Identification of the Source of Francisella tularensis Infection by Multiple-Locus Variable-Number Tandem Repeat Analysis
Tularemia is a zoonotic disease caused by Francisella tularensis. Most patients in Japan have reportedly acquired such infections through direct contact with infected Japanese hares. We recently encountered a patient who contracted tularemia after skinning and butchering a dead hare. Because the rem...
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Veröffentlicht in: | Japanese Journal of Infectious Diseases 2013, Vol.66(6), pp.543-545 |
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creator | Fujita, Osamu Hotta, Akitoyo Uda, Akihiko Yamamoto, Yoshie Fujita, Hiromi Shinya, Fumiaki Asano, Shigeyuki Morikawa, Shigeru Tanabayashi, Kiyoshi Yamada, Akio |
description | Tularemia is a zoonotic disease caused by Francisella tularensis. Most patients in Japan have reportedly acquired such infections through direct contact with infected Japanese hares. We recently encountered a patient who contracted tularemia after skinning and butchering a dead hare. Because the remains of the hare were available, we attempted to determine whether the patient actually contracted infection by handling the carcass. F. tularensis-specific sequences were successfully amplified by PCR from the patient specimens as well as from the remnants of discarded hare carcass. PCR amplification of the ISFtu2 and RD1 regions indicated infection by F. tularensis subsp. holarctica, which was considered as a prevalent strain in Japan. Furthermore, high-resolution multiple-locus variable-number tandem repeat analysis (MLVA) showed that the combination of repeat numbers in sequences from the patient and hare were indistinguishable, thus indicating that the patient had been infected with F. tularensis strain that had also infected the hare. These findings demonstrated that MLVA is a useful epidemiological investigational tool to identify possible sources of certain zoonotic diseases such as tularemia. |
doi_str_mv | 10.7883/yoken.66.543 |
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Most patients in Japan have reportedly acquired such infections through direct contact with infected Japanese hares. We recently encountered a patient who contracted tularemia after skinning and butchering a dead hare. Because the remains of the hare were available, we attempted to determine whether the patient actually contracted infection by handling the carcass. F. tularensis-specific sequences were successfully amplified by PCR from the patient specimens as well as from the remnants of discarded hare carcass. PCR amplification of the ISFtu2 and RD1 regions indicated infection by F. tularensis subsp. holarctica, which was considered as a prevalent strain in Japan. Furthermore, high-resolution multiple-locus variable-number tandem repeat analysis (MLVA) showed that the combination of repeat numbers in sequences from the patient and hare were indistinguishable, thus indicating that the patient had been infected with F. tularensis strain that had also infected the hare. These findings demonstrated that MLVA is a useful epidemiological investigational tool to identify possible sources of certain zoonotic diseases such as tularemia.</description><identifier>ISSN: 1344-6304</identifier><identifier>EISSN: 1884-2836</identifier><identifier>DOI: 10.7883/yoken.66.543</identifier><identifier>PMID: 24270148</identifier><language>eng</language><publisher>Japan: National Institute of Infectious Diseases, Japanese Journal of Infectious Diseases Editorial Committee</publisher><subject>Animals ; DNA, Bacterial - genetics ; Francisella tularensis ; Francisella tularensis - classification ; Francisella tularensis - genetics ; Francisella tularensis - isolation & purification ; Hares - microbiology ; Humans ; Male ; Middle Aged ; Minisatellite Repeats ; Molecular Typing - methods ; multi-locus variable-number tandem repeat analysis (MLVA) ; transmission ; tularemia ; Tularemia - diagnosis ; Tularemia - microbiology ; Zoonoses - diagnosis ; Zoonoses - microbiology</subject><ispartof>Japanese Journal of Infectious Diseases, 