scholarly journals Leptospirosis in native mixed-breed sheep slaughtered in a semiarid region of Brazil

2017 ◽  
Vol 47 (2) ◽  
Author(s):  
Diego Figueiredo da Costa ◽  
Aline Ferreira da Silva ◽  
Arthur Willian de Lima Brasil ◽  
Ana Paula Pereira Loureiro ◽  
Fabrine Alexandre dos Santos ◽  
...  
Keyword(s):  
Bacterial Culture ◽  
Renal Tissue ◽  
Agglutination Test ◽  
Urine Samples ◽  
Semiarid Region ◽  
Tissue Samples ◽  
Mixed Breed ◽  
Leptospira Spp ◽  
Low Prevalence ◽  
Breed Sheep

ABSTRACT: Sheep breeding is an economic activity of great value for the Brazilian livestock industry, and infectious diseases can significantly compromise its productivity. The aim of this study was to detect Leptospira spp. in mixed breed sheep from a semiarid region of the State of Paraíba, Northeast Brazil. In total, 49 blood and renal tissue samples, as well as 25 urine samples, were collected from 49 sheep in the slaughter line. The microscopic agglutination test (MAT) was used to verify the presence of anti -Leptospira spp. antibodies in blood samples. Renal tissue and urine samples were analyzed by both PCR and bacterial culture. Sero reactivity was observed in 8.2% (4/49) of animals. Three renal samples were positive for leptospiral DNA by PCR although all urine samples were negative. No leptospires in pure culture were recovered from the samples tested. Low prevalence of Leptospira spp. observed by serology and PCR suggested that the rusticity of the mixed-breed sheep may have contributed to the low occurrence of leptospirosis in the semiarid region investigated.

scholarly journals Chronic prostatitis in a dog infected with a smooth strain of Brucella spp.

2021 ◽  
Vol 14 (1) ◽  
pp. 61-65
Author(s):  
Maria Rüegger ◽  
◽  
Maria Gorordo ◽  
Maria Luciani ◽  
Denise Pautasso ◽  
...  
Keyword(s):  
Prostate Gland ◽  
Perineal Hernia ◽  
Agglutination Test ◽  
Farm Animals ◽  
Serological Tests ◽  
Tissue Samples ◽  
Veterinary Clinic ◽  
Mixed Breed ◽  
Smooth Strain ◽  
Serum Agglutination

Dogs may be occasionally infected by smooth strains of Brucella spp. The infection is usually associated with the ingestion of contaminated material from parturition or abortion, or other tissues from infected farm animals, particularly cattle and pigs. A 6-year-old, male mixed breed dog from a rural area was admitted at a veterinary clinic for clinical examination. The dog had bilateral perineal hernia with dysuria and dyschezia, as well as small firm testicles with scrotal adhesions. Serological tests, including buffered plate antigen, serum agglutination test, and 2-mercaptoethanol test, were positive for smooth Brucella spp. strains, whereas a rapid slide agglutination test was negative for B. canis. Blood and prostate tissue samples yielded no bacterial isolates. Histopathology demonstrated interstitial lymphoplasmacytic and histiocytic infiltration of the prostate gland, with fibrosis and occasional disruption of glandular architecture. Immunohistochemistry demonstrated abundant Brucella spp. antigens in the cytoplasm of macrophages. This report supports the notion that not only B. canis, but also smooth Brucella spp. must be considered in the differential diagnosis of prostatitis in dogs.

scholarly journals Antibodies produced by dogs successfully challenged with live Leptospira spp. did not cross-react to Brucella antigen in a commercial rapid slide agglutination test that detects antibodies to Brucella canis

2018 ◽  
Vol 31 (1) ◽  
pp. 83-85
Author(s):  
Matthew R. Krecic
Keyword(s):  
Cross Reactivity ◽  
Agglutination Test ◽  
Slide Agglutination ◽  
Serologic Tests ◽  
Experimental Infections ◽  
Negative Results ◽  
Brucella Canis ◽  
Slide Agglutination Test ◽  
Leptospira Spp ◽  
Canine Brucellosis

