Cellular reactions of the white grub larvae, Polyphylla adspersa, against entomopathogenic nematodes

Nematology ◽  
2014 ◽  
Vol 16 (9) ◽  
pp. 1047-1058 ◽  
Author(s):  
Jamileh Alvandi ◽  
Javad Karimi ◽  
Gary B. Dunphy

The haemocyte reactions of the white grub larvae Polyphylla adspersa to entomopathogenic nematodes (EPN), together with the host haemocyte types, have been studied. Six types of identified haemocytes included the prohaemocytes, granulocytes, plasmatocytes, oenocytoids, coagulocytes and spherulocytes. The granulocytes were the dominant (65.2%) haemocyte type followed by the plasmatocytes (22.1%). Both haemocyte types encapsulate EPN. White grub larvae and last larval stage of Galleria mellonella were individually infected with monoxenic Heterorhabditis bacteriophora or Steinernema glaseri. The maximum total haemocyte counts (THC) level of the white grub larvae against the nematode S. glaseri occurred at 12 h post-injection. In addition, by 8 h post-injection, the granulocyte and plasmatocyte levels decreased. The cell reactions of the grubs against H. bacteriophora in terms of THC and differential haemocyte counts and the encapsulation rate started earlier and were more pronounced than those against S. glaseri. The maximum percentage of the encapsulation observed in the white grub larvae against S. glaseri (27.3 ± 0.7%) and H. bacteriophora (36.5 ± 3.5%) occurred at 12 and 8 h post-injection, respectively. EPN-triggered encapsulation in P. adspersa larvae was more extensive than in G. mellonella larvae.

Nematology ◽  
2009 ◽  
Vol 11 (1) ◽  
pp. 107-116 ◽  
Author(s):  
Naser Eivazian Kary ◽  
Gholamreza Niknam ◽  
Seyed Abolgasem Mohammadi ◽  
Christine Griffin ◽  
Mohammad Moghaddam

AbstractDuring 2002-2004, a survey of entomopathogenic nematodes was conducted for the first time in Iran throughout the three provinces in the north-west of the country. Soil samples were tested for the presence of steinernematid and heterorhabditid nematodes by baiting with Galleria mellonella larvae. Of the 833 soil samples studied 27 were positive for entomopathogenic nematodes (3.2%), with 17 (2.0%) containing Heterorhabditis and ten (1.2%) Steinernema isolates. Morphological and molecular studies were carried out to characterise isolates. The Heterorhabditis isolates were identified as Heterorhabditis bacteriophora and Steinernema as Steinernema carpocapsae, S. bicornutum and S. feltiae. Heterorhabditis bacteriophora was the most common species, which was isolated from 17 sites across the three provinces. Steinernema feltiae was the most common species of Steinernema, which was isolated from eight sites but in only two provinces. Steinernema carpocapsae and S. bicornutum were each isolated from only one site. Steinernema spp. were isolated mainly from orchards and grasslands but Heterorhabditis was isolated mainly from grasslands and alfalfa fields.


Nematology ◽  
2000 ◽  
Vol 2 (4) ◽  
pp. 473-476
Author(s):  
María Bertolotti ◽  
Gladys De Sousa ◽  
Mónica Valenzuela ◽  
María M.A. De Doucet

AbstractEntomopathogenic nematodes of the genus Heterorhabditis are associated with symbiotic bacteria Photorhabdus spp. (Enterobacteriaceae). Taxonomic studies confirm that each species of nematode has a specific natural association with only one species of bacterium (Boemare & Doucet, 1996). Except in a few cases, the bacteria change the colour of the parasitized insect to different reddish tones and produce bioluminescence (Grimont et al., 1984; Boemare & Doucet, 1996). These distinct colours would be assumed to be due to the different species of Photorhabdus and, consequently, to indicate different species of Heterorhabditis. Therefore, the colour of the cadaver has been used as a taxonomic character (Stock, 1993). In a single soil sample from Córdoba City, Argentina, two isolates of Heterorhabditis were found that were clearly distinguished by the colour of the parasitized Galleria mellonella larva: isolate A, violet-brown; B, reddish. These different phenotypes led us to suppose that the nematode isolates were associated with different symbiotic bacteria and that the nematodes were different species. The purposes of this work were: to establish the identity of the isolates and to compare them on the basis of morphological and morphometric characters, and isozyme patterns.


2015 ◽  
Vol 52 (2) ◽  
pp. 118-122 ◽  
Author(s):  
I. A. Susurluk ◽  
T. C. Ulu

Summary Entomopathogenic nematodes (EPNs) are environmentally safe alternative control agents. Nematodes in the Heterorhabditidae and Steinernematidae families are widely used in biological control frameworks, especially for soil-inhabiting insect pests. In this experiment, Heterorhabditis bacteriophora (Poinar, 1976), Steinernema feltiae (Filipjev, 1934) and S. carpocapsae (Weiser, 1955) adapted at high temperature were assessed in order to detect differences in virulence between adapted and non-adapted populations. All species were exposed to 38 °C for 2 h. After this treatment, live infective juveniles (IJs) were used to infect to last instar Galleria mellonella (Linnaeus, 1758). larvae at the following doses: 1, 2, 3, 4 and 5 IJs/larva. The LD50 and LD90 were obtained for these species. Non-adapted populations of the nematode species were used as controls for this experiment. The results indicated that differences in S. feltiae and S. carpocapsae virulence between the adapted and non-adapted populations were significant; no significant difference was observed between the adapted and non-adapted H. bacteriophora populations.


