An Aphid Effector Targets Trafficking Protein VPS52 in a Host-Specific Manner to Promote Virulence

Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although for plant pathogenic microbes it is well established that effectors target host proteins to modulate host cell processes and promote disease,...

Full description

Saved in:
Bibliographic Details
Published inPlant physiology (Bethesda) Vol. 173; no. 3; pp. 1892 - 1903
Main Authors Rodriguez, Patricia A., Escudero-Martinez, Carmen, Bos, Jorunn I.B.
Format Journal Article
LanguageEnglish
Published United States American Society of Plant Biologists 01.03.2017
Subjects
Online AccessGet full text
ISSN0032-0889
1532-2548
1532-2548
DOI10.1104/pp.16.01458

Cover

Abstract Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although for plant pathogenic microbes it is well established that effectors target host proteins to modulate host cell processes and promote disease, the host cell targets of herbivorous insects remain elusive. Here, we show that the existing plant pathogenic microbe effector paradigm can be extended to herbivorous insects in that effector-target interactions inside host cells modify critical host processes to promote plant susceptibility. We showed that the effector Mp1 from Myzus persicae associates with the host Vacuolar Protein Sorting Associated Protein52 (VPS52). Using natural variants, we provide a strong link between effector virulence activity and association with VPS52, and show that the association is highly specific to M. persicae-host interactions. Also, coexpression of Mp1, but not Mp1-like variants, specifically with host VPS52s resulted in effector relocalization to vesicle-like structures that associate with prevacuolar compartments. We show that high VPS52 levels negatively impact virulence, and that aphids are able to reduce VPS52 levels during infestation, indicating that VPS52 is an important virulence target. Our work is an important step forward in understanding, at the molecular level, how a major agricultural pest promotes susceptibility during infestation of crop plants. We give evidence that an herbivorous insect employs effectors that interact with host proteins as part of an effective virulence strategy, and that these effectors likely function in a species-specific manner.
AbstractList A secreted salivary protein from an herbivorous insect targets a protein in host plants to promote infestation. Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although for plant pathogenic microbes it is well established that effectors target host proteins to modulate host cell processes and promote disease, the host cell targets of herbivorous insects remain elusive. Here, we show that the existing plant pathogenic microbe effector paradigm can be extended to herbivorous insects in that effector-target interactions inside host cells modify critical host processes to promote plant susceptibility. We showed that the effector Mp1 from Myzus persicae associates with the host Vacuolar Protein Sorting Associated Protein52 (VPS52). Using natural variants, we provide a strong link between effector virulence activity and association with VPS52, and show that the association is highly specific to M . persicae -host interactions. Also, coexpression of Mp1, but not Mp1-like variants, specifically with host VPS52s resulted in effector relocalization to vesicle-like structures that associate with prevacuolar compartments. We show that high VPS52 levels negatively impact virulence, and that aphids are able to reduce VPS52 levels during infestation, indicating that VPS52 is an important virulence target. Our work is an important step forward in understanding, at the molecular level, how a major agricultural pest promotes susceptibility during infestation of crop plants. We give evidence that an herbivorous insect employs effectors that interact with host proteins as part of an effective virulence strategy, and that these effectors likely function in a species-specific manner.
Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although for plant pathogenic microbes it is well established that effectors target host proteins to modulate host cell processes and promote disease, the host cell targets of herbivorous insects remain elusive. Here, we show that the existing plant pathogenic microbe effector paradigm can be extended to herbivorous insects in that effector-target interactions inside host cells modify critical host processes to promote plant susceptibility. We showed that the effector Mp1 from Myzus persicae associates with the host Vacuolar Protein Sorting Associated Protein52 (VPS52). Using natural variants, we provide a strong link between effector virulence activity and association with VPS52, and show that the association is highly specific to M. persicae-host interactions. Also, coexpression of Mp1, but not Mp1-like variants, specifically with host VPS52s resulted in effector relocalization to vesicle-like structures that associate with prevacuolar compartments. We show that high VPS52 levels negatively impact virulence, and that aphids are able to reduce VPS52 levels during infestation, indicating that VPS52 is an important virulence target. Our work is an important step forward in understanding, at the molecular level, how a major agricultural pest promotes susceptibility during infestation of crop plants. We give evidence that an herbivorous insect employs effectors that interact with host proteins as part of an effective virulence strategy, and that these effectors likely function in a species-specific manner.
Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although for plant pathogenic microbes it is well established that effectors target host proteins to modulate host cell processes and promote disease, the host cell targets of herbivorous insects remain elusive. Here, we show that the existing plant pathogenic microbe effector paradigm can be extended to herbivorous insects in that effector-target interactions inside host cells modify critical host processes to promote plant susceptibility. We showed that the effector Mp1 from associates with the host Vacuolar Protein Sorting Associated Protein52 (VPS52). Using natural variants, we provide a strong link between effector virulence activity and association with VPS52, and show that the association is highly specific to -host interactions. Also, coexpression of Mp1, but not Mp1-like variants, specifically with host VPS52s resulted in effector relocalization to vesicle-like structures that associate with prevacuolar compartments. We show that high VPS52 levels negatively impact virulence, and that aphids are able to reduce VPS52 levels during infestation, indicating that VPS52 is an important virulence target. Our work is an important step forward in understanding, at the molecular level, how a major agricultural pest promotes susceptibility during infestation of crop plants. We give evidence that an herbivorous insect employs effectors that interact with host proteins as part of an effective virulence strategy, and that these effectors likely function in a species-specific manner.
Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although for plant pathogenic microbes it is well established that effectors target host proteins to modulate host cell processes and promote disease, the host cell targets of herbivorous insects remain elusive. Here, we show that the existing plant pathogenic microbe effector paradigm can be extended to herbivorous insects in that effector-target interactions inside host cells modify critical host processes to promote plant susceptibility. We showed that the effector Mp1 from Myzus persicae associates with the host Vacuolar Protein Sorting Associated Protein52 (VPS52). Using natural variants, we provide a strong link between effector virulence activity and association with VPS52, and show that the association is highly specific to Mpersicae-host interactions. Also, coexpression of Mp1, but not Mp1-like variants, specifically with host VPS52s resulted in effector relocalization to vesicle-like structures that associate with prevacuolar compartments. We show that high VPS52 levels negatively impact virulence, and that aphids are able to reduce VPS52 levels during infestation, indicating that VPS52 is an important virulence target. Our work is an important step forward in understanding, at the molecular level, how a major agricultural pest promotes susceptibility during infestation of crop plants. We give evidence that an herbivorous insect employs effectors that interact with host proteins as part of an effective virulence strategy, and that these effectors likely function in a species-specific manner.Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although for plant pathogenic microbes it is well established that effectors target host proteins to modulate host cell processes and promote disease, the host cell targets of herbivorous insects remain elusive. Here, we show that the existing plant pathogenic microbe effector paradigm can be extended to herbivorous insects in that effector-target interactions inside host cells modify critical host processes to promote plant susceptibility. We showed that the effector Mp1 from Myzus persicae associates with the host Vacuolar Protein Sorting Associated Protein52 (VPS52). Using natural variants, we provide a strong link between effector virulence activity and association with VPS52, and show that the association is highly specific to Mpersicae-host interactions. Also, coexpression of Mp1, but not Mp1-like variants, specifically with host VPS52s resulted in effector relocalization to vesicle-like structures that associate with prevacuolar compartments. We show that high VPS52 levels negatively impact virulence, and that aphids are able to reduce VPS52 levels during infestation, indicating that VPS52 is an important virulence target. Our work is an important step forward in understanding, at the molecular level, how a major agricultural pest promotes susceptibility during infestation of crop plants. We give evidence that an herbivorous insect employs effectors that interact with host proteins as part of an effective virulence strategy, and that these effectors likely function in a species-specific manner.
Author Bos, Jorunn I.B.
Rodriguez, Patricia A.
