Predatory Activity of Nematode Trapping Fungi against the Larvae of Trichostrongylus axei and Ostertagia ostertagi: A Possible Method of Biological Control

1973 ◽  
Vol 47 (1) ◽  
pp. 35-48 ◽  
Author(s):  
V. S. Pandey
Keyword(s):  
Biological Control ◽  
Growth Rate ◽  
Arthrobotrys Oligospora ◽  
Ostertagia Ostertagi ◽  
Predatory Activity ◽  
Infective Larvae

Growth rate and activity of 10 nematode trapping fungi, (Hyphomycetes)—Arthrobotrys oligospora, Dactylaria brochopaga, D. gamsospora, D. polycephala, D. thaumasia, D. vermicola, Monacrosporium (Dactylella) bembicodes, M. {D.) cionopaga, M. {D.) ellipsospora, Trichothecium cystosporium—against the infective larvae of Ostertagia ostertagi and Trichostrongylus axei were studied. Species forming adhesive networks grew faster than the others. Species producing adhesive knobs, adhesive branches and constricting rings were, in general, slow growers.

Biological control of Ostertagia ostertagi by feeding selected nematode-trapping fungi to calves

1993 ◽  
Vol 67 (1) ◽  
pp. 31-36 ◽  
Author(s):  
J. Grønvold ◽  
J. Wolstrup ◽  
M. Larsen ◽  
S. A. Henriksen ◽  
P. Nansen
Keyword(s):  
Biological Control ◽  
Present Experiment ◽  
Alimentary Tract ◽  
Field Experiments ◽  
Gastrointestinal Nematodes ◽  
Not Given ◽  
Duddingtonia Flagrans ◽  
Arthrobotrys Oligospora ◽  
Ostertagia Ostertagi ◽  
Infective Larvae

AbstractThree nematode-trapping fungi, one Arthrobotrys oligospora and two Duddingtonia flagrans isolates, were fed to Ostertagia ostertagi-infected calves to test their ability to destroy larvae of this parasite in faeces and consequently to reduce the transmission of infective larvae to herbage. The fungi had previously been selected for their capability to pass the alimentary tract of cattle without losing growth and nematode-trapping potentials. Dung was collected from three calves each fed one of the three fungi and placed as 1-kg cow pats on a parasite-free grass plot together with control cow pats from a calf that was not given fungi. The cow pats contained comparable concentrations of parasite eggs. The two D. flagrans isolates were highly effective in that they reduced herbage larval infectivity by 74–85%. In contrast, A. oligospora did not show any effect in the present experiment. Field experiments will demonstrate if D. flagrans represents a potential organism for biological control of bovine gastrointestinal nematodes under practical agricultural management conditions.

Induction of traps by Ostertagia ostertagi larvae, chlamydospore production and growth rate in the nematode-trapping fungus Duddingtonia flagrans

1996 ◽  
Vol 70 (4) ◽  
pp. 291-297 ◽  
Author(s):  
J. Grønvold ◽  
P. Nansen ◽  
S.A. Henriksen ◽  
M. Larsen ◽  
J. Wolstrup ◽  
...  
Keyword(s):  
Biological Control ◽  
Growth Rate ◽  
Domestic Animals ◽  
Ageing Process ◽  
Parasitic Nematodes ◽  
Duddingtonia Flagrans ◽  
Ostertagia Ostertagi ◽  
Trap Formation ◽  
Nematode Larvae

AbstractBiological control of parasitic nematodes of domestic animals can be achieved by feeding host animals chlamydospores of the nematode-trapping fungus Duddingtonia flagrans. In the host faeces, D. flagrans develop traps that may catch nematode larvae. In experiments on agar, D. flagrans had a growth rate between 15 and 60 mm/week at temperatures between 20 and 30°C. The presence of nematodes induces the fungus to produce traps. The rate of trap formation in D. flagrans has an optimum at 30°C, producing 700–800 traps/cm2/2 days, when induced by 20 nematodes/cm2 on agar. Approaching 10 and 35°C the ability to produce traps is gradually reduced. The response of chlamydospore production on agar to changes in temperature is the same as that for trap formation. On agar, at 10, 20 and 30°C D. flagrans loses its trap inducibility after 2–3 weeks. During the ageing process, increasing numbers of chlamydospores are produced up to a certain limit. The time for reaching maximum chlamydospore concentration coincided with the time for loss of induction potential. The implications of these results in relation to biological control in faeces are discussed.

scholarly journals In vitro biological control of infective larvae of Ancylostoma ceylanicum

