除草剂"大田净"防除烟田杂草的效果

通过除草剂"大田净"的不同时期和不同浓度施用,观测其对烟田杂草的防除效果.试验结果表明,揭膜培土时(移栽后25d)喷施杂草防除效果较好;喷施不同浓度间,400倍液、550倍液比800倍液防治效果好.建议在揭膜培土时喷施550倍"大田净"进行除草.     

Polymerization of Tobacco Mosaic Virus Protein and its Control

Near neutral pH₉ TMV protein sub-units polymerize into two-layer aggregates culminating in the 20S disk, whereas the helical rod forms cooperatively at acid pH. The mode of aggregation is controlled by the state of ionization of two abnormally titrating carboxyl groups.     

Hormonal Control of Elongation of Tobacco Cells Derived from Protoplasts

Spherical protoplasts (30–40 µm in diameter), isolatedfrom cultured tobacco cells, elongated rapidly during a cultureperiod of 3 to 8 days and finally assumed a long cylindricalform (300–400 µm in length). The optimum concentrationof a-naphthaleneacetic acid and benzyladenine for the elongationwas 0.1 mg/liter and 1 mg/liter respectively. (Received August 10, 1982; Accepted November 12, 1982)     

Strategies for Tobacco Control in India: A Systematic Review

Background

Tobacco control needs in India are large and complex. Evaluation of outcomes to date has been limited.

Aim

To review the extent of tobacco control measures, and the outcomes of associated trialled interventions, in India.

Methods

Information was identified via database searches, journal hand-searches, reference and citation searching, and contact with experts. Studies of any population resident in India were included. Studies where outcomes were not yet available, not directly related to tobacco use, or not specific to India, were excluded. Pre-tested proformas were used for data extraction and quality assessment. Studies with reliability concerns were excluded from some aspects of analysis. The Framework Convention on Tobacco Control (FCTC) was use as a framework for synthesis. Heterogeneity limited meta-analysis options. Synthesis was therefore predominantly narrative.

Results

Additional to the Global Tobacco Surveillance System data, 80 studies were identified, 45 without reliability concerns. Most related to education (FCTC Article 12) and tobacco-use cessation (Article 14). They indicated widespread understanding of tobacco-related harm, but less knowledge about specific consequences of use. Healthcare professionals reported low confidence in cessation assistance, in keeping with low levels of training. Training for schoolteachers also appeared suboptimal. Educational and cessation assistance interventions demonstrated positive impact on tobacco use. Studies relating to smoke-free policies (Article 8), tobacco advertisements and availability (Articles 13 and 16) indicated increasingly widespread smoke-free policies, but persistence of high levels of SHS exposure, tobacco promotions and availability—including to minors. Data relating to taxation/pricing and packaging (Articles 6 and 11) were limited. We did not identify any studies of product regulation, alternative employment strategies, or illicit trade (Articles 9, 10, 15 and 17).

Conclusions

Tobacco-use outcomes could be improved by school/community-based and adult education interventions, and cessation assistance, facilitated by training for health professionals and schoolteachers. Additional tobacco control measures should be assessed.     

Ontogeny and Hormonal Control of Polyphenoloxidase Isozymes in Tobacco Pith

Isozymes of tobacco pith polyphenoloxidases (o-diphenol oxidase, EC 1.10.3.1) were separated electrophoretically from fresh pith of intact plants and from cultured pith sections. Extracts of fresh pith contained a poorly resolved complex of two to three anodic bands after starch gel electrophoresis at alkaline pH. This anodic complex was more active with chlorogenic acid than with 3,4-dihydroxyphenylalanine and was found in greater activity per gram fresh weight of tissue in younger internodes than in older ones. The longitudinal gradient of activity was thus the opposite of that found for the constitutive isozymes of peroxidase.A well defined cathodic band of polyphenoloxidase activity appeared after culture of pith in modified White's medium with shaking. This band, which was more active with 3,4-dihydroxyphenylalanine than with chlorogenic acid, could be detected after 1 to 2 days of incubation. Its appearance was enhanced by the addition of 10 mum indoleacetic acid; kinetin (1 mum tended to prevent this indoleacetic acid effect). Such hormonal control is opposite to that previously reported for the rapidly appearing new isozymes of peroxidase.The pattern of the major isozymes associated with polyphenoloxidase activities differs from that of peroxidase.     