Escudero-Martinez, Carmen
Author_xml – sequence: 1
  givenname: Patricia A.
  surname: Rodriguez
  fullname: Rodriguez, Patricia A.
– sequence: 2
  givenname: Carmen
  surname: Escudero-Martinez
  fullname: Escudero-Martinez, Carmen
– sequence: 3
  givenname: Jorunn I.B.
  surname: Bos
  fullname: Bos, Jorunn I.B.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28100451$$D View this record in MEDLINE/PubMed
BookMark eNptkd1vFCEUxYmpsdvqk88aHk3MrBcGGObFZNNUa1Jjk659JQwDW-osjMCa-N_Luq1f8ene5P7uORfOCToKMViEnhNYEgLszTwviVgCYVw-QgvCW9pQzuQRWgDUHqTsj9FJzncAQFrCnqBjKgkA42SBhlXAq_nWj_jcOWtKTHit08aWjNdJO-fNFx82-CrFYn3AN1fXnOLaaHwRc2muZ2t8hfBHHYJNuMQ9uq0wvvFpN9lg7FP02Okp22f39RR9fne-PrtoLj-9_3C2umwME31pemNhGKQRoieadZRwOYoRtJP1Ad1ozEhpS3vWVrBzPcDQcy1FB24YxNC79hS9PejOu2FrR2NDSXpSc_Jbnb6rqL36exL8rdrEb4q3rRRCVIFX9wIpft3ZXNTWZ2OnSQcbd1kRKQjvOLC2oi__9Ppl8vCxFSAHwKSYc7JOGV908XFv7SdFQO3DU_OsiFA_w6s7r__ZeZD9P_3iQN_lmtrvC1gPlEHX_gCy3KQr
CitedBy_id crossref_primary_10_1093_plcell_koac058
crossref_primary_10_1111_nph_17620
crossref_primary_10_1093_jxb_erac010
crossref_primary_10_1242_jcs_246728
crossref_primary_10_1093_gbe_evac069
crossref_primary_10_1016_j_heliyon_2024_e29201
crossref_primary_10_1111_tpj_13773
crossref_primary_10_1093_ee_nvaa036
crossref_primary_10_1093_plcell_koac009
crossref_primary_10_1111_1744_7917_12470
crossref_primary_10_1016_j_ibmb_2020_103363
crossref_primary_10_1094_MPMI_06_17_0139_R
crossref_primary_10_1016_j_cois_2018_01_003
crossref_primary_10_1002_ps_8225
crossref_primary_10_3389_fpls_2020_00605
crossref_primary_10_1002_ps_6252
crossref_primary_10_3390_microorganisms10101980
crossref_primary_10_1038_s41598_020_66217_0
crossref_primary_10_1111_nph_15475
crossref_primary_10_2174_0929866526666191014145839
crossref_primary_10_3389_fpls_2021_661141
crossref_primary_10_1007_s10340_023_01717_2
crossref_primary_10_1094_MPMI_10_23_0154_FI
crossref_primary_10_1002_ece3_8209
crossref_primary_10_1111_1744_7917_12648
crossref_primary_10_3389_fpls_2018_01057
crossref_primary_10_1007_s44281_024_00038_3
crossref_primary_10_1111_nph_18184
crossref_primary_10_1073_pnas_1918410117
crossref_primary_10_3390_biology10080753
crossref_primary_10_1002_pld3_246
crossref_primary_10_1016_j_plantsci_2018_04_027
crossref_primary_10_3389_fpls_2023_1326726
crossref_primary_10_1007_s41348_024_01002_z
crossref_primary_10_3390_insects14090760
crossref_primary_10_1016_j_cois_2020_11_005
crossref_primary_10_3390_ijms24076069
crossref_primary_10_1007_s11829_024_10071_8
crossref_primary_10_1111_nph_18507
crossref_primary_10_12688_f1000research_21502_1
crossref_primary_10_3390_ijms232113433
crossref_primary_10_1007_s10529_020_02961_7
crossref_primary_10_1073_pnas_1915396116
crossref_primary_10_1093_jxb_eraa015
crossref_primary_10_3389_fpls_2019_01452
crossref_primary_10_1073_pnas_1714990116
