Bacteria Pasteurella Multocida Research Articles

Porcine reproductive and neonatal infections: Importance and threats of bacterial virophoria

The provisions of the doctrine of transfer the epizootic process of dangerous viral infections to the enzootic process and their rooting in pig production through the integration of their pathogen into the pig microbiome in the form of comorbid viral and bacterial infections are substantiated. The aim of the study is to systematize the bacterial virophoria in the epizootology of porcine reproductive and neonatal infections (PRNI) as a component of the enzootic cycle of emergent infections in the pig industry of Ukraine. Classical swine fever (CSF) virus: attenuated strain ‘IECVM 03’; Aujeszky’s disease (AD) virus: epizootic strains of Ukrainian origin of AD virus ‘18v UNDIEV’; Teschen disease (TD) virus: epizootic strain ‘Bucha’. Epizootic strains: pasteurella bacteria, streptococcus, lacto- and bifidobacteria. According to the results of the study, it was found that the rotating magnetic field of the right direction promoted the adsorption of the CSF virus on pasteurella cells. The Aujeszky’s disease virus was adsorbed on the bacteria Salmonella choleraesuis No. 34, Bacterium bifidum and Lactobacillus casei with an efficiency of 15–45% in the pH range of 8.5–9.5, at neutral pH (7.4) no more than 1.5% of the virus was adsorbed, and at acidic pH (3.0) the AD virus was not adsorbed et all. On bacteria Pasteurella multocida No. 7, AD virus was adsorbed in the pH range of 8.5–9.5 with an efficiency of no more than 1.5%; at neutral pH (7.4), up to 50% of the virus was adsorbed, and at acidic pH (3.0), no more than 1.5% of AD virus was adsorbed. The interaction of TD virus with bifidobacteria inhibited viral reproduction in the body of infected polecats, but preserved the reproductive activity of teschovirus in the presence of streptococci. The rooting of dangerous viral infections (AD and TD, circovirus and parvovirus infections, reproductive and respiratory syndrome, and endemic porcine diarrhea) in pig production has always been accompanied by the ‘engraftment’ of their pathogens in the microbiome of pig production facilities in the form of comorbid (i. e. clinically manifested) and/or associated infections (i. e. similar to the group of Minimal Residual Human Diseases — Maladie Résiduelle Minimale, MRD). A key role in the establishment of these diseases and the formation of their stationary centers in pig production is played by the virophoria of bacteria synergistic with their pathogens, in particular as part of the etiologic microflora of reproductive and neonatal infections in pigs

Isolasi Bakteri Endofit Balakacida (Chromolaena odorata) Asal Banda Aceh dan Uji Aktivitas Antimikroba terhadap Bakteri Patogen Pasteurella multocida dan Bacillus subtilis

Endophytic bacteria are bacteria that live in plant tissue without causing negative effects. Endophytic bacteria can produce bioactive compounds that can be used as antibacterial, anti-fungal, antiviral, anti-cancer, anti-diabetic, antimalarial and anti-immunosuppressive properties. Endophytic bacteria are found in all higher plants, one of which is balakacida (Chromolaena odorata). This study aims to isolate the endophytic bacteria balakacida plant from Banda Aceh, to test the antimicrobial activity against the pathogenic bacteria Pasteurella multocida and Bacillus subtilis. The samples used were young leaves of balakacida plant with the method of isolation and purification of endophytic bacteria and in vitro tests.The results showed that endophytic bacteria could be isolated from balakacida plant and showed inhibitory activity against the pathogenic bacteria Pasteurella multocida and Bacillus subtilis. Thus, the endophytic bacteria from balakacida have bioactive compounds that have potential as antimicrobials.

STUDY ON PATHOGENICITY OF PASTEURELLA MULTOCIDA WHICH ISOLATED FROM FARM ANIMALS AND MAN

This study was described for the nature of the pathpgenesis of bacteria Pasteurella multocida which was isolated from infected man made comparison between these bacteria and those from infected farm animals. The percentage of Pasteurella multcida diagnosed bacteria from animals and human was 29.4% and 16.9% respectively. Comparing to other culture media Pasteurella multocida selective agar medium was characterized by its selectivity and sensitivity and then was attempt for biotyping species and subspecies of isolated Pasteurella from animals and human samples were successfully achieved. Pathogenicity test was performed on mice, only nine human isolatetes and twenty-one animal isolates from Pasteurella multocida were virulent. Todistinguish between the pathogenesis of human and animal isolates, one isolated from human and animal were chosed, in addition to the standared strain. The mice had been experimentally infected by three different ways, I/P, I/T, I/Eye. The results were showed that Pasteurella multocida can produce lesions as fibrinous suppurative pneumonia in lungs, liver and spleen which were detected histopatho logically. However the animal isolates were more virulent than human or standared strain.

