A species of MORGANELLA formerly classified as a Proteus species. It is found in the feces of humans, dogs, other mammals, and reptiles. (From Bergey's Manual of Determinative Bacteriology, 9th ed)
A genus of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in the intestines of humans and a wide variety of animals, as well as in manure, soil, and polluted waters. Its species are pathogenic, causing urinary tract infections and are also considered secondary invaders, causing septic lesions at other sites of the body.
A family of gram-negative, facultatively anaerobic, rod-shaped bacteria that do not form endospores. Its organisms are distributed worldwide with some being saprophytes and others being plant and animal parasites. Many species are of considerable economic importance due to their pathogenic effects on agriculture and livestock.
A genus of gram-negative, facultatively anaerobic, straight rods which are motile by peritrichous flagella. These organisms are chemoorganotrophic and have both a respiratory and fermentative type of metabolism. (From Bergey's Manual of Determinative Bacteriology, 9th ed)
Gram-negative rods isolated from human urine and feces.
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
Infections with bacteria of the genus PROTEUS.
Infections with bacteria of the family ENTEROBACTERIACEAE.
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that is frequently isolated from clinical specimens. Its most common site of infection is the urinary tract.
Enzymes found in many bacteria which catalyze the hydrolysis of the amide bond in the beta-lactam ring. Well known antibiotics destroyed by these enzymes are penicillins and cephalosporins.
A group of antibiotic aminoglycosides differing only in the number of repeating residues in the peptide side chain. They are produced by Streptomyces and Actinomyces and may have broad spectrum antimicrobial and some antiviral properties.
Bacteria which lose crystal violet stain but are stained pink when treated by Gram's method.
Any tests that demonstrate the relative efficacy of different chemotherapeutic agents against specific microorganisms (i.e., bacteria, fungi, viruses).
An enzyme that catalyzes the decarboxylation of histidine to histamine and carbon dioxide. It requires pyridoxal phosphate in animal tissues, but not in microorganisms. EC 4.1.1.22.
An enzyme that catalyzes the conversion of urea and water to carbon dioxide and ammonia. EC 3.5.1.5.
A genus of gram-negative, facultatively anaerobic, rod-shaped bacteria whose organisms arrange singly, in pairs, or short chains. This genus is commonly found in the intestinal tract and is an opportunistic pathogen that can give rise to bacteremia, pneumonia, urinary tract and several other types of human infection.
A group of broad-spectrum antibiotics first isolated from the Mediterranean fungus ACREMONIUM. They contain the beta-lactam moiety thia-azabicyclo-octenecarboxylic acid also called 7-aminocephalosporanic acid.
One of the three domains of life (the others being Eukarya and ARCHAEA), also called Eubacteria. They are unicellular prokaryotic microorganisms which generally possess rigid cell walls, multiply by cell division, and exhibit three principal forms: round or coccal, rodlike or bacillary, and spiral or spirochetal. Bacteria can be classified by their response to OXYGEN: aerobic, anaerobic, or facultatively anaerobic; by the mode by which they obtain their energy: chemotrophy (via chemical reaction) or PHOTOTROPHY (via light reaction); for chemotrophs by their source of chemical energy: CHEMOLITHOTROPHY (from inorganic compounds) or chemoorganotrophy (from organic compounds); and by their source for CARBON; NITROGEN; etc.; HETEROTROPHY (from organic sources) or AUTOTROPHY (from CARBON DIOXIDE). They can also be classified by whether or not they stain (based on the structure of their CELL WALLS) with CRYSTAL VIOLET dye: gram-negative or gram-positive.

The hybrid-cluster protein ('prismane protein') from Escherichia coli. Characterization of the hybrid-cluster protein, redox properties of the [2Fe-2S] and [4Fe-2S-2O] clusters and identification of an associated NADH oxidoreductase containing FAD and [2Fe-2S]. (1/33)

Hybrid-cluster proteins ('prismane proteins') have previously been isolated and characterized from strictly anaerobic sulfate-reducing bacteria. These proteins contain two types of Fe/S clusters unique in biological systems: a [4Fe-4S] cubane cluster with spin-admixed S = 3/2 ground-state paramagnetism and a novel type of hybrid [4Fe-2S-2O] cluster, which can attain four redox states. Genomic sequencing reveals that genes encoding putative hybrid-cluster proteins are present in a range of bacterial and archaeal species. In this paper we describe the isolation and spectroscopic characterization of the hybrid-cluster protein from Escherichia coli. EPR spectroscopy shows the presence of a hybrid cluster in the E. coli protein with characteristics similar to those in the proteins of anaerobic sulfate reducers. EPR spectra of the reduced E. coli hybrid-cluster protein, however, give evidence for the presence of a [2Fe-2S] cluster instead of a [4Fe-4S] cluster. The hcp gene encoding the hybrid-cluster protein in E. coli and other facultative anaerobes occurs, in contrast with hcp genes in obligate anaerobic bacteria and archaea, in a small operon with a gene encoding a putative NADH oxidoreductase. This NADH oxidoreductase was also isolated and shown to contain FAD and a [2Fe-2S] cluster as cofactors. It catalysed the reduction of the hybrid-cluster protein with NADH as an electron donor. Midpoint potentials (25 degrees C, pH 7.5) for the Fe/S clusters in both proteins indicate that electrons derived from the oxidation of NADH (Em NADH/NAD+ couple: -320 mV) are transferred along the [2Fe-2S] cluster of the NADH oxidoreductase (Em = -220 mV) and the [2Fe-2S] cluster of the hybrid-cluster protein (Em = -35 mV) to the hybrid cluster (Em = -50, +85 and +365 mV for the three redox transitions). The physiological function of the hybrid-cluster protein has not yet been elucidated. The protein is only detected in the facultative anaerobes E. coli and Morganella morganii after cultivation under anaerobic conditions in the presence of nitrate or nitrite, suggesting a role in nitrate-and/or nitrite respiration.  (+info)

Phosphorylation of nucleosides by the mutated acid phosphatase from Morganella morganii. (2/33)

