Transient expression of a viral histone H4, CpBV-H4, suppresses immune-associated genes of Plutella xylostella and Spodoptera exigua

2010 ◽  
Vol 13 (4) ◽  
pp. 313-318 ◽  
Author(s):  
Jaehyun Kim ◽  
Yonggyun Kim
2008 ◽  
Vol 89 (4) ◽  
pp. 931-938 ◽  
Author(s):  
Wael Gad ◽  
Yonggyun Kim

Histone H4 is highly conserved and forms a central-core nucleosome with H3 in eukaryotic chromatin. Its covalent modification at the protruding N-terminal region from the nucleosomal core can change the chromatin conformation in order to regulate gene expression. A viral H4 was found in the genome of Cotesia plutellae bracovirus (CpBV). The obligate host of the virus is an endoparasitoid wasp, C. plutellae, which parasitizes the diamondback moth, Plutella xylostella, and interrupts host development and immune reactions. CpBV has been regarded as a major source for interrupting the physiological processes during parasitization. CpBV H4 shows high sequence identity with the amino acid sequence of P. xylostella H4 except for an extended N-terminal region (38 aa). This extended N-terminal CpBV H4 contains nine lysine residues. CpBV H4 was expressed in P. xylostella parasitized by C. plutellae. Western blot analysis using a wide-spectrum H4 antibody showed two H4s in parasitized P. xylostella. In parasitized haemocytes, CpBV H4 was detected predominantly in the nucleus and was highly acetylated. The effect of CpBV H4 on haemocytes was analysed by transient expression using a eukaryotic expression vector, which was injected into non-parasitized P. xylostella. Expression of CpBV H4 was confirmed in the transfected P. xylostella by RT-PCR and immunofluorescence assays. Haemocytes of the transfected larvae lost their spreading ability on an extracellular matrix. Inhibition of the cellular immune response by transient expression was reversed by RNA interference using dsRNA of CpBV H4. These results suggest that CpBV H4 plays a critical role in suppressing host immune responses during parasitization.


2020 ◽  
Vol 11 (2) ◽  
pp. 60
Author(s):  
I G.A.A. INDRAYANI ◽  
A. A. AGRA GOTHAMA

