Bacteria Of Brucella Research Articles

Spatial prediction of human brucellosis susceptibility using an explainable optimized adaptive neuro fuzzy inference system

Brucellosis, a zoonotic disease caused by Brucella bacteria, poses significant risks to human, livestock, and wildlife health, alongside economic losses from livestock morbidity and mortality. This study improves Human Brucellosis Susceptibility Mapping (HBSM) by integrating the Adaptive Neuro-Fuzzy Inference System (ANFIS) with meta-heuristic algorithms, including Genetic Algorithm (GA) and Particle Swarm Optimization (PSO). Boruta-XGBoost identified key covariates, while VIF and tolerance tests addressed collinearity, and Shapley additive explanation (SHAP) values enhanced model interpretability. In Mazandaran province, Iran (2012–2018), the hybrid ANFIS-PSO model demonstrated superior performance (RMSE: 0.5076; R2: 0.6980). SHAP analysis highlighted mean elevation, NDVI, and relative humidity as the most impactful covariates, while max evaporation and precipitation had minimal influence. ANFIS-based models outperformed Support Vector Regression (SVR), offering a robust framework for brucellosis control. This approach enables effective interventions and resource allocation, with potential for improvement through advanced algorithms and greater interpretability.

Rapid detection of Brucella cells using a gold nanoparticle-based aptasensor via a simple colorimetric method

BackgroundBrucellosis is a major worldwide zoonotic disease that is caused by Brucella spp. and threatens the health of communities. Novel methods for rapid detection of Brucella bacteria are beneficial and necessary in preventing infection and subsequent economic losses. Constructing biosensors with nanoparticles is a promising approach for identification of pathogenic bacteria in a short time. This study aimed to introduce a new detection method of Brucella cells using a biosensor, based on gold nanoparticles and a specific aptamer, via a colorimetric reaction. In this work, gold nanoparticles (GNPs) were synthesized and attached to the aptamer through electrostatic bonding. The binding of aptamer to gold nanoparticles was confirmed by Uv/vis spectrophotometry, FT-IR, transmission electron microscope (TEM) and zeta sizer (DLS).ResultsIn the presence of the bacterial cells, aptamers were bound to their targets, and the surfaces of the nanoparticles were depleted from aptamers resulting in intensified peroxidation activity of GNPs, and with the addition of 3, 3′, 5, 5′-tetramethylbenzidine (TMB), the color of the solution was changed from red to purple, which indicated the presence of Brucella. The sensitivity of the aptasensor was investigated using different concentrations of Brucella cells and its specificity was confirmed against several species of bacteria. The results showed that the designed aptasensor was more sensitive compared to PCR assay method with the ability to detect 1.5 × 101 CFU/mL of the bacterial cells.ConclusionThese findings indicate that the designed aptasensor can be used as a simple and rapid diagnostic tool to detect Brucella cells without need to experts and expensive laboratory equipment.

Using ELISA to detect pathogen antibodies in wild mammal carcasses: a systematic literature review

Abstract Carcasses of wild mammals provide convenient samples for wildlife disease investigators. Specifically, antibodies can persist in the blood and tissues of animals up to a few days after death and can provide information on exposure to specific pathogens, including microorganisms with zoonotic implications, such as Toxoplasma gondii, Trichinella spp., Brucella spp., and Mycobacterium spp. Although screening samples from decaying wildlife for antibodies is not a new method, an overview of the literature with clear recommendations on best practices is lacking. Here, we present results from a systematic review of 115 studies using enzyme‐linked immunosorbent assay (ELISA) to detect pathogen antibodies in wild mammals across 298 individual research projects. We discuss the range of mammalian hosts and the pathogens most represented in the literature and suggest improvements to consider when using samples from decaying animals for seroinvestigation. Our results indicate that the most examined mammals were artiodactyl ungulates and that antibodies against the bacteria Brucella spp. are those most examined to date, followed by the protozoan Toxoplasma gondii, malignant catarrhal fever virus, Schmallenberg orthobunyavirus, and the coccidian Neospora caninum. The effect of haemolysis in serum samples on ELISA results was considered in only 3.7% of the research projects we reviewed, sample size decisions were not outlined in 83% of research projects, and half of the projects did not examine seroprevalence in different age classes. Nevertheless, these details are important for replicability and accurate interpretation of results. We highlight the benefits and limitations of detecting antibodies against pathogens in carcasses from wild mammalian groups. Wild mammals are reservoirs for a wide range of pathogens including those with zoonotic potential and investigating their carcasses can help wildlife investigators to better understand the epidemiology of many diseases with implications for wildlife, livestock, and human health.

