A molecular and morphological study of Ascaris suum in a human-pig contact scenario in northeastern Brazil / Estudo molecular e morfológico de Ascaris suum em um cenário de contato entre suínos e humanos no nordeste brasileiro

The aim of the present study was to assess morphologic and genetic data on ascariasis in swine (Sus scrofa domesticus) and humans in low-resource rural and periurban communities in the state of Piauí, Brazil. Our cross-sectional survey included 100 fecal samples obtained from swine and 682 samples from humans. Fifteen pigs were necropsied. Human and porcine fecal samples were examined to identify Ascaris eggs. Parasites obtained in the swine necropsies were studied using scanning electron microscopy (SEM), and the mitochondrial gene encoding the cytochrome oxidase 1 (cox1) enzyme was partially amplified and sequenced for molecular taxonomy and phylogenetic analyses. The overall prevalence of Ascaris eggs in the swine fecal samples was 16/100 (16%). No Ascaris eggs were identified in the human fecal samples. SEM of six worms recovered from pigs demonstrated morphological characteristics of A. suum. Cox1 sequences were compatible with A. suum reference sequences. Original and reference (GenBank) nucleotide sequences were organized into clusters that did not segregate the parasites by host species or and region. The largest haplogroups were dominated by haplotypes H01, H02 and H31. In the communities studied, there was no epidemiological evidence of the zoonotic transmission of ascariasis at the human-swine interface.(AU)

O presente estudo teve como objetivo acessar dados morfológicos e genéticos sobre a ascaridíase em suínos (Sus scrofa domesticus) e humanos, em comunidades rurais e periurbanas no estado do Piauí. O estudo transversal incluiu 100 amostras fecais de suínos e 682 amostras obtidas de humanos. Quinze suínos foram necropsiados. Amostras fecais suínas e humanas foram examinadas para detecção de ovos de Ascaris. Os parasitas adultos, obtidos nas necropsias, foram estudados através de microscopia eletrônica de varredura (MEV), e o gene mitocondrial codificante da enzima citocromo oxidase 1 (cox1) foi parcialmente amplificado e sequenciado para análises filogenéticas e de taxonomia molecular. A prevalência de Ascaris em amostras fecais de suínos foi 16/100 (16%), não sendo identificado nenhum caso de infecção por este parasita em humanos. A análise por MEV de parasitas recuperados de suínos demonstrou características morfológicas de Ascaris suum. As sequências nucleotídicas de cox1 foram compatíveis com A. suum. As sequências originais e de referência (obtidas no GeneBank) foram organizadas em clusters que não segregaram os parasitas por hospedeiro ou região geográfica. Os maiores haplogrupos foram dominados pelos haplótipos H01, H02 e H31. Nas comunidades estudadas, não foi evidenciada transmissão zoonótica de A. suum na interface suíno-humana.(AU)

Expression of antimicrobial peptide Cecropin P1 in Saccharomyces cerevisiae and its antibacterial and antiviral activity in vitro

BACKGROUND: Cecropin P1, acting as an antimicrobial, has a broad-spectrum antibacterial activity with some antiviral and antifungal properties. It is a promising natural alternative to antibiotics which is originally isolated from the pig intestinal parasitic nematode Ascaris suum. Many studies have shown that Cecropin P1 is helpful for the prevention or treatment of clinical diseases. Therefore, it is very necessary to establish a safe, nontoxic, and efficient expression method of Cecropin P1. RESULTS: The results indicated that the recombinant protein was about 5.5 kDa showed by Tricine­SDS­ PAGE and Western blot. And Cecropin P1 was efficiently secreted and expressed after 12 h of induction, with an increasing yield over the course of the induction. Its maximum concentration was 7.83 mg/L after concentration and purification. In addition, in vitro experiments demonstrated that Cecropin P1 not only exerted a strong inhibitory effect on Escherichia coli, Salmonella sp., Shigella sp., and Pasteurella sp., but also displayed an antiviral activity against PRRSV NADC30-Like strain. CONCLUSIONS: Collectively, the strategy of expressing Cecropin P1 in Saccharomyces cerevisiae is harmless, efficient, and safe for cells. In addition, the expressed Cecropin P1 has antiviral and antibacterial properties concurrently.

Extract of Ascaris suum induces TGF-ß and early production of IgG1 in experimental autoimmune hepatitis / Extrato de Ascaris suum induz TGF-ß e produção precoce de IgG1 na hepatite autoimune experimental

Abstract In experimental autoimmune hepatitis (EAH) of Th1 profile, an extract of adult Ascaris suum worms (ASC) was previously found to deviate the immune response to a Th2/IL-10 pattern. Here, the effects of treatment with ASC on production of TGF-β and the anti-Ascaris isotypes IgG1 and IgG2a in EAH were evaluated. EAH was induced in BALB/c mice, intravenously with concanavalin A. Two hours later, these animals received ASC (EAH+ASC group) or PBS vehicle (EAH group). IgG1 and IgG2a were evaluated 8 h, 24 h and 7 d after induction. TGF-β was measured in a splenocyte culture at this last time. The isotype levels in the EAH group were low throughout the kinetics. In the EAH+ASC group, there was significant production of IgG1 at 24 h and 7 d, but of IgG2a only at 7 d. There was statistically greater production of TGF-β in the EAH+ASC group. The higher levels of IgG1 and TGF-β in this group suggest that an additional Th1 response control route exists in EAH, which needs to be investigated.