Brucella canis is a cause of canine infertility and abortion. Veterinarians and veterinary laboratorians screen for antibodies to B. canis with serologic tests including a rapid slide agglutination test (RSAT; D-Tec CB, Zoetis, San Diego, CA). False-positive results are possible because of cross-reactivity to antibodies to some gram-negative bacteria. Cross-reactivity has been reported between antibodies of Brucella abortus and Leptospira spp. with serologic tests for bovine brucellosis; however, this has not been documented with serologic tests for canine brucellosis, to the author’s knowledge. The RSAT was evaluated with the sera from dogs experimentally challenged with 1 of 4 serovars of Leptospira spp.: L. kirschneri serovar Grippotyphosa, or L. interrogans serovars Canicola, Icterohaemorrhagiae, or Pomona. Experimental infections were confirmed through results of microscopic agglutination testing and/or lateral flow immunochromatography testing. The sera of 32 dogs collected at day 0 and days 7, 10, and 14 yielded negative results with the RSAT. Antibodies produced through experimental infections to these 4 serovars of Leptospira spp. did not cross-react with Brucella antigen with the RSAT; therefore, cross-reactivity of anti-leptospiral antibodies may not be of concern for B. canis rapid slide agglutination testing of dogs.

scholarly journals DIRECT AGGLUTINATION TEST WITH URINE SAMPLES FOR THE DIAGNOSIS OF VISCERAL LEISHMANIASIS

2004 ◽  
Vol 70 (1) ◽  
pp. 78-82 ◽  
Author(s):  
MOHAMMAD ZAHIDUL ISLAM ◽  
IFTIKHAR AHMED ◽  
ABDUL HALIM SARDER ◽  
RUSELLA MIRZA ◽  
EISAKU KIMURA ◽  
...  
Keyword(s):  
Visceral Leishmaniasis ◽  
Agglutination Test ◽  
Urine Samples ◽  
Direct Agglutination Test

FGFR testing from matched tissue and urine samples within the prospective real world clinico-pathological register trial BRIDGister.

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. e16532-e16532
Author(s):  
Ralph M. Wirtz ◽  
Richard Watts ◽  
Ronny Kellner ◽  
Reinhard Ortmann ◽  
Torsten Horns ◽  
...  
Keyword(s):  
Real World ◽  
Benign Lesion ◽  
Digital Pcr ◽  
Urine Samples ◽  
Urine Test ◽  
Tissue Samples ◽  
Before And After ◽  
Commercial Kits ◽  
Urine Testing ◽  
Matched Tissue

e16532 Background: The objective of the present study was to assess FGFR mutattions and fusions from matched urine and tissue samples from patients suspicious of bladder cancer and undergoing first TURB at the pilot center of the multicentric BRIDGister RealWorld Experience trial Methods: For this pilot study paraffin fixed pretreatment tissue samples from the first TURB of 28 pts participating in the BRIDGister trial and matched urine samples were prospectively collected and analyzed. RNA from FFPE tissues were extracted by commercial kits and analyzed by Therascreen FGFR IVD kit (Qiagen GmbH, Hilden). In addition urine samples were shipped for central isolation of extracellular vesicles and extraction of RNA (exoRNA.Exosome Diagnostics GmbH, Martinsried) and subsequently centrally analyzed by QIAcuity digital PCR (Qiagen, Hilden). Additional urine testing was performed by further technologies including central cytology. Concordance, Kruskal-Wallis, MannWhitney and Sensitivity/Specificity tests were analyzed by JMP 9.0.0 (SAS software). Results: The pilot cohort of the BRIDGister trial consisted of 28 patients (median age: 73, male 71% vs female 29%) of diverse clinical stages (Benign lesions/no tumor 21%, pTa 32%, pT1 21%, pT2 21%) and WHO 1973 grade (G1 7%, G2 43%, G3 21%). Based on FFPE tissue testing using Therascreen FGFR IVD kit 9 out of 28 patients exhibited FGFR alterations (32%). Based on exosomal RNA (exoRNA) and subsequent dPCR testing 8 out of 21 matched urine sampels were FGFR positive (38%). Comparison with tissue testing as probable gold standard revealed 71% sensitivity, 78% specificity, 63% PPV and 85%NPV. There were 3 patients being FGFR positive for exoRNA from urine with no mutation found in the corresponding TUR biopsy. One of these mutations could be validated by independent urine test. Furthermore one tumor harbored two tissue mutations (R248C, Y373C) but three urine mutations (R248C, Y373C, G370C) indicating substantial tumor heterogeneity. One FGFR3-TACC3 fusion was detected from a benign lesion, which was not found by the exosomal urine test. Conclusions: Extraction of exosomal RNA from urine followed by highly sensitive dPCR mutation testing is feasible with good concordance to matched tissue testing. Urine testing bears the potential of detecting additional mutations in a real world setting and might evolve as alternative approach for FGFR3 screening in a non invasive fashion without the need of transurethral biopsy. Discordant cases are further followed up and might reveal validation of mutation status in upcoming recurrences.Further exploration is warranted and includes the potential of monitoring patients with FGFR before and after therapeutic intervention. By the time of the congress an update of the data with approximately 50 matched pairs will be presented.