crossref_primary_10_1016_j_xplc_2020_100050
crossref_primary_10_1093_gbe_evy183
crossref_primary_10_1111_1744_7917_12856
crossref_primary_10_1146_annurev_phyto_021622_123232
crossref_primary_10_3389_fpls_2023_1104275
crossref_primary_10_1016_j_pbi_2017_07_001
crossref_primary_10_1094_MPMI_04_23_0044_R
crossref_primary_10_1186_s12864_022_08712_4
crossref_primary_10_3390_v12020148
crossref_primary_10_3389_fpls_2023_1176048
crossref_primary_10_1016_j_tplants_2020_10_009
crossref_primary_10_1016_j_cropro_2022_106122
crossref_primary_10_1093_jxb_eraa043
crossref_primary_10_1146_annurev_ento_120220_020526
crossref_primary_10_1093_pcp_pcae059
crossref_primary_10_1186_s12870_020_02749_x
crossref_primary_10_1093_gbe_evy097
crossref_primary_10_3390_plants8100374
crossref_primary_10_1038_s41598_020_62856_5
crossref_primary_10_1111_eea_13297
crossref_primary_10_1016_j_plantsci_2021_111120
crossref_primary_10_1094_MPMI_10_23_0167_FI
crossref_primary_10_1007_s42690_021_00546_z
crossref_primary_10_1016_j_bbrc_2021_07_066
crossref_primary_10_1007_s11829_020_09769_2
crossref_primary_10_3390_insects15120935
crossref_primary_10_1016_j_jia_2024_05_018
crossref_primary_10_3390_ijms252312951
ContentType Journal Article
Copyright Copyright © 2017 American Society of Plant Biologists
2017 American Society of Plant Biologists. All Rights Reserved.
2017 American Society of Plant Biologists. All Rights Reserved. 2017
Copyright_xml – notice: Copyright © 2017 American Society of Plant Biologists
– notice: 2017 American Society of Plant Biologists. All Rights Reserved.
– notice: 2017 American Society of Plant Biologists. All Rights Reserved. 2017
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOI 10.1104/pp.16.01458
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList

MEDLINE
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Botany
EISSN 1532-2548
EndPage 1903
ExternalDocumentID PMC5338666
28100451
10_1104_pp_16_01458
24902407
Genre Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: Biotechnology and Biological Sciences Research Council
  grantid: BB/J005258/1
– fundername: European Research Council
  grantid: 310190
GroupedDBID ---
-DZ
-~X
0R~
123
29O
2AX
2WC
2~F
4.4
5VS
5WD
85S
8R4
8R5
AAHBH
AAHKG
AAPXW
AARHZ
AAUAY
AAVAP
AAXTN
ABBHK
ABDFA
ABEJV
ABGNP
ABJNI
ABMNT
ABPLY
ABPPZ
ABPTD
ABTLG
ABVGC
ABXSQ
ABXVV
ABXZS
ACBTR
ACGOD
ACHIC
ACNCT
ACPRK
ACUFI
ADBBV
ADGKP
ADIPN
ADIYS
ADQBN
ADULT
ADVEK
ADYHW
AEEJZ
AENEX
AEUPB
AFAZZ
AFFZL
AFGWE
AFRAH
AGORE
AGUYK
AHMBA
AHXOZ
AICQM
AJBYB
AJEEA
AJNCP
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALXQX
AQVQM
ATGXG
BAWUL
BCRHZ
BEYMZ
BTFSW
CBGCD
CS3
DATOO
DIK
DU5
E3Z
EBS
ECGQY
EJD
F5P
FLUFQ
FOEOM
H13
IPSME
JAAYA
JBMMH
JBS
JENOY
JHFFW
JKQEH
JLS
JLXEF
JPM
JST
JXSIZ
KOP
KQ8
KSI
KSN
MV1
NOMLY
NU-
OBOKY
OJZSN
OK1
