scholarly journals Rapid serum agglutination and agar gel immunodiffusion tests associated to clinical signs in rams experimentally infected with Brucella ovis

2011 ◽  
Vol 41 (8) ◽  
pp. 1441-1446 ◽  
Author(s):  
Cristiane Nakada Nozaki ◽  
Nair Silva Cavalcanti de Lira ◽  
Otávio Augusto Filho ◽  
Hymerson Costa Azevedo ◽  
Leandro Rodello ◽  
...  
Keyword(s):  
Experimental Infection ◽  
Clinical Signs ◽  
Large Fluctuation ◽  
Agar Gel ◽  
Brucella Ovis ◽  
Serological Profile ◽  
Serum Agglutination

The purpose of this study was to evaluate the agar gel immunodiffusion and the rapid serum agglutination tests associated to clinical signs in rams experimentally infected with Brucella ovis. The serological profile during the 12 months of infection showed a large fluctuation of antibodies that favors the failure in the diagnostic. The evaluation of tests after the experimental infection allowed to suggest that none of the tests were able to detect the infection throughout the period of study. The study reinforces the importance of considering the clinical signs to support the diagnosis of Brucella ovis infection in rams.

scholarly journals Leptospirosis and brucellosis seroepidemiology in sheep and dogs from non-mechanized rural properties in the northwestern region in the state of Paraná

2016 ◽  
Vol 37 (5) ◽  
pp. 3147
Author(s):  
Leila Alves de Oliveira ◽  
Melissa Marchi Zaniolo ◽  
Eduardo Herrera Dias ◽  
Hermes Bianki Silva Brandão ◽  
Kariny Aparecida Jardim Rubio ◽  
...  
Keyword(s):  
Animal Species ◽  
Severe Disease ◽  
Clinical Signs ◽  
The State ◽  
Reproductive Disorders ◽  
Agar Gel ◽  
Brucella Ovis ◽  
Leptospira Spp ◽  
Northwestern Region ◽  
Variable Exchange

Sheep breeding has been important in agribusiness, transforming the Brazilian productive scenario. However, it is still deficient due to the damages caused by infectious diseases. Leptospirosis is a severe disease with global distribution, caused by bacteria from the Leptospira genre affecting both humans and animals. The general infection is unapparent, or its clinical signs, when present, are similar to other infections. Brucellosis is an infectious disease caused by bacteria from the Brucella genre responsible for reproductive disorders in animals, especially ruminants. The purpose of this paper was to seroepidemiological study of Leptospira spp. and Brucella ovis in sheep and dogs from nonmechanized rural properties from the northwestern region in the state of Paraná, Brazil. In order to detect anti-Leptospira antibodies, microscopic agglutination (MAT) was performed. For anti-Brucella antibodies, the agar gel immunodiffusion assay (AGID) was performed. From the total 542 samples from sheep sera analyzed, 11.25% were considered reagent to Leptospira spp. and 18.26% to Brucella ovis. From the 36 dog samples, 25% were reagent to MAT and AGID. From the 32 properties analyzed, 75% were considered positive for leptospirosis and 56.25% for brucellosis. Antibodies against the most probable serovars were Hardjo (34.42%) and Butembo (44.44%) in sheep and dogs, respectively, and the variable exchange of animals among properties was associated to leptospiric infection (p=0.028) in sheep. Leptospirosis and brucellosis are present in the sheep herd and dogs in the rural properties studied, and such result is a warning of the zoonotic importance and the need to establish sanitary programs directed to these animal species.

scholarly journals Experimental infection of indigenous North African goats with goatpox virus

2021 ◽  
Vol 63 (1) ◽  
Author(s):  
Jihane Hamdi ◽  
Zahra Bamouh ◽  
Mohammed Jazouli ◽  
Meryem Alhyane ◽  
Najet Safini ◽  
...  
Keyword(s):  
Antibody Response ◽  
Experimental Infection ◽  
Subcutaneous Tissue ◽  
Severe Disease ◽  
Clinical Signs ◽  
Economic Losses ◽  
North African ◽  
Cutaneous Lesions ◽  
Viral Dna ◽  
Goatpox Virus

