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A molecular diagnostic method for detecting Nacobbus in soil and in potato tubers
Abstract Species of the genus Nacobbus have the potential to reduce yields of major food crops such as potato, sugar beet and tomato in many parts of the world, thus warranting a quarantine effort to avoid their introduction. Molecular studies offer a new method for routine quarantine diagnostics fo...
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Published in: | Nematology : international journal of fundamental and applied nematological research 2005-01, Vol.7 (2), p.193-202 |
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container_title | Nematology : international journal of fundamental and applied nematological research |
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creator | Atkins, Simon D Manzanilla-López, Rosa H Franco, Javier Peteira, Belkis Kerry, Brian R |
description | Abstract
Species of the genus Nacobbus have the potential to reduce yields of major
food crops such as potato, sugar beet and tomato in many parts of the world,
thus warranting a quarantine effort to avoid their introduction. Molecular
studies offer a new method for routine quarantine diagnostics for this
nematode that will be faster and more sensitive than previous methods. A
primer set was designed from Nacobbus ITS sequences and their specificity
confirmed. DNA was extracted from nematodes, soil and potato tubers for use
in PCR. Optimised PCR conditions were established and the PCR products were
separated on 2% agarose gels, showing that specific ITS primers for the
detection of Nacobbus generated a single PCR product, although band size
varied slightly between species and soil isolates. The product was generated
from DNA extracted from all the Nacobbus samples but not from other
nematodes tested (Pratylenchus, Radopholus, Meloidogyne, Globodera,
Heterodera). No bands were generated from the uninfested control soil and
control tuber DNA samples, thus demonstrating the specificity of the
primers. For the first time, Nacobbus was detected in soil and tuber samples
using molecular approaches. These results have important applications not
only in analysing advisory samples but also in the screening of material for
quarantine purposes. |
doi_str_mv | 10.1163/1568541054879539 |
format | article |
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Species of the genus Nacobbus have the potential to reduce yields of major
food crops such as potato, sugar beet and tomato in many parts of the world,
thus warranting a quarantine effort to avoid their introduction. Molecular
studies offer a new method for routine quarantine diagnostics for this
nematode that will be faster and more sensitive than previous methods. A
primer set was designed from Nacobbus ITS sequences and their specificity
confirmed. DNA was extracted from nematodes, soil and potato tubers for use
in PCR. Optimised PCR conditions were established and the PCR products were
separated on 2% agarose gels, showing that specific ITS primers for the
detection of Nacobbus generated a single PCR product, although band size
varied slightly between species and soil isolates. The product was generated
from DNA extracted from all the Nacobbus samples but not from other
nematodes tested (Pratylenchus, Radopholus, Meloidogyne, Globodera,
Heterodera). No bands were generated from the uninfested control soil and
control tuber DNA samples, thus demonstrating the specificity of the
primers. For the first time, Nacobbus was detected in soil and tuber samples
using molecular approaches. These results have important applications not
only in analysing advisory samples but also in the screening of material for