2012 ◽  
Vol 21 (3) ◽  
pp. 283-286 ◽  
Author(s):  
Fernanda Mara Fernandes ◽  
Jackson Victor Araújo ◽  
Fabio Ribeiro Braga ◽  
Pedro Henrique Gazzinelli-Guimarães ◽  
Juliana Milani Araujo ◽  
...  
Keyword(s):  
Biological Control ◽  
Gastrointestinal Transit ◽  
Live Weight ◽  
Treated Group ◽  
Control Group ◽  
Ancylostoma Ceylanicum ◽  
Predatory Activity ◽  
Infective Larvae ◽  
Group 10

The aim of this study was to evaluate the predatory activity of the fungus Duddingtonia flagrans (AC001) on infective larvae of Ancylostoma ceylanicum after gastrointestinal transit in hamsters. Twenty animals were used in the experiment, divided into two groups: a treated group (10 animals) and a control group (10 animals). In the group treated with D. flagrans, each animal received mycelium from the AC001 isolate, at an oral dose of 5 mg/25 g of live weight. To evaluate the predatory activity of the fungus, fecal samples were collected from the animals in both groups, at the times of 6, 8, 12, 24 and 36 hours after the treatment. Then, subsamples of 2 g of feces were placed in Petri dishes containing 2% water-agar (2% WA) culture medium and 1000 L3 of A. ceylanicum. Over the study period, the following percentage reductions were observed: 43.2% (6 hours), 30.8% (8 hours), 25.8% (12 hours), 30% (24 hours) and 11% (36 hours). The fungus D. flagrans presented predatory activity on the L3 of A. ceylanicum, after passing through the hamsters' gastrointestinal tract. It was therefore concluded that the fungus D. flagrans may be an alternative for biological control of the L3 of A. ceylanicum.

Predatory activity of nematophagus fungus Duddingtonia flagrans in infective larvae after gastrointestinal transit: biological control in pasture areas and in vitro

2021 ◽  
Vol 95 ◽  
Author(s):  
Barbara Haline Buss Baiak ◽  
Jennifer Mayara Gasparina ◽  
Letícia Ianke ◽  
Karolini Tenffen de Sousa ◽  
Matheus Deniz ◽  
...  
Keyword(s):  
Biological Control ◽  
Gastrointestinal Transit ◽  
Treated Group ◽  
Gastrointestinal Nematodes ◽  
Control Group ◽  
Duddingtonia Flagrans ◽  
Predatory Activity ◽  
Infective Larvae ◽  
Pasture Area

Abstract Biological control is a strategy to decrease parasitic populations, and the action takes place through natural antagonists in the environment. We studied the predatory activity of the fungus Duddingtonia flagrans in infective larvae (L3) of gastrointestinal nematodes after gastrointestinal transit. Ten heifers were divided into two groups: treated (animals received pellets containing fungus) and control (animals received pellets without fungus). Twelve hours after administration, faeces samples were collected for in vitro efficacy tests. The animals then remained for 7 h in the experimental pasture area. At the end of this period, 20 faecal pads (ten treated and ten control) were selected at random. Pasture, faecal pad and soil collections occurred with an interval of 7 days, totalling four assessments. In vitro activity demonstrated that fungi effectively preyed on L3, achieving a reduction percentage of 88%. In the faecal pad of the pasture area, there was a difference (P < 0.05) between collections 3 and 4 for both groups; in the treated group a reduction of 65% was obtained, while in the control group there was an increase of 217% in the number of L3. The recovery of L3 in the soil and in the pasture was similar in both groups. There was no influence (P = 0.87) of the passage time on the fungus predatory activity. Duddingtonia flagrans demonstrated the ability to survive gastrointestinal transit in the animals, reducing the number of L3 in the faeces, indicating that this biological control has great potential in the control of worm infections.

scholarly journals In vitro predatory activity of nematophagous fungi isolated from water buffalo feces and from soil in the Mexican southeastern

2019 ◽  
Vol 28 (2) ◽  
pp. 314-319 ◽  
Author(s):  
Nadia Florencia Ojeda-Robertos ◽  
Liliana Aguilar-Marcelino ◽  
Agustín Olmedo-Juárez ◽  
Carlos Luna-Palomera ◽  
Jorge Alonso Peralta-Torres ◽  
...  
Keyword(s):  
Haemonchus Contortus ◽  
Room Temperature ◽  
Water Buffalo ◽  
Reduction Rate ◽  
Nematophagous Fungi ◽  
Arthrobotrys Oligospora ◽  
Predatory Activity ◽  
Infective Larvae ◽  
Petri Dishes