Resumo Na hepatite autoimune experimental (HAE) de perfil Th1, o extrato de vermes adultos Ascaris suum (ASC) desviou a resposta imune para um padrão Th2/IL-10. Neste trabalho, foram avaliados os efeitos do tratamento com ASC na produção TGF-β e dos isótipos de IgG1 e IgG2a anti-Ascaris na HAE. Esta foi induzida em camundongos BALB/c intravenosamente com Concanavalina A. Após duas horas, os animais receberam ASC (grupo HAE+ASC) ou veículo PBS (grupo HAE). IgG1 e IgG2a foram avaliados em 8 horas, 24 horas e 7 dias após indução. TGF-β foi mensurado em cultura de esplenócitos nesse último tempo. Os níveis dos isótipos no grupo HAE foram baixos durante toda a cinética. No grupo HAE+ASC, houve produção significativa de IgG1 em 24 horas e 7 dias, mas somente em 7 dias para IgG2a. A produção de TGF-β foi estatisticamente maior no grupo HAE+ASC. Níveis mais altos de IgG1 e TGF-β nesse grupo sugerem uma via adicional de controle da resposta Th1 na HAE que precisa ser investigada.

Absence of mutations associated with resistance to benzimidazole in the beta-tubulin gene of Ascaris suum

Abstract INTRODUCTION: Benzimidazoles are commonly used for the control of veterinary nematodes. Resistance to benzimidazoles has been associated with three single nucleotide polymorphisms in the β-tubulin gene of common nematodes. However, these mutations are infrequent in the genus Ascaris spp. METHODS: In order to determine mutations associated with benzimidazole resistance in Ascaris suum, worms were collected from slaughtered pigs and a partial region of the β-tubulin gene was sequenced. RESULTS: All parasites showed the wildtype genotype for codons 167, 198, and 200 of the β-tubulin gene. CONCLUSIONS: This is the first report of genetic sequences associated with benzimidazole resistance in A. suum.

Effect of endoparasites occurrence in sows from intensive production system / Efeito da ocorrência de endoparasitas em matrizes suínas de sistema de produção intensivo

Abstract The goal of this study was to assess the effect of farm size (FS) and farrowing order (FO) on the occurrence of endoparasites eggs in commercial sows housed in maternity and gestation areas during the period from May to July 2014. Forty-three piglet production units were classified by FS: small (100 to 250 sows), medium (251 to 510 sows), large (511 to 1,000 sows) and very large (more than 1,000 sows). Sows were classified by FO: up to two, three to five or more than five parturitions. Faecal samples were processed using the simple flotation technique in a hypersaturated salt solution (30-35% NaCl). The results revealed that the overall prevalence of gastrointestinal endoparasites obtained in this study was 12.47%, in that 4.64% were positive for Ascaris suum, 0.56% for Trichuris suis and 8.27% for coccidia oocysts. The prevalence of endoparasites obtained for small and medium size farm, and for large and very large farm was 34.58% and 15.52%, respectively. In conclusion, the study shows that more than half of the farms were positive for A. suum and coccidia oocysts, but mainly for younger females. In general, sows with up to two parturitions and small farms showed a higher endoparasites percentage.

Resumo O objetivo deste estudo foi o de avaliar o efeito de tamanho de granja (TG) e a ordem de parição (OP) sobre a ocorrência de ovos de endoparasitas em matrizes suínas comerciais alojadas na maternidade e gestação durante o período de maio a julho de 2014. Quarenta e três unidades produtoras de leitões foram classificadas por TG: pequena (100 a 250 porcas), média (251 a 510 porcas), grande (511 a 1.000 porcas) e muito grande (mais de 1.000 porcas). As porcas foram classificadas por OP: até dois, três a cinco e mais que cinco partos. As amostras fecais foram processadas usando a técnica de flotação em solução salina hipersaturada a 30-35%. Os resultados revelaram que a prevalência global de endoparasitas gastrointestinais obtidos neste estudo foi de 13,59%, em que 4,64% foram positivas para Ascaris suum, 0,56% para Trichuris suis e 8,27% para oocistos de coccídeos. A prevalência de endoparasitas obtidos para fazendas de pequeno e médio porte, e para fazendas grandes e muito grandes foi de 34,58% e 15,52%, respectivamente. Em conclusão, o estudo mostra que mais da metade das fazendas foram positivas para A. suum e oocistos de coccídeos, mas principalmente para as fêmeas mais jovens. Em geral, as porcas com até dois partos e pequenas propriedades mostraram uma porcentagem maior de endoparasitas.

