Autophagy and apoptosis function as important early cellular defense mechanisms in infections and other diseases. The outcome of an infection is determined by a complex interplay between the pathogenic microorganism and these intracellular pathways. To better understand the cytopathogenicity of Herpes simplex virus types 1 and 2 (HSV-1 and -2), we studied the effect of these viruses on the autophagic and apoptotic processes in the SIRC corneal cell line. Infection with the KOS strain of HSV-1 and a wild-type strain of HSV-2 enhanced autophagosome formation, triggered cytoplasmic acidification, increased LC3B lipidation and elevated the ratio of apoptotic cells. The autophagy inhibitor bafilomycin A1 triggered a significant increase in the apoptotic responses of HSV-1- and HSV-2-infected cells. Thus, both HSV types affect autophagy and apoptosis in a coordinated fashion, and autophagy plays cytoprotective role in HSV-infected cells via antagonizing apoptosis. Together these data implicate autophagy in the pathogenic mechanism of herpetic keratitis.

Our earlier research showed that an interspecific tobacco hybrid ( Nicotiana edwardsonii ‘Columbia’ [NEC]) displays elevated levels of salicylic acid (SA) and enhanced resistance to localized necrotic symptoms (hypersensitive response [HR]) caused by tobacco mosaic virus (TMV) and tobacco necrosis virus (TNV), as compared with another interspecific hybrid ( Nicotiana edwardsonii [NE]) derived from the same parents. In the present study, we investigated whether symptomatic resistance in NEC is indeed associated with the inhibition of TMV and TNV and whether SA plays a role in this process. We demonstrated that enhanced viral resistance in NEC is manifested as both milder local necrotic (HR) symptoms and reduced levels of TMV and TNV. The presence of an adequate amount of SA contributes to the enhanced defense response of NEC to TMV and TNV, as the absence of SA resulted in seriously impaired viral resistance. Elevated levels of subcellular tripeptide glutathione (GSH) in NEC plants in response to viral infection suggest that in addition to SA, GSH may also contribute to the elevated viral resistance of NEC. Furthermore, we found that NEC displays an enhanced resistance not only to viral pathogens but also to bacterial infections and abiotic oxidative stress induced by paraquat treatments. [ ] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .

Our previous research has demonstrated the role of optimal temperatures and reactive oxygen species (ROS) in maintaining symptomless nonhost resistance (NHR) of barley to powdery mildews. However, the exact functions of temperature and ROS in NHR of plants, including barley, to viral infections are not known. Although barley is a nonhost for Tobacco mosaic virus (TMV), this virus can replicate in barley leaves at temperatures of ca. 30 °C. Here we elucidated the influence of short-term heat stress pre-treatments (30 °C, 3 h; heat shock at 49 °C, 20 s) on the symptomless NHR of barley to TMV and the role of the ROS superoxide (O₂^.−) in maintaining NHR. Heat stress and antioxidant (superoxide dismutase and catalase, SOD + CAT) treatments resulted in 50–100% higher TMV levels, while combined heat shock and SOD + CAT application caused further increases in TMV and appearance of cell and tissue death resembling a hypersensitive response (HR). An early (from 2 h after inoculation) burst of O₂^.− was essentially absent in TMV-infected barley exposed to short-term heat stress pre-treatments. Expression of barley genes regulating ROS (O₂^.−) metabolism (HvRBOHF2, HvSOD1) and cell death (HvBI-1) displayed an inverse correlation with TMV levels even at later time points (1–4 days after inoculation), implying a role in symptomless NHR, while increased levels of the antioxidant glutathione marked heat stress-induced suppression of NHR. We demonstrated that short-term heat stress and antioxidant treatments result in compromised NHR of barley to TMV, pointing to the role of optimal temperatures and ROS (O₂^.−) in symptomless NHR to virus infections.

A Hungarian cherry pepper (Capsicum annuum var. cerasiformé) cultivar ('Szentesi') displays resistance to pepper powdery mildew caused by Leveillula taurica. Resistance also develops in susceptible sweet pepper (C. annuum) when grafted on resistant cherry pepper cv. Szentesi rootstocks. Powdery mildew (PM) resistance is correlated with high levels of the defense regulator reactive oxygen species superoxide (O2 ') even in healthy plants. In order to further elucidate the mechanisms of preformed defense responses in cherry pepper cv. Szentesi we have monitored levels of salicylic acid (SA), a key molecule of plant defense signaling and expression of so-called pathogenesis/defense related (PR) genes in healthy pepper plants. Assays of free and bound (glycosylated) SA by high performance liquid chromatography (HPLC) revealed that in leaves of PM-resistant pepper levels of free SA are ca. twice as high compared to that of PM-sensitive plants. No difference occurred in levels of bound (glycosylated) SA. Expression of the CaPR-1 gene was several times higher in leaves of PM-resistant pepper than in sensitive plants as assayed by real time reverse transcription quantitative polymerase chain reaction (real time RT-qPCR). On the other hand, high expression levels of the CaPR-2 (glucanase) gene did not entirely correlate with PM-resistance, being detectable only in PM-resistant cv. Szentesi plants but neither in PM-resistant sweet pepper cv. Totál grafted on cv. Szentesi rootstocks nor in susceptible controls (cv. Totál). It seems that graft-transmissible PMresistance of the cherry pepper cv. Szentesi is correlated not only with high levels of superoxide but also with elevated levels of free salicylic acid and enhanced expression of the defense-related CaPR-1 gene.

Muscari species are widely cultivated, popular ornamental plants in Europe, but are susceptible to rust fungi, which can substantially reduce their aesthetic value and overall fitness. In May 2023, characteristic rust fungus-like symptoms were observed on M. armeniacum plants in Solymár (Hungary). The causal agent, designated as isolate UmHu2, was identified as Uromyces muscari based on morphological studies and results of molecular phylogenetic analyses, which included three reference specimens from Hungary and one from Canada collected on other Muscari species. Features of the rust infections and spores produced were consistent with previous descriptions. Sequences generated four gene regions, ITS and LSU rDNA, β-tubulin and translation elongation factor 1-alpha, showed 98-100 % identity and grouped with strong support together in multi-gene maximum likelihood phylogenetic analyses with selected Pucciniaceae rusts. Pathogenicity was confirmed by artificial inoculation of healthy M. armeniacum plants. Microscopic investigation and sequencing verified consistency with the inoculum, thereby fulfilling Koch's postulates. Cross-infection experiments demonstrated that U. muscari isolates from different Muscari species are genus-specific but not species-specific. To our knowledge, this is the first report of U. muscari infecting M. armeniacum in Hungary.