Exploration of the Molecular and Phylogenetic Aspects of Brucella intermedia (Ochrobactrum intermedia)

Brucella bacteria are among the oldest known zoonotic pathogens and they have become iconic case studies in infectious diseases. Genome comparisons have led to the reclassification of the genus Ochrobactrum, with its individual species now being categorized as Brucella. This study aims to isolate and molecularly identify Ochrobactrum intermedia from Iraqi patients. One hundred seventy urine samples were collected from patients with various conditions suspected of brucellosis. Based on identification by the VITEK compact system, two of the bacterial isolates were identified as Brucella intermedia (Ochrobactrum intermedia) species. This was confirmed by polymerase chain reaction using genus-specific primers for the 16S rRNA and recA genes which are specific for B.intermedia. The 16S rRNA gene sequences were aligned using BLAST and the BioEdit program. It was observed that there was a remarkable 99% similarity among the Brucella intermedia sequences. The affiliation of the two novel strains of B. intermedia, identified as Brucella intermedia strain BC-TCC 16S ribosomal RNA gene (OP415407) and Brucella intermedia strain Baghdadies 16S ribosomal RNA gene (OP415409), was confirmed through the analysis of both 16S rRNA and recA genes. These findings suggest that the use of 16S RC-PCR and sequencing in clinical settings can improve patient care by increasing the sensitivity of detection and identification of bacterial pathogens, resulting in more diagnoses of bacterial infections. By studying novel strains in a phylogenetic tree, researchers can learn more about the diversity of a species and can identify potential new threats to human and animal health.

Potential Piperolactam A Isolated From Piper betle as Natural Inhibitors of Brucella Species Aminoacyl-tRNA Synthetase for Livestock Infections: In Silico Approach.

Brucellosis is an important global zoonosis caused by the bacterium Brucella sp. Brucellosis causes abortions, reproductive failure and reduced milk production, resulting in significant economic losses. Brucella species are reported to be resistant to antibiotics, which makes treatment difficult. The urgency of discovering new drug candidates to combat Brucella's infection necessitates the exploration of novel alternative agents with unique protein targets. Aminoacyl-tRNA synthetases (aaRSs), which have fundamental functions in translation, inhibit this process, stop protein synthesis and ultimately inhibit bacterial growth. The purpose of this study was to isolate piperolactam A compounds from the methanol extract of Piper betle leaves that have potential as antibacterials to inhibit the growth of Brucella sp. causing brucellosis in livestock and to analyse the mechanism of inhibitory activity of piperolactam A compounds against the aaRS enzyme through a molecular docking approach in silico. Piperolactam A was isolated from P. betle by column chromatography and characterized by UV, IR, 1D and 2D NMRs and MS, then tested for their inhibition mechanism against the enzymes threonyl-tRNA synthetase, leucyl-tRNA synthetase (LeuRS) and methionyl-tRNA synthetase in silico. The result in silico test is that piperolactam A has the potential to inhibit LeuRS enzyme with the greater binding affinity.

Brucella Species Circulating in Smallholder Dairy Cattle in Tanzania.

Brucellosis is a zoonosis caused by bacteria of the genus Brucella, which results in economic losses relating to livestock and threatens public health. A cross-sectional study was conducted to determine the molecular prevalence of Brucella species in smallholder dairy cattle in six regions of Tanzania from July 2019 to October 2020. Dairy cattle (n = 2048) were sampled from 1371 farms. DNA extracted from blood and vaginal swabs was tested for Brucella using qPCR targeting the IS711 gene and positives were tested for the alkB marker for B. abortus and BMEI1172 marker for B. melitensis. The molecular prevalence was 3.5% (95% CI: 2.8-4.4) with the highest prevalence 8.1% (95% CI: 4.6-13.0) in Njombe region. B. melitensis was the predominant species detected (66.2%). Further studies are recommended to understand the source of B. melitensis and its implications for veterinary public health. Livestock keepers should be informed of the risks and biosecurity practices to reduce the introduction and control of Brucella. Cattle and small ruminant vaccination programs could be implemented to control brucellosis in high-risk populations in the country.

