Identification of the coat protein gene of a sweet potato sunken vein closterovirus isolate from Kenya and evidence for a serological relationship among geographically diverse closterovirus isolates from sweet potato

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Ute Hoyer
  • Edgar Maiss
  • Wilhelm Jelkmann
  • Dietrich E. Lesemann
  • H. Josef Vetten

Organisationseinheiten

Externe Organisationen

  • Julius Kühn-Institut (JKI) Bundesforschungsinstitut für Kulturpflanzen
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)744-750
Seitenumfang7
FachzeitschriftPHYTOPATHOLOGY
Jahrgang86
Ausgabenummer7
PublikationsstatusVeröffentlicht - Juli 1996

Abstract

A Kenyan isolate of sweet potato sunken vein virus (SPSVV- Ke), a tentative member of the genus Closterovirus, was transmitted to Ipomoea setosa by the whitefly Bemisia tabaci. Cross-banded filamentous particles about 850 nm in length were detected in infected plants by immunoelectron microscopy (IEM) with an antiserum to virions of an Israeli isolate of SPSVV (SPSVV-Is). Vital double-stranded RNA species of about 10 and 9 kbp were extracted from infected I. setosa and used as templates for complementary DNA (cDNA) synthesis. Sequencing of selected cDNA clones revealed an open reading frame of 774 nucleotides that encodes a protein with an estimated molecular mass of 29,028 Da. Computer analysis of the deduced amino acid sequence of this protein indicated a distinct affinity to the coat protein (CP) of lettuce infectious yellows closterovirus (LIYV) and a lesser similarity to the CPs of beet yellows and citrus tristeza closteroviruses, suggesting that it is the CP of SPSYV-Ke. After expression of the CP gene of SPSVV-Ke in Escherichia coli, its identity as the viral CP was confirmed by Western blot analysis with the SPSVV-Is antiserum. This antiserum and a rabbit antiserum raised against the bacterially expressed CP of SPSYV-Ke were used in Western blot and IEM experiments for assessing the serological relationships among SPSVV-Ke, SPSVV-Is, and sweet potato virus disease associated closterovirus isolates from Nigeria and the United States. Results showed that SPSVV-Ke is closely related serologically to similar closterovirus isolates infecting sweet potato in Israel, Nigeria, and the United States but differs from them in reacting weakly with an antiserum to LIYV in IEM and Western blots.

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Identification of the coat protein gene of a sweet potato sunken vein closterovirus isolate from Kenya and evidence for a serological relationship among geographically diverse closterovirus isolates from sweet potato. / Hoyer, Ute; Maiss, Edgar; Jelkmann, Wilhelm et al.
in: PHYTOPATHOLOGY, Jahrgang 86, Nr. 7, 07.1996, S. 744-750.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Identification of the coat protein gene of a sweet potato sunken vein closterovirus isolate from Kenya and evidence for a serological relationship among geographically diverse closterovirus isolates from sweet potato",
abstract = "A Kenyan isolate of sweet potato sunken vein virus (SPSVV- Ke), a tentative member of the genus Closterovirus, was transmitted to Ipomoea setosa by the whitefly Bemisia tabaci. Cross-banded filamentous particles about 850 nm in length were detected in infected plants by immunoelectron microscopy (IEM) with an antiserum to virions of an Israeli isolate of SPSVV (SPSVV-Is). Vital double-stranded RNA species of about 10 and 9 kbp were extracted from infected I. setosa and used as templates for complementary DNA (cDNA) synthesis. Sequencing of selected cDNA clones revealed an open reading frame of 774 nucleotides that encodes a protein with an estimated molecular mass of 29,028 Da. Computer analysis of the deduced amino acid sequence of this protein indicated a distinct affinity to the coat protein (CP) of lettuce infectious yellows closterovirus (LIYV) and a lesser similarity to the CPs of beet yellows and citrus tristeza closteroviruses, suggesting that it is the CP of SPSYV-Ke. After expression of the CP gene of SPSVV-Ke in Escherichia coli, its identity as the viral CP was confirmed by Western blot analysis with the SPSVV-Is antiserum. This antiserum and a rabbit antiserum raised against the bacterially expressed CP of SPSYV-Ke were used in Western blot and IEM experiments for assessing the serological relationships among SPSVV-Ke, SPSVV-Is, and sweet potato virus disease associated closterovirus isolates from Nigeria and the United States. Results showed that SPSVV-Ke is closely related serologically to similar closterovirus isolates infecting sweet potato in Israel, Nigeria, and the United States but differs from them in reacting weakly with an antiserum to LIYV in IEM and Western blots.",
keywords = "coat protein expression, dsRNA",
author = "Ute Hoyer and Edgar Maiss and Wilhelm Jelkmann and Lesemann, {Dietrich E.} and Vetten, {H. Josef}",
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volume = "86",
pages = "744--750",
journal = "PHYTOPATHOLOGY",
issn = "0031-949X",
publisher = "American Phytopathological Society",
number = "7",