Effects of Disinfectants on Larval Development of Ascaris suum Eggs

The objective of this study was to evaluate the effects of several different commercial disinfectants on the embryogenic development of Ascaris suum eggs. A 1-ml aliquot of each disinfectant was mixed with approximately 40,000 decorticated or intact A. suum eggs in sterile tubes. After each treatment time (at 0.5, 1, 5, 10, 30, and 60 min), disinfectants were washed away, and egg suspensions were incubated at 25℃ in distilled water for development of larvae inside. At 3 weeks of incubation after exposure, ethanol, methanol, and chlorohexidin treatments did not affect the larval development of A. suum eggs, regardless of their concentration and treatment time. Among disinfectants tested in this study, 3% cresol, 0.2% sodium hypochlorite and 0.02% sodium hypochlorite delayed but not inactivated the embryonation of decorticated eggs at 3 weeks of incubation, because at 6 weeks of incubation, undeveloped eggs completed embryonation regardless of exposure time, except for 10% povidone iodine. When the albumin layer of A. suum eggs remained intact, however, even the 10% povidone iodine solution took at least 5 min to reasonably inactivate most eggs, but never completely kill them with even 60 min of exposure. This study demonstrated that the treatment of A. suum eggs with many commercially available disinfectants does not affect the embryonation. Although some disinfectants may delay or stop the embryonation of A. suum eggs, they can hardly kill them completely.

Seropositivity for ascariosis and toxocariosis nd cytokine expression among the indigenous people in the Venezuelan delta region / Seropositividad para ascariosis y toxocariosis y expresión de citocinas entre la población indígena de la región del delta Venezolano

The present study aimed at measuring seropositivities for infection by Ascaris suum and Toxocara canis using the excretory/secretory (E/S) antigens from Ascaris suum (AES) and Toxocara canis (TES) within an indigenous population. In addition, quantification of cytokine expressions in peripheral blood cells was determined. A total of 50 Warao indigenous were included; of which 43 were adults and seven children. In adults, 44.1% were seropositive for both parasites; whereas children had only seropositivity to one or the other helminth. For ascariosis, the percentage of AES seropositivity in adults and children was high; 23.3% and 57.1%, respectively. While that for toxocariosis, the percentage of TES seropositivity in adults and children was low; 9.3% and 14.3%, respectively. The percentage of seronegativity was comparable for AES and TES antigens in adults (27.9%) and children (28.6%). When positive sera were analyzed by Western blotting technique using AES antigens; three bands of 97.2, 193.6 and 200.2 kDas were mostly recognized. When the TES antigens were used, nine major bands were mostly identified; 47.4, 52.2, 84.9, 98.2, 119.1, 131.3, 175.6, 184.4 and 193.6 kDas. Stool examinations showed that Blastocystis hominis, Hymenolepis nana and Entamoeba coli were the most commonly observed intestinal parasites. Quantification of cytokines IFN-γ, IL-2, IL-6, TGF-β, TNF-α, IL-10 and IL-4 expressions showed that there was only a significant increased expression of IL-4 in indigenous with TES seropositivity (p < 0.002). Ascaris and Toxocara seropositivity was prevalent among Warao indigenous.

El objetivo del presente estudio fue determinar la seropositividad de infección por Ascaris suum y Toxocara canis, utilizando antígenos de excreción/secreción (E/S) de Ascaris suum (AES) y Toxocara canis (TES) en una población indígena. Adicionalmente, se cuantificó la expresión de citocinas a partir de células de sangre periférica. Un total de 50 indígenas Warao se incluyeron en el estudio; 43 fueron adultos y 7 niños. Entre los adultos, 44,1% fueron seropositivos para ambos parásitos; mientras que los niños sólo mostraron seropositividad a uno u otro de los helmintos. Para ascariosis, el porcentaje de seropositividad para los antígenos AES fue alto tanto en adultos como en niños; 23,3% y 57,1%, respectivamente. Para toxocariosis, el porcentaje de seropositividad para los antígenos TES fue bajo en adultos así como en niños; 9,3% y 14,3%, respectivamente. El porcentaje de seronegatividad fue similar tanto para los antígenos AES como para TES en adultos (27,9%) y niños (28,6%). Cuando la seropositividad fue analizada a través de la técnica de Western blotting utilizando los antígenos AES; 3 bandas de 97,2, 193,6 y 200,2 kDas fueron principalmente reconocidas. Para los antígenos TES, 9 bandas fueron mayormente identificadas; 47,4, 52,2, 84,9, 98,2, 119,1, 131,3, 175,6, 184,4 y 193,6 kDas. Los análisis coproparasitológicos mostraron que los parásitos Blastocystis hominis, Hymenolepis nana y Entamoeba coli fueron los parásitos intestinales más comúnmente observados. La cuantificación de la expresión de las citocinas IFN-γ, IL-2, IL-6, TGF-β, TNF-α, IL-10 e IL-4 mostró que hubo un significante incremento de la expresión de IL-4 entre los indígenas con seropositividad para los antígenos TES (p < 0.002). La seropositividad para Ascaris y Toxocara fue prevalente entre los indígenas Warao.

