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Efficacy of Monacrosporium thaumasium in the control of goat gastrointestinal helminthiasis in a semi-arid region of Brazil
(Parasitology Research, 2013-02) Braga, Fabio Ribeiro; Araújo, Jackson Victor de; Vilela, Vinícius Longo Ribeiro; Feitosa, Thais Ferreira; Lucena, Samuel Cavalcante de; Dantas, Elaine Silva; Athayde, Ana Célia Rodrigues; Silva, Wilson Wouflan
The aim of the present study was to test a pellet formulation of Monacrosporium thaumasium in a sodium alginate matrix in the biological control of goat gastrointestinal helminthiasis in a semi-arid region of northeastern Brazil. An area of 2.4 ha was divided into three paddocks, with seven goats kept on each paddock, during the months of March to August 2011: group 1 received 3 g/10 kg live weight of M. thaumasium pellets (NF34a) twice a week; group 2 was given 0.2 mg/kg of 0.2 % moxidectin orally every 30 days; and group 3 received 3 g/10 kg live weight of pellets without fungus twice per week. Each month, two tracer goats was placed in each group for 30 days and then killed and necropsied. The M. thaumasium group showed a 34 % reduction in eggs per gram, higher packed cell volume rates and a lower parasitic load in the tracers compared with the other groups. The 0.2 % moxidectin group had weight gain of 5.7 kg; the M. thaumasium group, 3.6 kg; and the control group had an average reduction in weight of 1.1 kg. The use of M. thaumasium pellets may be effective as an alternative method to control goat gastrointestinal helminthiasis in the semi-arid region of northeastern Brazil.
Fungi predatory activity on embryonated Toxocara canis eggs inoculated in domestic chickens (Gallus gallus domesticus) and destruction of second stage larvae
(Parasitology Research, 2015-09) Araújo, Jackson Victor de; Fonseca, Leandro Abreu da; Hiura, Emy; Lopes, Aline del Carmen Garcia; Paz, Jeanne Saraiva da; Gava, Maylla Garschagen; Flecher, Mayra Cunha; Colares, Manuela; Soares, Filippe Elias de Freitas; Lacerda, Tracy; Braga, Fabio Ribeiro
The objective of this study was to evaluate the infectivity of Toxocara canis eggs after interacting with isolated nematophagous fungi of the species Duddingtonia flagrans (AC001) and Pochonia chlamydosporia (VC4), and test the predatory activity of the isolated AC001 on T. canis second stage larvae after 7 days of interaction. In assay A, 5000 embryonated T. canis eggs previously in contact with the AC001 and VC4 isolated for 10 days were inoculated into domestic chickens (Gallus gallus domesticus), and then these animals were necropsied to collect material (digested liver, intestine, muscles and lungs) at 3-, 7-, 14-, and 21-day intervals after inoculation. In assay A, the results demonstrated that the prior interaction of the eggs with isolated AC001 and VC4 decreases the amount of larvae found in the collected organs. Difference (p < 0.01) was observed in the medium larvae counts recovered from liver, lung, intestine, and muscle of animals in the treated groups when compared to the animals in the control group. At the end of assay A, a percentage reduction of 87.1 % (AC001) and 84.5 % (VC4) respectively was recorded. In the result of assay B, the isolated AC001 showed differences (p < 0.01) compared to the control group, with a reduction of 53.4 % in the recovery of L2. Through these results, it is justified to mention that prior interaction of embryonated T. canis eggs with the tested fungal isolates were efficient in reducing the development and migration of this parasite, in addition to the first report of proven predatory activity on L2.