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TY - JOUR

T1 - Identification of the coat protein gene of a sweet potato sunken vein closterovirus isolate from Kenya and evidence for a serological relationship among geographically diverse closterovirus isolates from sweet potato

AU - Hoyer, Ute

AU - Maiss, Edgar

AU - Jelkmann, Wilhelm

AU - Lesemann, Dietrich E.

AU - Vetten, H. Josef

PY - 1996/7

Y1 - 1996/7

N2 - A Kenyan isolate of sweet potato sunken vein virus (SPSVV- Ke), a tentative member of the genus Closterovirus, was transmitted to Ipomoea setosa by the whitefly Bemisia tabaci. Cross-banded filamentous particles about 850 nm in length were detected in infected plants by immunoelectron microscopy (IEM) with an antiserum to virions of an Israeli isolate of SPSVV (SPSVV-Is). Vital double-stranded RNA species of about 10 and 9 kbp were extracted from infected I. setosa and used as templates for complementary DNA (cDNA) synthesis. Sequencing of selected cDNA clones revealed an open reading frame of 774 nucleotides that encodes a protein with an estimated molecular mass of 29,028 Da. Computer analysis of the deduced amino acid sequence of this protein indicated a distinct affinity to the coat protein (CP) of lettuce infectious yellows closterovirus (LIYV) and a lesser similarity to the CPs of beet yellows and citrus tristeza closteroviruses, suggesting that it is the CP of SPSYV-Ke. After expression of the CP gene of SPSVV-Ke in Escherichia coli, its identity as the viral CP was confirmed by Western blot analysis with the SPSVV-Is antiserum. This antiserum and a rabbit antiserum raised against the bacterially expressed CP of SPSYV-Ke were used in Western blot and IEM experiments for assessing the serological relationships among SPSVV-Ke, SPSVV-Is, and sweet potato virus disease associated closterovirus isolates from Nigeria and the United States. Results showed that SPSVV-Ke is closely related serologically to similar closterovirus isolates infecting sweet potato in Israel, Nigeria, and the United States but differs from them in reacting weakly with an antiserum to LIYV in IEM and Western blots.

AB - A Kenyan isolate of sweet potato sunken vein virus (SPSVV- Ke), a tentative member of the genus Closterovirus, was transmitted to Ipomoea setosa by the whitefly Bemisia tabaci. Cross-banded filamentous particles about 850 nm in length were detected in infected plants by immunoelectron microscopy (IEM) with an antiserum to virions of an Israeli isolate of SPSVV (SPSVV-Is). Vital double-stranded RNA species of about 10 and 9 kbp were extracted from infected I. setosa and used as templates for complementary DNA (cDNA) synthesis. Sequencing of selected cDNA clones revealed an open reading frame of 774 nucleotides that encodes a protein with an estimated molecular mass of 29,028 Da. Computer analysis of the deduced amino acid sequence of this protein indicated a distinct affinity to the coat protein (CP) of lettuce infectious yellows closterovirus (LIYV) and a lesser similarity to the CPs of beet yellows and citrus tristeza closteroviruses, suggesting that it is the CP of SPSYV-Ke. After expression of the CP gene of SPSVV-Ke in Escherichia coli, its identity as the viral CP was confirmed by Western blot analysis with the SPSVV-Is antiserum. This antiserum and a rabbit antiserum raised against the bacterially expressed CP of SPSYV-Ke were used in Western blot and IEM experiments for assessing the serological relationships among SPSVV-Ke, SPSVV-Is, and sweet potato virus disease associated closterovirus isolates from Nigeria and the United States. Results showed that SPSVV-Ke is closely related serologically to similar closterovirus isolates infecting sweet potato in Israel, Nigeria, and the United States but differs from them in reacting weakly with an antiserum to LIYV in IEM and Western blots.

KW - coat protein expression

KW - dsRNA

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U2 - 10.1094/Phyto-86-744

DO - 10.1094/Phyto-86-744

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SP - 744

EP - 750

JO - PHYTOPATHOLOGY

JF - PHYTOPATHOLOGY

SN - 0031-949X

IS - 7

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