Ascaris suum in pigs of the Zona da Mata, Minas Gerais State, Brazil / Ascaris suum em suínos da Zona da Mata, Estado de Minas Gerais, Brasil

Among the parasites that affect pigs, Ascaris suum stands out for causing the greatest losses to livestock production systems. This parasite can be monitored during the slaughter of animals through the identification of milk spots or white patches on the liver caused by its larval migration. However, infection in the herd is usually subclinical, which is why the presence of this parasite in industrial pig production has been overlooked. The aim of the study was therefore to evaluate the occurrence of milk spots on the liver of animals slaughtered in the micro-region of Ponte Nova in the Zona da Mata - Minas Gerais, Brazil, and to associate these lesions with the time of year, herd size and source of origin of the animals. An evaluation was made of 1,069 lots, totaling 108,073 animals, based on data extracted from the Federal Inspection Service. The animals were slaughtered during the period of January 2011 to June 2013. Out of the total number of slaughtered animals, 10,535 (9.75%) tested positive for these lesions. Therefore, veterinarians and producers should be warned about the inefficiency of the deworming protocols that are used, and the need to develop and/or review control strategies for this parasite in production systems.

Dentre os parasitas que acometem os suínos, Ascaris suumdestaca-se como o mais impactante nos sistemas de criação. Seu monitoramento pode ser realizado durante o abate dos animais, por meio da identificação de milk spots ou manchas de leite presentes no fígado, decorrentes da sua migração larval. Entretanto devido ao fato da infecção ocorrer no rebanho normalmente de forma subclínica, a presença desse parasita na produção industrial de suínos vem sendo negligenciada. O objetivo do estudo foi avaliar a ocorrência de manchas de leite no fígado de animais abatidos na micro-região de Ponte Nova, na Zona da Mata de Minas Gerais - Brasil, e associar tais lesões com a época do ano, tamanho do rebanho e local de origem dos animais. Foram avaliados 1.069 lotes, totalizando 108.073 animais. Os dados foram extraídos do Serviço de Inspeção Federal, e eram referentes aos animais abatidos, durante o período de janeiro de 2011 a junho de 2013. Do total de animais abatidos, 10.535 (9,75%) foram positivos para a lesão. Portanto, veterinários e produtores devem ser alertados quanto à ineficiência dos protocolos de vermifugação utilizados e a necessidade do desenvolvimento e/ou revisão de estratégias de controle para este parasita na produção.

Effects of Some Pesticides on Development of Ascaris suum Eggs

To evaluate the effects of pesticides to parasite eggs, Ascaris suum eggs were incubated with 5 different pesticides (1:1,500-1:2,000 dilutions of 2% emamectin benzoate, 5% spinetoram, 5% indoxacarb, 1% deltamethrin, and 5% flufenoxuron; all v/v) at 20degrees C for 6 weeks, and microscopically evaluated the egg survival and development on a weekly basis. The survival rate of A. suum eggs incubated in normal saline (control eggs) was 90+/-3% at 6 weeks. However, the survival rates of eggs treated with pesticides were 75-85% at this time, thus significantly lower than the control value. Larval development in control eggs commenced at 3 weeks, and 73+/-3% of eggs had internal larvae at 6 weeks. Larvae were evident in pesticide-treated eggs at 3-4 weeks, and the proportions of eggs carrying larvae at 6 weeks (36+/-3%-54+/-3%) were significantly lower than that of the control group. Thus, pesticides tested at levels similar to those used in agricultural practices exhibited low-level ovicidal activity and delayed embryogenesis of A. suum eggs, although some differences were evident among the tested pesticides.