scholarly journals Cryo-Gel embedding compound for renal biopsy biobanking

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Malou L. H. Snijders ◽  
Marina Zajec ◽  
Laurens A. J. Walter ◽  
Remco M. A. A. de Louw ◽  
Monique H. A. Oomen ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Cutting Temperature ◽  
Renal Tissue ◽  
Tissue Samples ◽  
Normal Spleen ◽  
Renal Biopsies ◽  
Optimal Cutting Temperature ◽  
Embedding Medium ◽  
Rna And Dna

Abstract Optimal preservation and biobanking of renal tissue is vital for good diagnostics and subsequent research. Optimal cutting temperature (OCT) compound is a commonly used embedding medium for freezing tissue samples. However, due to interfering polymers in OCT, analysis as mass spectrometry (MS) is difficult. We investigated if the replacement of OCT with Cryo-Gel as embedding compound for renal biopsies would enable proteomics and not disturb other common techniques used in tissue diagnostics and research. For the present study, fresh renal samples were snap-frozen using Cryo-Gel, OCT and without embedding compound and evaluated using different techniques. In addition, tissue samples from normal spleen, skin, liver and colon were analyzed. Cryo-Gel embedded tissues showed good morphological preservation and no interference in immunohistochemical or immunofluorescent investigations. The quality of extracted RNA and DNA was good. The number of proteins identified using MS was similar between Cryo-Gel embedded samples, samples without embedding compound and OCT embedded samples. However, polymers in the OCT disturbed the signal in the MS, while this was not observed in the Cryo-Gel embedded samples. We conclude that embedding of renal biopsies in Cryo-Gel is an excellent and preferable alternative for OCT compound for both diagnostic and research purposes, especially in those cases where proteomic analysis might be necessary.

High frequency of seropositive and carriers of Leptospira spp. in pigs in the semiarid region of northeastern Brazil

2020 ◽  
Vol 52 (4) ◽  
pp. 2055-2061
Author(s):  
Juciê Jales Fernandes ◽  
João Pessoa Araújo Júnior ◽  
Camila Dantas Malossi ◽  
Leila Sabrina Ullmann ◽  
Diego Figueiredo da Costa ◽  
...  
Keyword(s):  
High Frequency ◽  
Northeastern Brazil ◽  
Semiarid Region ◽  
Leptospira Spp

scholarly journals Prevalencia de leptospirosis en perros de trabajo vacunados y en población humana con riesgo ocupacional

Biomédica ◽  
2020 ◽  
Vol 40 (Supl. 1) ◽  
pp. 62-75
Author(s):  
César A. Murcia ◽  
Miryam Astudillo ◽  
Marlyn H. Romero
Keyword(s):  
Agglutination Test ◽  
Microscopic Agglutination Test ◽  
Leptospira Spp