quarantine purposes.</description><identifier>ISSN: 1388-5545</identifier><identifier>EISSN: 1568-5411</identifier><identifier>EISSN: 1388-5545</identifier><identifier>DOI: 10.1163/1568541054879539</identifier><language>eng</language><publisher>The Netherlands: Brill</publisher><subject>Biological and medical sciences ; detection ; DNA ; FALSE ROOT-KNOT NEMATODE ; Fundamental and applied biological sciences. Psychology ; Generalities ; internal transcribed spacers ; molecular systematics ; NACOBBUS ; nucleotide sequences ; Phytopathology. Animal pests. Plant and forest protection ; plant parasitic nematodes ; polymerase chain reaction ; potatoes ; Protozoa. Invertebrates ; QUARANTINE ; ribosomal DNA ; soil ; Solanum tuberosum ; SPECIES-SPECIFIC PCR PRIMERS ; tubers</subject><ispartof>Nematology : international journal of fundamental and applied nematological research, 2005-01, Vol.7 (2), p.193-202</ispartof><rights>2005 Koninklijke Brill NV, Leiden, The Netherlands</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b440t-c71df69cbe0aba2733094a55227fb4913fd8baadad02b8d5b6f279a01de489e43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17126059$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Atkins, Simon D</creatorcontrib><creatorcontrib>Manzanilla-López, Rosa H</creatorcontrib><creatorcontrib>Franco, Javier</creatorcontrib><creatorcontrib>Peteira, Belkis</creatorcontrib><creatorcontrib>Kerry, Brian R</creatorcontrib><title>A molecular diagnostic method for detecting Nacobbus in soil and in potato tubers</title><title>Nematology : international journal of fundamental and applied nematological research</title><addtitle>NEMY</addtitle><description>Abstract
Species of the genus Nacobbus have the potential to reduce yields of major
food crops such as potato, sugar beet and tomato in many parts of the world,
thus warranting a quarantine effort to avoid their introduction. Molecular
studies offer a new method for routine quarantine diagnostics for this
nematode that will be faster and more sensitive than previous methods. A
primer set was designed from Nacobbus ITS sequences and their specificity
confirmed. DNA was extracted from nematodes, soil and potato tubers for use
in PCR. Optimised PCR conditions were established and the PCR products were
separated on 2% agarose gels, showing that specific ITS primers for the
detection of Nacobbus generated a single PCR product, although band size
varied slightly between species and soil isolates. The product was generated
from DNA extracted from all the Nacobbus samples but not from other
nematodes tested (Pratylenchus, Radopholus, Meloidogyne, Globodera,
Heterodera). No bands were generated from the uninfested control soil and
control tuber DNA samples, thus demonstrating the specificity of the
primers. For the first time, Nacobbus was detected in soil and tuber samples
using molecular approaches. These results have important applications not
only in analysing advisory samples but also in the screening of material for
quarantine purposes.</description><subject>Biological and medical sciences</subject><subject>detection</subject><subject>DNA</subject><subject>FALSE ROOT-KNOT NEMATODE</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Generalities</subject><subject>internal transcribed spacers</subject><subject>molecular systematics</subject><subject>NACOBBUS</subject><subject>nucleotide sequences</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>plant parasitic nematodes</subject><subject>polymerase chain reaction</subject><subject>potatoes</subject><subject>Protozoa. Invertebrates</subject><subject>QUARANTINE</subject><subject>ribosomal DNA</subject><subject>soil</subject><subject>Solanum tuberosum</subject><subject>SPECIES-SPECIFIC PCR PRIMERS</subject><subject>tubers</subject><issn>1388-5545</issn><issn>1568-5411</issn><issn>1388-5545</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp1UE1v1DAUjKoi0Rbu3OpLj1ns2I7jY9UvoBXQsj1bz19bt9l4ZXsl-Pc4CqISEqc3mjczGk3TfCB4RUhPPxLeD5wRzNkgJKfyoDmaqbZy5LBiOlTMGX_bHOf8jDHmkpOj5v4cbePozH6EhGyAzRRzCQZtXXmKFvlYWVecKWHaoK9gotb7jMKEcgwjgsnOeBcLlIjKXruU3zVvPIzZvf9zT5rH66v1xaf27tvN54vzu1YzhktrBLG-l0Y7DBo6QSmWDDjvOuE1k4R6O2gACxZ3erBc974TEjCxjg3SMXrS4CXXpJhzcl7tUthC-qUIVvMk6t9JquVssewgGxh9gsmE_OoTpOvrLlXXLrqQi_v59w_pRfWCCq6-3K7V-vZSrtnDdzVXOV30HqKCTaqZjz86TCgmmFIm5sTVotApjKN6jvs01XH-X_U3gAiHAA</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Atkins, Simon D</creator><creator>Manzanilla-López, Rosa H</creator><creator>Franco, Javier</creator><creator>Peteira, Belkis</creator><creator>Kerry, Brian R</creator><general>Brill</general><general>BRILL</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050101</creationdate><title>A molecular diagnostic