Abstract Background Goatpox is a viral disease caused by infection with goatpox virus (GTPV) of the genus Capripoxvirus, Poxviridae family. Capripoxviruses cause serious disease to livestock and contribute to huge economic losses. Goatpox and sheeppox are endemic to Africa, particularly north of the Equator, the Middle East and many parts of Asia. GTPV and sheeppox virus are considered host-specific; however, both strains can cause clinical disease in either goats or sheep with more severe disease in the homologous species and mild or sub-clinical infection in the other. Goatpox has never been reported in Morocco, Algeria or Tunisia despite the huge population of goats living in proximity with sheep in those countries. To evaluate the susceptibility and pathogenicity of indigenous North African goats to GTPV infection, we experimentally inoculated eight locally bred goats with a virulent Vietnamese isolate of GTPV. Two uninfected goats were kept as controls. Clinical examination was carried out daily and blood was sampled for virology and for investigating the antibody response. After necropsy, tissues were collected and assessed for viral DNA using real-time PCR. Results Following the experimental infection, all inoculated goats displayed clinical signs characteristic of goatpox including varying degrees of hyperthermia, loss of appetite, inactivity and cutaneous lesions. The infection severely affected three of the infected animals while moderate to mild disease was noticed in the remaining goats. A high antibody response was developed. High viral DNA loads were detected in skin crusts and nodules, and subcutaneous tissue at the injection site with cycle threshold (Ct) values ranging from 14.6 to 22.9, while lower viral loads were found in liver and lung (Ct = 35.7 and 35.1). The results confirmed subcutaneous tropism of the virus. Conclusion Clinical signs of goatpox were reproduced in indigenous North African goats and confirmed a high susceptibility of the North African goat breed to GTPV infection. A clinical scoring system is proposed that can be applied in GTPV vaccine efficacy studies.

scholarly journals Virus Adaptation Following Experimental Infection of Chickens with a Domestic Duck Low Pathogenic Avian Influenza Isolate from the 2017 USA H7N9 Outbreak Identifies Polymorphic Mutations in Multiple Gene Segments

Viruses ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 1166
Author(s):  
Klaudia Chrzastek ◽  
Karen Segovia ◽  
Mia Torchetti ◽  
Mary Lee Killian ◽  
Mary Pantin-Jackwood ◽  
...  
Keyword(s):  
Avian Influenza ◽  
Experimental Infection ◽  
Clinical Signs ◽  
Interspecies Transmission ◽  
Clinical Samples ◽  
Domestic Duck ◽  
Receptor Binding Site ◽  
Synonymous Mutations ◽  
Field Samples ◽  
Virus Adaptation

In March 2017, highly pathogenic (HP) and low pathogenic (LP) avian influenza virus (AIV) subtype H7N9 were detected from poultry farms and backyard birds in several states in the southeast United States. Because interspecies transmission is a known mechanism for evolution of AIVs, we sought to characterize infection and transmission of a domestic duck-origin H7N9 LPAIV in chickens and genetically compare the viruses replicating in the chickens to the original H7N9 clinical field samples used as inoculum. The results of the experimental infection demonstrated virus replication and transmission in chickens, with overt clinical signs of disease and shedding through both oral and cloacal routes. Unexpectedly, higher levels of virus shedding were observed in some cloacal swabs. Next generation sequencing (NGS) analysis identified numerous non-synonymous mutations at the consensus level in the polymerase genes (i.e., PA, PB1, and PB2) and the hemagglutinin (HA) receptor binding site in viruses recovered from chickens, indicating possible virus adaptation in the new host. For comparison, NGS analysis of clinical samples obtained from duck specimen collected during the outbreak indicated three polymorphic sides in the M1 segment and a minor population of viruses carrying the D139N (21.4%) substitution in the NS1 segment. Interestingly, at consensus level, A/duck/Alabama (H7N9) had isoleucine at position 105 in NP protein, similar to HPAIV (H7N9) but not to LPAIV (H7N9) isolated from the same 2017 influenza outbreak in the US. Taken together, this work demonstrates that the H7N9 viruses could readily jump between avian species, which may have contributed to the evolution of the virus and its spread in the region.