A novel nucleoside phosphorylation process using the food additive pyrophosphate as the phosphate source was investigated. The Morganella morganii gene encoding a selective nucleoside pyrophosphate phosphotransferase was cloned. It was identical to the M. morganii PhoC acid phosphatase gene. Sequential in vitro random mutagenesis was performed on the gene by error-prone PCR to construct a mutant library. The mutant library was introduced into Escherichia coli, and the transformants were screened for the production of 5'-IMP. One mutated acid phosphatase with an increased phosphotransferase reaction yield was obtained. With E. coli overproducing the mutated acid phosphatase, 101 g of 5'-IMP per liter (192 mM) was synthesized from inosine in an 88% molar yield. This improvement was achieved with two mutations, Gly to Asp at position 92 and Ile to Thr at position 171. A decreased K(m) value for inosine was responsible for the increased productivity.  (+info)

TEM-72, a new extended-spectrum beta-lactamase detected in Proteus mirabilis and Morganella morganii in Italy. (3/33)

A new natural TEM-2 derivative, named TEM-72, was identified in a Proteus mirabilis strain and in a Morganella morganii strain isolated in Italy in 1999. Compared to TEM-1, TEM-72 contains the following amino acid substitutions: Q39K, M182T, G238S, and E240K. Kinetic analysis showed that TEM-72 exhibits an extended-spectrum activity, including activity against oxyimino-cephalosporins and aztreonam. Expression of bla(TEM-72) in Escherichia coli was capable of decreasing the host susceptibility to the above drugs.  (+info)

Immunohistopathologic demonstration of pleuropneumonia associated with Morganella morganii in a piglet. (4/33)

Serofibrinous pleuropneumonia in a piglet was examined microbiologically and immunohistopathologically. Large numbers of Morganella morganii were isolated from the pneumonic lesion, but no other pathogens were identified. A large amount of M. morganii antigen was demonstrated, and its distribution was closely associated with the histologic lesion. This finding suggests that pleuropneumonia in piglets might be caused by M. morganii.  (+info)

Necrotizing fasciitis in a newborn infant: a case report. (5/33)

We report the case of a one-day-old newborn infant, female, birth weight 1900 g, gestational age 36 weeks presenting with necrotizing fasciitis caused by E. coli and Morganella morganii. The newborn was allowed to fall into the toilet bowl during a domestic delivery. The initial lesion was observed at 24 hours of life on the left leg at the site of the venipuncture for the administration of hypertonic glucose solution. Despite early treatment, a rapid progression occurred resulting in a fatal outcome. We call attention to the risk presented by this serious complication in newborns with a contaminated delivery, and highlight the site of the lesion and causal agents.  (+info)

Antibacterial effect of human V gamma 2V delta 2 T cells in vivo. (6/33)

V gamma 2V delta 2 cells, a class of T cells found only in primates, are reactive to nonpeptide organophosphate and alkylamine antigens secreted by bacteria and parasites. These cells make up 2-5% percent of human peripheral blood T cells but expand to make up 8-60% of peripheral blood T cells during bacterial and parasitic infections. We show here, using a chimeric severe combined immunodeficiency (SCID) mouse (hu-SCID) model, that human V gamma 2V delta 2 T cells mediate resistance to extracellular gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli and Morganella morganii) bacteria, as assessed by survival, body weight, bacterial loads, and histopathology. Surprisingly, this bacterial resistance was evident 1 day after infection, and bacteria were cleared well before gamma delta T cell expansion was detected 6 days after infection. Decreased resistance in V delta 2 T cell-depleted hu-SCID mice correlated with decreased serum IFN-gamma titers. Intravenous treatment of infected, reconstituted hu-SCID mice with pamidronate, a human V gamma 2V delta 2 T cell-specific aminobisphosphonate antigen, markedly increased the in vivo antibacterial effect of V gamma 2V delta 2 T cells. Therefore, this large pool of antigen-specific, yet immediately reactive memory human V gamma 2V delta 2 T cells is likely to be an important mediator of resistance against extracellular bacterial infection and may bridge the gap between innate and acquired immunity.  (+info)

Human V gamma 2V delta 2 T cells produce IFN-gamma and TNF-alpha with an on/off/on cycling pattern in response to live bacterial products. (7/33)

Whereas cytokine production in alphabeta T cells is rapidly regulated by exposure to peptide Ag, the mechanisms regulating cytokine production by gammadelta T cells are unknown. In this study, we demonstrate that human Vgamma2Vdelta2 T cells produce IFN-gamma and TNF-alpha as early as 2 h after Ag exposure, and that they produce these cytokines in a dose- and time- dependent manner in response to stimulation with a live bacterial product, iso-butylamine (IBA), but not to dead bacteria or LPS. gammadelta T cells began, ceased, and then resumed IFN-gamma and TNF-alpha generation in an on/off/on cycling pattern, both in vitro and in vivo, depending on the presence or absence of IBA. IFN-gamma and TNF-alpha, whose optimum production was dependent on IBA-stimulated gammadelta T cells, were critical for monocyte-mediated killing of Escherichia coli. By limiting cytokine production to periods of direct contact with live bacteria, gammadelta T cells focus their resources at the site of infection, while limiting systemic immunopathology. Thus, human gammadelta T cells may mediate innate resistance to extracellular bacteria via tightly regulated cytokine production without necessarily expanding in number.  (+info)

Enhancement of nucleoside phosphorylation activity in an acid phosphatase. (8/33)