Biological control of goat gastrointestinal helminthiasis by Duddingtonia flagrans in a semi-arid region of the northeastern Brazil
(Veterinary Parasitology, 2012-08-13) Braga, Fabio Ribeiro; Araújo, Jackson Victor de; Vilela, Vinícius Longo Ribeiro; Feitosa, Thais Ferreira; Souto, Diego Vagner de Oliveira; Santos, Herbis Eduardo da Silva; Silva, Gabriela Lucena Longo da; Athayde, Ana Célia Rodrigues
The aim of this study was to test a pellet formulation in a sodium alginate matrix of Duddingtonia flagrans in the biological control of goat gastrointestinal helminths kept in a native pasture in a semi-arid region of Paraíba state, northeastern Brazil. An area of 2.4 ha was divided into three paddocks, where groups of seven goats ware formed. Each group received the following treatments during the months of March to August 2011: D. flagrans group, received 3 g of pellets containing D. flagrans (AC001) for each 10 kg/l. w., twice a week; Moxidectin 0.2% group, received 0.2 mg/kg of Moxidectin 0.2% orally, every 30 days; Control group, received 3 g of pellets without fungi per 10 kg/l. w., twice a week. Each month, a tracer goat was placed in each group for 30 days and then sacrificed and necropsied. The D. flagrans group showed a greater reduction in EPG, increased weight gain, higher rates of packed cell volume and lower parasitic load burden in the tracer goats compared to Moxidectin 0.2% and Control groups. D. flagrans was efficient in controlling goat gastrointestinal helminthiasis in a semi-arid region of northeastern Brazil.
Activity of the nematophagous fungi Pochonia chlamydosporia, Duddingtonia flagrans and Monacrosporium thaumasium on egg capsules of Dipylidium caninum
(Veterinary Parasitology, 2009-12-03) Araujo, Juliana Milani; Araújo, Jackson Victor de; Braga, Fabio Ribeiro; Carvalho, Rogério Oliva; Ferreira, Sebastião Rodrigo
Nematophagous fungi are potential biological control agents of helminths. The in vitro ovicidal effect of four isolates of the nematophagous fungi Pochonia chlamydosporia (VC1 and VC4), Duddingtonia flagrans (AC001) and Monacrosporium thaumasium (NF34) was evaluated on egg capsules of Dipylidium caninum, a cestode parasite of dogs, cats and humans. One thousand egg capsules of D. caninum were plated on 2% water-agar with the grown isolates and control without fungus. The ovicidal activity of these fungi was evaluated 5, 10 and 15 days after incubation. Only P. chlamydosporia showed ovicidal activity (p < 0.05) on D. caninum egg capsules, of 19.6% (VC1) and 20% (VC4) on the 5th day; 44.2% (VC1) and 31.5% (VC4) on the 10th day; and 49.2% (VC1) and 41.9% (VC4) on the 15th day. D. flagrans and M. thaumasium caused no morphological damage to egg capsules. The results demonstrated that P. chlamydosporia was in vitro effective against capsules and eggs of D. caninum, and can be considered as a potential biological control agent for this helminth.
In vitro predatory activity of nematophagous fungi Duddingtonia flagrans on infective larvae of Oesophagostomum spp. after passing through gastrointestinal tract of pigs
(Tropical Animal Health and Production, 2011-04-06) Ferreira, Sebastião Rodrigo; Araújo, Jackson Victor de; Braga, Fabio Ribeiro; Araujo, Juliana Milani; Fernandes, Fernanda Mara
One isolate of predator fungi Duddingtonia flagrans (AC001) was assessed in vitro regarding the capacity of supporting the passage through pigs' gastrointestinal tract without loss of the ability of preying infective larvae Oesophagostomum spp. Fungal isolates survived the passage and were efficient in preying L3 since the first 8 h of collection (p < 0.01) in relation to the control group (without fungus). Compared with control, there was a significant decrease (p < 0.01) of 59.6% (8 h), 71.7% (12 h), 76.8% (24 h), 81.0% (36 h), 78.0% (48 h), 76.1% (72 h), and 82.7% (96 h) in means of infective larvae Oesophagostomum spp. recovered from treatments with isolate AC001. Linear regression coefficients of L3 of recovered Oesophagostomum spp. regarding the collections due to time were −0.621 for control, −1.40 for AC001, and −2.64 for NF34. Fungi D. flagrans (AC001) had demonstrated to be promising for use in the biological control of pig parasite Oesophagostomum spp.