Identificación de fracciones electroforéticas de unión a IgE en extractos de Ascaris sp. / Identification of electrophoretic fractions of the IgE-binding in Ascaris sp. extracts

Introducción: Ascaris lumbricoides infecta a una cuarta parte de la población mundial, constituyéndose en un problema de salud pública. La ascariosis humana está asociada con morbilidad crónica y aguda, especialmente en niños. Recientemente se ha planteado la existencia de anticuerpos IgE en el suero sanguíneo de pacientes alérgicos, que tienen reacción cruzada con alérgenos de artrópodos domésticos y antígenos de Ascaris sp., esto podría aumentar el número de muestras seropositivas a Ascaris sp, en poblaciones sensibilizadas a los ácaros del polvo intradomiciliario. Objetivo: Producir extractos de cuerpo entero de A. lumbricoides y A. suum, evaluar sus propiedades antigénicas y capacidad de unión a la IgE de pacientes alérgicos al ácaro Dermatophagoides pteronyssinus. Métodos: Los extractos fueron obtenidos por homogenización y lisis osmótica de las células en presencia de Tween-20 e inhibidores de proteasas. El perfil de proteínas de cada extracto fue identificado por electroforesis en geles de poliacrilamida con dodecilsulfato sódico (SDS-PAGE). La reactividad antigénica se determinó por Western blotting usando once sueros de pacientes alérgicos con diagnóstico de asma. Resultados: SDS-PAGE reveló 20 fracciones electroforéticas mayoritarias (20-200 kDa). Western Blotting reveló diferencias en el perfil de proteínas de unión a la inmunoglobulina IgE de los extractos. Conclusiones: Proteínas del cuerpo entero de A. lumbricoides y A. suum mostraron un perfil de unión a IgE diferente en el Western blotting, con sueros de pacientes alérgicos al ácaro D. pteronyssinus, sugiriendo la presencia de marcadores especie específicos entre los dos parásitos, los cuales podrían usarse en futuras investigaciones biomédicas.

Background: Ascaris lumbricoides infects a quarter of the world's population, thus becoming a public health problem. Human ascariasis is associated with chronic and acute morbidity, especially in children. Recently, it has been stated that the existence of IgE antibodies in the blood serum of allergic patients that have cross reactivity with domestic arthropods and antigens of Ascaris sp. could increase the number of samples seropositive for Ascaris sp. in populations who are sensitized to house dust mites. Objective: To produce whole body extracts of both A. lumbricoides and A. suum, and to evaluate their antigenic properties and the IgE-binding capacity in patients allergic to the house dust mite (Dermatophagoides pteronyssinus). Methods: The extracts were obtained by homogenization and osmotic lysis in the presence of Tween-20 and protease inhibitors. The protein profile of each extract was identified by sodium dodecyl sulphate-polyacrylamide gel elctrophoresis (SDS-PAGE). Antigen reactivity was determined by Western blotting, using eleven sera from allergic patients with the diagnosis of asthma. Results: SDS-PAGE revealed 20 major electrophoretic fractions (20-200 kDa). Western Blotting revealed differences in the protein profile of the immunologlobulin IgE-binding of the extracts. Conclusions: Whole body proteins of both A. lumbricoides and A. suum showed a different IgE-binding profile in the Western blotting, with sera from patients allergic to the D. pteronyssinus mite, suggesting the presence of species-specific markers between the two parasites, which could be used in further biomedical research.

IgG Antibody responses in mice coinfected with Toxocara canis and other helminths or protozoan parasites / Anticorpos IgG em camundongos coinfectados por Toxocara canis e outros helmintos e por protozoários parasitos

The immune response expressed by IgG antibodies in BALB/c mice experimentally infected with Toxocara canis, was studied with the aim of verifying the possible in vivo cross-reactivity between antigens of T. canis and other parasites (Ascaris suum, Taenia crassiceps, Schistosoma mansoni, Strongyloides venezuelensis and Toxoplasma gondii). Experiments included three groups of mice: one infected only by T. canis, another with one of the other species of parasites and a third concomitantly infected with T. canis and the other species in question. Animals were bled by orbital plexus at 23, 38 and 70 days post infection (p.i.). Sera were analyzed for anti-Toxocara antibodies by ELISA and Immunoblotting, using excretion-secretion antigens (ES), obtained from culture of third-stage larvae of T. canis. For all experiments a control group comprised by ten non-infected mice was used. Only in the case of A. suum infection, in these experimental conditions, the occurrence of cross-reactivity with T. canis was observed. However, in the case of co-infection of T. canis - S. mansoni, T. canis - S. venezuelensis and T. canis - T. crassiceps the production of anti-Toxocara antibodies was found at levels significantly lower than those found in mice infected with T. canis only. Co-infection with S. mansoni or S. venezuelensis showed lower mortality rates compared to what occurred in the animals with single infections. Results obtained in mice infected with T. canis and T. gondii showed significant differences between the mean levels of the optical densities of animals infected with T. canis and concomitantly infected with the protozoan only in the 23rd day p.i.