Escherichia blattae non-specific acid phosphatase (EB-NSAP) possesses a pyrophosphate-nucleoside phosphotransferase activity, which is C-5'-position selective. Current mutational and structural data were used to generate a mutant EB-NSAP for a potential industrial application as an effective and economical protein catalyst in synthesizing nucleotides from nucleosides. First, Gly74 and Ile153 were replaced by Asp and Thr, respectively, since the corresponding replacements in the homologous enzyme from Morganella morganii reduced the K(m) value for inosine and thus increased the productivity of 5'-IMP. We determined the crystal structure of G74D/I153T, which has a reduced K(m) value for inosine, as expected. The tertiary structure of G74D/I153T was virtually identical to that of the wild-type. In addition, neither of the introduced side chains of Asp74 and Thr153 is directly involved in the interaction with inosine in a hypothetical binding mode of inosine to EB-NSAP, although both residues are situated near a potential inosine-binding site. These findings suggested that a slight structural change caused by an amino acid replacement around the potential inosine-binding site could significantly reduce the K(m) value. Prompted by this hypothesis, we designed several mutations and introduced them to G74D/I153T, to decrease the K(m) value further. This strategy produced a S72F/G74D/I153T mutant with a 5.4-fold lower K(m) value and a 2.7-fold higher V(max) value as compared to the wild-type EB-NSAP.  (+info)

"Morganella morganii" is a species of gram-negative, facultatively anaerobic, rod-shaped bacteria that is commonly found in the environment, including in soil, water, and associated with various animals. In humans, it can be part of the normal gut flora but can also cause infections, particularly in immunocompromised individuals or following surgical procedures. It is known to cause a variety of infections, such as urinary tract infections, wound infections, pneumonia, and bacteremia (bloodstream infection). The bacteria can produce a number of virulence factors, including enzymes that help it evade the host's immune system and cause tissue damage. It is resistant to many antibiotics, which can make treatment challenging.

'Proteus' doesn't have a specific medical definition itself, but it is related to a syndrome in medicine. Proteus syndrome is a rare genetic disorder characterized by the overgrowth of various tissues and organs in the body. The name "Proteus" comes from the Greek god Proteus, who could change his form at will, reflecting the diverse and ever-changing nature of this condition's symptoms.

People with Proteus syndrome experience asymmetric overgrowth of bones, skin, and other tissues, leading to abnormalities in body shape and function. The disorder can also affect blood vessels, causing benign tumors called hamartomas to develop. Additionally, individuals with Proteus syndrome are at an increased risk of developing certain types of cancer.

The genetic mutation responsible for Proteus syndrome is found in the AKT1 gene, which plays a crucial role in cell growth and division. This disorder is typically not inherited but instead arises spontaneously as a new mutation in the affected individual. Early diagnosis and management of Proteus syndrome can help improve patients' quality of life and reduce complications associated with the condition.

Enterobacteriaceae is a family of gram-negative, rod-shaped bacteria that are commonly found in the intestines of humans and animals. Many species within this family are capable of causing various types of infections, particularly in individuals with weakened immune systems. Some common examples of Enterobacteriaceae include Escherichia coli (E. coli), Klebsiella pneumoniae, Proteus mirabilis, and Salmonella enterica.

These bacteria are typically characterized by their ability to ferment various sugars and produce acid and gas as byproducts. They can also be distinguished by their biochemical reactions, such as their ability to produce certain enzymes or resist specific antibiotics. Infections caused by Enterobacteriaceae can range from mild to severe, depending on the species involved and the overall health of the infected individual.

Some infections caused by Enterobacteriaceae include urinary tract infections, pneumonia, bloodstream infections, and foodborne illnesses. Proper hygiene, such as handwashing and safe food handling practices, can help prevent the spread of these bacteria and reduce the risk of infection.

"Morganella" is a genus of gram-negative, facultatively anaerobic, rod-shaped bacteria that are commonly found in the environment, including in soil, water, and the gastrointestinal tracts of animals. The most well-known species within this genus is "Morganella morganii," which can cause various types of infections in humans, particularly in individuals with weakened immune systems.

"Morganella morganii" is a common cause of healthcare-associated infections, such as urinary tract infections, wound infections, and bacteremia (bloodstream infections). It can also cause traveler's diarrhea and other types of gastrointestinal infections.

In addition to its clinical importance, "Morganella morganii" is also notable for its ability to produce a variety of enzymes, including proteases, lipases, and hemolysins, which can contribute to its virulence and invasiveness in humans. It is resistant to many antibiotics, making it a challenging organism to treat in some cases.

"Providencia" is a term that refers to a type of bacteria that can cause infections in humans. The scientific name for this bacterium is "Providencia stuartii." It is part of the Enterobacteriaceae family and is commonly found in the gastrointestinal tract of humans and animals.

Providencia stuartii can cause a variety of infections, including urinary tract infections, wound infections, and bloodstream infections. It is often resistant to many antibiotics, which can make it difficult to treat. People who are hospitalized, have weakened immune systems, or use catheters are at increased risk for Providencia infections.

It's important to note that while "Providencia" refers to a specific type of bacteria, the term is not typically used in medical diagnoses or treatment. Instead, healthcare providers would specify the type of infection and the name of the bacterium causing it.

Proteus vulgaris is a species of Gram-negative, facultatively anaerobic, rod-shaped bacteria that are commonly found in soil, water, and the human digestive tract. They are named after the Greek god Proteus, who could change his shape at will, as these bacteria are known for their ability to undergo various morphological changes.

Proteus vulgaris is a member of the family Enterobacteriaceae and can cause opportunistic infections in humans, particularly in individuals with weakened immune systems or underlying medical conditions. They can cause a variety of infections, including urinary tract infections, wound infections, pneumonia, and bacteremia (bloodstream infections).

Proteus vulgaris is also known for its ability to produce urease, an enzyme that breaks down urea into ammonia and carbon dioxide. This can lead to the formation of urinary stones and contribute to the development of chronic urinary tract infections. Additionally, Proteus vulgaris can form biofilms, which can make it difficult to eradicate the bacteria from infected sites.

In a medical context, identifying Proteus vulgaris is important for determining appropriate antibiotic therapy and managing infections caused by this organism.

Proteus infections are caused by the bacterium Proteus mirabilis or other Proteus species. These bacteria are gram-negative, opportunistic pathogens that can cause various types of infections, including urinary tract infections (UTIs), wound infections, and bacteremia (bloodstream infections). Proteus infections are often associated with complicated UTIs, catheter-associated UTIs, and healthcare-associated infections. They can be difficult to treat due to their ability to produce enzymes that inactivate certain antibiotics and form biofilms.