BACTERIAL, FUNGAL AND VIRAL ZOONOSES OF PETS

Today, pets are the source of numerous infectious diseases that can be transmitted to humans, as a result of their increasingly frequent contact. The most important viruses with zoonotic potential include rabies and influenza viruses as well as rotaviruses and noroviruses. However, the importance of individual viruses varies depending on the climate and infectious disease control systems in certain countries. Dogs, cats, and other increasingly popular types of pets can transmit bacterial zoonotic agents to humans in various ways. In addition to known pathogens such as the bacteria causing leptospirosis, salmonellosis, campylobacteriosis, or brucellosis, the bacteria Pasteurella multocida and Bartonella henselae transmitted by bites or scratches are also significant in human pathology. There has been a significant increase in the prevalence of methicillin-resistant strains of Staphylococcus aureus in isolates originating from pets and the transmission of these strains between humans and animals requires special attention. Furthermore, fungi causing diseases such as sporotrichosis or dermatophytosis are linked to long-term and persistent infections in humans. The epidemiological situation caused by SARS-CoV-2, and the assumption of an interspecies jump of this virus from animals to humans, including its documented presence in domestic cats, dogs, tigers, and martens, have raised the question of the possibility of virus transmission from pets to humans. However, the current pandemic is caused exclusively by SARS-CoV-2 transmission in the human population, and these animals are not a source of infection for humans. A significant number of zoonoses originating from pets is a threat to public health, thus requiring the "One Health" approach through close cooperation between human and veterinary medicine to develop and implement effective health measures for both humans and animals. As part of responsible ownership, pet owners must be informed by veterinarians about measures to prevent infectious diseases and certain risks that are related to keeping certain species of animals.

DEVELOPMENT OF MEANS FOR THE SPECIFIC PREVENTION OF MYXOMATOSIS AND PASTEURELLOSIS IN RABBITS

In the course of the work, an epizootic strain of the rabbit myxoma virus was isolated, and its adaptation to continuous cell cultures was carried out. When assessing the possibility of using an epizootic strain of myxoma of rab-bits for the manufacture of a vaccine, it was found that the isolated strain has low immunogenicity.
 For the manufacture of a vaccine for the prevention of pasteurellosis, bordetelliosis and myxomatosis in rab-bits, the rabbit myxoma virus (strain KMIEV-V141), bacteria Pasteurella multocida (strain KMIEV-B166), and Bor-detella bronchiseptica (strain KMIEV-B212) were used; parameters of cultivation of strains of myxoma of rabbits, pas-teurella and bordetella were worked out, inactivants and adjuvants were selected, methods of inactivation of pasteurel-la and bordetella of rabbits were worked out. A vaccine sample for the prevention of pasteurellosis, bordetelliosis and myxomatosis in rabbits has been prepared.

Heterologous Hyaluronic Acid Production in Kluyveromyces lactis.

Hyaluronic Acid (HA) is a biopolymer composed by the monomers Glucuronic Acid (GlcUA) and N-Acetyl Glucosamine (GlcNAc). It has a broad range of applications in the field of medicine, being marketed between USD 1000–5000/kg. Its primary sources include extraction of animal tissue and fermentation using pathogenic bacteria. However, in both cases, extensive purification protocols are required to prevent toxin contamination. In this study, aiming at creating a safe HA producing microorganism, the generally regarded as safe (GRAS) yeast Kluyveroymyces lactis is utilized. Initially, the hasB (UDP-Glucose dehydrogenase) gene from Xenopus laevis (xlhasB) is inserted. After that, four strains are constructed harboring different hasA (HA Synthase) genes, three of humans (hshasA1, hshasA2, and hshasA3) and one with the bacteria Pasteurella multocida (pmhasA). Transcript values analysis confirms the presence of hasA genes only in three strains. HA production is verified by scanning electron microscopy in the strain containing the pmHAS isoform. The pmHAS strain is grown in a 1.3 l bioreactor operating in a batch mode, the maximum HA levels are 1.89 g/L with a molecular weight of 2.097 MDa. This is the first study that reports HA production in K. lactis and it has the highest HA titers reported among yeast.