Global Health Governance and the Commercial Sector: A Documentary Analysis of Tobacco Company Strategies to Influence the WHO Framework Convention on Tobacco Control

Background

In successfully negotiating the Framework Convention on Tobacco Control (FCTC), the World Health Organization (WHO) has led a significant innovation in global health governance, helping to transform international tobacco control. This article provides the first comprehensive review of the diverse campaign initiated by transnational tobacco corporations (TTCs) to try to undermine the proposed convention.

Methods and Findings

The article is primarily based on an analysis of internal tobacco industry documents made public through litigation, triangulated with data from official documentation relating to the FCTC process and websites of relevant organisations. It is also informed by a comprehensive review of previous studies concerning tobacco industry efforts to influence the FCTC. The findings demonstrate that the industry''s strategic response to the proposed WHO convention was two-fold. First, arguments and frames were developed to challenge the FCTC, including: claiming there would be damaging economic consequences; depicting tobacco control as an agenda promoted by high-income countries; alleging the treaty conflicted with trade agreements, “good governance,” and national sovereignty; questioning WHO''s mandate; claiming the FCTC would set a precedent for issues beyond tobacco; and presenting corporate social responsibility (CSR) as an alternative. Second, multiple tactics were employed to promote and increase the impact of these arguments, including: directly targeting FCTC delegations and relevant political actors, enlisting diverse allies (e.g., mass media outlets and scientists), and using stakeholder consultation to delay decisions and secure industry participation.

Conclusions

TTCs'' efforts to undermine the FCTC were comprehensive, demonstrating the global application of tactics that TTCs have previously been found to have employed nationally and further included arguments against the FCTC as a key initiative in global health governance. Awareness of these strategies can help guard against industry efforts to disrupt the implementation of the FCTC and support the development of future, comparable initiatives in global health. Please see later in the article for the Editors'' Summary     

Parental Smoking in the Vicinity of Children and Tobacco Control Policies in the European Region

Objective

To ascertain patterns of parental smoking in the vicinity of children in Eastern and Western Europe and their relation to Tobacco Control Scale (TCS) scores.

Methods

Data on parental smoking patterns were obtained from the School Child Mental Health Europe (SCMHE), a 2010 cross-sectional survey of 5141 school children aged 6 to 11 years and their parents in six countries: Germany, Netherlands, Lithuania, Romania, Bulgaria and Turkey ranked by TCS into three level categories toward tobacco control policies.

Results

A slightly higher proportion of Eastern compared to Western European mothers (42.4 vs. 35.1%) were currently smoking in but the difference was not statistically significant after adjusting for maternal age and maternal educational attainment. About a fifth (19.3%) and a tenth (10.0%) of Eastern and Western European mothers, respectively, smoked in the vicinity of their children, and the difference was significant even after adjustment for potential confounders (p<0.001). Parents with the highest educational attainment were significantly less likely to smoke in the vicinity of their children than those with the lowest attainment. After control of these covariates lax tobacco control policies, compared to intermediate policies, were associated with a 50% increase in the likelihood of maternal smoking in the vicinity of children adjusted odds ratio (AOR) = 1.52 and 1.64. Among fathers, however, the relationship with paternal smoking and TCS seems more complex since strict policy increases the risk as well AOR = 1,40. Only one country, however belongs to the strict group.

Significance

Tobacco control policies seem to have influenced maternal smoking behaviors overall to a limited degree and smoking in the vicinity of children to a much greater degree. Children living in European countries with lax tobacco control policies are more likely to be exposed to second hand smoking from maternal and paternal smoking.     

黄瓜花叶病毒卫星RNA生防制剂在烟草上的防病作用

用人工组装的黄瓜花叶病毒卫星RNA生防制剂在烟草生产品种进行了田间保护试验。由于使用了生防制剂,经处理的烟草发病率降低84.9～86.4％,同时比对照早熟5天,上等烟比率增加151.3～173.5％,平均每亩收入增加43.3～65.7％。另外发现生防制剂能增强烟草对真菌病害的抵抗作用。     

防烟叶霉变菌株培养条件的研究

为有效防治烟叶霉变．对防烟叶霉变最好的3个菌株B112、B329、JMB142的发酵条件进行了初步探讨,通过测定吸光度值计算孢子浓度,确定了3个菌株生长的最适pH值与最适培养基。结果表明菌株JMB142在pH为7．2到8．4时,生长较好,菌株B112和329在PH6.3到PH7.9之间生长较好;当PH小于4.2时,三个菌株均不能正常生长,PH大于9.0时,三个菌株的生长都呈下降趋势。通过方差分析,比较了7种培养基对3株防烟叶霉变菌株产菌量的影响,结果表明,B112、JMB142菌株最佳培养基分别为6^#、5^#培养基,而5^#、7^#培养基更适合B329生长。     