Succession changes of microbial community for inferring the time since deposition of saliva.

Saliva is a common biological examination material at crime scenes and has high application value in forensic case investigations. It can reflect the suspect's time of crime at the scene and provide evidence of the suspect's criminal facts. Even though many researchers have proposed their experimental protocols for estimating the time since deposition (TsD) of saliva, there is still a relative lack of research on the use of microorganisms to estimate TsD. In the current study, the succession change of microbial community in saliva with different TsD values was explored to discern the microbial markers related to TsD of saliva. We gathered saliva samples from six unrelated healthy Han individuals living in Guizhou, China and exposed these samples to indoor conditions at six time points (0, 1, 3, 7, 15, and 28 days). Temporal changes of microbial compositions in these samples were investigated by 16S rRNA sequencing (V3-V4 regions). By assessing temporal variation patterns of microbial abundance at the genus level, four bacteria (Brucella, Prevotella, Pseudomonas, and Fusobacterium) were observed to show good time dependence in these samples. In addition, the hierarchical clustering and principal co-ordinates analysis results revealed that these saliva samples could be classified into t-short (≤7 days) and t-long (>7 days) groups. In the end, the random forest model was developed to predict the TsD of these samples. For the model, the root mean square error, R2, and mean absolute error between predicted and actual TsD values were 1.5213, 0.9851, and 1.1969, respectively. To sum up, we identified TsD-related microbial markers in saliva samples, which could be viewed as valuable markers for inferring the TsD of saliva.

Study of the Prevalence of Bovine Brucellosis (Brucella abortus) in General Proaño Parish: Evaluation using Rose Bengal Test and Confirmation through Competitive ELISA

Bovine brucellosis is an infectious pathology that compromises animal well-being and causes significant economic losses for livestock farmers. This disease leads to abortions and is caused by the bacterium Brucella abortus. In this research, the prevalence of bovine brucellosis (Brucella abortus) was estimated in General Proaño Parish using the Rose Bengal test and confirmation through competitive ELISA. Methodologically, The research was carried out between February and August 2023 on 100 animals from 25 locations in the Proaño parish, in the Morona canton, Ecuador. Blood serum was obtained from five breeds of cattle: Charolais, Holstein, Brown Swiss, Mestiza and Jersey. The collected samples were transported to the laboratory for their respective analysis. Five milliliters of venous blood were collected from the coccygeal vein, from which 1 mL of blood serum was obtained. The serum was used for disease diagnosis through the Rose Bengal test, and those that tested seropositive were reconfirmed using the competitive ELISA immunoassay method. The clinical analyses determined that there is a 0% prevalence of the pathology; based on these results, we can state that the null prevalence of Brucella may be due to environmental and geographical factors that influence its presence and transmission. Furthermore, the precision and sensitivity of the diagnostic methods used are crucial; however, the ELISA and Rose Bengal methods may have been insensitive and did not detect mild infections. Finally, Brucella infection may not be present during sampling due to temporal fluctuations in its prevalence. In conclusion, there is no scientific evidence of bovine brucellosis as the primary cause of abortions and gestational losses in the study area.

Applying a Fluorescence Polarization Assay for Detection of Brucellosis in Animals Using the Fluorescently Labeled Synthetic Oligosaccharides as Biosensing Tracer.

Brucellosis in animals is an infectious disease caused by bacteria of the genus Brucella. Known methods for diagnosing brucellosis face some challenges, due to the difficulties in isolating and standardizing the natural brucellosis antigen. In this work, we investigated the possibility of using the fluorescence polarization assay (FPA) with synthetic glycoconjugate biosensing tracers to detect antibodies against Brucella as a new methodology for diagnosing brucellosis. Based on the received results, the synthetic fluorescein-labeled trisaccharide tracer is most effective for Brucellosis detection. This tracer is structurally related to the immune determinant fragment of the Brucella LPS buildup of N-formyl-d-perosamine units, connected via α-(1→3)-linkage at the non-reducing end and α-(1→2)-linkage at the reducing end. The sensitivity and specificity in the case of the use of trisaccharide tracer 3b were 71% and 100% (Yuden's method) and 87% and 88% (Euclidean method), respectively, which is comparable with the diagnostic efficiency of traditionally used serological methods, such as the agglutination test (AT), complement fixation test (CFT), and Rose Bengal test (RBT). Given the known advantages of FPA (e.g., speed, compactness of the equipment, and standard reagents) and the increased specificity of the developed test system, it would be appropriate to consider its widespread use for the diagnosis of brucellosis in animals, including rapid testing in the field.

