Anhydrobiotic nematodes were fixed and extracted from dry Mojave desert soils with hot and cold fixatives (5% formalin and 4% gluteraldehyde). Morphologically, extracted nematodes were tightly coiled and shrunken in size. Various concentrations of KCl, ethylene glycol, and sucrose solutions were compared for their effectiveness in extracting viable nematodes still in the anhydrobiotic state. Ap...

Background: The social amoeba Dictyostelium discoideum is a soil-dwelling microbe, which lives most of its life cycle in the vegetative stage as a predator of bacteria and as prey for nematodes. When bacteria are sparse, amoebae aggregate into a multicellular fruiting body. Some clones of D. discoideum have agriculture (Brock et al., 2011). They carry bacteria through the social stage, eat them...

The infectivity of four species of entomopathogenic nematodes, Steinernema carpocapsae (Weiser) [Breton strain], Steinernema riobrave Cabanillas, Poinar & Raulston [Weslaco strain], Heterorhabditis bacteriophora Poinar [HP88 strain], and Heterorhabditis indica Poinar, Karunakar & David [Coimbatore strain] was examined in the laboratory against two subterranean termites: Reticulitermes flavipes ...

It has long been recognized that chemotaxis is the primary means by which nematodes locate host plants. Nonetheless, chemotaxis has received scant attention. We show that chemotaxis is predicted to take nematodes to a source of a chemo-attractant via the shortest possible routes through the labyrinth of air-filled or water-filled channels within a soil through which the attractant diffuses. The...

Infection with parasitic nematodes is characterized by the induction of a profound type 2 immune response. We have studied the role of glycans in the induction of the skewed type 2 response by antigens of the parasitic nematode Brugia malayi as well as the free-living nematode Caenorhabditis elegans. Lymph node cells from BALB/c mice immunized with soluble extracts of the two nematodes showed d...

in order to identify the plant parasitic nematodes of pulse fields in northern khorasan province, 41 soil and root samples were collected from rhizosphere of pisum sp., phaseoulus sp., lens sp. during 2011 and 2012. the nematodes were extracted by combined sieving and centrifugal-flotation method of jenkins (1969) and transferred to glycerin by using method of de grisse (1969). the permanent sl...

Effects of live and dead (heat-killed) infective juveniles (IJs) of the entomopathogenic nematode Steinernema carpocapsae on nematodes associated with boxwood Buxus spp. were evaluated in field experiments during 1999 and 2000. Both living and dead IJs of S. carpocapsae were equally effective, causing more than 50% reduction in total populations of plant-parasitic nematodes relative to the cont...

Trophic interactions of introduced biocontrol fungi with soil animals can bea key determinant in the fungal proliferation and activity.This study investigated trophic interaction of an introduced biocontrol fungus with soil nematodes. The biocontrol fungusTrichoderma harzianum ThzID1-M3 and the fungivorous nematode Aphelenchoides sp. (10 per gram of soil) were added to nonsterile soil, and micr...

Bacteria serve as live food and nutrients for bacterial-feeding nematodes (BFNs) in soils, and influence nematodes behavior and physiology through their metabolism. Five bacterial taxa (Bacillus amyloliquefaciens JX1, Variovorax sp. JX14, Bacillus megaterium JX15, Pseudomonas fluorescens Y1 and Escherichia coli OP50) and the typical BFN Caenorhabditis elegans were selected to study the effects ...

Inactivity in nematodes is often correlated with survival of adverse environments. The non-feeding second-stage juvenile (J2) of Heterodera glycines must survive in a soil environment that may contain numerous toxins. In this report, we show that quiescent J2 of H. glycines survived higher concentrations of both ethanol and the plant-derived compound, allyl isothiocyanate, compared with activel...