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Publications

NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.

2021

Abstract

In 2018–2019, establishment problems were encountered, after reseeding creeping bentgrass (Agrostis stolonifera) on a sand-based putting green after ice encasement at the NIBIO Turfgrass Research Center, Norway. Seeds germinated, but the seedlings attained a purple color and died in large patches. Replacement of the top 3 cm layer with new sand amended with Sphagnum peat or garden compost did not solve the problem. To explain this phenomenon, we (1) analyzed the original substrate for nematodes in patches with and without reestablishment failure; and (2) conducted a factorial pot trial with creeping bentgrass and Chewings fescue (Festuca rubra ssp. commutata) seeded on different substrates, some of them in layers, and with and without phosphorus (P) fertilization. The nematode counts showed six times more stubby-root nematodes and two times more spiral nematodes and needle nematodes in the patches with dead seedlings than in the patches with healthy seedings. In the pot trial, the fastest and slowest reestablishment was observed with new sand amended with garden compost and in the two treatments that included the original substrate, respectively. Replacement of the top 3 cm of the old substrate with new garden compost resulted in stagnation of bentgrass seedlings from four weeks after seeding, while fescue seedlings were unaffected. We conclude that the failure to reestablish creeping bentgrass was primarily due to nematodes, which are likely to be more critical for seedlings than for established turf. The green was later reestablished successfully with a 100 % red fescue seed blend.

2020

Abstract

I 2019 års kartlegging av furuvednematoden Bursaphelenchus xylophilus i Norge ble 400 prøver tatt fra hogstavfall og vindfall av Pinus sylvestris L. med angrep av furubukk Monochamus spp. Prøvene ble tatt ut i Akershus, Buskerud, Østfold, Telemark, Aust-Agder og Vest-Agder. Prøvene som besto av flis ble inkubert ved +25oC i to uker før de ble ekstrahert med Baermanntrakt og undersøkt i mikroskop. Furuvednematoden B. xylophilus ble ikke påvist i prøvene, men den naturlig forekommende arten Bursaphelenchus mucronatus kolymensis ble oppdaget i fire prøver fra Agderfylkene. Feller med feromoner for fangst av furubukk ble satt opp i Hedmark (Elverum, Romedal, Stange og ved Geitholmsjøen), Møre og Romsdal (Kvanne) og Østfold (Fredrikstad og Vestby). I laboratoriet ble billene kuttet i biter og ekstrahert med en modifisert Baermanntrakt. Suspensjonen fra ekstraksjonene ble undersøkt i stereomikroskop for forekomst av infektive stadier av Bursaphelenchus spp.. Ingen nematoder kunne påvises i de 106 undersøkte billene. I perioden 2000 – 2019 er totalt 8123 vedprøver analysert. Flest prøver er tatt i Østfold, fulgt av Hedmark, Telemark, Buskerud og Aust-Agder. I kartleggingen 2019 ble B. mucronatus kolymensis påvist i fire av de 400 vedprøvene, tilsvarende en frekvens på 0,01 (1 %). For hele perioden 2000 - 2019 ble Bursaphelenchus mucronatus kolymensis + B. macromucronatus, oppdaget i 73 av 8123 vedprøver som gir en eteksjonsfrekvens på 0,009 (ca. 1 %). I perioden 2014-2019 har Bursaphelenchus mucronatus kolymensis blitt påvist fem av totalt 581 biller, som gir den samme frekvensen som for vedprøver. B. mucronatus kolymensis og B. macromucronatus likner på B. xylophilus i generell biologi og habitatvalg. Hvis vi antar en hypotetisk frekvens i forekomsten til B. xylophilus som er 100 ganger lavere enn for disse naturlig forekommende nematodene, dvs. 0,00009, kan det antall prøver som trengs for en påvisning av B. xylophilus med 95 % konfidensintervall estimeres til 30 801. Dette indikerer at vi i dag hypotetisk sett har nådd bare 26 % av det antall prøver som trengs for å kunne erklære Norge fri for furuvednematoden B. xylophilus.