1998 ◽  
Vol 33 (1) ◽  
pp. 40-48 ◽  
Author(s):  
Monica L. Townsend ◽  
Donn T. Johnson ◽  
Don C. Steinkraus

In the laboratory, four nematode species differed significantly in the percentage mortality that each caused in second-instar green June beetles (grubs), Cotinis nitida (L.). Water suspensions of 1,000 infective juveniles (IJ)/one grub/Petri dish each of Heterorhabditis bacteriophora, Steinernema glaseri, and S. feltiae caused 34, 22 and 18% grub mortality, respectively. These values were significantly (P = 0.05) greater than the grub mortality caused by either S. carpocapsae (12%) or the water check (0%) that were similar. Several factors affected third- and fourth-instar susceptibility in the laboratory when exposed to 10,000 S. carpocapsae or H. bacteriophora IJ in 75 g of soil (133 IJ/cm3 soil)/plastic cup. Soil at 30% moisture by weight resulted in significantly more (P= 0.006) dead grubs (6.6%) than at 10% soil moisture (2.8%). Significantly more (P = 0.03) grubs died when at a grub density of 2 grubs/plastic cup (5.6%) than at 1 grub/plastic cup (3.8%). Significantly more (P = 0.01) grubs were killed by either S. carpocapsae and H. bacteriophora at a soil temperature of 25°C (6.5%) than at 12°C (2.8%). There was also a significant interaction of temperature and nematode species. Heterorhabditis bacteriophora killed significantly more (P= 0.02) grubs at 25°C (9.5%) than at 12°C (1.9%) and more than S. carpocapsae killed at either 12°C or 25°C (<3.9%). More virulent nematode strains or species than these four nematode species must be identified if green June beetles are to be controlled by nematodes.


Nematology ◽  
2008 ◽  
Vol 10 (1) ◽  
pp. 137-141 ◽  
Author(s):  
I. Alper Susurluk

Abstract The vertical movement of Turkish isolates of Steinernema feltiae (TUR-S3) and Heterorhabditis bacteriophora (TURH2) was compared at different temperatures in the presence and absence of larvae of the host insect, Galleria mellonella. Nematodes of both species moved faster towards the bottom of the column when an insect was placed there. Steinernema feltiae showed greater vertical dispersal ability than H. bacteriophora. The vertical movement of both species increased as the temperature increased and lower temperatures depressed the movement of H. bacteriophora more than S. feltiae. The nematodes that had migrated different distances were compared for their infectivity to G. mellonella and the positive correlations between distance travelled and infectivity indicate that there is a link between host searching behaviour and infection behaviour in S. feltiae and, to a lesser extent, also in H. bacteriophora.


2016 ◽  
Vol 10 (1) ◽  
pp. 26 ◽  
Author(s):  
Yuliantoro Baliadi ◽  
E. Kondo ◽  
T. Yoshiga

The non-feeding developmentally arrested infective juveniles (IJs) of entomopathogenic nematodes in the family of Steinernematidae and Heterorhabditidae seek out a susceptible insect host and initiate infections. The aim of the research was to examine the continual<br />forming and contribution of IJs produced via endotokia matricida (IJs-EM) of Heterorhabditis bacteriophora, Steinernema glaseri, and S. carpocapsae. The research was conducted at the Laboratory of Nematology of the Saga University, Japan (April 2001-April<br />2002) and the Laboratory of Nematology of the Indonesian Legume and Tuber Crops Research Institute (June 2003-October 2004). The nematode progenies were investigated using the greater wax moth, Galleria mellonella, pre-inoculated with 50 IJs at 25°C.<br />Results showed that three reproductive adult generations were observed at day 18th. There were 135,000, 128,000 and 133,000 IJs per insect cadaver produced in H. bacteriophora, S. glaseri and S. carpocapsae, respectively. Endotokia matricida contributed a higher number of IJs than that of a normal mode of IJs production. The ratios are 81%, 28% and 64% for H. bacteriophora, S. glaseri, and S. carpocapsae of the IJs total production, respectively. Among the generations, the highest contribution of IJs was come from the<br />third adult generation bearing endotokia matricida, i.e., 63%, 24% and 51% for the three nematode species. Although the IJs-EM were more transparent compared to the normal IJs, they were morphologically similar. The results show that endotokia matricida has a pivotal role in a species maintenance and survival strategy of entomopathogenic nematodes in extreme environmental conditions.


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