Molecular investigation on the occurrence of Toxoplasma gondii oocysts in cat feces using TOX-element and ITS-1 region targets

•By light microscopy, 49/254 (19.3%) of feline fecal specimens contained coccidian oocysts.•PCR analysis demonstrated 2/254 (0.8%) positive results using Tox primers.•Sixteen ITS-1 sequences were identified as Toxoplasma gondii (n = 12; 4.7%) and Hammondia hammondi (n = 4; 1.6%).•Most PCR-positive s...

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Veröffentlicht in:The veterinary journal (1997) 2016-09, Vol.215, p.118-122
Hauptverfasser: Chemoh, W., Sawangjaroen, N., Nissapatorn, V., Sermwittayawong, N.
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container_start_page 118
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creator Chemoh, W.
Sawangjaroen, N.
Nissapatorn, V.
Sermwittayawong, N.
description •By light microscopy, 49/254 (19.3%) of feline fecal specimens contained coccidian oocysts.•PCR analysis demonstrated 2/254 (0.8%) positive results using Tox primers.•Sixteen ITS-1 sequences were identified as Toxoplasma gondii (n = 12; 4.7%) and Hammondia hammondi (n = 4; 1.6%).•Most PCR-positive specimens were negative for coccidian oocysts by microscopy.•ITS-1 regions have potential as alternative makers for the detection of T. gondii. [Display omitted] One of the most important routes of transmission for Toxoplasma gondii infection is the ingestion of foods contaminated with cat feces containing sporulated oocysts. The diagnosis of T. gondii infection by fecal microscopy is complicated, as other similar coccidian oocysts are often present in the same fecal specimen. This study aimed to identify T. gondii oocysts in cat feces using a novel PCR technique. Feline fecal specimens (n = 254) were screened for coccidian oocysts by light microscopy using the Sheather's flotation method. PCR analysis performed on the same specimens targeted a 529 bp repeat element and internal transcribed spacer-1 (ITS-1) regions were used to confirm the presence of Toxoplasma oocysts. By light microscopy, 49/254 (19.3%) of specimens contained coccidian oocysts. PCR analysis demonstrated 2/254 (0.8%) and 17/254 (6.7%) positive results using Tox and ITS-1 primers, respectively. However, coccidian oocysts were not identified on microscopic examination of specimens that were PCR-positive by Tox primers. Coccidian oocysts were identified on microscopic examination of 6/17 (35.3%) of the PCR-positive fecal specimens using ITS-1 primers. The BLAST results of 16 ITS-1 sequences were identified as T. gondii (n = 12; 4.7%) and Hammondia hammondi (n = 4; 1.6%). There was slight agreement between the 529 bp and ITS-1 PCR results (κ = 0.148). This is the first report of the detection of Toxoplasma oocysts using PCR analysis on feline fecal specimens from Southern Thailand. The ITS-1 region has potential as an alternative marker to identify T. gondii oocysts in feline fecal specimens.
doi_str_mv 10.1016/j.tvjl.2016.05.018
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[Display omitted] One of the most important routes of transmission for Toxoplasma gondii infection is the ingestion of foods contaminated with cat feces containing sporulated oocysts. The diagnosis of T. gondii infection by fecal microscopy is complicated, as other similar coccidian oocysts are often present in the same fecal specimen. This study aimed to identify T. gondii oocysts in cat feces using a novel PCR technique. Feline fecal specimens (n = 254) were screened for coccidian oocysts by light microscopy using the Sheather's flotation method. PCR analysis performed on the same specimens targeted a 529 bp repeat element and internal transcribed spacer-1 (ITS-1) regions were used to confirm the presence of Toxoplasma oocysts. By light microscopy, 49/254 (19.3%) of specimens contained coccidian oocysts. PCR analysis demonstrated 2/254 (0.8%) and 17/254 (6.7%) positive results using Tox and ITS-1 primers, respectively. However, coccidian oocysts were not identified on microscopic examination of specimens that were PCR-positive by Tox primers. Coccidian oocysts were identified on microscopic examination of 6/17 (35.3%) of the PCR-positive fecal specimens using ITS-1 primers. The BLAST results of 16 ITS-1 sequences were identified as T. gondii (n = 12; 4.7%) and Hammondia hammondi (n = 4; 1.6%). There was slight agreement between the 529 bp and ITS-1 PCR results (κ = 0.148). This is the first report of the detection of Toxoplasma oocysts using PCR analysis on feline fecal specimens from Southern Thailand. 