Proteus infections can cause symptoms such as fever, chills, fatigue, and discomfort in the affected area. In UTIs, patients may experience symptoms like burning during urination, frequent urges to urinate, and cloudy or foul-smelling urine. Wound infections caused by Proteus can lead to delayed healing, increased pain, and pus formation. Bacteremia can cause sepsis, a life-threatening condition that requires immediate medical attention.

Treatment for Proteus infections typically involves antibiotics, such as fluoroquinolones, trimethoprim-sulfamethoxazole, or carbapenems. The choice of antibiotic depends on the severity and location of the infection, as well as the patient's overall health status and any underlying medical conditions. In some cases, surgical intervention may be necessary to drain abscesses or remove infected devices like catheters.

Enterobacteriaceae are a large family of gram-negative bacteria that are commonly found in the human gut and surrounding environment. Infections caused by Enterobacteriaceae can occur when these bacteria enter parts of the body where they are not normally present, such as the bloodstream, urinary tract, or abdominal cavity.

Enterobacteriaceae infections can cause a range of symptoms depending on the site of infection. For example:

* Urinary tract infections (UTIs) caused by Enterobacteriaceae may cause symptoms such as frequent urination, pain or burning during urination, and lower abdominal pain.
* Bloodstream infections (bacteremia) caused by Enterobacteriaceae can cause fever, chills, and sepsis, a potentially life-threatening condition characterized by a whole-body inflammatory response to infection.
* Pneumonia caused by Enterobacteriaceae may cause cough, chest pain, and difficulty breathing.
* Intra-abdominal infections (such as appendicitis or diverticulitis) caused by Enterobacteriaceae can cause abdominal pain, fever, and changes in bowel habits.

Enterobacteriaceae infections are typically treated with antibiotics, but the increasing prevalence of antibiotic-resistant strains of these bacteria has made treatment more challenging in recent years. Preventing the spread of Enterobacteriaceae in healthcare settings and promoting good hygiene practices can help reduce the risk of infection.

Proteus mirabilis is a species of Gram-negative, facultatively anaerobic, rod-shaped bacteria that are commonly found in the environment, particularly in soil and water. In humans, P. mirabilis can be part of the normal gut flora but can also cause opportunistic infections, particularly in the urinary tract. It is known for its ability to produce urease, which can lead to the formation of urinary stones and blockages.

P. mirabilis infections are often associated with underlying medical conditions such as diabetes, kidney disease, or urinary catheterization. Symptoms of a P. mirabilis infection may include fever, cloudy or foul-smelling urine, and pain or burning during urination. Treatment typically involves antibiotics that are effective against Gram-negative bacteria, although resistance to certain antibiotics is not uncommon in P. mirabilis isolates.

Beta-lactamases are enzymes produced by certain bacteria that can break down and inactivate beta-lactam antibiotics, such as penicillins, cephalosporins, and carbapenems. This enzymatic activity makes the bacteria resistant to these antibiotics, limiting their effectiveness in treating infections caused by these organisms.

Beta-lactamases work by hydrolyzing the beta-lactam ring, a structural component of these antibiotics that is essential for their antimicrobial activity. By breaking down this ring, the enzyme renders the antibiotic ineffective against the bacterium, allowing it to continue growing and potentially causing harm.

There are different classes of beta-lactamases (e.g., Ambler Class A, B, C, and D), each with distinct characteristics and mechanisms for breaking down various beta-lactam antibiotics. The emergence and spread of bacteria producing these enzymes have contributed to the growing problem of antibiotic resistance, making it increasingly challenging to treat infections caused by these organisms.

To overcome this issue, researchers have developed beta-lactamase inhibitors, which are drugs that can bind to and inhibit the activity of these enzymes, thus restoring the effectiveness of certain beta-lactam antibiotics. Examples of such combinations include amoxicillin/clavulanate (Augmentin) and piperacillin/tazobactam (Zosyn).

Streptothricins are a type of antibiotic produced by certain strains of the bacterium Streptomyces lavendulae. These antibiotics are known to be highly toxic to many species of bacteria, including some that are resistant to other antibiotics. They work by inhibiting protein synthesis in bacterial cells.

Streptothricins are not commonly used in clinical medicine due to their narrow therapeutic index and high toxicity to mammalian cells. However, they have been used experimentally in research settings to study bacterial physiology and as a topical treatment for skin infections in veterinary medicine.

It's worth noting that exposure to streptothricins can cause allergic reactions and other adverse effects in some individuals, so handling and use of these substances should be done with caution and under the guidance of trained professionals.

Gram-negative bacteria are a type of bacteria that do not retain the crystal violet stain used in the Gram staining method, a standard technique used in microbiology to classify and identify different types of bacteria based on their structural differences. This method was developed by Hans Christian Gram in 1884.

The primary characteristic distinguishing Gram-negative bacteria from Gram-positive bacteria is the composition and structure of their cell walls:

1. Cell wall: Gram-negative bacteria have a thin peptidoglycan layer, making it more susceptible to damage and less rigid compared to Gram-positive bacteria.
2. Outer membrane: They possess an additional outer membrane that contains lipopolysaccharides (LPS), which are endotoxins that can trigger strong immune responses in humans and animals. The outer membrane also contains proteins, known as porins, which form channels for the passage of molecules into and out of the cell.
3. Periplasm: Between the inner and outer membranes lies a compartment called the periplasm, where various enzymes and other molecules are located.

Some examples of Gram-negative bacteria include Escherichia coli (E. coli), Pseudomonas aeruginosa, Klebsiella pneumoniae, Salmonella enterica, Shigella spp., and Neisseria meningitidis. These bacteria are often associated with various infections, such as urinary tract infections, pneumonia, sepsis, and meningitis. Due to their complex cell wall structure, Gram-negative bacteria can be more resistant to certain antibiotics, making them a significant concern in healthcare settings.