Diagnosis of an atypical fever in a 55-year-old man.

The paper describes a diagnostically challenging case of recurrent fever with an atypical course in a 55-year-old man. The authors highlight the significant difficulty in reaching a correct diagnosis, as well as the doubts and problems associated with the diagnostics. They suggest considering brucellosis as a diagnosis based on the patient's history and the course of the disease characterized by fluctuating, intermittent, and nocturnal fever. The aim of the study was to present an atypical and diagnostically challenging case of recurrent febrile episodes in a 55-year-old man. A comprehensive diagnostic workup, including laboratory tests, imaging, and specialist consultations, was conducted. The patient's medical history, physical examination, and various diagnostic tests were analyzed. In a patient with recurrent episodes of fever, an infection with Brucella spp. was detected, which was effectively treated with long-term antibiotic therapy. Imaging and laboratory diagnostics, along with specialist consultations, helped rule out other potential causes of the symptoms. The patient achieved lasting improvement following the treatment. There is a high probability that the patient was infected with Brucella bacteria. Diagnostic challenges and the rarity of the disease, considered non-existent in Poland, hinder prompt confirmation or exclusion of infection. The authors aimed to highlight the possibility of a higher frequency of brucellosis in Poland. They suggest that Brucella bacteria may still be present, causing chronic, unrecognized, recurrent fevers. Based on the case analysis, the authors indicate that the frequent occurrence of this disease in Poland might be higher than reported by statistics.

Seroprevalence of Brucella among Patients Visiting a Single-Center Hospital: A Cross-Sectional Study

Introduction: Brucellosis is a disease that can be contracted by humans through contact with infected animals or animal products. It can be transmitted through contaminated dairy products, so caution must be exercised when handling and preparing food. By taking precautions, the spread of this disease can be mitigated to protect both humans and animals. (1) Brucella spp is a type of bacteria that can cause an infection. The symptoms of this infection can range from mild flu-like symptoms to severe complications that affect different parts of the body. Because Brucella is able to invade the body and avoid the immune system, it's important to get an accurate diagnosis and start treatment as soon as possible. (2). (3)  Method: The study was conducted at Kalkaal Hospital from 2019 to 2023, spanning three years. Patients who went to the hospital's Outpatient department and were screened for Brucella were included in the study. Data on patients' demographics, including their residence, gender, age, and Brucella screening results, were collected and recorded over the study period. The participants' blood samples were gathered and analyzed for Brucella infection through a variety of diagnostic The clinical assessment included an examination of symptoms, medical history, and possible exposure to Brucella. To detect specific antibodies (IgM and IgG) against Brucella present in the blood serum, serological tests such as the Serum Agglutination Test (SAT), ELISA, and Rose Bengal Test were conducted. The blood samples were analyzed to identify the Brucella bacteria through blood cultures. In addition, the presence of Brucella DNA was confirmed in various clinical samples using Polymerase Chain Reaction (PCR). The Kalkaal Hospital Research Review Board gave approval for the study protocol. Data cleaning was carried out with the help of Excel. The analysis of data was performed using SPSS software version 25.  Results: According to the analysis of the data, 30.3% of patients were men, and 69.7% of patients were women. The age ranges were 0–19: 1245 (8.1%), 20–29: 3951 (25.7%), 30-39: 3027 (19.7%), 40–49: 1786 (11.6%), and 50+: 4582. (29.9 percent). In addition, 14884 (97.0%) of the outcomes were negative, while only 465 (3.0%) were positive.  Conclusion: The research carried out at Kalkaal Hospital in Mogadishu, Somalia, has revealed important information about the prevalence of Brucella infection in the area. The results suggest that a significant number of patients have tested positive for Brucella antibodies, which indicates that the disease is a significant burden on the local population. These findings add to the global knowledge of brucellosis and emphasize its severe and long-term effects. It is important for experts in this field to have further discussions and come to a consensus on how to address this issue.

Brucella NpeA is a secreted Type IV effector containing an N-WASP-binding short linear motif that promotes niche formation.