<p>ABSTRAK<br />Nematoda  entomopatogen  Steinernema  sp.  telah  banyak<br />dimanfaatkan sebagai agens hayati untuk mengendalikan serangga hama di<br />luar negeri, namun di Indonesia masih terbatas. Tujuan penelitian adalah<br />mengevaluasi efektivitas 3 strain Steinernema sp. lokal terhadap beberapa<br />hama utama tanaman perkebunan dan hortikultura. Penelitian ini dilakukan<br />di Laboratorium Entomologi dan Kebun Percobaan, Balai Penelitian<br />Tanaman Tembakau dan Serat Malang, Jawa Timur, mulai April 2001<br />sampai Mei 2002. Tiga strain nematoda lokal, yaitu BT02, ML07, dan<br />AB05 diuji masing-masing pada konsentrasi 50; 100; 200; 400; dan 800<br />Juvenil infektif (JI)/ml dan satu kontrol (tanpa JI). Sembilan spesies<br />serangga hama yang diuji yaitu Helicoverpa armigera, dan Pectinophora<br />gossypiella (hama kapas), H. assulta dan Myzus persicae (tembakau),<br />Plutella xylostella, dan Crocidolomia binotalis (kubis), Spodoptera exigua<br />(bawang merah), Liriomyza sp. dan S. litura (bunga krisan). Setiap spesies<br />serangga mewakili satu unit pengujian. Setiap perlakuan dalam unit<br />disusun dalam rancangan acak lengkap (RAL) dengan empat ulangan.<br />Aplikasi perlakuan dilakukan dengan metode vial, kultur sel, dan sumuran,<br />tergantung perilaku serangga uji dan menggunakan spray chamber. Di<br />laboratorium, parameter yang diamati adalah sublethal (LC 25 ) dan lethal<br />concentration (LC 50 ), sublethal and lethal time (LT), dan produksi JI. Di<br />lapang, hanya satu perlakuan tunggal yang digunakan yaitu LC 50 dari<br />setiap strain nematoda. Sebanyak masing-masing 20 inang serangga<br />dipajankan daun atau bagian tanaman yang telah disemprot dengan<br />suspensi nematoda di lapang, kemudian serangga uji diamati di<br />laboratorium hingga mati. Hasil penelitian menunjukkan bahwa ketiga<br />strain nematoda menunjukkan efektif membunuh C. binotalis (BT02), P.<br />xylostella, M. persicae (ML07), dan P. gossypiella (AB05), tetapi kurang<br />efektif terhadap H. armigera (AB05), S. exigua dan S. litura (ML07), dan<br />Liriomyza sp. (BT02). Waktu efektif yang diperlukan nematoda untuk<br />membunuh inang (Lethal Time) pada ketiga strain berkisar antara 1-4 hari.<br />Selain efektif membunuh stadia larva, Steinernema sp. juga efektif<br />terhadap prepupa dan pupa.<br />Kata kunci : Tanaman  perkebunan,  hortikultura,  Steinernema  sp.,<br />Helicoverpa armigera, Pectinophora gossypiella, H.<br />assulta, Myzus persicae, Plutella xylostella, Crocidolomia<br />binotalis, Spodoptera exigua, S. litura, Liriomyza sp., juvenil<br />infektif, mortalitas</p><p><br />ABSTRACT<br />Effectiveness of entomopathogenic nematode Steiner-<br />nema sp. against major insect pests of plantation and<br />horticulture<br />Entomopathogenic nematode of family Steinernematidae is a<br />prospective agent for biological control of insect pests. It has been known<br />that many species of insects can be infected by nematode and sometimes<br />showed different levels of infection. Laboratory and field study on the<br />effectiveness of Steinernema sp. against major insect pests of plantation<br />and horticulture was carried out in Laboratory of Entomology and<br />Experimental Station of Indonesian Tobacco and Fiber Crops Research<br />Institute (IToFCRI), Malang, East Java. The objective was to find out the<br />effectiveness of three local strains of Steinernema sp. to any different<br />major of insect pests of plantation and horticulture. Three local strains of<br />nematode tested as BT02, ML07, and AB05 which each consist of five<br />level concentrations of IJ, viz. 50, 100, 200, 400 and 800 IJ/ml and one<br />untreated with IJ as control were tested against nine species of insect, viz.<br />H. armigera, P. gossypiella (cotton), H. assulta and M. persicae (tobacco),<br />P. xylostella and C. binotalis (cabbage), S. exigua (red onion), Liriomyza<br />sp. and S. litura (chrysanthemum). Each species of insect was tested as<br />one unit of test and treated with the same level of concentration. Each<br />treatment in every unit of test was arranged in randomized complete<br />design with four replications. Application method of treatment used were<br />vial, cell culture plate, and well, depends on insect behaviour. Nematode<br />suspension was applied by using spray chamber. Parameters observed<br />were sublethal and lethal concentration, sublethal and lethal time and IJ<br />production. In field study, only one single treatment LC 50 was used to<br />observe the insect mortality. In this study, twenty of insect hosts were fed<br />on treated-sample leaves collected from the field and observed till death.<br />The result showed that all strains of Steinernema sp. were more<br />pathogenic and effective against C. binotallis (BT02), P. xylostella and M.<br />persicae (ML07), and P. gossypiella (AB05), but less pathogenic against<br />H. armigera (AB05), S. exigua and S. litura (ML07), and Liriomyza sp.<br />(BT02). Time needed (LT) to kill the insect host was ranged from one to<br />four days. Strains of nematode tested were not only effective against larvae<br />but also effective to kill prepupae and pupae of insect host.<br />Key words : Estate crops, horticulture, Steinernema sp., H. armigera, P.<br />gossypiella, H. assulta, M. persicae, P. xylostella, C.<br />binotalis, S. exigua, Liriomyza sp, S. litura, infective<br />juvenile, mortality</p>


2004 ◽  
Vol 39 (1) ◽  
pp. 30-45 ◽  
Author(s):  
Robert R. Farrar ◽  
Martin Shapiro ◽  
A. H. McIntosh

The nucleopolyhedrovirus of the diamondback moth, Plutella xylostella (L.), (PxMNPV) was the most potent of three viruses tested against this insect. The potency of PxMNPV could be increased by the addition of certain diaminostilbene disulfonic acid-derived fluorescent brighteners, including Blankophor P167® at a concentration of 1%. Other fluorescent brighteners, including Blankophor HRS® at 1%, reduced the activity of PxMNPV, though lower concentrations of Blankophor HRS (0.25 to 0.5%) enhanced activity. In contrast, Blankophor HRS at 1% enhanced the nucleopolyhedrovirus of the celery looper, Anagrapha falcifera (Kirby), (AfMNPV) against the diamondback moth. Similar results were found in the corn earworm, Helicoverpa zea (Boddie), and the beet armyworm, Spodoptera exigua (Hübner), which are also susceptible to both PxMNPV and AfMNPV. Consumption of foliage treated with Blankophor HRS (0.5 to 1.0%) did not differ from that of foliage treated with similar concentrations of Blankophor P167. These results indicate a negative effect of higher concentrations of Blankophor HRS on PxMNPV, rather than on the host insect.


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