Integrative and Conjugative Elements (ICEs) in Pasteurellaceae Species and Their Detection by Multiplex PCR.

Strains of the Pasteurellaceae bacteria Pasteurella multocida and Mannheimia haemolytica are major etiological agents of bovine respiratory disease (BRD). Treatment of BRD with antimicrobials is becoming more challenging due to the increasing occurrence of resistance in infecting strains. In Pasteurellaceae strains exhibiting resistance to multiple antimicrobials including aminoglycosides, beta-lactams, macrolides and sulfonamides, the resistance determinants are often chromosomally encoded within integrative and conjugative elements (ICEs). To gain a more comprehensive picture of ICE structures, we sequenced the genomes of six strains of P. multocida and four strains of M. haemolytica; all strains were independent isolates and eight of them were multiple-resistant. ICE sequences varied in size from 49 to 79 kb, and were comprised of an array of conserved genes within a core region and varieties of resistance genes within accessory regions. These latter regions mainly account for the variation in the overall ICE sizes. From the sequence data, we developed a multiplex PCR assay targeting four conserved core genes required for integration and maintenance of ICE structures. Application of this assay on 75 isolates of P. multocida and M. haemolytica reveals how the presence and structures of ICEs are related to their antibiotic resistance phenotypes. The assay is also applicable to other members of the Pasteurellaceae family including Histophilus somni and indicates how clustering and dissemination of the resistance genes came about.

Avian cholera outbreaks threaten seabird species on Amsterdam Island.

Infectious diseases may be particularly critical for the conservation of endangered species. A striking example is the recurrent outbreaks that have been occurring in seabirds on Amsterdam Island for the past 30 years, threatening populations of three Endangered seabird species and of the endemic, Critically Endangered Amsterdam albatross Diomedea amsterdamensis. The bacteria Pasteurella multocida (avian cholera causative agent), and to a lesser extent Erysipelothrix rhusiopathiae (erysipelas causative agent), were both suspected to be responsible for these epidemics. Despite this critical situation, demographic trends were not available for these threatened populations, and the occurrence and characterization of potential causative agents of epizootics remain poorly known. The aims of the current study were to (i) provide an update of population trends for four threatened seabird species monitored on Amsterdam Island, (ii) assess the occurrence of P. multocida, and E. rhusiopathiae in live birds from five species, (iii) search for other infectious agents in these samples and, (iv) isolate and genotype the causative agent(s) of epizooties from dead birds. Our study shows that the demographic situation has worsened substantially in three seabird species during the past decade, with extremely low reproductive success and declining populations for Indian yellow-nosed albatrosses Thalassarche carteri, sooty albatrosses Phoebetria fusca, and northern rockhopper penguins Eudyptes moseleyi. Pasteurella multocida or E. rhusiopathiae were detected by PCR in live birds of all five investigated species, while results were negative for eight additional infectious agents. A single strain of P. multocida was repeatedly cultured from dead birds, while no E. rhusiopathiae could be isolated. These results highlight the significance of P. multocida in this particular eco-epidemiological system as the main agent responsible for epizootics. The study stresses the urgent need to implement mitigation measures to alter the course of avian cholera outbreaks threatening the persistence of seabird populations on Amsterdam Island.

Identification of a chondroitin synthase from an unexpected source, the green sulfur bacterium Chlorobium phaeobacteroides.

Glycosaminoglycans (GAGs) are known to be present in all animals as well as some pathogenic microbes. Chondroitin sulfate is the most abundant GAG in mammals where it has various structural and adhesion roles. The Gram-negative bacteria Pasteurella multocida Type F and Escherichia coli K4 produce extracellular capsules composed of unsulfated chondroitin or a fructosylated chondroitin, respectively. Such polysaccharides that are structurally related to host molecules do not generally provoke a strong antibody response thus are thought to be employed as molecular camouflage during infection. We observed a sequence from the photosynthetic green sulfur bacteria, Chlorobium phaeobacteroides DSM 266, which was very similar (~62% identical) to the open reading frames of the known bifunctional chondroitin synthases (PmCS and KfoC); some segments are strikingly conserved amongst the three proteins. Recombinant E. coli-derived Chlorobium enzyme preparations were found to possess bona fide chondroitin synthase activity in vitro. This new catalyst, CpCS, however, has a more promiscuous acceptor usage than the prototypical PmCS, which may be of utility in novel chimeric GAG syntheses. The finding of such a similar chondroitin synthase enzyme in C. phaeobacteroides is unexpected for several reasons including (a) a free-living nonpathogenic organism should not "need" an animal self molecule for protection, (b) the Proteobacteria and the green sulfur bacterial lineages diverged ~2.5-3 billion years ago and (c) the ecological niches of these bacteria are not thought to overlap substantially to facilitate horizontal gene transfer. CpCS provides insight into the structure/function relationship of this class of enzymes.