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Abstract

Shallot (Allium cepa var. aggregatum), a small bulb onion, is widely grown in the world. We previously reported a droplet-vitrification for cryopreservation of in vitro-grown shoot tips of shallot genotype ‘10603’. The present study further evaluated rooting, vegetative growth, bulb production and contents of biochemical compounds, as well as genetic stability in cryo-derived plants. The results showed no significant differences in rooting, vegetative growth, bulb production and contents of soluble sugars and flavonols between the cryo- and in vitro-derived plants. Analyses of ISSR and AFLP markers did not detect any polymorphic bands in the cryo-derived plants. These results indicate rooting and vegetative growth ability, biochemical compounds and genetic stability were maintained in cryo-derived plants. The present study provides experimental evidences that support the use of cryopreservation method for long-term preservation of genetic resources of shallots and other Allium species.

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Abstract

Enset (Ensete ventricosum) is an important starch staple crop, cultivated primarily in south and southwestern Ethiopia. Enset is the main crop of a sustainable indigenous African system that ensures food security in a country that is food deficient. Related to the banana family, enset is similarly affected by plant-parasitic nematodes. Plant-parasitic nematodes impose a huge constraint on agriculture. The distribution, population density and incidence of plant-parasitic nematodes of enset was determined during August 2018. A total of 308 fields were sampled from major enset-growing zones of Ethiopia. Eleven plant-parasitic nematode taxa were identified, with Pratylenchus (lesion nematode) being the most prominent genus present with a prominence value of 1460. It was present in each sample, with a highest mean population density per growing zone of 16 050 (10 g root)−1, although densities as high as 25 000 were observed in fields at higher altitudes in Guraghe (2200-3000 m a.s.l.). This lesion nematode is found in abundance in the cooler mountainous regions. Visible damage on the roots and corms was manifested as dark purple lesions. Using a combination of morphometric and molecular data, all populations were identified as P. goodeyi and similar to populations from Kenya, Uganda and Spain (Tenerife). Differences in population densities amongst cultivars indicate possible resistance of enset to P. goodeyi.

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Abstract

The present study described a combining thermotherapy with meristem culture for improved eradication of onion yellow dwarf virus (OYDV) and shallot latent virus (SLV) from co‐infected in vitro‐cultured shallot shoots. In vitro‐cultured shoots infected with OYDV and SLV were thermo‐treated at a constant temperature of 36°C for 0, 2 and 4 weeks, and then meristems (0.5 mm) containing 1–2 leaf primordia were excised and cultured for shoot regrowth. Meristem culture without thermotherapy produced much higher levels of survival (100%) and shoot regrowth (55%) than those (62% survival and 32% shoot regrowth) produced by the procedure combining 4 weeks of thermotherapy with meristem culture. However, much higher virus‐free frequencies (70% for OYSV, 80% for SLV and 50% for both viruses) were obtained in the latter than those (10% for OYSV, 15% for SLV and 10% for both viruses) obtained in the former. Histological and subcellular studies showed that thermotherapy imposed stress or damage to the cells of meristems, thus resulting in reduced meristem survival and shoot regrowth. Studies on virus location revealed considerable alternations of virus distribution patterns in the thermo‐treated meristems. The results of histological and subcellular studies and analysis of virus distribution pattern added valuable experimental data in the combining thermotherapy with meristem culture for virus eradication. These data provided explanations as to why combining thermotherapy with meristem culture improved the eradication of OYDV and SLV from the virus‐infected in vitro shallot shoots.

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Abstract

Diseases caused by viruses threaten the production industry and food safety of aquaculture which is a great animal protein source. Grass carp reovirus (GCRV) has caused tremendous loss, and the molecular function of viral proteins during infection needs further research, as for most aquatic viruses. In this study, interaction between GCRV major outer capsid protein VP4 and RIG-I, a critical viral RNA sensor, was screened out by GST pull-down, endogenous immunoprecipitation and subsequent LC-MS/MS, and then verified by co-IP and an advanced farred fluorescence complementation system. VP4 was proved to bind to the CARD and RD domains of RIG-I and promoted K48-linked ubiquitination of RIG-I to degrade RIG-I. VP4 reduced mRNA and promoter activities of key genes of RLR pathway and sequential IFN production. As a consequence, antiviral effectors were suppressed and GCRV replication increased, resulting in intensified cytopathic effect. Furthermore, results of transcriptome sequencing of VP4 stably expressed CIK (C. idella kidney) cells indicated that VP4 activated the MyD88-dependent TLR pathway. Knockdown of VP4 obtained opposite effects. These results collectively revealed that VP4 interacts with RIG-I to restrain interferon response and assist GCRV invasion. This study lays the foundation for anti-dsRNA virus molecular function research in teleost and provides a novel insight into the strategy of immune evasion for aquatic virus.