Estudou-se a resposta imune humoral expressa por anticorpos da classe IgG em camundongos BALB/c experimentalmente infectados com Toxocara canis em duas situações distintas. Na primeira, com o objetivo de verificar in vivo a possível reatividade cruzada entre Toxocara canis e outros parasitos (Ascaris suum, Taenia crassiceps, Schistosoma mansoni, Strongyloides venezuelensis e Toxoplasma gondii), foram realizados experimentos constituídos por três grupos de camundongos: um infectado apenas por Toxocara canis, outro com uma das demais espécies de parasitos estudados e um terceiro concomitantemente infectado por Toxocara canis e a espécie em questão. Todos os animais foram sangrados, através do plexo orbitário, 23, 38 e 70 dias após infecção. Os soros foram analisados para a presença de anticorpos anti-Toxocara por meio de teste imunoenzimático (ELISA) e por Immunoblotting, empregando-se antígeno de excreção-secreção (ES), obtido a partir da cultura de larvas de terceiro estádio de Toxocara canis. Para todos os experimentos utilizou-se grupo controle negativo constituído por 10 camundongos não infectados. Apenas no caso da infecção por Ascaris suum, nas condições experimentais observadas, logrou-se demonstrar ocorrência de reatividade cruzada com antígenos de Toxocara canis. Verificou-se, entretanto, no caso das coinfecções entre Toxocara canis-Schistosoma mansoni, Toxocara canis-Strongyloides venezuelensis e Toxocara canis-Taenia crassiceps produção de anticorpos anti-Toxocara em níveis significativamente inferiores do que os encontrados nos camundongos infectados somente por Toxocara canis. Nas coinfecções com Schistosoma mansoni ou Strongyloides venezuelensis observou-se, também, menor taxa de letalidade quando comparada à ocorrida nos animais com as respectivas infecções simples.

Effects of Kimchi Extract and Temperature on Embryostasis of Ascaris suum Eggs

To determine the effects of kimchi extracts at different temperatures on larval development, Ascaris suum eggs were mixed with soluble part of 7 different brands of commercially available kimchi and preserved at either 5degrees C or 25degrees C for up to 60 days. A. suum eggs incubated at 25degrees C showed marked differences in larval development between kimchi extract and control group. While all eggs in the control group completed embryonation by day 21, only 30% of the eggs in the kimchi extract group became embryonated by day 36 and about 25% never became larvated even at day 60. At 5degrees C, however, none of the eggs showed larval development regardless of the incubation period or type of mixture group. To determine the survival rate of A. suum eggs that showed no embryonation after being preserved at 5degrees C, eggs preserved in kimchi extracts for 14, 28, and 60 at 5degrees C were re-incubated at 25degrees C for 3 weeks in distilled water. While all eggs in the control group became larvated, eggs in the kimchi extract group showed differences in their embryonation rates by the incubation period; 87.4 % and 41.7% of the eggs became embryonated after being refrigerated for 14 days and 28 days, respectively. When refrigerated for 60 days, however, no eggs mixed in kimchi extract showed larval development. Our results indicate that embryogenesis of A. suum eggs in kimchi extract was affected by duration of refrigeration, and that all eggs stopped larval development completely in kimchi kept at 5degrees C for up to 60 days.

Effect of Temperature on Embryonation of Ascaris suum Eggs in an Environmental Chamber

The influence of temperature on the development and embryonation of Ascaris suum eggs was studied using coarse sand medium in an environmental chamber with 50% humidity. The time required for development and embryonation of eggs was examined under 3 different temperature conditions, 5degrees C, 25degrees C, and 35degrees C. A. suum eggs did not develop over 1 month at the temperature of 5degrees C. However, other temperature conditions, 25degrees C and 35degrees C, induced egg development to the 8-cell-stage at days 5-6 after incubation. All eggs examined developed to the 8-cell stage at day 6 after incubation in the sand medium at 25degrees C. The higher temperature, 35degrees C, slightly accelerated the A. suum egg development compared to 25degrees C, and the development to the 8-cell stage occurred within day 5 after incubation. The formation of larvae in A. suum eggs at temperatures of 35degrees C and 25degrees C appeared at days 17 and 19 after incubation, respectively. These findings show that 35degrees C condition shortens the time for the development of A. suum eggs to the 8-cell-stage in comparison to 25degrees C, and suggest the possibility of accelerated transmission of this parasite, resulting from global warming and ecosystem changes.

Quantitative Evaluation of Viability- and Apoptosis-Related Genes in Ascaris suum Eggs under Different Culture-Temperature Conditions

Ascaris suum eggs are inactivated by composting conditions; however, it is difficult to find functional changes in heat-treated A. suum eggs. Here, unembryonated A. suum eggs were incubated at 20degrees C, 50degrees C, and 70degrees C in vitro, and the gene expression levels related to viability, such as eukaryotic translation initiation factor 4E (IF4E), phosphofructokinase 1 (PFK1), and thioredoxin 1 (TRX1), and to apoptosis, such as apoptosis-inducing factor 1 (AIF1) and cell death protein 6 (CDP6), were evaluated by real-time quantitative RT-PCR. No prominent morphological alterations were noted in the eggs at 20degrees C until day 10. In contrast, the eggs developed rapidly, and embryonated eggs and hatched larvae began to die, starting on day 2 at 50degrees C and day 1 at 70degrees C. At 20degrees C, IF4E, PFK1, and TRX1 mRNA expression was significantly increased from days 2-4; however, AIF1 and CDP6 mRNA expression was not changed significantly. IF4E, PFK1, and TRX1 mRNA expression was markedly decreased from day 2 at 50degrees C and 70degrees C, whereas AIF1 and CDP6 mRNA expression was significantly increased. The expressions of HSP70 and HSP90 were detected for 9-10 days at 20degrees C, for 3-5 days at 50degrees C, and for 2 days at 70degrees C. Taken together, incremental heat increases were associated with the rapid development of A. suum eggs, decreased expression of genes related to viability, and earlier expression of apoptosis-related genes, and finally these changes of viability- and apoptosis-related genes of A. suum eggs were associated with survival of the eggs under temperature stress.