烟草黑胫病生物防治研究进展(综述)

随着烟草生产向无公害发展,黑胫病作为烟草生产上的主要病害之一,其生物防治取得较大的进展。本文就其诱抗剂、生防菌等生物防治方面的研究作简要综述。     

Master Settlement Agreement (MSA) Spending and Tobacco Control Efforts

We investigate whether the distributions to the states from the Tobacco Master Settlement Agreement (MSA) in 1998 is associated with stronger tobacco control efforts. We use state level data from 50 states and the District of Columbia from four time periods post MSA (1999, 2002, 2004, and 2006) for the analysis. Using fixed effect regression models, we estimate the relationship between MSA disbursements and a new aggregate measure of strength of state tobacco control known as the Strength of Tobacco Control (SoTC) Index. Results show an increase of $1 in the annual per capita MSA disbursement to a state is associated with a decrease of −0.316 in the SoTC mean value, indicating higher MSA payments were associated with weaker tobacco control measures within states. In order to achieve the initial objectives of the MSA payments, policy makers should focus on utilizing MSA payments strictly on tobacco control activities across states.     

Patterns and Predictors of Smokeless Tobacco Use among Adults in Bangladesh: Findings from the International Tobacco Control (ITC) Bangladesh Survey

Background

Although smokeless tobacco (SLT) use is prevalent in South Asian countries including Bangladesh, information about the pattern and correlates of SLT use is scarce. This study described the pattern and predictors of SLT use among Bangladeshi adults.

Methods

The data for this study were derived from the International Tobacco Control Policy Evaluation Bangladesh (ITC BD) Survey, a prospective cohort survey of a nationally representative sample of smokers and non-smokers, conducted during November 2011 and May 2012. The study included 5522 adults aged 15 or above. We used multiple logistic regression models to identify predictors of SLT use.

Results

Of the respondents (N = 5522), 20% were SLT users. In general, SLT use was significantly higher among women, the illiterate and residents of the Dhaka slums or non-tribal/non-border areas outside Dhaka; SLT use increased with age. Several attitudinal factors were also associated with SLT use. Multivariable logistic regression analyses revealed several predictors of SLT use: being female (OR = 1.96, 95% confidence interval, CI: 1.18–3.24), an increasing age, being a resident of a Dhaka slum (OR = 5.86; 95% CI: 3.73–9.21) or non-tribal/non-border areas outside Dhaka (OR = 3.42; 95% CI: 1.94–6.03), being illiterate (OR = 3.37; 95% CI: 1.99–5.71), holding positive opinion towards societal approval of SLT use (OR = 5.84; 95% CI: 3.38–10.09), holding positive opinion towards SLT use by women (OR = 2.63; 95% CI: 1.53–4.54), believing that SLT is addictive (OR = 2.96; 95% CI: 1.51–5.81), and believing SLT is less harmful than bidi (OR = 2.22; 95% CI: 1.36–3.62).

Conclusion

The findings suggest that coordinated efforts of governmental and non-governmental organizations, targeting both smoked tobacco and SLT use reduction and cessation, could be modified to reach each level of population including those who are marginalized, female, less educated and elderly. As most tobacco control programs in Bangladesh target mainly cigarette or bidi smoking, coordinated programs are needed that will also include SLT use within the tobacco control policy and prevention strategies.     

Transgenic Tobacco Plants with a Fully Synthesized GFM CryIA Gene Provide Effective Tobacco Bollworm (Heliothis armigera) Control