​​Differential Disease Resistance of Indian Native Chicken Breeds to Experimental P. multocida Infection

2021 ◽  
Author(s):  
T.R. Kannaki ◽  
E. Priyanka ◽  
M. Abhilash ◽  
Santosh Haunshi
Keyword(s):  
Experimental Infection ◽  
Pasteurella Multocida ◽  
Clinical Signs ◽  
Mortality Rates ◽  
Susceptibility Pattern ◽  
Intranasal Route ◽  
Bacterial Diseases ◽  
Death Time ◽  
Native Chicken ◽  
Chicken Breeds

Background: Native chicken breeds are considered more disease tolerant than exotic chicken breeds especially for the bacterial diseases. Aseel, Ghagus and Vanaraja chicken breeds/ variety were evaluated for the disease tolerance/susceptibility pattern after experimental infection with P. multocida A:1 isolate. Methods: A total of 72 birds of three breeds viz., Aseel, Ghagus and Vanaraja (n=24 each) were divided into three groups. The birds were inoculated with 2.5x106 CFU/ml of virulent Pasteurella multocida A:1 isolate through intraperitoneal (I/P) and intranasal (I/N) routes at 12 weeks of age. Clinical signs, morbidity, mortality rates and lesions were observed in the infected birds. Result: The mortality rates were 83.3% in Assel breed against 100% in both Ghagus and Vanaraja breed in intraperitoneally infected groups. Upon intranasal infection, the mortality was 83.3% in Assel and Vanaraja breed against 100% in Ghagus breed. Aseel birds showed significantly better survivability and longer death time than Ghagus breed upon experimental infection with Pasteureall multocida A:1 isolate. Vanaraja breed showed tolerance comparable to Aseel in experimental infection via intranasal route.

Recent advances in the laboratory diagnosis of peste des petits ruminants

2021 ◽  
Vol 77 (05) ◽  
pp. 226-231
Author(s):  
WIESŁAW NIEDBALSKI ◽  
ANDRZEJ FITZNER ◽  
KRZYSZTOF BULENGER ◽  
ANDRZEJ KĘSY
Keyword(s):  
Reverse Transcription ◽  
Animal Health ◽  
Clinical Signs ◽  
Small Ruminants ◽  
Clinical Diagnostics ◽  
Molecular Diagnostic ◽  
Molecular Diagnostic Techniques ◽  
Peste Des Petits Ruminants ◽  
Rt Pcr ◽  
Agar Gel

Peste des petits ruminants (PPR) is a highly contagious and economically important, viral disease of small ruminants caused by the peste des petits ruminants virus (PPRV), which belongs to the genus Morbilivirus in the family Paramyxoviridae. PPR control is achieved mostly through vaccination and/or slaughter of susceptible animals coupled with clinical or laboratory-based diagnosis. Since clinical signs of PPR are not disease-specific and clinical diagnostics is not reliable, it should be confirmed by laboratory testing. Laboratory confirmation of clinical suspicions is made by detection of PPRV in blood, swabs or post-mortem tissues through classical virus isolation (VI), agar gel immunodiffusion (AGID)/agar gel precipitation test (AGPT), counter-immunoelectrophoresis (CIE), immunoperoxidase test (IPT) or enzyme-linked immunosorbent (ELISA) assays. However, these conventional methods have been superseded by more rapid, sensitive and accurate molecular diagnostic techniques based on the amplification of parts of either nucleocapsid (N) or fusion (F) protein gene, such as RT-PCR, real-time RT-PCR, reverse transcription loop-mediated isothermal amplification (RT-LAMP), reverse transcription recombinase polymerase amplification (RT-RPA) and Oxford nanopore MinION technology. Although these molecular diagnostic assays are accurate, rapid and sensitive, they have to be performed in laboratory settings, and samples must be transported under appropriate conditions from the field to the laboratory, which can delay the confirmation of PPRV infection. The recently developed immunochromatographic lateral flow device (IC-LFD) assay can be used in the field (“pen-side”) without the need for expensive equipment, so a well-established laboratory is not required. The control and eventual eradication of PPR is now one of the top priorities for the Food and Agriculture Organization (FAO) and the World Organization for Animal Health (OIE). In 2015, the international community agreed on a global strategy for PPR eradication, setting 2030 as a target date for elimination of the disease

scholarly journals Hematological alterations during experimental canine infection by Trypanosoma cruzi

2012 ◽  
Vol 21 (2) ◽  
pp. 151-156 ◽  
Author(s):  
Paulo Marcos Matta Guedes ◽  
Vanja Maria Veloso ◽  
Tiago Wilson Patriarca Mineo ◽  
Juliana Santiago-Silva ◽  
Geovan Crepalde ◽  
...  
Keyword(s):  
Trypanosoma Cruzi ◽  
Experimental Model ◽  
Chagas Disease ◽  
Experimental Infection ◽  
Clinical Signs ◽  
Beagle Dogs ◽  
Canine Infection ◽  
Loss Of Appetite ◽  
Experimental Canine ◽  
Hematological Alterations