Ocorrência de Ascaris suum em suínos abatidos na Zona da Mata, Minas Gerais / Occurence of the Ascaris suum in slaughtered swine in Zona da Mata region, Minas Gerais State

Os suínos são acometidos por diversas enfermidades e as verminoses se constituem como as principais causas de nãoganho de peso, competição e diminuição da conversão alimentar, descarte de vísceras ao abate e perdas financeiras. Onematoide Ascaris suum se constitui na principal parasitose na suinocultura nacional. Esse trabalho teve como objetivoavaliar o nível de infestação por A. suum em suínos em idade de abate provenientes de granjas tecnificadas localizadasna região do município de Piranga, região oeste da Zona da Mata, Minas Gerais, latitude 20º45’45’’S, longitude43º18’10’’W. Os animais foram abatidos em três matadouros localizados no município de Piranga, e foram observadosos tratos gastrintestinais dos suínos abatidos quanto à presença desse parasito. Foi observada a presença do nematoideem animais provenientes de 90% das granjas e a ocorrência total foi 22,4%, média de todo o período experimental.Também foi observado que, durante o período experimental, a ocorrência de A. suum no lume intestinal dos animaisnão apresentou diminuição e os protocolos de everminação não foram eficazes para a diminuição da ocorrência desseshelmintos nas propriedades onde foram empregados.

Swine are affected by several diseases and worms constitute the main causes of absence of weight gain, competitionand decreased feed conversion, discards of slaughter viscera and financial losses. The nematode Ascaris suum remainsa major parasitic disease in national livestock pigs. The objective of this work was to evaluate the level of infestationby A. suum in pigs at slaughter age provenient from intensive production systems located in Zona da Mata region,latitude 20º45’45’’S, longitude 43°18’10’’W, in tropical Southeastern, Brazil. The animals were slaughtered at threeslaughterhouses located in the municipality of Piranga, and their gastrointestinal tracts were observed in order toidentify the presence of those helminthes. We observed the presence of nematode in animals from 90% of the farms andthe total occurrence was 22.4%, media of all the experimental period. It was also observed that, during the experimentalperiod, the occurrence of A. suum in the gastrointestinal tube did not present reduction and the protocol to administeranthelmintic were not efficient to decrease the occurrence this helminthes in proprieties in which they were applied...

Boosting the suppressive effects of Ascaris suum components in IFN-γ-deficient mice / Potencialização do efeito supressor de componentes do Ascaris suum em camundongos deficientes em IFN-γ

High molecular weight components from Ascaris suum extract suppress ovalbumin-specific immunity in mice. In IFN-γ-deficient mice, ovalbumin-specific delayed-type hypersensitivity reactions are more strongly downregulated by these suppressive components. Here, the cellularity of the delayed-type hypersensitivity reaction in IFN-γ-deficient mice and the increased downregulation induced by Ascaris suum components were analyzed. IL-12p40-dependent neutrophilic influx was predominant. Suboptimal doses of the suppressive fraction from this nematode completely inhibited the hypersensitivity reaction, thus indicating intensification of the immunosuppression under conditions of intense recruitment of IFN-γ-independent neutrophils.

Componentes de alto peso molecular do extrato de Ascaris suum suprimem a imunidade específica à ovalbumina em camundongos. Em camundongos geneticamente deficientes de IFN-γ a reação de hipersensibilidade tardia específica para ovalbumina foi mais fortemente prejudicada por estes componentes supressivos. Aqui, a celularidade da reação de hipersensibilidade tardia em camundongos deficientes de IFN-γ e o incremento na supressão induzida por componentes do Ascaris suum foram analisados. Influxo neutrofílico, dependente de IL-12p40, foi predominante. Dose sub-ótima da fração supressiva do nematódeo inibiu completamente a reação de hipersensibilidade, indicando uma intensificação da imunossupressão em condições de recrutamento intenso de neutrófilos independente de IFN-γ.