English

Respiratory diseases in sheep are a multifactorial etiology syndrome, causing great economic losses. This study was carried out with the aim of establishing a bacteriological diagnosis of respiratory diseases in sheep, on the basis of lungs with macroscopic lesions taken from sheep slaughtered at the Blida abattoir. A total of 150 samples (swabs and lung parenchyma) from 75 Ouled Djellal sheep, aged six to twelve months old, with pulmonary lesions, were collected to determine possible correlations between the etiological agents and the type of lesion. Hepatization (or consolidation) was the main lesion observed (70%), preferentially localized on the right apical lobe (88% of the cases). This is a special form of pneumonia called atypical pneumonia. A varied microbial flora was isolated, alone or in association, namely bacteria with respiratory tropism as well as others of secondary infection. The bacteria most frequently isolated were γ-hemolytic streptococci (18%), Escherichia coli (17.5%), Micrococcus species (14.5%), and coagulase-negative staphylococci (10.5%); the large family of Enterobacteriaceae represented nearly 43% of the isolates. The pneumotropic bacteria (Mannheimia haemolytica and Pasteurella multocida) which count for 5.6% of the isolates, turned out to be correlated with the hepatization lesions. Key words: Mannheimia haemolytica, Pasteurella multocida, pneumonia, sheep, Algeria.

Development of the method for identification and genotyping of the bacteria Pasteurella multocida and Mannheimia haemolytica on the basis of the pcr and phylogenetic analysis of bacterial cultures isolated from cattle

The results of development of a method for detection and genotyping of the bacteria Pasteurella multocida capsular five groups and Mannheimia haemolytica Al based on the multiplex polymerase chain reaction (PCR) with electrophoretic detection are submitted. Diagnostic sensitivity of the developed method was 103 CFU/ml in the study of the pure cultures and 105 CFU/g in the study of biological material. A study of 260 samples of biological material from infected animals revealed Pasteurella multocida in 50.0%, and Mannheimia haemolytica in 11.2% of the investigated samples. Circulation among the tested livestock of capsular groups B and E of Pasteurella multocida was not revealed. The majority of the tested samples contained group A, in some cases, group D, and, in one case, group F. On the basis of the phylogenetic analysis circulation of two different genetic types of Pasteurella multocida of the capsular group A was revealed.

Ocorrência de genes tad associados à formação de biofilme em isolados de Pasteurella multocida de pulmões de suínos com pneumonia

Os atuais sistemas de criação intensiva de suínos aumentam a pressão de seleção microbiana propiciando a disseminação de doenças respiratórias. A bactéria Pasteurella multocida é associada a diversas patologias respiratórias em animais submetidos a esse tipo de criação, causando grandes perdas econômicas. A formação de biofilme foi descrita in vitro em P. multocida e fatores analisados indicaram a facilitação na colonização dos tecidos, aumentando a resistência às defesas do hospedeiro e aos antibióticos. Os objetivos deste trabalho foram analisar a ocorrência de P. multocida em pneumonias de suínos e na microbiota de pulmões sem lesão e a ocorrência dos genes do lócus tad nestes isolados. Foram analisados 70 isolados de P. multocida de pulmões, sendo sessenta e sete com lesão e três sem lesão. Isolados do sorotipo A ocorreram principalmente em pulmões com lesões (85,71%), enquanto em pulmões sem lesão observou-se somente o sorotipo D. Os genes tadA, tadB, tadC, tadD, tadE tadF e tadG estavam presentes em 89,55% dos isolados de pulmões com lesões. Os genes tadA, tadB e tadC estavam presentes em todos os isolados de pulmões sem lesão, porém os genes tadD, tadE, tadF e tadG estavam presentes em 0%, 33,3%, 33,3% e 66,6%, dos isolados sem lesão, respectivamente. Neste trabalho observou-se a associação da ocorrência dos genes tadD, tadE e tadF em isolados de P. multocida e a presença de lesões em pulmões.