Microbial sensitivity tests, also known as antibiotic susceptibility tests (ASTs) or bacterial susceptibility tests, are laboratory procedures used to determine the effectiveness of various antimicrobial agents against specific microorganisms isolated from a patient's infection. These tests help healthcare providers identify which antibiotics will be most effective in treating an infection and which ones should be avoided due to resistance. The results of these tests can guide appropriate antibiotic therapy, minimize the potential for antibiotic resistance, improve clinical outcomes, and reduce unnecessary side effects or toxicity from ineffective antimicrobials.

There are several methods for performing microbial sensitivity tests, including:

1. Disk diffusion method (Kirby-Bauer test): A standardized paper disk containing a predetermined amount of an antibiotic is placed on an agar plate that has been inoculated with the isolated microorganism. After incubation, the zone of inhibition around the disk is measured to determine the susceptibility or resistance of the organism to that particular antibiotic.
2. Broth dilution method: A series of tubes or wells containing decreasing concentrations of an antimicrobial agent are inoculated with a standardized microbial suspension. After incubation, the minimum inhibitory concentration (MIC) is determined by observing the lowest concentration of the antibiotic that prevents visible growth of the organism.
3. Automated systems: These use sophisticated technology to perform both disk diffusion and broth dilution methods automatically, providing rapid and accurate results for a wide range of microorganisms and antimicrobial agents.

The interpretation of microbial sensitivity test results should be done cautiously, considering factors such as the site of infection, pharmacokinetics and pharmacodynamics of the antibiotic, potential toxicity, and local resistance patterns. Regular monitoring of susceptibility patterns and ongoing antimicrobial stewardship programs are essential to ensure optimal use of these tests and to minimize the development of antibiotic resistance.

Histidine Decarboxylase is a medical term that refers to an enzyme found in various organisms, including humans. This enzyme plays a crucial role in the conversion of the amino acid L-histidine into histamine, which is a biogenic amine that acts as a neurotransmitter and inflammatory mediator in the human body.

Histidine decarboxylase is found in several tissues, including the central nervous system, gastrointestinal tract, and skin. It requires pyridoxal 5'-phosphate (PLP) as a cofactor for its enzymatic activity. Abnormal levels or activity of histidine decarboxylase have been implicated in several medical conditions, including allergic reactions, inflammation, and neuropsychiatric disorders.

Inhibitors of histidine decarboxylase are being investigated as potential therapeutic agents for the treatment of various diseases, such as mast cell-mediated disorders, gastrointestinal disorders, and neurological conditions associated with abnormal histamine levels.

Urease is an enzyme that catalyzes the hydrolysis of urea into ammonia and carbon dioxide. It is found in various organisms, including bacteria, fungi, and plants. In medicine, urease is often associated with certain bacterial infections, such as those caused by Helicobacter pylori, which can produce large amounts of this enzyme. The presence of urease in these infections can lead to increased ammonia production, contributing to the development of gastritis and peptic ulcers.

Klebsiella is a genus of Gram-negative, facultatively anaerobic, encapsulated, non-motile, rod-shaped bacteria that are part of the family Enterobacteriaceae. They are commonly found in the normal microbiota of the mouth, skin, and intestines, but can also cause various types of infections, particularly in individuals with weakened immune systems.

Klebsiella pneumoniae is the most common species and can cause pneumonia, urinary tract infections, bloodstream infections, and wound infections. Other Klebsiella species, such as K. oxytoca, can also cause similar types of infections. These bacteria are resistant to many antibiotics, making them difficult to treat and a significant public health concern.

Cephalosporins are a class of antibiotics that are derived from the fungus Acremonium, originally isolated from seawater and cow dung. They have a similar chemical structure to penicillin and share a common four-membered beta-lactam ring in their molecular structure.

Cephalosporins work by inhibiting the synthesis of bacterial cell walls, which ultimately leads to bacterial death. They are broad-spectrum antibiotics, meaning they are effective against a wide range of bacteria, including both Gram-positive and Gram-negative organisms.

There are several generations of cephalosporins, each with different spectra of activity and pharmacokinetic properties. The first generation cephalosporins have a narrow spectrum of activity and are primarily used to treat infections caused by susceptible Gram-positive bacteria, such as Staphylococcus aureus and Streptococcus pneumoniae.

Second-generation cephalosporins have an expanded spectrum of activity that includes some Gram-negative organisms, such as Escherichia coli and Haemophilus influenzae. Third-generation cephalosporins have even broader spectra of activity and are effective against many resistant Gram-negative bacteria, such as Pseudomonas aeruginosa and Klebsiella pneumoniae.

Fourth-generation cephalosporins have activity against both Gram-positive and Gram-negative organisms, including some that are resistant to other antibiotics. They are often reserved for the treatment of serious infections caused by multidrug-resistant bacteria.

Cephalosporins are generally well tolerated, but like penicillin, they can cause allergic reactions in some individuals. Cross-reactivity between cephalosporins and penicillin is estimated to occur in 5-10% of patients with a history of penicillin allergy. Other potential adverse effects include gastrointestinal symptoms (such as nausea, vomiting, and diarrhea), neurotoxicity, and nephrotoxicity.

Bacteria are single-celled microorganisms that are among the earliest known life forms on Earth. They are typically characterized as having a cell wall and no membrane-bound organelles. The majority of bacteria have a prokaryotic organization, meaning they lack a nucleus and other membrane-bound organelles.

Bacteria exist in diverse environments and can be found in every habitat on Earth, including soil, water, and the bodies of plants and animals. Some bacteria are beneficial to their hosts, while others can cause disease. Beneficial bacteria play important roles in processes such as digestion, nitrogen fixation, and biogeochemical cycling.

Bacteria reproduce asexually through binary fission or budding, and some species can also exchange genetic material through conjugation. They have a wide range of metabolic capabilities, with many using organic compounds as their source of energy, while others are capable of photosynthesis or chemosynthesis.

Bacteria are highly adaptable and can evolve rapidly in response to environmental changes. This has led to the development of antibiotic resistance in some species, which poses a significant public health challenge. Understanding the biology and behavior of bacteria is essential for developing strategies to prevent and treat bacterial infections and diseases.