The modulation of actin polymerization is a common theme among microbial pathogens. Even though microorganisms show a wide repertoire of strategies to subvert the activity of actin, most of them converge in the ones that activate nucleating factors, such as the Arp2/3 complex. Brucella spp. are intracellular pathogens capable of establishing chronic infections in their hosts. The ability to subvert the host cell response is dependent on the capacity of the bacterium to attach, invade, avoid degradation in the phagocytic compartment, replicate in an endoplasmic reticulum-derived compartment and egress. Even though a significant number of mechanisms deployed by Brucella in these different phases have been identified and characterized, none of them have been described to target actin as a cellular component. In this manuscript, we describe the identification of a novel virulence factor (NpeA) that promotes niche formation. NpeA harbors a short linear motif (SLiM) present within an amphipathic alpha helix that has been described to bind the GTPase-binding domain (GBD) of N-WASP and stabilizes the autoinhibited state. Our results show that NpeA is secreted in a Type IV secretion system-dependent manner and that deletion of the gene diminishes the intracellular replication capacity of the bacterium. In vitro and ex vivo experiments demonstrate that NpeA binds N-WASP and that the short linear motif is required for the biological activity of the protein.IMPORTANCEThe modulation of actin-binding effectors that regulate the activity of this fundamental cellular protein is a common theme among bacterial pathogens. The neural Wiskott-Aldrich syndrome protein (N-WASP) is a protein that several pathogens target to hijack actin dynamics. The highly adapted intracellular bacterium Brucella has evolved a wide repertoire of virulence factors that modulate many activities of the host cell to establish successful intracellular replication niches, but, to date, no effector proteins have been implicated in the modulation of actin dynamics. We present here the identification of a virulence factor that harbors a short linear motif (SLiM) present within an amphipathic alpha helix that has been described to bind the GTPase-binding domain (GBD) of N-WASP stabilizing its autoinhibited state. We demonstrate that this protein is a Type IV secretion effector that targets N-WASP-promoting intracellular survival and niche formation.

Human brucellosis and associated risk factors in the Middle East region: A comprehensive systematic review, meta-analysis, and meta-regression

IntroductionHuman brucellosis, caused by the bacteria Brucella, is a significant infectious disease globally, also known as Mediterranean fever or Malta fever. MethodsThis meta-analysis and systematic review focuses on the prevalence rate, risk factors, and diagnostic methods of human brucellosis in Middle Eastern countries, where the disease remains a significant public health issue. The analysis included 92 studies conducted between 1993 and 2024, following specified inclusion and exclusion criteria among symptomatic patients across these countries. The prevalence rate was calculated by dividing positive samples by total samples. The I2 index and Chi-squared test assessed study heterogeneity. Significant heterogeneity occurred when I2 exceeded 50 %. ResultsThe highest prevalence rate was observed in Oman, Lebanon, and Kuwait countries, emphasizing a notable burden of Brucella infection in these regions. Risk factors associated with human brucellosis were identified, with unpasteurized dairy consumption and close animal contact being predominant. Various professions such as farmers, dairy factory workers, and agriculture workers showed higher prevalence rate. Gender analysis indicated a prevalence rate of 18.02 % (95 % CI: 11.55–25.51 %) in males and 13.61 % (95 % CI: 10.8–16.68 %) in females, with no significant difference in hospitalization rates. The prevalence rate of Brucella spp. was varied across detection methods, with immunocapture agglutination assay (Brucellacapt) showing the highest estimated prevalence rate of (44.04 %, 95 % CI: 27.71–61.04), followed by PCR (39.84 %, 95 % CI: 20.14–61.39) and culture (29.22 %, 95 % CI: 17.89–42.03). Among Brucella species, Brucella melitensis (B. melitensis) and Brucella abortus (B. abortus) were the highest prevalence rate. Although statistically insignificant, the meta-analysis also revealed an upward trend in prevalence rate from 1993 to 2024, (P value = 0.277). DiscussionThis comprehensive review emphasizes the need for tailored strategies to control brucellosis in the Middle East, highlighting the importance of timely diagnosis, public awareness, and effective treatment protocols. These findings provide valuable insights for policymakers and healthcare professionals working to mitigate the impact of this disease in the region.