GFM CrylA gene is a fully modified synthetic gene derived from insecticidal crystal prorein gene of Bacillus thuringiensis Berliner (Bt). It was synthesized based on the codon usage of plant genes instead of changing the primary sequences of amino acids of insecticidal crystal protein (ICP) gene of Bacillus thuringiensis Htibner. To test the function of the synthetic GFM CrylA gene, we introduced the GFM CrylA gene into tobacco plant cells via an Agrobacterium tumefacieus (Smith et Townsedn) Conn binary vector system. As expected, the GFM CrylA gene is expressed under control of the cauliflower mosaic virus (CaMV) 35S promoter and allows efficient production of lepidopteran insectspecific toxic proteins in the transformed tobacco plants. Bioassays using transgenic tobacco plants with tobacco bollworm showed that the transgenic tobacco plants expressing proteins of GFM CrylA gene had effective control to tobacco bollworm. In this paper the authors firstly report the complete synthesis of GFM CryIA gene and the construction of plant expression vector pGBI4AB. The authors performed introduction of the synthetic GFM CrylA gene into the tobacco plants, and the integration of GFM CrylA gene into tobacco genome was confirmed by Southern blot analysis of the tobacco genomic DNA. The gene was efficiently expressed in the transgenic tobacco plants and effective tobacco bollworm control was verified by the insect-bioassays.     

Desiccation and the Control of Expression of {beta}-Phaseolin in Transgenic Tobacco Seeds

Drying of seeds at certain stages prior to maturation, i.e.premature desiccation, will terminate synthetic events uniqueto development, for example, storage protein synthesis, andinitiate processes associated with germination. In this studywe have investigated the role of desiccation in the expressionof a storage protein gene, ß-phaseolin, to determineif such a developmentally-regulated gene remains sensitive todrying when controlled by a promoter that has no known sensitivityto this treatment. We compared, in transgenic tobacco seeds,the effects of maturation and premature drying on the expressionof a full ß-phaseolin gene, and ß-phaseolingenes driven by a cauliflower mosaic virus 35S promoter withor without an alfalfa mosaic virus (AMV) 5' untranslated leadersequence. The results indicate that the ß-phaseolinpromoter is directly down-regulated by desiccation during maturationand, although activated during the drying phase of a prematuredesiccation event, it is not active upon rehydration or imbibition.The 35S promoter is down-regulated also by both maturation dryingand premature desiccation but unlike the ß-phaseolinpromoter it is reactivated upon rehydration or imbibition. Key words: Desiccation, ß-phaseolin, gene regulation, Phoseolus vulgaris, seed development     

Hormonal Control of Gene Expression During Reactivation of the Cell Cycle in Tobacco Mesophyll Protoplasts

The roles of auxin and cytokinin in cell cycle reactivation were studied during the first 48 h of culture of mesophyll protoplasts of Nicotiana tabacum. Using hormone delay and withdrawal studies we found that auxin was required by 0–4 h of culture, whereas cytokinin was not required until hour 10–12, which is 6–10 h before S phase. Cycloheximide blocks division, indicating that protein synthesis is required. In an effort to detect a molecular response to either hormone, we examined the expression of the cell cycle marker, cdc2. Cdc2 expression was detected by 12 h of culture, coincident with the timing of the cytokinin requirement and well before the entry into S. However, cdc2 was partially induced by either auxin or cytokinin alone, suggesting that cdc2 expression is not the primary target of either hormone. Our hormone delay experiments suggest that there are separate signal transduction pathways leading from auxin and from cytokinin to reactivation of the cell cycle and that these pathways converge before S. The underlying mechanisms for these distinct pathways remain to be elucidated. Received November 4, 1997; accepted October 7, 1998     

芽胞杆菌防治烟草病虫害的研究进展

烟草病虫害严重影响烟草产业的可持续发展,更为安全的生物防治方法已成为烟草病虫害防治研究的热点领域。芽胞杆菌属(Bacillus)是一类比较理想的生防微生物,在植病生物防治领域显示出了广阔的应用前景。本文论述了芽胞杆菌属细菌的生物学特性及其在烟草黑胫病、赤星病、青枯病、炭疽病、根黑腐病、花叶病、白粉病、烟草斜纹夜蛾和甲虫等烟草病虫害防治中的应用。     

防治烟草赤星病有益内生细菌的筛选及抑菌作用

从健康烟草的叶、茎中分离到302株非病原内生细菌,通过平板对峙培养,筛选出对烟草赤星病菌［Alternaria alternata（Fr.）Keissl］不同致病力的4个代表菌株均有拮抗作用的11个菌株。室内测定其对赤星病菌抑菌带的宽度达5.5～13.2mm;拮抗、防病试验测定,来自叶片内的内生菌株Itb162对赤星病菌有较强和稳定的拮抗作用,对赤星病有52.0%的防病效果。无菌滤液实验表明,拮抗内生细菌Itb162无菌滤液在一定浓度范围内均能有效地抑制菌丝生长,减少孢子萌发,且浓度越高,抑制能力越强。     