Control of sheep gastrointestinal nematodes using the combination of Duddingtonia flagrans and Levamisole Hydrochloride 5%
(Revista Brasileira de Parasitologia Veterinária, 2018-02-05) Braga, Fabio Ribeiro; Vilela, Vinícius Longo Ribeiro; Braga, Fabio Ribeiro; Vieira, Vanessa Diniz; Lucena, Samuel Cavalcante de; Araújo, Jackson Victor de
The objective was to evaluate the action of D. flagrans pellets in association with Levamisole Hydrochloride 5% for controlling sheep gastrointestinal nematodes in the northeastern Brazil. Three groups of six sheep each were formed: group 1 received 3 g of the pellets (0.6 g of D. flagrans mycelium) for each 10 kg b.w., twice a week for six months, and deworming with Levamisole Hydrochloride 5% when EPG ≥ 1500; group 2 received a dosage of Levamisole Hydrochloride 5% when EPG ≥ 1500; and group 3 received 3 g of pellets without fungi for each 10 kg b.w., twice a week for six months. EPG counts, larval cultures, packed cell volume (PCV) and weighing were performed every 15 days; monthly, samples of grass from each paddock were collected. The mean EPG of the groups began to statistically differ from day 30 (p < 0.05). Group 1 required less deworming with Levamisole Hydrochloride 5% and showed superiority of PCV values throughout the experiment (p < 0.05). There was a significant reduction (p < 0.05) in L3 recovery in the group 1 paddock from day 30 onwards. The use of D. flagrans pellets in association with Levamisole Hydrochloride 5% was effective for controlling gastrointestinal nematodes.
Effect of the fungus Pochonia chlamydosporia on Echinostoma paraensei (Trematoda: Echinostomatidae)
(Acta Tropica, 2014-07-10) Lelis, Rosane Teixeira; Braga, Fabio Ribeiro; Carvalho, Lorendane Millena de; Paula, Alessandra Teixeira de; Araujo, Juliana Milani; Fausto, Mariana Costa; Rodrigues, João Victor Facchini; Soares, Filippe Eliasde Freitas; Araújo, Jackson Victor de; Maldonado Junior, Arnaldo; Garcia, Juberlan Silva
Echinostoma paraensei is a trematode of the genus Echinostoma that causes echinostomiasis in humans. The objectives of this study were to: evaluate the ovicidal activity of the nematophagous fungus Pochonia chlamydosporia (VC1 and VC4) on a solid medium 2% water–agar (2% WA) against E. paraensei eggs (assay A); evaluate ovicidal effect (destruction of eggs) of the isolate VC4 in supplemented culture media (assay B); and evaluate the ovicidal ability of the crude extract (VC4) on E. paraensei eggs (assay C). Eggs of E. paraensei (assay A) were placed in Petri dishes containing 2% WA with an isolate of the fungus P. chlamydosporia (VC1 and VC4) grown for 10 days, and without fungus as a control and evaluated regarding their destruction. In assay B, eggs of E. paraensei were placed in Petri dishes with different supplemented culture media and with VC4 isolate and the destruction of eggs was examined at the end of 25 days of interaction. In assay C, effects of the crude extract of P. chlamydosporia (VC4) on eggs were evaluated at the end of 7 days. In assay A, there was no difference (p > 0.05) in ovicidal activity among the tested isolates (VC1 and VC4); however, the highest percentage for ovicidal activity (type 3 effect) was demonstrated by the isolate VC4. In assay B, the culture medium starch–agar showed the best results for the destruction of the eggs, with a percentage of 46.6% at the end of the assay. In assay C, the crude extract of VC4 was effective in the destruction of E. paraensei eggs, with a percentage reduction of 53%. The results of this study demonstrate that a rich culture medium with a greater availability of carbon and nitrogen may interfere directly in the predatory characteristics of ovicidal fungi.
Duddingtonia flagrans formulated in rice bran in the control of Oesophagostomum spp. intestinal parasite of swine
(Experimental Parasitology, 2017-11-10) Rodrigues, Joao Victor Facchini; Braga, Fabio Ribeiro; Campos, Artur Kanadani; Carvalho, Lorendane Millena de; Araujo, Juliana Milani; Aguiar, Anderson Rocha; Ferraz, Carolina Magri; Silveira, Wendeo Ferreira da; Valadao, Marisa Caixeta; Oliveira, Thais de; Freitas, Samuel Galvao de; Araújo, Jackson Victor de
Three experimental assays with Duddingtonia flagrans (isolated AC001) were carried out. The growth of the genus Duddingtonia present in formulation of rice bran, its predatory capability on Oesophagostomum spp. infective larvae (L3) in petri dishes (assay 1), its action in faecal cultures with eggs of that parasite (assay 2) and isolate's capability of predation after passing through gastrointestinal tract of swine (assay 3) was evaluated. At assay 3, feces were collected at time intervals of 12, 24, 36, 48, and 60 h after feed animals with the formulation. Assays 1 and 2 showed a statistical difference (p < 0.01) by the F test when comparing the treated group with the control group. At the both assays, was observed in the treated group a reduction percentage of 74.18% and 88.38%, respectively. In assay 3, there was a statistical difference between the treated group and the control group at all collection times (p < 0.01). Regarding the collection periods, there was no statistical difference over time in the treatment group (p > 0.05). The results demonstrate that the fungal isolate AC001 formulated in rice bran can prey on L3 of Oesophagostomum spp., in vitro and after passing through the gastrointestinal tract, without loss of viability. This isolate may be an alternative in the control of Oesophagostomum spp. in swine.
