Literature DB >> 9195730

Experimental toxoplasmosis in broiler chicks.

C N Kaneto1, A J Costa, A C Paulillo, F R Moraes, T O Murakami, M V Meireles.   

Abstract

To evaluate chicken toxoplasmosis both as an economic and a public health subject, 84 broiler chicks of a commercial strain, 30 days old, were distributed into seven groups of 12 birds (three replications of four chicks) experimentally infected with three developing T. gondii stages of the P strain as follows: tachyzoites, intravenous (two groups: 5.0 x 10(5) and 5.0 x 10(6)), cysts, per os (two groups: 1.0 x 10(2) and 1.0 x 10(3)) and oocysts, per os (three groups: 5.0 x 10(2), 5.0 x 10(3) and 5.0 x 10(4)). Twelve chicks received only a placebo (control group). During the next 30 days the following parameters were estimated: productivity (weight gain and feed conversion), clinical signs, including rectal temperature and parasitemia (bioassay). No clinical signs suggesting toxoplasmosis were seen and no statistical differences on productivity standards were found in comparison between inoculated and control chicks. However, fowls inoculated with tachyzoites and oocysts occasionally showed hyperthermia. Some haematological changes were detected in fowls inoculated with T. gondii. Anatomo-histopathological changes were not observed. From 14 parasitemias detected, 35.7% appeared on the 5th day after inoculation and 57.1% of them resulted from oocysts inoculation. After 30-35 days all birds were slaughtered: fragments from 12 organs or tissues from each of them were subjected to artificial peptic digestion and after that injected into T. gondii antibody-free mice (IIFR). T. gondii was detected in brain (12), pancreas (five), spleen (five), retina (five), kidney (two), heart (four), proventriculus (three), liver (two), intestine (two), lung (one), and skeletal muscle (one). Similar to observations with parasitemia, from 42 T. gondii isolations, 59.5% came from chicks which had received oocysts. It can thus be inferred that the developing form, expelled by cats, is the most important for T. gondii chicken infection and that brain is the most infected organ in birds. Attention must be paid to the potential importance of chicken meat in public health, since T. gondii was isolated from skeletal and heart muscles.

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Year:  1997        PMID: 9195730     DOI: 10.1016/s0304-4017(96)01126-0

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  9 in total

1.  Long-term investigations on Toxoplasma gondii-infected primary chicken macrophages.

Authors:  Irene Malkwitz; Angela Berndt; Arwid Daugschies; Berit Bangoura
Journal:  Parasitol Res       Date:  2013-06-10       Impact factor: 2.289

2.  Tissue tropism of Toxoplasma gondii in turkeys (Meleagris gallopavo) after parenteral infection.

Authors:  B Zöller; M Koethe; M Ludewig; S Pott; A Daugschies; R K Straubinger; K Fehlhaber; B Bangoura
Journal:  Parasitol Res       Date:  2013-02-14       Impact factor: 2.289

3.  Experimental Toxoplasma gondii and Eimeria tenella co-infection in chickens.

Authors:  Lysanne Hiob; M Koethe; G Schares; T Goroll; A Daugschies; B Bangoura
Journal:  Parasitol Res       Date:  2017-10-05       Impact factor: 2.289

4.  Strain-dependent host transcriptional responses to Toxoplasma infection are largely conserved in mammalian and avian hosts.

Authors:  Yi-Ching Ong; Jon P Boyle; John C Boothroyd
Journal:  PLoS One       Date:  2011-10-13       Impact factor: 3.240

5.  Evaluation of Toxoplasma gondii as a live vaccine vector in susceptible and resistant hosts.

Authors:  Jun Zou; Xiao-Xi Huang; Guang-Wen Yin; Ye Ding; Xian-Yong Liu; Heng Wang; Qi-Jun Chen; Xun Suo
Journal:  Parasit Vectors       Date:  2011-08-28       Impact factor: 3.876

6.  Pathogenicity of Five Strains of Toxoplasma gondii from Different Animals to Chickens.

Authors:  Shuai Wang; Guang-Wei Zhao; Wang Wang; Zhen-Chao Zhang; Bo Shen; I A Hassan; Qing Xie; Ruo-Feng Yan; Xiao-Kai Song; Li-Xin Xu; Xiang-Rui Li
Journal:  Korean J Parasitol       Date:  2015-04-22       Impact factor: 1.341

7.  Exploring early and late Toxoplasma gondii strain RH infection by two-dimensional immunoblots of chicken immunoglobulin G and M profiles.

Authors:  Saeed El-Ashram; Ximeng Sun; Qing Yin; Xianyong Liu; Xun Suo
Journal:  PLoS One       Date:  2015-03-24       Impact factor: 3.240

Review 8.  The Influence of Parasite Infections on Host Immunity to Co-infection With Other Pathogens.

Authors:  Neil A Mabbott
Journal:  Front Immunol       Date:  2018-11-08       Impact factor: 7.561

9.  CCp5A Protein from Toxoplasma gondii as a Serological Marker of Oocyst-driven Infections in Humans and Domestic Animals.

Authors:  Silas S Santana; Luiz C Gebrim; Fernando R Carvalho; Heber S Barros; Patrício C Barros; Ana C A M Pajuaba; Valeria Messina; Alessia Possenti; Simona Cherchi; Edna M V Reiche; Italmar T Navarro; João L Garcia; Edoardo Pozio; Tiago W P Mineo; Furio Spano; José R Mineo
Journal:  Front Microbiol       Date:  2015-11-24       Impact factor: 5.640

  9 in total

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