To confirm that Beagle dogs are a good experimental model for Chagas disease, we evaluated hematological alterations during the acute and chronic phases in Beagle dogs infected with the Y, Berenice-78 (Be-78) and ABC strains of Trypanosomacruzi, correlating clinical signs with the parasitemia curve. We demonstrate that the acute phase of infection was marked by lethargy and loss of appetite. Simultaneously, we observed anemia, leukocytosis and lymphocytosis. Also,we describe hematological alterations and clinical signs that were positively correlated with the parasitemia during the experimental infection with the three strains of T.cruzi, and demonstrate that experimental infection of Beagle is a trustworthy model for Chagas disease.

Immunological Studies on Experimental Infection of Pigs with Ascaris suum Goeze, 1782. III.—The Antibody Response and Acquired Immunity

1964 ◽  
Vol 38 (1-2) ◽  
pp. 129-150 ◽  
Author(s):  
L. F. Taffs
Keyword(s):  
Antibody Response ◽  
Experimental Infection ◽  
Larval Growth ◽  
Clinical Signs ◽  
Acquired Immunity ◽  
Absorption Test ◽  
Challenge Dose ◽  
Larval Migration ◽  
Antibody Titres ◽  
Two Peaks

Two experiments are described in which antibodies against A. suum were detected in the circulation of infected pigs by means of the conglutinating complement absorption test. The pattern and nature of the antibody response was studied. In 21 out of 24 cases the sera antibody titres rose after test doses of infective eggs were given, and on 18 of these occasions a rise in titre was observed within seven days. Following infection two peaks of antibody were detected. At three to four weeks the antibody content of the serum reached its highest concentration, and a further rise was apparent between the 37th and 56th days.The phenomenon of “self-cure” was demonstrated following reinfection. This was manifested by a depression of the egg count and the elimination of Ascaris worms from the intestine, with a concomitant rise in the antibody content of the serum.In three out of five pigs which were initially infected, the infection became patent between the 51st and 58th days. On only one occasion out of thirteen were any superimposed larvae able to reach maturity.Pigs which had been previously infected exhibited resistance to a challenge dose. This was shown by (1) the absence of clinical signs, (2) a resistance to larval migration, and (3) an inhibition of larval growth. In this demonstration of an active acquired immunity to A. suum infection in pigs, a correlation between resistance and high sera titres was observed.

Experimental oral and ocularEncephalitozoon cuniculiinfection in rabbits

Parasitology ◽  
2010 ◽  
Vol 137 (12) ◽  
pp. 1749-1757 ◽  
Author(s):  
E. JEKLOVA ◽  
L. LEVA ◽  
K. KOVARCIK ◽  
J. MATIASOVIC ◽  
V. KUMMER ◽  
...  
Keyword(s):  
Antibody Response ◽  
Experimental Infection ◽  
Post Infection ◽  
Clinical Signs ◽  
High Dose ◽  
Cell Mediated Immunity ◽  
Specific Cell ◽  
Immunological Responses ◽  
Obligate Intracellular Pathogen ◽  
Dose Dependent

SUMMARYEncephalitozoon cuniculiis an obligate intracellular pathogen that has a wide host distribution, but primarily affects rabbits. The aim of this study was to characterize both the cell-mediated and the antibody response in rabbits after experimental infection using 2 different infection routes: oral and ocular. SPF rabbits were infected with low (103spores) and high (107spores) infection doses. Monitored parameters included clinical signs, detection of spores in urine, antibody response detected with ELISA, and cell-mediated immunity detected by antigen-driven lymphocyte proliferation. At week 13 post-infection, half of the rabbits in each group were suppressed by intramuscular administration of dexamethasone. At week 18 post-infection, animals were euthanized. Clinical signs were mild with exacerbation after immunosuppression. Spores in urine and antigen-specific cell-mediated immunity were detected from weeks 5 and 4 post-infection, respectively. Specific IgM was detected 1 week after infection, and IgG antibodies followed 1 week later in rabbits infected with the high dose. Immunological responses were dose dependent. The authors can conclude that both oral and ocular experimental infection withE. cuniculiresulted in an immune response of the infected animals. Rabbits could be used as an experimental model for the study of ocular microsporidiosis.

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