Introducción. Los perros de trabajo pueden infectarse con diversas serovariedades de Leptospira que se mantienen en sus túbulos renales e intersticios por mucho tiempo, por lo que se convierten en portadores y fuentes de infección para otros huéspedes.Objetivo. Establecer la prevalencia de Leptospira spp. en perros de trabajo vacunados y en población humana con riesgo ocupacional de seis unidades policiales en Colombia.Materiales y métodos. Mediante tres instrumentos estructurados, se evaluaron 92 perros de trabajo con inmunización previa contra Leptospira spp. (65 machos y 27 hembras) y 69 personas de seis unidades policiales de los municipios de Manizales, Pereira, Armenia, Ibagué, Tuluá y Cali. Se obtuvieron muestras sanguíneas de las personas y de los perros, las cuales se evaluaron mediante la prueba de microaglutinación (Microscopic Agglutination Test, MAT) en 24 serogrupos. Se hizo un examen clínico de los perros y se obtuvieron muestras de orina para urocultivo.Resultados. La seroprevalencia de leptospirosis en las personas fue de 2,9 % (n=2) y en los perros de 57,61 % (n=53). Los serogrupos más prevalentes en los perros fueron Leptospira canicola y L. panama. El urocultivo fue positivo en 58,7 % (54/92) de las muestras y se encontró asociación estadísticamente significativa entre la edad de los perros (≥10 años; p=0,043) y la ubicación de la unidad policial (p=0,016).Conclusión. Las características epidemiológicas de la leptospirosis en los perros sugieren una presentación endémica de la infección. Se requieren algoritmos diagnósticos sensibles y específicos para investigar la leptospirosis canina y diferenciar los anticuerpos vacunales de la infección natural.

scholarly journals Epidemiological characterization and risk factors associated with leptospirosis and brucellosis in small ruminants sold at animal fair in the Sertão Region of Pernambuco State, a semiarid Region of Northeastern Brazil

2017 ◽  
Vol 38 (4) ◽  
pp. 1933 ◽  
Author(s):  
José Romero Alexandre Alves ◽  
Geilson Manoel de Souza Lima ◽  
José Dêvede da Silva ◽  
Diego Figueiredo da Costa ◽  
Fabrine Alexandre dos Santos ◽  
...  
Keyword(s):  
Risk Factors ◽  
Odds Ratio ◽  
Management System ◽  
Small Ruminants ◽  
Northeastern Brazil ◽  
Semiarid Region ◽  
Intensive Management ◽  
Serum Samples ◽  
Factors Associated ◽  
Leptospira Spp

The transit of infected animals may be a route for the introduction and dispersal of diseases, which necessitates protocols for the controlled entry of infected animals into herds. The objective of this study was to determine the prevalence of anti-Leptospira and anti-Brucella ovis antibodies in small ruminants sold at an animal fair in the Sertão region of the Pernambuco State, Northeastern Brazil, and to identify the possible risk factors associated with seropositivity. Serum samples were collected from 233 goats and 119 sheep, belonging to twelve different owners from November 2014 to June 2015. Diagnosis of Leptospira spp. infection was established using the microscopic agglutination test (MAT); for B. ovis infection, the agar gel immuno-diffusion (AGID) test was conducted. A total of 16/233 (6.87%; 95% CI = 4.27% – 10.83%) goats and 16/119 (13.45%; 95% CI = 8.67% – 21.24%) sheep were identified as seropositive for Leptospira spp. The most frequent serotype was Icterohaemorrhagiae. In goats, intensive management system (odds ratio = 15.8; p < 0.001) and consorted rearing of equines and goats (odds ratio = 7.3; p = 0.005) were identified as risk factors. There were no risk factors identified for sheep. Seven (5.88%; 95% CI = 2.88% – 11.65%) sheep were seropositive for B. ovis, and the intensive management system was identified as the risk factor (odds ratio = 11.5; p = 0.005). This suggests that Leptospira spp. and B. ovis infections occur in small ruminants commercialized in the Sertão region of the Pernambuco State. Thus, improvements to the sanitary conditions of the facilities and the control of synanthropic rodents are recommended.

scholarly journals ELISA is superior to bacterial culture and agglutination test in the diagnosis of brucellosis in an endemic area in China