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Other bacterial pathogens identified have been Chryseobacterium spp., Morganella morganii and Bacillus cereus spp.. Wild ...
Morganella morganii Providencia rettgeri Serratia spp. Pseudomonas spp. Listeria Cefazolin is pregnancy category B, indicating ...
M: Morganella morganii In vitro sensitivities are not applicable in vivo. In general, treatment with cephalosporins results in ...
Proteus mirabilis, Proteus vulgaris, and Morganella morganii are the most common organisms isolated; less common organisms ...
It is also active against some Enterobacter species, Morganella morganii, and Serratia species. Temocillin has no useful ...
"A bifunctional urease enhances survival of pathogenic Yersinia enterocolitica and Morganella morganii at low pH". Journal of ...
Escherichia coli Haemophilus influenzae Klebsiella species Morganella morganii Neisseria gonorrhoeae Proteus mirabilis Proteus ...
Common bacterial species include Pantoea, Citrobacter, Morganella morganii, Pseudomonas aeruginosa, Coagulase-Negative ...
Morganella morganii, and Pseudomonas aeruginosa. People with purple urine bag syndrome usually do not complain of any symptoms ...
Urinary tract infection caused by urease-producing organisms (Proteus, Pseudomonas aeruginosa, Klebsiella, Morganella morganii ...
Some Morganella morganii, Proteus vulgaris, Providencia rettgeri, Pseudomonas aeruginosa, Serratia marcescens and Klebsiella ...
Currently, bacteria like Enterobacter aerogenes, Morganella morganii and Pseudomonas aeruginosa are resistant to cefprozil, ...
Morganella morganii and members of the α, γ, and δ Proteobacteria. These may benefit the leech by providing nutrients which are ...
... and the petroleum extract exhibits a similar effect against Morganella morganii. The methanolic extract is also effective as a ...
... and Morganella morganii. The primary skin lesion usually starts with a macule that is painless, round and erythematous. Then, ...
... a genus of bacteria containing the single species Morganella morganii Morganella (fungus), a genus of puffball fungi in the ... Morganella may refer to: Surname Michel Morganella (born 17 May 1989), a Swiss footballer Michele Morganella (born 25 April ... family Agaricaceae Morganella (insect), a scale insect genus in the family Diaspididae Morganella (brachiopod), a Devonian ... period brachiopod in the family Araksalosiidae Specific epithet Phyllophaga morganella a species of New World scarab beetle in ...
Morganella morganii, Proteus mirabilis, P. vulgaris, Shigella sonnei, Yersinia enterocolitica, Salmonella, Haemophilus ...
1914 Morganella Zeller 1948 Peziza morganii Massee 1902 Physospora morganii Sacc. & Traverso 1911 Polyporus morganii Frost 1879 ... 1887 Stemonitis morganii Peck 1880 Steccherinum morganii Banker 1906 (now Steccherinum reniforme) Trametes morganii Lloyd 1919 ... now Hygrophoropsis morganii) Geastrum morganii Lloyd 1902 Hypoxylon morganii Ellis & Everh. 1892 Polyporus morgani Frost ... Agaricus morganii Peck 1879 Boletus morgani Peck 1883 (now Heimioporus betula) Cantharellus morgani Peck ( ...
... the biogenic amine histamine via the enzyme histidine decarboxylase produced by symbiotic bacteria such as Morganella morganii ...
Morganella MeSH B03.440.450.425.500.500 - Morganella morganii MeSH B03.440.450.425.580 - Pantoea MeSH B03.440.450.425.585 - ... Morganella MeSH B03.660.250.150.500.500 - Morganella morganii MeSH B03.660.250.150.540 - Pantoea MeSH B03.660.250.150.542 - ...
... now Morganella morganii) in mannitol. The culture with Flexner would always produce gas and acid, while the culture with Shiga ...
Morganella morganii (Proteus morganii) eMedicine. Morganella infections "Morganella infections". Medscape. Retrieved 5 December ... morganii and M. morganii subsp. sibonii. M. morganii subsp. sibonii is able to ferment trehalose, whereas subsp. morganii ... In 1936, though, Rauss renamed B. morganii as Proteus morganii. Fulton, in 1943, showed that B. columbensis and P. morganii ... thereby removing that organism from the genus Morganella. Morganella morganii is facultatively anaerobic and oxidase-negative. ...
Morganella morganii answers are found in the Tabers Medical Dictionary powered by Unbound Medicine. Available for iPhone, iPad ... "Morganella Morganii." Tabers Medical Dictionary, 24th ed., F.A. Davis Company, 2021. Nursing Central, nursing.unboundmedicine. ... com/nursingcentral/view/Tabers-Dictionary/757605/0/Morganella_morganii. Morganella morganii. In: Venes DD, ed. Tabers Medical ... Morganella Morganii [Internet]. In: Venes DD, editors. Tabers Medical Dictionary. F.A. Davis Company; 2021. [cited 2023 ...
individuals with type I BD showed higher IgM responses to Morganella morganii than patients with MDD and type II BD. ... individuals with type I BD showed higher IgM responses to Morganella morganii than patients with MDD and type II BD ... lactis, #Lactobacillus plantarum, #Streptococcus thermophilus, #Escherichia coli, Morganella morganii, #Klebsiella pneumoniae, ... including multiple Morganella morganii strains) directly damaged DNA in cell-free assays and induced the expression of the DSB ...
What is the cell morphology of morganella morganii?. Morganella morganii is a gram negative bacteria that grows as yellowish ... Is proteus morganii motile?. Proteus morganii is a type of bacteria that is found in the human gut. Yes, morganii is motile ... Is Morganella morganii positive for a citrate test?. M. Morganii is citrate negative ... What is the birth name of Joe Morganella?. Joe Morganellas birth name is Joseph Paul Morganella III. ...
Review MicroSwab Morganella morganii WDCM 00112-ATCC® 25830™. Anuluj pisanie odpowiedzi. Twój adres e-mail nie zostanie ...