2013, Vol.66(6), pp.543-545</ispartof><rights>Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c592t-ebc8d523351ded8882ab2d0ca324a9b69eed8f4ec7a89555ea6bdacf6d202013</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24270148$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujita, Osamu</creatorcontrib><creatorcontrib>Hotta, Akitoyo</creatorcontrib><creatorcontrib>Uda, Akihiko</creatorcontrib><creatorcontrib>Yamamoto, Yoshie</creatorcontrib><creatorcontrib>Fujita, Hiromi</creatorcontrib><creatorcontrib>Shinya, Fumiaki</creatorcontrib><creatorcontrib>Asano, Shigeyuki</creatorcontrib><creatorcontrib>Morikawa, Shigeru</creatorcontrib><creatorcontrib>Tanabayashi, Kiyoshi</creatorcontrib><creatorcontrib>Yamada, Akio</creatorcontrib><title>Identification of the Source of Francisella tularensis Infection by Multiple-Locus Variable-Number Tandem Repeat Analysis</title><title>Japanese Journal of Infectious Diseases</title><addtitle>Jpn J Infect Dis</addtitle><description>Tularemia is a zoonotic disease caused by Francisella tularensis. Most patients in Japan have reportedly acquired such infections through direct contact with infected Japanese hares. We recently encountered a patient who contracted tularemia after skinning and butchering a dead hare. Because the remains of the hare were available, we attempted to determine whether the patient actually contracted infection by handling the carcass. F. tularensis-specific sequences were successfully amplified by PCR from the patient specimens as well as from the remnants of discarded hare carcass. PCR amplification of the ISFtu2 and RD1 regions indicated infection by F. tularensis subsp. holarctica, which was considered as a prevalent strain in Japan. Furthermore, high-resolution multiple-locus variable-number tandem repeat analysis (MLVA) showed that the combination of repeat numbers in sequences from the patient and hare were indistinguishable, thus indicating that the patient had been infected with F. tularensis strain that had also infected the hare. These findings demonstrated that MLVA is a useful epidemiological investigational tool to identify possible sources of certain zoonotic diseases such as tularemia.</description><subject>Animals</subject><subject>DNA, Bacterial - genetics</subject><subject>Francisella tularensis</subject><subject>Francisella tularensis - classification</subject><subject>Francisella tularensis - genetics</subject><subject>Francisella tularensis - isolation & purification</subject><subject>Hares - microbiology</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Minisatellite Repeats</subject><subject>Molecular Typing - methods</subject><subject>multi-locus variable-number tandem repeat analysis (MLVA)</subject><subject>transmission</subject><subject>tularemia</subject><subject>Tularemia - diagnosis</subject><subject>Tularemia - microbiology</subject><subject>Zoonoses - diagnosis</subject><subject>Zoonoses - microbiology</subject><issn>1344-6304</issn><issn>1884-2836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1vEzEURS1ERUthxxp5yYIJ_o6zQlXVQqTQSiVia73xvKEuM55gexbz75k0ISxZ2fe94yNZl5B3nC2W1spP0_AL48KYhVbyBbng1qpKWGleznepVGUkU-fkdc5PjAmtOXtFzoUSS8aVvSDTusFYQhs8lDBEOrS0PCL9PozJ4z7dJog-ZOw6oGXsIGHMIdN1bNE_v6gn-m3sSth1WG0GP2b6A1KAeo53Y19joluIDfb0AXcIhV5F6KZZ8YactdBlfHs8L8n29mZ7_bXa3H9ZX19tKq9XolRYe9toIaXmDTbWWgG1aJgHKRSsarPCedoq9EuwK601gqkb8K1pBBOMy0vy4aDdpeH3iLm4PmS__07EYcyOa6msEsLq_6PKcLvU0soZ_XhAfRpyTti6XQo9pMlx5va1uOdanDFurmXG3x_NY91jc4L_9jADnw_AUy7wE08ApBJ8h_9s5qg8bfwjJIdR_gGF-6L1</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Fujita, Osamu</creator><creator>Hotta, Akitoyo</creator><creator>Uda, Akihiko</creator><creator>Yamamoto, Yoshie</creator><creator>Fujita, Hiromi</creator><creator>Shinya, Fumiaki</creator><creator>Asano, Shigeyuki</creator><creator>Morikawa, Shigeru</creator><creator>Tanabayashi, Kiyoshi</creator><creator>Yamada, Akio</creator><general>National Institute of Infectious Diseases, Japanese Journal of Infectious Diseases Editorial Committee</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>2013</creationdate><title>Identification of the Source of Francisella tularensis Infection by Multiple-Locus Variable-Number Tandem Repeat Analysis</title><author>Fujita, Osamu ; Hotta, Akitoyo ; Uda, Akihiko ; Yamamoto, Yoshie ; Fujita, Hiromi ; Shinya, Fumiaki ; Asano, Shigeyuki ; Morikawa, Shigeru ; Tanabayashi, Kiyoshi ; Yamada, Akio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c592t-ebc8d523351ded8882ab2d0ca324a9b69eed8f4ec7a89555ea6bdacf6d202013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>DNA, Bacterial - genetics</topic><topic>Francisella tularensis</topic><topic>Francisella tularensis - classification</topic><topic>Francisella tularensis - genetics</topic><topic>Francisella tularensis - isolation & purification</topic><topic>Hares - microbiology</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Minisatellite Repeats</topic><topic>Molecular Typing - methods</topic><topic>multi-locus variable-number tandem repeat analysis (MLVA)</topic><topic>transmission</topic><topic>tularemia</topic><topic>Tularemia - diagnosis</topic><topic>Tularemia - microbiology</topic><topic>Zoonoses - diagnosis</topic><topic>Zoonoses - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujita, Osamu</creatorcontrib><creatorcontrib>Hotta, Akitoyo</creatorcontrib><creatorcontrib>Uda, Akihiko</creatorcontrib><creatorcontrib>Yamamoto, Yoshie</creatorcontrib><creatorcontrib>Fujita, Hiromi</creatorcontrib><creatorcontrib>Shinya, Fumiaki</creatorcontrib><creatorcontrib>Asano, Shigeyuki</creatorcontrib><creatorcontrib>Morikawa, Shigeru</creatorcontrib><creatorcontrib>Tanabayashi, Kiyoshi</creatorcontrib><creatorcontrib>Yamada, Akio</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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Japanese Journal of Infectious Diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujita, Osamu</au><au>Hotta, Akitoyo</au><au>Uda, Akihiko</au><au>Yamamoto, Yoshie</au><au>Fujita, Hiromi</au><au>Shinya, Fumiaki</au><au>Asano, Shigeyuki</au><au>Morikawa, Shigeru</au><au>Tanabayashi, Kiyoshi</au><au>Yamada, Akio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of the Source of Francisella tularensis Infection by Multiple-Locus Variable-Number Tandem Repeat Analysis</atitle><jtitle>Japanese Journal of Infectious Diseases</jtitle><addtitle>Jpn J Infect Dis</addtitle><date>2013</date><risdate>2013</risdate><volume>66</volume><issue>6</issue><spage>543</spage><epage>545</epage><pages>543-545</pages><issn>1344-6304</issn><eissn>1884-2836</eissn><abstract>Tularemia is a zoonotic disease caused by Francisella tularensis. Most patients in Japan have reportedly acquired such infections through direct contact with infected Japanese hares. We recently encountered a patient who contracted tularemia after skinning and butchering a dead hare. Because the remains of the hare were available, we attempted to determine whether the patient actually contracted infection by handling the carcass. F. tularensis-specific sequences were successfully amplified by PCR from the patient specimens as well as from the remnants of discarded hare carcass. PCR amplification of the ISFtu2 and RD1 regions indicated infection by F. tularensis subsp. holarctica, which was considered as a prevalent strain in Japan. Furthermore, high-resolution multiple-locus variable-number tandem repeat analysis (MLVA) showed that the combination of repeat numbers in sequences from the patient and hare were indistinguishable, thus indicating that the patient had been infected with F. tularensis strain that had also infected the hare. These findings demonstrated that MLVA is a useful epidemiological investigational tool to identify possible sources of certain zoonotic diseases such as tularemia.</abstract><cop>Japan</cop><pub>National Institute of Infectious Diseases, Japanese Journal of Infectious Diseases Editorial Committee</pub><pmid>24270148</pmid><doi>10.7883/yoken.66.543</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals DNA, Bacterial - genetics Francisella tularensis Francisella tularensis - classification Francisella tularensis - genetics Francisella tularensis - isolation & purification Hares - microbiology Humans Male Middle Aged Minisatellite Repeats Molecular Typing - methods multi-locus variable-number tandem repeat analysis (MLVA) transmission tularemia Tularemia - diagnosis Tularemia - microbiology Zoonoses - diagnosis Zoonoses - microbiology |
title | Identification of the Source of Francisella tularensis Infection by Multiple-Locus Variable-Number Tandem Repeat Analysis |
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