Porcine Respiratory Pathogens in Swine Farms Environment in Mexico

Respiratory pathogens are the main health problem in the swine industry worldwide. These pathogens are transmitted by direct contact between animals or by aerosols and however are not well known yet, if the environment works as its reservoir, inoculum and/or dispersion medium. The objective of this study was to determine the presence of respiratory pathogens in environmental samples from swine farms in Aguascalientes, Mexico, through of PCR and RT-PCR techniques. The bacteria Actinobacillus pleuropneumoniae and Pasteurella multocida were found viable in samples from water, food, soil and air. Streptococcus suis was found in a viable state in water samples. Haemophilus parasuis, Porcine Reproductive and Respiratory Syndrome virus and Swine Influenza virus (H1N1 and H3N2) were detected in drinking water samples. Mycoplasma hyopneumoniae and Porcine Circovirus type 2 (PCV2) were not detected in environmental samples. These results suggest that the environment of the farms acts as a reservoir, inoculum and/or vehicle of dispersion for these pathogens except for M. hyopneumoniae and PCV2.

Chemoenzymatic Synthesis with Distinct Pasteurella Heparosan Synthases: MONODISPERSE POLYMERS AND UNNATURAL STRUCTURES

Heparosan (-GlcUA-beta1,4-GlcNAc-alpha1,4-)(n) is a member of the glycosaminoglycan polysaccharide family found in the capsule of certain pathogenic bacteria as well as the precursor for the vertebrate polymers, heparin and heparan sulfate. The two heparosan synthases from the Gram-negative bacteria Pasteurella multocida, PmHS1 and PmHS2, were efficiently expressed and purified using maltose-binding protein fusion constructs. These relatively homologous synthases displayed distinct catalytic characteristics. PmHS1, but not PmHS2, was able to produce large molecular mass (100-800 kDa) monodisperse polymers in synchronized, stoichiometrically controlled reactions in vitro. PmHS2, but not PmHS1, was able to utilize many unnatural UDP-sugar analogs (including substrates with acetamido-containing uronic acids or longer acyl chain hexosamine derivatives) in vitro. Overall these findings reveal potential differences in the active sites of these two Pasteurella enzymes. In the future, these catalysts should allow the creation of a variety of heparosan and heparinoids with utility for medical applications.

Lipid composition-dependent incorporation of multiple membrane proteins into liposomes

Membrane proteins from bacteria Pasteurella multocida were used as a model for studying its incorporation into liposomes. An important step to achieve efficient high yield protein incorporation in proteoliposomes is the study of the more suitable lipid composition. To this end, we compared the amount of total protein, reconstituted by co-solubilization methods, into liposomes of phospholipids with different polar head groups and acyl chain lengths. The liposomes and proteoliposomes were characterised by isopycnic centrifugation in sucrose gradient and by dynamic light scattering. Experimental and theoretical results were compared considering the effects exerted through the hydrocarbon chain length, volume, and optimal cross-sectional area of the phospholipid (combined in the geometrical critical packing parameter, lipid–protein matching), critical spontaneous radius of curvature of the bilayer vesicle, phase transition temperature of the lipid and ratio of lipid–protein molecules present in the vesicles. The highest incorporation of multiple proteins was found with dipalmitoylphosphatidylcholine (DPPC), reaching a yield of 93% compared to the lower relative amounts incorporated in proteoliposomes of the other lipids. The incorporation of multiple proteins induces a proportional enhancement of vesicular dimension, since DPPC–proteoliposomes have an average diameter of 1850 Å, compared to the 1430 Å for pure DPPC vesicles.

Humoral immunity in cats infected with feline immunodeficiency virus or leukaemia virus

The humoral antibody responses of 82 domestic cats to the common commensal bacteria Pasteurella multocida and Staphylococcus aureus were measured by an indirect immunofluorescence assay to give a subjective quantification of specific IgG in serum. There was no significant difference in specific serum IgG levels between sick cats which tested antibody-positive to feline immunodeficiency virus or antigen-positive to feline leukaemia virus and sick, virus-negative cats. This finding suggested that there was no change in immune status, as measured by this method, in both feline leukemia and feline immunodeficiency virus infections, although, based on clinical signs shown by the virus-positive cats, overall immunosuppression was indicated. Feline immunodeficiency virus and feline leukemia virus infection may have an effect on cellular immunity, as is the case with human immunodeficiency virus.