Transfer of resistance to beet cyst nematode from Beta patellaris to sugar beet

Euphytica ◽  
1983 ◽  
Vol 32 (2) ◽  
pp. 287-298 ◽  
Author(s):  
W. Heijbroek ◽  
A. J. Roelands ◽  
J. H. De Jong
2021 ◽  
pp. 394-399
Author(s):  
Matthias Daub

Abstract The beet cyst nematode (BCN) was one of the first discovered plant parasitic nematodes. Heterodera schachtii was observed in 1859 in Halle in Central Germany by the botanist Herman Schacht and described later by Adolf Schmidt in 1871, who named this cyst nematode species after its original discoverer. Partly due to the lack of knowledge about the effect of sugar beet monocultures on the population build-up of BCN, this nematode had a devastating impact on sugar production in 1876 that led to the shutdown of 24 sugar factories in Germany. This chapter discusses the economic importance, distribution, host range, damage symptoms, biology and life cycle, interactions with other nematodes and pathogens, recommended integrated management, and management optimization of H. schachtii. Future research requirements and future developments are also mentioned.


Agronomy ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 355
Author(s):  
Daub Matthias

The integration of oilseed rape (OSR) into sugar beet rotation systems is restricted due to the very good host status of OSR for the beet cyst nematode (BCN) Heterodera schachtii. In contrast to sugar beet, the cultivation of winter OSR covers a longer period, but at a lower soil temperature regime. Thus, presumably one or two generations of BCN may develop during the cultivation of winter OSR, resulting in moderate multiplication rates of 1–2 in the present study. This multiplication rate was year-dependent, but not affected by different sowing times. For the first time, the present study identified volunteer OSR emerging in high densities post-harvest as a major risk for a high multiplication of BCN at optimum temperatures. The emergence of BCN females with offspring was observed very early, resulting in a significant population increase before 350-degree days (>8 °C) in inoculation experiments and in field investigations. Conducting treatment trials with glyphosate to control volunteer OSR in micro-plots and field experiments confirmed effective suppression of BCN reproduction when growth of volunteer OSR was interrupted at 250–350-degree days. Thus, data gained from BCN reproduction studies under controlled and field conditions provided a unique basis for the development of a trap crop method. The degree day model has been successfully implemented as part of an open access management tool.


2017 ◽  
Vol 119 ◽  
pp. 192-196 ◽  
Author(s):  
Saeed Sadeghzadeh Hemayati ◽  
Mohammad-Reza Jahad-e Akbar ◽  
Ali-Reza Ghaemi ◽  
Parviz Fasahat

Life ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1358
Author(s):  
Chen Jiang ◽  
Yingdong Zhang ◽  
Ke Yao ◽  
Sulaiman Abdulsalam ◽  
Guangkuo Li ◽  
...  

Sugar beet cyst nematode (SBCN, Heterodera schachtii) is an important nematode that causes significant yield losses of 25–50% or more in most areas of sugar beet production worldwide. Rapid and accurate identification of this species is essential to support decisions on pest management. However, the difference between H. schachtii and other Heterodera spp. based on morphology is a challenging task. In the present study, a SCAR-PCR assay was developed to identify and differentiate H. schachtii in infected root and soil samples. H. schachtii-species-specific SCAR-PCR primers OPA06-HsF and OPA06-HsR were designed from the randomly amplified polymorphic DNA (RAPD) marker amplified with random primer OPA06. The developed primers specifically amplify a 922-bp fragment from the target populations but did not amplify DNA from non-target cyst nematodes including Heterodera, Globodera, Cactodera, and other related species tested in this study. The sensitivity detection indicated that 5 × 10−4 of a single cyst, 1/320 of a single second-stage juvenile (J2), or 10 pg of genomic DNA could be detected. The assay accurately identifies the different stages of H. schachtii in sugar beet and oilseed rape roots as well as a single J2 in 10 g of soil. Finally, the SCAR-PCR assay detected H. schachtii in seven samples out of the fifteen field samples. The assay will not only be useful for differentiating H. schachtii from mixed populations of Heterodera spp. but also for effective detection of the species directly from infested samples. The assay also requires no expertise in the taxonomy and morphology of the species but serves to improve the diagnosis of H. schachtii in infested fields.


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