Abstract Nematophagous fungi from the feces of water buffalo and soil from southeastern Mexico were isolated, and their in vitro predatory activity against Haemonchus contortus infective larvae (L3) (HcL3) was assessed. The fungi were isolated by sprinkling soil or feces on water agar plates. Six series of 10 Petri dishes containing a 7-day-old culture of each fungus and a series without fungi as the control were prepared. Five hundred HcL3 were added to each plate. The plates were incubated at room temperature. The average of recovered HcL3 was considered to estimate the larval reduction rate. Four nematophagous fungi isolates corresponding to Arthrobotrys oligospora, var microspora (strains 4-276, 269 and 50-80) and one identified as A. oligospora,var. oligospora (isolates 48-80) were obtained from water buffalo feces. From the soil, five isolates were isolated; three corresponded to A. musiformis (Bajío, Yumca and Macuspana isolates), and two isolates were identified as A. oligospora (Comalcalco and Jalapa de Méndez isolates). The predatory activity of isolates from water buffalo feces ranged between 85.9 and 100%. Meanwhile, the fungi from the soil ranged between 55.5 and 100% (p≤0.05). The nematophagous fungi obtained could have important implications in the control of parasites of importance in the livestock industry.

The capability of the predacious fungus Arthrobotrys oligospora (Hyphomycetales) to reduce numbers of infective larvae of Ostertagia ostertagi (Trichostrongylidae) in cow pats and herbage during the grazing season in Denmark

1988 ◽  
Vol 62 (4) ◽  
pp. 271-280 ◽  
Author(s):  
J. Grønvold ◽  
P. Nansen ◽  
S. A. Henriksen ◽  
J. Thylin ◽  
J. Wolstrup
Keyword(s):  
The Other ◽  
Arthrobotrys Oligospora ◽  
Ostertagia Ostertagi ◽  
Significant Lowering ◽  
Grazing Season ◽  
Infective Larvae

AbstractArtificially prepared cow pats containing Ostertagia ostertagi eggs were deposited on two pasture plots in May, June and July 1986. Half of the cow pats, placed on one plot, were inoculated with 2000 conidia per gram faeces of the predacious fungus Arthrobotrys oligospora. On the other plot fungus-free control cow pats were placed at the same time. In the faeces generally fewer infective O. ostertagi larvae developed in the inoculated than in the control cow pats. On the herbage around the control cow pats deposited in May, June and July a maxium concentration of infective larvae was found at the same time on the 6th of August 1986. At that time the herbage larval infectivity around inoculated cow pats deposited in May, June and July was subject to a reduction of 48%, 89% and 46%, respectively, compared with fungus-free control cow pats. This experiment indicates that a concentration of 2000 A. oligospora conidia per gram faeces results in a significant lowering of the herbage larval infectivity during the grazing season in Denmark.

scholarly journals Predatory activity of Arthrobotrys oligospora and Duddingtonia flagrans on pre-parasitic larval stages of cyathostominae under different constant temperatures

2001 ◽  
Vol 31 (5) ◽  
pp. 839-842 ◽  
Author(s):  
Clóvis de Paula Santos ◽  
Terezinha Padilha ◽  
Maria de Lurdes de Azevedo Rodrigues
Keyword(s):  
Optimum Temperature ◽  
Duddingtonia Flagrans ◽  
Arthrobotrys Oligospora ◽  
Egg Development ◽  
Free Living ◽  
Predatory Activity ◽  
Larval Stages ◽  
Different Temperatures ◽  
Reduction Percentage

The effect of different temperatures on the predatory activity of Arthrobotrys oligospora and Duddingtonia flagrans on the free-living larval stages of cyathostomes were evaluated in an experiment where feces of horses containing the parasites’ eggs were treated with these fungi and incubated under different constant temperatures (10°C, 15°C, 20°C, 25°C and 30°C ). The results indicated that the optimum temperature for egg development was 25°C. At 10°C the number of L3 recovered was practically zero, and at 15°C and 20°C, the percentage of larvae recovered was less than 3% of the total number of eggs per gram of feces. When these cultures subsequently were incubated for an additional period of 14 days at 27°C, they allowed the development of L3. In all the cultures inoculated with fungi a significant reduction in the number of larvae was observed. When incubated at 25°C or 30°C, the fungi caused reductions above 90%, in the number of L3. The samples cultivated at 10°C, 15°C, 20°C, 25°C and 30°C, when incubated for an additional period of 14 days at 27°C the reduction percentage of larvae was above 90% for A. oligospora. However, the same did not occur for D. flagrans. Here a reduction percentage between 47.5% and 41.8% was recorded when the cultures were incubated at 10°C and 20°C, respectively. The two species of fungi tested showed to be efficient in reducing the number of L3 when mixed with equine feces and maintained at the same temperature for the development of larval pre-parasitic stages of cyathostomes.

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