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Nannan Xu ◽  
Wei Wang ◽  
Fengzhe Chen ◽  
Wen Li ◽  
Gang Wang
Keyword(s):  
Healthy Volunteers ◽  
Chinese Population ◽  
Bacterial Culture ◽  
Clinical Symptoms ◽  
Characteristic Curve ◽  
High Sensitivity ◽  
Agglutination Test ◽  
Specific Method ◽  
Elisa Assay ◽  
Positive Rate

Abstract Background Brucellosis is endemic in many areas in China. The current diagnosis of Brucellosis predominantly relies on the traditional bacterial culture and serum agglutination test. In this study, we aimed to explore the value of ELISA in the diagnosis of Brucellosis in Chinese population. Methods We recruited 235 patients with a diagnosis of Brucellosis at different clinical stages: 117 in acute, 78 in subacute, and 40 in chronic. We also recruited 248 control patients who presented with similar clinical symptoms but with a different diagnosis other than Brucellosis. In addition, 90 healthy volunteers were also recruited. Bacterial culture, agglutination test and ELISA assay were performed to detect Brucella spp. Results Among 235 patients with Brucellosis, 51 (21.7%) was positive for bacterial culture, 150 (63.8%) were positive by agglutination test, and 232 (98.7%) were positive by ELISA (IgG and/or IgM). When we stratified the patients based on the disease stages (acute, subacute and chronic), ELISA was the most sensitive method and showed a highest positive rate in all stages. By Receiver Operating Characteristic Curve analysis of ELISA results, we found that measurement of IgG level was superior to measurement of IgM level (AUC, 0.993 versus 0.877). Since the measurement of IgG itself missed rare cases in acute phase, we recommended measuring IgG and IgM simultaneously by ELISA for the diagnosis of Brucellosis. In term of the specificity of ELISA in the diagnosis of Brucellosis, our study showed that only 1.6% (4/248) non-Brucellosis patients were positive by ELISA; all positive cases were IgM only and none showed positive IgG. Similar results were found in healthy volunteers. In summary, our study concluded that ELISA is the most sensitive and specific method to detect Brucellosis in Chinese population. Conclusions ELISA assay is sensitive, fast, and convenient to detect Brucellosis. It shows the high sensitivity and specifity and should be used as a routine lab test when Brucellosis is suspected in clinical practice.

scholarly journals Development of a Genus-Specific Brucella Real-Time PCR Assay Targeting the 16S-23S rDNA Internal Transcribed Spacer from Different Specimen Types

2020 ◽  
Vol 7 (4) ◽  
pp. 175
Author(s):  
Rejoice Nyarku ◽  
Ayesha Hassim ◽  
Annelize Jonker ◽  
Melvyn Quan
Keyword(s):  
Sensitivity And Specificity ◽  
Internal Transcribed Spacer ◽  
Bacterial Culture ◽  
Limit Of Detection ◽  
Quantitative Polymerase Chain Reaction ◽  
Surface Protein ◽  
Qpcr Assay ◽  
Rapid Screening ◽  
Analytical Sensitivity ◽  
Tissue Samples

The aim of this study was to develop a 16S-23S ribosomal deoxyribonucleic acid internal transcribed spacer (ITS) quantitative polymerase chain reaction (qPCR) assay for the early diagnosis and rapid screening of brucellosis. Blood, milk, and tissue samples were spiked with B. abortus biovar 1 (B01988-18 strain) to determine the analytical sensitivity and specificity of the assay. The 95% limit of detection of the ITS qPCR assay was highest in tissue, followed by blood, then milk, i.e., 0.48, 4.43, and 15.18 bacteria/PCR reaction, respectively. The diagnostic performance of the assay was compared to the Brucella cell surface protein (BCSP) 31 qPCR assay and bacterial culture. Out of 56 aborted foetal tissue samples from bovine, ovine, and caprine, 33% (19/56) were positive for Brucella spp. The sensitivity and specificity of the ITS qPCR assay was 87% and 95% respectively, compared to 92% and 89% for the BCSP31 qPCR assay and 47% and 55% for bacterial culture, respectively. The assay was efficient, sensitive, and specific, making it a valuable tool in the early detection of the Brucella pathogen.

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