OWPYF
P2P
Q2X
RHI
ROX
RPB
RWL
RXW
SA0
TAE
TN5
TR2
W8F
WH7
WOQ
XSW
YBU
YKV
YNT
YSK
YZZ
ZCA
ZCN
~02
~KM
53G
7X2
7X7
88E
88I
8AF
8AO
8CJ
8FE
8FH
8FI
8FJ
8FW
8G5
AAWDT
AAYJJ
AAYXX
ABIME
ABPIB
ABUWG
ABZEO
ACFRR
ACIPB
ACUTJ
ACVCV
ACZBC
ADXHL
AEUYN
AFFDN
AFKRA
AFYAG
AGMDO
AHGBF
AIDAL
AIDBO
AJDVS
ANFBD
APJGH
AQDSO
AS~
ATCPS
AZQEC
BBNVY
BENPR
BHPHI
BPHCQ
BVXVI
C1A
CCPQU
CITATION
D1J
DWQXO
FYUFA
GNUQQ
GTFYD
GUQSH
HCIFZ
HMCUK
HTVGU
LK8
LU7
M0K
M1P
M2O
M2P
M2Q
M7P
MVM
P0-
PHGZM
PHGZT
PQQKQ
PROAC
PSQYO
QZG
S0X
TCN
UBC
UKHRP
UKR
WHG
XOL
Y6R
ZCG
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
PQGLB
7X8
5PM
ID FETCH-LOGICAL-c469t-9ce0bb8c6691a472158d6d0af88897dccd22329439ce7f900b95a8670fbb6b9f3
ISSN 0032-0889
1532-2548
IngestDate Thu Aug 21 14:11:59 EDT 2025
Fri Sep 05 07:21:43 EDT 2025
Mon Jul 21 06:02:32 EDT 2025
Thu Apr 24 23:06:07 EDT 2025
Tue Jul 01 03:08:31 EDT 2025
Fri May 30 11:46:56 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Language English
License 2017 American Society of Plant Biologists. All Rights Reserved.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c469t-9ce0bb8c6691a472158d6d0af88897dccd22329439ce7f900b95a8670fbb6b9f3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
www.plantphysiol.org/cgi/doi/10.1104/pp.16.01458
The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Jorunn I.B. Bos (j.bos@dundee.ac.uk).
P.A.R. and J.I.B.B. designed the experiments; P.A.R., C.E.-M., and J.I.B.B. performed the experiments and analyzed the data; P.A.R. and J.I.B.B. wrote the manuscript; J.I.B.B. directed the project; all authors read and approved the final manuscript.
ORCID 0000-0003-3222-8643
0000-0002-5876-0331
0000-0002-2442-4516
OpenAccessLink http://www.plantphysiol.org/content/plantphysiol/173/3/1892.full.pdf
PMID 28100451
PQID 1861575043
PQPubID 23479
PageCount 12
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_5338666
proquest_miscellaneous_1861575043
pubmed_primary_28100451
crossref_citationtrail_10_1104_pp_16_01458
crossref_primary_10_1104_pp_16_01458
jstor_primary_24902407
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2017-03-01
PublicationDateYYYYMMDD 2017-03-01
PublicationDate_xml – month: 03
  year: 2017
  text: 2017-03-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Plant physiology (Bethesda)
PublicationTitleAlternate Plant Physiol
PublicationYear 2017
Publisher American Society of Plant Biologists
Publisher_xml – name: American Society of Plant Biologists
SSID ssj0001314
Score 2.514396
Snippet Plant- and animal-feeding insects secrete saliva inside their hosts, containing effectors, which may promote nutrient release and suppress immunity. Although...
A secreted salivary protein from an herbivorous insect targets a protein in host plants to promote infestation. Plant- and animal-feeding insects secrete...