Control of Tobacco mosaic virus Movement Protein Fate by CELL-DIVISION-CYCLE Protein48

Like many other viruses, Tobacco mosaic virus replicates in association with the endoplasmic reticulum (ER) and exploits this membrane network for intercellular spread through plasmodesmata (PD), a process depending on virus-encoded movement protein (MP). The movement process involves interactions of MP with the ER and the cytoskeleton as well as its targeting to PD. Later in the infection cycle, the MP further accumulates and localizes to ER-associated inclusions, the viral factories, and along microtubules before it is finally degraded. Although these patterns of MP accumulation have been described in great detail, the underlying mechanisms that control MP fate and function during infection are not known. Here, we identify CELL-DIVISION-CYCLE protein48 (CDC48), a conserved chaperone controlling protein fate in yeast (Saccharomyces cerevisiae) and animal cells by extracting protein substrates from membranes or complexes, as a cellular factor regulating MP accumulation patterns in plant cells. We demonstrate that Arabidopsis (Arabidopsis thaliana) CDC48 is induced upon infection, interacts with MP in ER inclusions dependent on the MP N terminus, and promotes degradation of the protein. We further provide evidence that CDC48 extracts MP from ER inclusions to the cytosol, where it subsequently accumulates on and stabilizes microtubules. We show that virus movement is impaired upon overexpression of CDC48, suggesting that CDC48 further functions in controlling virus movement by removal of MP from the ER transport pathway and by promoting interference of MP with microtubule dynamics. CDC48 acts also in response to other proteins expressed in the ER, thus suggesting a general role of CDC48 in ER membrane maintenance upon ER stress.Plant viruses are obligate intracellular pathogens that replicate in association with host membranes (Laliberté and Sanfaçon, 2010) and subvert host intra- and intercellular trafficking pathways to achieve cell-to-cell and systemic spread (Harries and Ding, 2011; Niehl and Heinlein, 2011). In the case of the well-studied Tobacco mosaic virus (TMV), viral replication factories form on membranes of the endoplasmic reticulum (ER; Heinlein et al., 1995, 1998). As the plant ER is continuous between cells through plasmodesmata (PD; Ding et al., 1992), this membrane network provides a direct pathway for the spread of replicated virus from the replication sites in infected cells into the ER network of noninfected cells. The spread of plant viruses depends on virus-encoded movement proteins (MPs; Deom et al., 1987; Lucas, 2006). The MP of TMV facilitates the cell-to-cell passage of the infectious particle by forming a ribonucleoprotein complex with the viral RNA (Citovsky et al., 1990) and by increasing the size exclusion limit of PD (Wolf et al., 1989).During the course of infection, as well as when ectopically expressed, the MP associates with PD, the ER/actin network, and microtubules (Heinlein et al., 1995, 1998; Reichel and Beachy, 1998; Wright et al., 2007; Sambade et al., 2008; Hofmann et al., 2009; Boutant et al., 2010; Peña and Heinlein, 2012; Supplemental Fig. S1). Shortly after infection of a new cell, the MP localizes to small, mobile, ER-associated particles proposed to play a role in PD targeting of the viral RNA (Boyko et al., 2007; Sambade et al., 2008). Similar small, mobile MP particles are observed early upon ectopic expression of the protein. These particles colocalize with RNA and undergo stop-and-go movements in association with the ER (Sambade et al., 2008). The particle movements pause at microtubule proximal sites and their detachment requires microtubule polymerization (Sambade et al., 2008). These observations suggest that the interaction with the microtubule system plays a critical role in the maturation and ER-mediated delivery of infectious viral RNA particles to PD during early infection stages. Consistently, tobacco (Nicotiana tabacum) mutants with reduced microtubule dynamics exhibit reduced TMV movement (Ouko et al., 2010). Following virus movement, the previously infected cell further accumulates MP at the ER, a process that coincides with the formation of large ER inclusions that contain viral replicase and viral RNA in addition to MP and likely function as virus factories (Heinlein et al., 1998; Más and Beachy, 1999). In mature form, these inclusions may represent the so-called viroplasms or X-bodies described in the classical literature (Bawden and Sheffield, 1939; Esau and Cronshaw, 1967; Hills et al., 1987). Their formation is associated with rearrangements of the ER membrane and likely mediated by the accumulated MP since the inclusions diminish and reconstitute a native ER structure when MP becomes degraded