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[Display omitted] One of the most important routes of transmission for Toxoplasma gondii infection is the ingestion of foods contaminated with cat feces containing sporulated oocysts. The diagnosis of T. gondii infection by fecal microscopy is complicated, as other similar coccidian oocysts are often present in the same fecal specimen. This study aimed to identify T. gondii oocysts in cat feces using a novel PCR technique. Feline fecal specimens (n = 254) were screened for coccidian oocysts by light microscopy using the Sheather's flotation method. PCR analysis performed on the same specimens targeted a 529 bp repeat element and internal transcribed spacer-1 (ITS-1) regions were used to confirm the presence of Toxoplasma oocysts. By light microscopy, 49/254 (19.3%) of specimens contained coccidian oocysts. PCR analysis demonstrated 2/254 (0.8%) and 17/254 (6.7%) positive results using Tox and ITS-1 primers, respectively. However, coccidian oocysts were not identified on microscopic examination of specimens that were PCR-positive by Tox primers. Coccidian oocysts were identified on microscopic examination of 6/17 (35.3%) of the PCR-positive fecal specimens using ITS-1 primers. The BLAST results of 16 ITS-1 sequences were identified as T. gondii (n = 12; 4.7%) and Hammondia hammondi (n = 4; 1.6%). There was slight agreement between the 529 bp and ITS-1 PCR results (κ = 0.148). This is the first report of the detection of Toxoplasma oocysts using PCR analysis on feline fecal specimens from Southern Thailand. 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purification</topic><topic>Toxoplasma oocyst</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chemoh, W.</creatorcontrib><creatorcontrib>Sawangjaroen, N.</creatorcontrib><creatorcontrib>Nissapatorn, V.</creatorcontrib><creatorcontrib>Sermwittayawong, N.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The veterinary journal (1997)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chemoh, W.</au><au>Sawangjaroen, N.</au><au>Nissapatorn, V.</au><au>Sermwittayawong, N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular investigation on the occurrence of Toxoplasma gondii oocysts in cat feces using TOX-element and ITS-1 region targets</atitle><jtitle>The veterinary journal (1997)</jtitle><addtitle>Vet J</addtitle><date>2016-09</date><risdate>2016</risdate><volume>215</volume><spage>118</spage><epage>122</epage><pages>118-122</pages><issn>1090-0233</issn><eissn>1532-2971</eissn><abstract>•By light microscopy, 49/254 (19.3%) of feline fecal specimens contained coccidian oocysts.•PCR analysis demonstrated 2/254 (0.8%) positive results using Tox primers.•Sixteen ITS-1 sequences were identified as Toxoplasma gondii (n = 12; 4.7%) and Hammondia hammondi (n = 4; 1.6%).•Most PCR-positive specimens were negative for coccidian oocysts by microscopy.•ITS-1 regions have potential as alternative makers for the detection of T. gondii. [Display omitted] One of the most important routes of transmission for Toxoplasma gondii infection is the ingestion of foods contaminated with cat feces containing sporulated oocysts. The diagnosis of T. gondii infection by fecal microscopy is complicated, as other similar coccidian oocysts are often present in the same fecal specimen. This study aimed to identify T. gondii oocysts in cat feces using a novel PCR technique. Feline fecal specimens (n = 254) were screened for coccidian oocysts by light microscopy using the Sheather's flotation method. PCR analysis performed on the same specimens targeted a 529 bp repeat element and internal transcribed spacer-1 (ITS-1) regions were used to confirm the presence of Toxoplasma oocysts. By light microscopy, 49/254 (19.3%) of specimens contained coccidian oocysts. PCR analysis demonstrated 2/254 (0.8%) and 17/254 (6.7%) positive results using Tox and ITS-1 primers, respectively. However, coccidian oocysts were not identified on microscopic examination of specimens that were PCR-positive by Tox primers. Coccidian oocysts were identified on microscopic examination of 6/17 (35.3%) of the PCR-positive fecal specimens using ITS-1 primers. The BLAST results of 16 ITS-1 sequences were identified as T. gondii (n = 12; 4.7%) and Hammondia hammondi (n = 4; 1.6%). There was slight agreement between the 529 bp and ITS-1 PCR results (κ = 0.148). This is the first report of the detection of Toxoplasma oocysts using PCR analysis on feline fecal specimens from Southern Thailand. The ITS-1 region has potential as an alternative marker to identify T. gondii oocysts in feline fecal specimens.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27325616</pmid><doi>10.1016/j.tvjl.2016.05.018</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-2899-8955</orcidid></addata></record>
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subjects Animals
Cat Diseases - epidemiology
Cat Diseases - parasitology
Cats
Coccidiosis - epidemiology
Coccidiosis - parasitology
Coccidiosis - veterinary
DNA, Protozoan - analysis
DNA, Ribosomal Spacer - analysis
Feces - parasitology
ITS-1 region
Oocysts - cytology
Polymerase Chain Reaction - veterinary
Prevalence
Sarcocystidae - isolation & purification
Sequence Analysis, DNA - veterinary
Thailand - epidemiology
TOX-element
Toxoplasma - isolation & purification
Toxoplasma oocyst
title Molecular investigation on the occurrence of Toxoplasma gondii oocysts in cat feces using TOX-element and ITS-1 region targets
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