Antígenos de larvas pulmonares de Ascaris suum reconocidos por anticuerpos producidos en Oryctolagus cuniculus / Ascaris suum lung larvae antigens recognized by antibodies produced in Oryctolagus cuniculus

El presente trabajo tuvo como objetivo determinar mediante la técnica de Western Blot los antígenos de larvas pulmonares de Ascaris suum que son detectados por anticuerpos producidos en Oryctolagus cuniculus inmunizado experimentalmente. Las larvas pulmonares (L3 y L4) fueron obtenidas en 120 ejemplares de Mus musculus cepa BALB/c ratón infectados experimentalmente por vía oral con huevos infectivos de A. suum. Parte de estas larvas fueron cultivadas en el medio Eagle (MEM) para la obtención de antígenos de excreción/secreción y la otra fue sonificada para la obtención de antígenos somáticos, los cuales sirvieron para inmunizar dos ejemplares de O. cuniculus, utilizando Adyuvante Completo e Incompleto de Freund. A las 5 semanas de inmunización se obtuvo sangre de los conejos por punción cardiaca a fin de recuperar el suero, parte del cual fue purificado parcialmente por precipitación salina y diálisis. Mediante la técnica de electroinmuno-transferencia (Western Blot) y usando sueros de los conejos inmunizados se detectaron en los antígenos de excreción/secreción de 20 horas de cultivo reducidos con dithiothreitol, 12 bandas antigénicas de 100, 72.4, 56.2, 42.7, 39.8, 34.6, 31.6, 30.2, 19.5, 16.9, 15.5 y 14.9 KDa, siendo las más reactivas las de 100, 72.4, 16.9, 15.5 y 14.9 KDa. En los antígenos somáticos bajo condiciones de reducción, se detectaron solamente seis bandas de 42.7, 39.8, 34.6, 30.2, 28 y 25.2 KDa de poca reactividad. Estos resultados permiten afirmar que los antígenos de excreción/secreción de A. suum de 20 horas de incubación en el medio MEM inducen la producción de un mayor número de anticuerpos de tipo IgG en conejos inmunizados experimen-talmente.

Excretory/secretory antigens (E/SAg) and somatic antigens (SAg) of Ascaris suum lung larvae that induce the immunoglobulin G antibodies production in Oryctolagus cuniculus experimentally immunized was determined. For this purposes, specimens of Mus musculus BALB/c were inoculated orally with infective eggs of A. suum obtained from pigs naturally parasitized in order to obtain the lung larvae. Part of these larvae was cultured in Minimum Essential Medium (MEM) to obtain E/SAg and another part was sonicated to obtain the SAg too. Both, E/SAg and SAg mixed with complete and incomplete Freund's adjuvant were used for rabbits immunization. Five weeks after the immunization, the rabbits were bled by cardiac puncture obtaining the immunosera by centrifugation, which was purified partially by saline precipitation and dialysis. By using an Western blot technique with purified immunoserum and E/SAg obtained to 20 hours and reduced with dithiothreitol, fourteen antigens bands of 100, 72.4, 56.2, 42.7, 39.8, 34.6, 31.6, 30.2, 19.5, 16.9, 15.5 y 14.9 KD, were detected. The bands of 100, 72.4, 16.9, 15.5 and 14.9 KDa were been the most reactives. Thereby the SAg, also reduced with dithiothreitol, seven bands of 42.7, 39.8, 34.6, 30.2, 28.0 and 25.2 KDa were detected. They were a bit clear. In conclusion, the E/SAg induce the highest production of immunoglobulin G antibodies in rabbits experimentally immunized.

PRELIMINARY STUDIES OF ALBENDAZOLE (ABZ),ALBENDAZOLE-SULFOXIDE (ABZSX) AND AIBENDAZOLE-SULFONE(ABZSN) ON THE ENZYME COMPLEXES ACTIVITIES IN MITOCHONDRIA OF ASCARIS SUUM MUSCLE / 中国人兽共患病学报

AimTo study the mechanism of ABZ,ABZSX and ABZSN on Ascaris Suum. MethodsThe activities of enzyme complexes in mitochondria were detected by spectrophotometer for the study of effects of ABZ, ABZSX and ABZSN on the anaerobic respiratory chain of enzyme complexes in mitochondria of Ascaris Suum muscle and rat liver. ResultsThe activity of succinate CoQ reductase in Ascaris muscle mitochondria was apparently suppressed by ABZ ,ABZSX. Conclusion Preliminary study on the mechanism and toxicity of ABZ through enzyme studies,in order to find a more effective and satisfactory drug with low toxicity for clinical use.

Comparative Studies on the Difference Between Ascaris lumbricoides and Ascaris suum / 中国寄生虫学与寄生虫病杂志

There has been continued controversy on the taxonomy of Ascaris lumbricoides Linnaeus,1758 from humans and Ascaris suum Goeze,1782 from pigs.This article reviews a range of comparative studies related to host susceptibility,morphology,karyotype,immunology and biochemistry,as well as molecular genetics in recent years.