by the 26S proteasome (Reichel and Beachy, 1998, 2000). Transfected cells accumulate MP in similar inclusions as those formed during infection, indicating that accumulated MP is indeed necessary and sufficient to form inclusions in association with the ER (Reichel and Beachy, 1998; Supplemental Fig. S1). Following accumulation of MP in virus factories, the infected cells accumulate the MP also along microtubules (Heinlein et al., 1998). The accumulation of MP in virus factories and on microtubules in cells behind the leading front of infection is dispensable for virus movement (Heinlein et al., 1998; Boyko et al., 2000a). At these late infection stages, the virus factories may enable the virus to produce high virion titers (Laliberté and Sanfaçon, 2010; Tilsner et al., 2012), and the subsequent accumulation along microtubules may play a role in withdrawing MP from the cell-to-cell communication pathway (Curin et al., 2007) and in stockpiling MP prior to degradation (Padgett et al., 1996; Gillespie et al., 2002).The molecular mechanisms that guide the MP to the ER and subsequently to microtubules during infection are not known. The MP is a hydrophobic protein that behaves like a membrane-integral or tightly membrane-associated protein in differential fractionation experiments and contains two predicted transmembrane domains (Reichel and Beachy, 1998; Brill et al., 2000, 2004) involved in ER association (Fujiki et al., 2006). The association with microtubules depends on MP amino acids 1 to 213 required for MP function (Kahn et al., 1998; Boyko et al., 2000b,Boyko et al., 2000c, 2002; Kotlizky et al., 2001). Moreover, certain amino acid exchange mutations known to affect the function of MP in virus movement in a temperature-sensitive manner also affect the ability of MP to interact with microtubules (Boyko et al., 2007,Boyko et al., 2000b). Interestingly, these mutations cluster together in a short domain of 25 amino acids showing a structural similarity with the M-loop of tubulin involved in tubulin-tubulin interactions (Boyko et al., 2000b; Waigmann et al., 2007). Importantly, this M-loop similarity domain overlaps with the predicted transmembrane domain (Brill et al., 2000, 2004) thus suggesting that the association of MP with membranes or microtubules is an alternative event that may depend on specific posttranslational modifications or specific folds of MP. However, although the different subcellular localizations of MPs during the course of infection indicate directional transport of MP from the ER to microtubules and may indicate different folds and functions of the protein when associated with these different subcellular components, the mechanism that controls the subcellular localization and, thus, the fate and function of MP is not known.Here, we identify CELL-DIVISION-CYCLE protein48 (CDC48), named p97/VCP (Valosin-containing protein) in mammals and Cdc48p in yeast (Saccharomyces cerevisiae), as a cellular factor regulating MP subcellular accumulation patterns. CDC48 functions are well characterized in mammalian and yeast systems but remain poorly investigated in plants. Yeast and mammalian CDC48s are essential, conserved chaperones involved in diverse cellular processes by controlling protein fate through extraction of substrates from membranes or complexes (Tsai et al., 2002; Meusser et al., 2005; Römisch, 2005; Rumpf and Jentsch, 2006; Schrader et al., 2009; Eisele et al., 2010; Meyer et al., 2012; Yamanaka et al., 2012). We show that virus infection leads to the induction of Arabidopsis (Arabidopsis thaliana) CDC48 isoforms and demonstrate a function of CDC48 in ER maintenance upon ER stress conditions. We further demonstrate that CDC48 interacts with MP and that CDC48 activity is required for MP degradation. Interaction of CDC48 with MP depends on the MP N terminus, which is required for degradation of the protein, for PD localization and microtubule accumulation of MP, and for function of MP in cell-to-cell transport of the viral RNA. Overexpressed CDC48 shifts MP subcellular localization from ER inclusions to microtubules, suggesting that CDC48 extracts the MP from ER-associated inclusions, where it accumulates in midstages of infection, to the cytosol, where it accumulates along microtubules during late infection stages. Moreover, overexpression of active, but not inactive, CDC48 inhibits virus movement. Our data demonstrate that a CDC48-dependent pathway leading to the clearance of ER-associated protein inclusions exists in plants, that plant viral MPs are substrates for this pathway, and that this pathway determines viral protein fate during infection. We suggest that CDC48-mediated extraction of MP from the ER is part of a plant defense response to remove MP from the ER, the compartment the virus uses for replication and movement.