Nematophagous fungi for biological control of gastrointestinal nematodes in domestic animals
(Applied Microbiology and Biotechnology, 2013-11-22) Braga, Fabio Ribeiro; Araújo, Jackson Victor de
Several studies have been conducted using fungi in the biological control of domestic animals and humans. In this respect, a large amount of research has been undertaken to understand the particularities of each fungus used. These fungi have been demonstrated to act on all classes of helminthes. Therefore, they should not only be called nematophagous but also helmintophagous. Evidence of enzymatic action has also revealed their mechanism of action, as well as potential metabolites that could be synthesized as bioactive molecules. Cultural barriers to the use of fungi should be broken down, since the impact on the environment is minimal. In this context, much is already known about the mechanism of interaction of these organisms with their ‘targets’. Recent research has pointed to the search for substances derived from nematophagous fungi that have demonstrated their ovicidal and/or larvicidal activity, thus being a global premise to be studied further. Crude extracts derived from nematophagous fungi of predator and ovicidal groups reduce the amount of larvae of gastrointestinal nematodes and prevent the hatching of their eggs, since they have been demonstrated to act with extracellular proteases and other enzymes. Furthermore, the activity of these enzymes has begun to be explored regarding their possible interaction with the exoskeleton of arthropods, which could emerge as an alternative method of tick control. Finally, it should be clear that nematophagous fungi in general are ‘old friends’ that are ready to the ‘fight with our old enemies’, the gastrointestinal helminth parasites harmful to human and animal health.
Fungal antagonism assessment of predatory species and producers metabolites and their effectiveness on Haemonchus contortus infective larvae
(BioMed Research International, 2015-07-21) Silva, Manoel Eduardo; Braga, Fabio Ribeiro; Gives, Pedro Mendoza de; Millán-Orozco, Jair; Uriostegui, Miguel Angel Mercado; Marcelino, Liliana Aguilar; Soares, Filippe Elias de Freitas; Araújo, Andréia Luiza; Vargas, Thainá Souza; Aguiar, Anderson Rocha; Senna, Thiago; Rodrigues, Maria Gorete; Froes, Frederico Vieira; Araújo, Jackson Victor de
The objective of this study was to assess antagonism of nematophagous fungi and species producers metabolites and their effectiveness on Haemonchus contortus infective larvae (L3). Assay A assesses the synergistic, additive, or antagonistic effect on the production of spores of fungal isolates of the species Duddingtonia flagrans, Clonostachys rosea, Trichoderma esau, and Arthrobotrys musiformis; Assay B evaluates in vitro the effect of intercropping of these isolates grown in 2% water-agar (2% WA) on L3 of H. contortus. D. flagrans (Assay A) produced 5.3 × 106 spores and associated with T. esau, A. musiformis, or C. rosea reduced its production by 60.37, 45.28, and 49.05%, respectively. T. esau produced 7.9 × 107 conidia and associated with D. flagrans, A. musiformis, or C. rosea reduced its production by 39.24, 82.27, and 96.96%, respectively. A. musiformis produced 7.3 × 109 spores and associated with D. flagrans, T. esau, or C. rosea reduced its production by 99.98, 99.99, and 99.98%, respectively. C. rosea produced 7.3 × 108 conidia and associated with D. flagrans, T. esau, or A. musiformis reduced its production by 95.20, 96.84, and 93.56%, respectively. These results show evidence of antagonism in the production of spores between predators fungi.

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