Morganella morganii TK forms histamine in each pack. At the end of the incubation period, histamine levels in MAP 1 packaging ... Morganella morganii TK 07 was incubated at room temperature and observed at 0,24,48, 72 and 96 hours. Bacterial growth was ... Selanjutnya Morganella morganii TK 07 diinkubasi pada suhu ruang dan dilakukan pengamatan pada jam ke 0,24,48,72, dan 96. ... Morganella morganii TK membentuk histamin disetiap kemasan. Pada akhir masa inkubasi kadar histamin pada kemasan MAP 1 sebesar ...
The complete genome sequence of Morganella morganii DG56-16 was sequenced. This strain was isolated from the liver of a dead ... Genome Sequence of Morganella morganii DG56-16, Isolated from Shinisaurus crocodilurus. Authors: Jiang, Hai-Ying and Lin, Li-Bo ... The complete genome sequence of Morganella morganii DG56-16 was sequenced. This strain was isolated from the liver of a dead ...
Subacute Osteomyelitis of the Pediatric Talus: A First Report of Brodies Abscess from Morganella morganii. Case Rep Orthop. ...
Morganella morganii SC01 protein. Ferrous iron transport peroxidase EfeB. I4L3H6_9PSED (I4L3H6). Pseudomonas synxantha BG33R ...
Morganella morganii, Proteus mirabilis, and Pseudomonas aeruginosa). The minimum inhibitory concentration (MIC) and the minimum ... Morganella morganii. ,20. ,20. 20. ,20. 20. ,20. 20. ,20. 20. ,20. ,0.0078. ,0.0078. nt. nt. ...
Morganella morganii. *Some Neisseria species. *Proteus mirabilis. *Most Proteus vulgaris strains. *Pseudomonas aeruginosa ...
Morganella morganii. Neisseria gonorrhoeae. Proteus mirabilis. Proteus vulgaris. Providencia spp.. Anaerobic bacteria. ... Urinary tract infections caused by Escherichia coli, Klebsiella species, Proteus mirabilis, Morganella morganii, Proteus ...
Morganella morganii. 1. 1. 2. Moraxella catarrhalis. 1. 1. Cutibacterium acnes. 2. 2. ...
Morganella morganii Proteus vulgaris Providencia rettgeri Providencia stuartii Serratia marcescens Susceptibility Tests ...
... and Morganella morganii (formerly Proteus morganii); Klebsiella spp.; Serratia spp. including S. marcescens; and Enterobacter ...
Morganella morganii Neisseria gonorrhoeae Neisseria meningitidis Proteus mirabilis Proteus vulgaris Pseudomonas aeruginosa ... Caused by Escherichia coli, Proteus mirabilis, Proteus vulgaris, Morganella morganii or Klebsiella pneumoniae. ... Morganella morganii*, Pseudomonas aeruginosa, Serratia marcescens, Acinetobacter calcoaceticus, Bacteroides fragilis* or ...
Morganella morganii. 39. 100. 77. 92. 100. 92. 82. Proteus mirabilis. 124. 100. 81. 94. 100. 89. 94. 100. R. 100. 95. 90. ...
Morganella morganii Providencia spp.. Pseudomonas sp.. Serratia sp.. Stenotrophomonas maltophilia $ Natural intermediate ...
Escherichia coli + Morganella morganii + Citrobacter freundii 1. Escherichia coli + Proteus vulgaris + Morganella morganii 1. ... 12.1%) and Raoultella ornithinolytica (8.7%). Proteus hauseri, Citrobacter spp., Morganella morgannii, Providencia rettgeri, ... 12,1%) e Raoultella ornithinolytica (8,7%). Proteus hauseri, Citrobacter spp., Morganella morgannii, Providencia rettgeri, ... 4.3%) and Proteus hauseri (4.3%) (Table 1). The identification of other genera such as Morganella morgannii (3.5%), Providencia ...
Morganella morganii. Proteus vulgaris. Providencia rettgeri. Serratia marcescens. Stenotrophomonas maltophilia. Susceptibility ...
Draft genome sequence of a Diarrheagenic Morganella morganii isolate. Genome Announc. (2015) 3:e01165-15. doi: 10.1128/genomeA. ... The dominant family in this case were the Morganellaceae, mainly comprising the genus Morganella, which is normally a rather ... identified as members of the Morganellaceae family with Morganella (1.17%) the dominating genus, 11.57% assigned to the ...
Categories: Morganella morganii Image Types: Photo, Illustrations, Video, Color, Black&White, PublicDomain, CopyrightRestricted ...
Morganella morganii, ,/em,and ,em,Aeromonas hydrophila,/em,, whose frequencies were 6(13.3%), 4(8.9%) and 1(2.2%) respectively ...
It is not active against most strains of Enterobacter spp., Morganella morganii, and Proteus vulgaris. It has no activity ...
Morganella morganii, Hafnia alvei, Aeromonas sp., and P. aeruginosa isolates can be assumed to be AmpC producers. These ...
Morganella morganii (2, 2.3%), Pantoea agglomerans (3, 3.4%), Pseudomonas luteola (2, 2.3%), Enterococcus faecalis (2, 2.3%), ...
Histamine food poisoning from gram-negative bacteria in fin-fish products is also common, and Morganella morganii and M ... Development of a real-time PCR method coupled with a selective pre-enrichment step for quantification of Morganella morganii ... and Morganella psychrotolerans in fish products. Int J Food Microbiol. 2015 Jun 16. 203:55-62. [QxMD MEDLINE Link]. ...
  • In 1936, though, Rauss renamed B. morganii as Proteus morganii. (wikipedia.org)
  • Morganella morganii (Proteus morganii) eMedicine. (wikipedia.org)
  • Is proteus morganii motile? (answers.com)
  • Proteus morganii is a type of bacteria that is found in the human gut. (answers.com)
  • Urinary tract infections caused by Escherichia coli, Klebsiella species, Proteus mirabilis, Morganella morganii, Proteus vulgaris and Providencia species (including P. rettgeri). (rxlist.com)
  • Morganella morganii , and Proteus vulgaris . (druglib.com)
  • Proteus vulgaris , Morganella morganii , Serratia marcescens , Providencia species may also overproduce AmpC, but clinically significant expression is less common. (merckmanuals.com)
  • En Proteus mirabilis, s'ha pogut observat al llarg dels deu anys un lleuger increment de la resistència a l'associació amoxicil·lina-àcid clavulànic i de manera puntual l'aparició de soques productores de pAmpCt (tres soques amb CMY-2) o de BLEA (una soca amb CTX-M-1). (uab.cat)