A Method Utilizing an Image Visibility Graph to Portray the Arrangement of Genomic Data Sequencing, Gene Frequencies for The Peptidoglycan-Associated Lipoprotein (Pal) Gene in Brucella Spp., and Prevalence of Brucellosis in Nineveh

Brucellosis is a disease triggered by various Gram-negative bacteria (Brucella spp.), impacting animals through miscarriages and causing fever in humans. The verified reality that peptidoglycan-associated lipoprotein (Pal) proteins eist in multiple bacteria and display remarkable vaccine potential shifts the spotlight to this protein and its importance within bacterial systems. Furthermore, gaining insight into the implications of mutations in this protein becomes of utmost importance. Biological informatics software was utilized to carry out a comparative study of the Pal gene across different species of Brucella bacteria. Computational methods were employed to represent sequences using both CGR and FCGR techniques. The Pal protein’s secondary and tertiary structures were built, and comparisons were drawn regarding mutations present among various Brucella species. An assessment of instances of infection was conducted, and statistical analyses were eecuted concerning brucellosis in the Nineveh region. While no significant differences were observed in the Pal gene among Brucella species, noticeable variations became evident when employing CGR and FCGR methodologies. FCGR proves to be more precise for visualization compared to CGR. Particularly, B. endophytica ehibited the most notable changes in the Pal protein when compared to the standard type within the species. The frequency of brucellosis infections increases in correlation with rising population numbers. The initial CGR images might not ehibit noticeable differences, but utilizing the FCGR method makes it easier to distinguish these variations. This affirms that FCGR is more effective for assessing the degree of dissimilarities. The presence of brucellosis poses a concern, especially in regions characterized by dense populations. It is important to emphasize public education regarding the adoption of suitable health precautions to thwart the disease, coupled with the importance of vaccination.

New synthesis of oligosaccharides modelling the M epitope of the Brucella O-polysaccharide.

Brucellosis is a dangerous zoonotic disease caused by bacteria of the genus Brucella. Diagnosis of brucellosis is based on the detection in animal and human sera of antibodies to the O-polysaccharide of Brucella lipopolysaccharide. The currently employed serodiagnosis of brucellosis relies on the use of the Brucella O-polysaccharide as a diagnostic antigen. However, the existence of bacterial species, which also express O-polysaccharides structurally similar to that of Brucella, may decrease the specificity of the brucellosis detection due to false-positive test results. It has been shown that the efficiency of the test can be significantly improved by using synthetic oligosaccharides that correspond to the so-called M epitope of the Brucella O-antigen. This epitope is characterized by an α-(1→3)-linkage between d-perosamine units and is unique to Brucella. Here we report on an efficient approach to the synthesis of oligosaccharides that model the M epitope of the Brucella O-polysaccharide. The approach is based on the use of the α-(1→3)-linked disaccharide thioglycoside as the key donor block. Its application allowed the straightforward assembly of a set of four protected oligosaccharides, which includes a disaccharide, two trisaccharides, and a tetrasaccharide, in five glycosylation steps. The synthesized oligosaccharides are planned to be used in the development of diagnostic tools for identifying brucellosis in humans and domestic animals, as well as a potential vaccine against it.

Seroprevalence and molecular detection of brucellosis among Pakistani women with spontaneous abortion.

Human brucellosis is a neglected disease transmitted to humans from animals such as cattle, goats, dogs, and swine. The causative agents are bacteria of the genus Brucella, intracellular pathogens usually confined to the reproductive organs of their animal hosts causing sterility and abortions. The objective of the study was to determine the seroprevalence of brucellosis among women with spontaneous abortions (SAW) and compare this seroprevalence with that of healthy pregnant women (HPW). The case-control study was designed to determine the seroprevalence and molecular detection of brucellosis in women who suffered from spontaneous abortion and healthy pregnant women of the Haripur District of Pakistan. A total of 770 blood samples (n = 385 for each group) were collected from 9 public and 11 private hospitals in Haripur District from December 2021-March 2023. Data on demographic features, epidemiological variables, and risk factors were collected from each participant by structured questionnaires. Initial screening for brucellosis was performed by Rose Bengal Plate Test followed by qRT-PCR for molecular detection of the genus-specific BCSP-31 gene of Brucella. The study showed that anti-Brucella antibodies were more found in SAW 23.63% (91/385) than in HPW 1.29% (5/385). Brucella specific DNA was amplified in 89.01% (81/91) seropositive samples of SAW. Demographic features and risk factors such as age, urbanicity, socioeconomic status, education, occupation, and animal contact were found significantly associated with brucellosis (p ≤ 0.05). Consumption of unpasteurized raw milk (OR = 18.28, 95%CI: 8.16-40.94) was found highly concomitant with seroprevalence. This study reports the first evidence of involvement of brucellosis in spontaneous abortions in women of Pakistan. The study can be used to develop strategies for risk management during pregnancy, to raise awareness for brucellosis, and develop control programs.