SourceID pubmedcentral
proquest
pubmed
crossref
jstor
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1892
SubjectTerms Amino Acid Sequence
Animals
Aphids - genetics
Aphids - pathogenicity
Aphids - physiology
Arabidopsis - genetics
Arabidopsis - metabolism
Arabidopsis - parasitology
Arabidopsis Proteins - genetics
Arabidopsis Proteins - metabolism
Gene Expression Regulation, Plant
Host-Parasite Interactions
Immunoblotting
Insect Proteins - genetics
Insect Proteins - metabolism
Microscopy, Confocal
Plant Diseases - genetics
Plant Diseases - parasitology
Plants, Genetically Modified
Protein Binding
Reverse Transcriptase Polymerase Chain Reaction
Sequence Homology, Amino Acid
SIGNALING AND RESPONSE
Solanum tuberosum - genetics
Solanum tuberosum - metabolism
Solanum tuberosum - microbiology
Species Specificity
Vesicular Transport Proteins - genetics
Vesicular Transport Proteins - metabolism
Virulence - genetics
Title An Aphid Effector Targets Trafficking Protein VPS52 in a Host-Specific Manner to Promote Virulence
URI https://www.jstor.org/stable/24902407
https://www.ncbi.nlm.nih.gov/pubmed/28100451
https://www.proquest.com/docview/1861575043
https://pubmed.ncbi.nlm.nih.gov/PMC5338666
Volume 173
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Jb9NAFB6FwoELYiukLBqknrBsvGXsOSYVqAWBKkir3qzZrEYCO3LsQ_kV_GTeLHacKofCxbKcmTjx-_ze92begtDxbKbiNFHUp4qW4KDQ0GcZS3wCipClQkhpQv6_fiOnF-nnq9nVZPJnFLXUtTwQv_fmlfyPVOEayFVnyf6DZIcvhQtwDvKFI0gYjneS8bwCFnm9kp6tQVw33tIEdm90zXJdG0Kvg-tcAN3S0rs8_zGL9foG091CWt-0nodBOgSmUo1moecmOE95l6umM9lIY-6q-xu1dinEFm4CcrrQ-cIbyUYLCt9rCR5_51amTQeAFfPmwcDdN6KTqql9W8HAjjthza9tUtqidrsTDdBr7yxYBOPFCTB4Q3RWr3CT2NeRVNbc9Do29sEvzXeUsG1o4tCWjFRqlNtmec48A4FJ9qv-MNX9itdBRAK9V5pvLVy_q3_L8A3hiMYRCtNivS4iUpjJ99D9OAM2pmn22ZfBtkeJrRbf_y2X8QmTP4zuvMNxbJjrPgfmdhzuiNgsH6NHziPBcwuvJ2iiqqfowaIGr-HmGeLzChuM4R5j2GEMjzCGHcawwRiGE4Z3MIYtxnBbY4cxPGDsObr49HF5cuq7vhy-SAltfSpUyHkuCKHwPmdAGnNJZMjKHJ5IJuEFB84ZU6C6QmUlDUNOZywnWVhyTjgtk0N0UNWVeolwSSVQaJmFcRalUgkO_j1PU8kkEcDF4yl63z_JQrii9bp3ys9ij8ym6HgYvLa1WvYPOzQiGcbEKdWV_rIpetfLqAAlq3fOWKXqblNEORB_3QghmaIXVmbb2XlkijRNUbYjzWGALuC--0m1ujaF3MHVygkhR3f73a_Qw-0r9hodtE2n3gAjbvlbA9K_c7O0mQ
linkProvider Flying Publisher
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=An+Aphid+Effector+Targets+Trafficking+Protein+VPS52+in+a+Host-Specific+Manner+to+Promote+Virulence&rft.jtitle=Plant+physiology+%28Bethesda%29&rft.au=Rodriguez%2C+Patricia+A.&rft.au=Escudero-Martinez%2C+Carmen&rft.au=Bos%2C+Jorunn+I.B.&rft.date=2017-03-01&rft.issn=0032-0889&rft.eissn=1532-2548&rft.volume=173&rft.issue=3&rft.spage=1892&rft.epage=1903&rft_id=info:doi/10.1104%2Fpp.16.01458&rft.externalDBID=n%2Fa&rft.externalDocID=10_1104_pp_16_01458
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0032-0889&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0032-0889&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0032-0889&client=summon