method for detecting Nacobbus in soil and in potato tubers</title><author>Atkins, Simon D ; Manzanilla-López, Rosa H ; Franco, Javier ; Peteira, Belkis ; Kerry, Brian R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b440t-c71df69cbe0aba2733094a55227fb4913fd8baadad02b8d5b6f279a01de489e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biological and medical sciences</topic><topic>detection</topic><topic>DNA</topic><topic>FALSE ROOT-KNOT NEMATODE</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Generalities</topic><topic>internal transcribed spacers</topic><topic>molecular systematics</topic><topic>NACOBBUS</topic><topic>nucleotide sequences</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>plant parasitic nematodes</topic><topic>polymerase chain reaction</topic><topic>potatoes</topic><topic>Protozoa. Invertebrates</topic><topic>QUARANTINE</topic><topic>ribosomal DNA</topic><topic>soil</topic><topic>Solanum tuberosum</topic><topic>SPECIES-SPECIFIC PCR PRIMERS</topic><topic>tubers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Atkins, Simon D</creatorcontrib><creatorcontrib>Manzanilla-López, Rosa H</creatorcontrib><creatorcontrib>Franco, Javier</creatorcontrib><creatorcontrib>Peteira, Belkis</creatorcontrib><creatorcontrib>Kerry, Brian R</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Nematology : international journal of fundamental and applied nematological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Atkins, Simon D</au><au>Manzanilla-López, Rosa H</au><au>Franco, Javier</au><au>Peteira, Belkis</au><au>Kerry, Brian R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A molecular diagnostic method for detecting Nacobbus in soil and in potato tubers</atitle><jtitle>Nematology : international journal of fundamental and applied nematological research</jtitle><addtitle>NEMY</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>7</volume><issue>2</issue><spage>193</spage><epage>202</epage><pages>193-202</pages><issn>1388-5545</issn><eissn>1568-5411</eissn><eissn>1388-5545</eissn><abstract>Abstract
Species of the genus Nacobbus have the potential to reduce yields of major
food crops such as potato, sugar beet and tomato in many parts of the world,
thus warranting a quarantine effort to avoid their introduction. Molecular
studies offer a new method for routine quarantine diagnostics for this
nematode that will be faster and more sensitive than previous methods. A
primer set was designed from Nacobbus ITS sequences and their specificity
confirmed. DNA was extracted from nematodes, soil and potato tubers for use
in PCR. Optimised PCR conditions were established and the PCR products were
separated on 2% agarose gels, showing that specific ITS primers for the
detection of Nacobbus generated a single PCR product, although band size
varied slightly between species and soil isolates. The product was generated
from DNA extracted from all the Nacobbus samples but not from other
nematodes tested (Pratylenchus, Radopholus, Meloidogyne, Globodera,
Heterodera). No bands were generated from the uninfested control soil and
control tuber DNA samples, thus demonstrating the specificity of the
primers. For the first time, Nacobbus was detected in soil and tuber samples
using molecular approaches. These results have important applications not
only in analysing advisory samples but also in the screening of material for
quarantine purposes.</abstract><cop>The Netherlands</cop><pub>Brill</pub><doi>10.1163/1568541054879539</doi><tpages>10</tpages></addata></record> |
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source | Alma/SFX Local Collection |
subjects | Biological and medical sciences detection DNA FALSE ROOT-KNOT NEMATODE Fundamental and applied biological sciences. Psychology Generalities internal transcribed spacers molecular systematics NACOBBUS nucleotide sequences Phytopathology. Animal pests. Plant and forest protection plant parasitic nematodes polymerase chain reaction potatoes Protozoa. Invertebrates QUARANTINE ribosomal DNA soil Solanum tuberosum SPECIES-SPECIFIC PCR PRIMERS tubers |
title | A molecular diagnostic method for detecting Nacobbus in soil and in potato tubers |
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