Survey of Incidence of Pigeonpea Cyst Nematode (Heterodera cajani) and Wilt Complex of Pigeonpea in parts of North Eastern Karnataka

2018 ◽  
Vol 6 (2) ◽  
pp. 1483-1487
Author(s):  
Saddamhusen Alase ◽  
ZooKeys ◽  
2011 ◽  
Vol 135 ◽  
pp. 1-19 ◽  
Author(s):  
Uma Rao ◽  
Sashi Rao ◽  
Anamika Rathi ◽  
Ragini Gothalwal ◽  
Howard Atkinson

Agronomy ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1457
Author(s):  
Yu Yu Min ◽  
Thu Htet Naing ◽  
Nwe Nwe Htun ◽  
Aung Kyaw Myint ◽  
Yuri Ichinose ◽  
...  

The pigeon pea cyst nematode, Heterodera cajani, is an economically important plant-parasitic nematode in sesame production. The objective of the study was to investigate distribution of H. cajani in the major sesame producing areas in Myanmar. Before cultivation, soil samples were collected in 96 local farmer’s fields: (19 fields in Magway, 20 fields in Mandalay, 14 fields in Sagaing and 43 in Nay Pyi Taw), and nematode density was quantified by real-time PCR. The cyst nematode was detected in 63.2% of the fields in Magway and the mean density was 22.6 eggs equivalent (20 g soil)−1. In Mandalay and Nay Pyi Taw, the cyst nematode was detected in 40.0% and 18.6% of the fields with the mean densities of 9.9 and 21.0 eggs equivalent (20 g soil)−1, respectively. By contrast, the cyst nematode was not detected in Sagaing fields, in which sesame is rotated with paddy rice. Infestation of root-knot nematodes (RKN, Meloidogyne spp.) was also evaluated, because sesame is generally rotated with rice and pulses, which are attacked by RKN. The results showed 25.6% infestation of RKN with a mean density of 34.3 eggs equivalent (20 g soil)−1 only in Nay Pyi Taw, while there was no infestation in Magway, Mandalay, and Sagaing. The relationships between the nematode infestation level and the cropping patterns in each sesame growing area in Myanmar were discussed.


Nematologica ◽  
1970 ◽  
Vol 16 (4) ◽  
pp. 477-482 ◽  
Author(s):  
C.L. Sethi ◽  
P.K. Koshy ◽  
G. Swarup

Author(s):  
Amit Kumar Maurya ◽  
Sobita Simon ◽  
Vinny John ◽  
Abhilasha A. Lal

A survey was conducted in selected villages of Prayagraj district to evaluate the disease incidence of Fusarium (Fusarium udum) wilt and cyst nematode (Heterodera cajani) of pigeon pea (Cajanus cajan). Soil and roots were collected from the rhizosphere of infested pigeonpea plants. The maximum wilt incidence was recorded (57.6%) in Dari village followed by Pump House (56%), Pahlu ka Purwa (51.2%) and the lowest incidence of wilt was recorded in Chaka (12.8%), Naini (11.2%) and Jhusi (9.6%) in the year 2016. For cyst nematode, soil samples was collected from selected fields, the soil was mixed thoroughly and 500 g of the soil was processed following Cobb’s sieving and decanting method where cyst and J2’s were separated in separate mesh size sieves. It was observed that infestation of Heterodera cajani was very high in Jari (51%) followed by Naini (41%). The minimum infestation of Heterodera cajani was found in Meza village which was responsible for wilt disease in pigeonpea concluding that Fusarium wilt of pigeonpea is a major problem in Prayagraj district of U.P. India.


Nematology ◽  
2021 ◽  
pp. 1-6
Author(s):  
Tatiana V. Roubtsova ◽  
Sergei A. Subbotin

Summary The pigeon pea cyst nematode, Heterodera cajani, is an important nematode pest of pigeon pea that is present in all major growing regions of this crop in India and reported from Pakistan, Egypt and Myanmar. In this study, a new real-time PCR assay for detection of H. cajani using a species-specific primer and a TaqMan probe was developed. The primers and a probe were designed to amplify the COI gene fragment. The specificity of the primer-probe set was tested in singleplex or multiplex reactions against target and non-target nematodes. In multiplex real-time PCR experiments with the specific and universal primer-probe sets, the signals were simultaneously observed for COI and D3 of 28S rRNA target genes. The results showed that the real-time PCR assay with species-specific primer and probe was sensitive enough to detect H. cajani DNA extracted from 0.003 egg or second-stage juvenile.


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