Biodegradation of polyethylene terephthalate (PET) by Brucella intermedia IITR130 and its proposed metabolic pathway.

Accumulation of polyethylene terephthalate (PET) polyester in ecosystems across the globe is a major pollution of concern. Microbial degradation recently generated novel insights into the biodegradation of varieties of plastics. In this study, a PET degrading bacterium Brucella intermedia IITR130 was isolated from a contaminated lake ecosystem at Pallikaranai, Chennai, India. Incubation of the bacterium along with the PET sheet (0.1mm thickness) for 60 days resulted in 26.06% degradation, indicating a half-life of 137.8 days. Considerable changes in the surface morphology of the PET sheet were found as holes, pits, and cracks on incubation with strain IITR130, as revealed by scanning electron microscopy (SEM). After bacterial treatment of PET, the formation of new functional groups, most notably in the area of 3326cm-1 suggestive of O-H stretch, leading to carboxylic acid and alcohol as products were suggested by fourier transform infrared (FTIR) analysis. Monomethyl terephthalate (MMT) and terephthalic acid (TPA) were identified by gas chromatography-mass spectrometry (GC-MS) analysis as PET degradation metabolites. Tributyrin clearance assay confirmed the presence of a lipase/esterase enzyme in the strain IITR130. In this study, a degradation pathway for PET by an isolated and identified bacterium Brucella intermedia IITR130 was characterized in detail.

Investigating the Rate of Contamination of Milk and Traditional Dairy Products with Brucella Bacteria by PCR Method, Mamasani District, Fars Province, South of Iran

Investigating the Rate of Contamination of Milk and Traditional Dairy Products with Brucella Bacteria by PCR Method, Mamasani District, Fars Province, South of Iran

Contrasting roles for IgM and B-cell MHCII expression in Brucella abortus S19 vaccine-mediated efficacy against B. melitensis infection.

Brucella is a neglected zoonotic pathogen with a worldwide distribution. Our study delves into B-cell effector functions in live vaccine-mediated immunity against brucellosis. Notably, we found antibody production, particularly secretory IgM, confers protection against virulent Brucella melitensis in vaccinated mice, which was associated with complement activation. By contrast, B-cell MHCII expression negatively impacted vaccine efficacy. In addition, B-cell depletion after vaccination, but before the B. melitensis challenge, enhanced protection against infection, suggesting a detrimental B-cell role during the challenge phase. Interestingly, deficiency of T follicular helper cells, which are crucial for aiding germinal center B cells, dampened vaccine efficacy at later stages of challenge independent of antibody production. This study underscores contrasting and phase-dependent roles of B-cell effector functions in vaccine-mediated immunity against Brucella.

Seroprevalence study of brucellosis in wild boar hunted for private consumption in northeast Portugal

Brucellosis is an important infectious disease caused by bacteria of the genus Brucella. In the northeast region of Portugal, infection with Brucella melitensis is endemic in small ruminants, and there are also humans’ cases. However, the epidemiological role of the wild boar in the dynamics of this disease in this region is unknown. In this study, a total of 332 blood samples were collected from wild boar hunted in thirty-six hunting areas during the 2022/2023 hunting season. All were taken by the hunters for private consumption, with no evisceration or examination in the field. Serum samples were tested by indirect ELISA (i-ELISA). It was observed that 88 wild boars were exposed to Brucella spp., pointing to a seroprevalence of 26.5% (95% CI: 21.8 – 31.3%). This high prevalence underlines the importance that wild boar may have in the dynamics of this disease in the region and its potential transmission to other animals, and to humans (for example, during the handling of carcasses). Increased awareness and knowledge of brucellosis in wild boar is essential for the implementation of effective practices and habits and, consequently, for the control and prevention of this important zoonosis.