intervals in the remaining (control) villages. Treatment was accompanied by a regimen of multivitamins with iron to be taken daily for 14 days after each treatment. Subjects were screened for ova and parasites prior to treatment and at 1-year intervals. In addition to A. lumbricoides, other parasites found on screening were recorded. RESULTS: Treatment resulted in a 92.5% cure rate for A. lumbricoides at the 2-year assessment. Growth and development assessments demonstrated fewer individuals below the 3 percentile for age-adjusted measurements when treated quarterly. CONCLUSIONS: Based on these limited data, single low-dose mebendazole administered quarterly appears to have a positive effect on the health of isolated village populations in the Amazon River basin.


Subject(s)
Antinematodal Agents/administration & dosage , Antinematodal Agents/therapeutic use , Ascariasis/drug therapy , Mebendazole/administration & dosage , Mebendazole/therapeutic use , Adolescent , Adult , Aged , Aged, 80 and over , Amazona/parasitology , Animals , Antinematodal Agents/pharmacology , Ascaris lumbricoides/drug effects , Child , Child, Preschool , Clinical Protocols , Drug Administration Schedule , Female , Humans , Infant , Male , Mebendazole/pharmacology , Middle Aged , Parasite Egg Count , Peru
6.
Parasitol Int ; 51(1): 41-51, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11880226

ABSTRACT

P-type ATPases are ion-transporting pumps that enable organisms to control cellular functions and survive changing environmental conditions by regulating internal ion concentrations. Eight P-type ATPases were identified in the amitochondriate protist Trichomonas vaginalis using polymerase chain reaction (PCR) amplification with oligonucleotide primers that recognize conserved motifs present in all P-type ATPases, the ATP phosphorylation site (DKTGTLT) and the ATP binding site (TGDGVND). Phylogenetic analysis and the presence of conserved motifs in predicted peptide sequences identify the Trichomonas ATPases as a sarcoplasmic-endoplasmic reticulum calcium pump (TVCA1); three additional Ca(2+) transporting pumps (TVCA2-4), three phospholipid translocases (TVAPLT1-3), and one P-type ATPase of unknown transport specificity (TVPATP8). Southern blot analyses indicate that the P-type ATPase genes are not linked and are present in single copy, except TVCA2 and TVCA4 which contain additional copies or closely related homologues within the genome. Transcripts of 3.1 kb for TVCA1, 3.0 kb for TVCA2, 2.9 kb for TVCA3, 4.0 kb for TVAPLT1, 4.2 kb for TVAPLT2, 3.9 kb for TVAPLT3, and 3.1 kb for TVPATP8 were detected by Northern blot analysis. No TVCA4 transcript was observed, however, RT-PCR amplification of a transcript product indicates that TVCA4 is expressed. RNA expression of the Trichomonas ATPases, except TVCA3, was constitutive over a range of environmental conditions. TVCA1, TVAPLT3 and TVPATP8 had the highest levels of RNA expression while TVAPLT1 and TVAPLT2 expression was the lowest.


Subject(s)
Adenosine Triphosphatases/genetics , Adenosine Triphosphatases/metabolism , Phospholipid Transfer Proteins , Trichomonas vaginalis/enzymology , Animals , Calcium-Transporting ATPases/metabolism , Carrier Proteins/metabolism , Endoplasmic Reticulum/enzymology , Gene Dosage , Humans , Membrane Proteins/metabolism , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , Sarcoplasmic Reticulum/enzymology , Sequence Analysis, DNA , Transcription, Genetic , Trichomonas vaginalis/genetics , Trichomonas vaginalis/growth & development
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