  • Successful joint arthroplasty following Proteus morganii (Morganella morganii) septic arthritis: a four-year study. (medscape.com)
  • Els estudis de sensibilitat en Escherichia coli i Klebsiella pneumoniae mostren un clar increment de la resistència a cefalosporines de tercera generació (C3G) i aztreonam, fruit d'una major prevalença de soques portadores de BLEA i pAMPCt. (uab.cat)
  • En Klebsiella oxytoca el principal mecanisme implicat és la hiperproducció de llur β-lactamasa cromosòmica que confereix resistència a l'aztreonam. (uab.cat)
  • Morganella morgannii , Providencia rettgeri , Enterobacter spp. (scielo.br)
  • Els estudis de sensibilitat mostren que en les espècies amb una β-lactamasa cromosòmica induïble tipus AmpC (Enterobacter, Citrobacter freundii i Morganella morganii) no hi ha hagut un increment de la resistència a C3G, indicatiu d'una possible desrepressió de l'enzim, essent el percentatge de soques amb fenotip de desrepressió del voltant del 30% en Enterobacter i C. freundii i del 7,5% en M. morganii. (uab.cat)
  • However, in 1962, a review article by Ewing reported that M. columbensis had been re-identified as Escherichia coli, thereby removing that organism from the genus Morganella. (wikipedia.org)
  • We show here, using a chimeric severe combined immunodeficiency (SCID) mouse (hu-SCID) model, that human Vγ2Vδ2 T cells mediate resistance to extracellular gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli and Morganella morganii) bacteria, as assessed by survival, body weight, bacterial loads, and histopathology. (jci.org)
  • This organism moves by way of peritrichous flagella, but some strains do not form flagella at 30 °C (86 °F). M. morganii is split into two subspecies: M. morganii subsp. (wikipedia.org)
  • citation needed]M. morganii has been regarded as a normally harmless opportunistic pathogen, but some strains carry "antibiotic-resistant plasmids" and have been associated with nosocomial outbreaks of infections. (wikipedia.org)
  • However, some M. morganii strains are resistant to penicillin, ampicillin/sulbactam, oxacillin, first-generation and second-generation cephalosporins, macrolides, lincosamides, fosfomycin, colistin, and polymyxin B. The emergence of highly resistant strains of M. morganii have been associated with use of third-generation cephalosporins. (wikipedia.org)
  • 1.1 ] - small-molecule metabolites from gram-positive bacteria (including #Clostridium perfringens and #Clostridium ramosum strains) and gram-negative bacteria (including multiple Morganella morganii strains) directly damaged DNA in cell-free assays and induced the expression of the DSB marker γ-H2AX and cell-cycle arrest in epithelial cells. (metabiom.org)
  • Yes, morganii is motile however, some strains are non-motile. (answers.com)
  • Morganella morganii is a species of Gram-negative bacteria. (wikipedia.org)
  • This study aimed to determine the effect of various packaging on the growth rate and histamine formation by Morganella morganii TK 07 bacteria in smoked mackerel tuna. (ugm.ac.id)
  • 0.05) on the growth rate of bacteria by Morganella morganii TK 07. (ugm.ac.id)
  • Histamine food poisoning from gram-negative bacteria in fin-fish products is also common, and Morganella morganii and M psychrotolerans are particularly strong histamine producers. (medscape.com)
  • Taking a large amount of sewage and returning it to the lab to isolate the bacteria within, the researchers discovered Morganella morganii (a gram-negative bacteria found as normal flora within the human and animal gut) with an mcr-9.1 gene. (iflscience.com)
  • C. freundii 3/44 (6.8%) , M. morganii 3/44 (6.8%) , P. aeruginosa 3/44 (6.8%) and S. enteritidis 3/44 (6.8%) isolates were the moderately identified bacterial species. (biomedcentral.com)
  • Although M. morganii has a wide distribution, it is considered an uncommon cause of community-acquired infection, and it is most often encountered in postoperative and other nosocomial infections, such as urinary tract infections. (wikipedia.org)
  • Morganella morganii, a newly reported, rare cause of neonatal sepsis. (visual-3d.es)
  • M morganii is usually opportunistic pathogen in hospitalized patients, particularly those on antibiotic therapy. (medscape.com)
  • Morganella morganii TK forms histamine in each pack. (ugm.ac.id)
  • Morganella morganii: epidemiology of bacteremic disease. (medscape.com)
  • En Salmonella enterica cal destacar l'aïllament de tres soques productores de BLEA (dues CTX-M-9 i una CTX-M-14) i una soca productora de CMY-2. (uab.cat)
  • Fulton, in 1943, showed that B. columbensis and P. morganii were the same and defined the genus Morganella, due to the DNA-DNA hybridization. (wikipedia.org)
  • The genus Morganella belongs to the tribe Proteeae of the family Enterobacteriaceae. (medscape.com)
  • In the late 1930s, M morganii was identified as a cause of urinary tract infections. (medscape.com)
  • Treatment of M. morganii infections may include:[citation needed] Ticarcillin Piperacillin Ciprofloxacin Third-generation and fourth-generation cephalosporins A study conducted at the University Hospital at Heraklion, Crete, Greece, showed a 92% success rate in the use of these antibiotics. (wikipedia.org)
  • Tucci and Isenberg reported a cluster epidemic of M morganii infections occurring over a 3-month period at a general hospital in 1977. (medscape.com)
  • Neonatal brain abscess caused by Morganella morgagni. (medscape.com)
  • Morganella morganii is a gram-negative rod commonly found in the environment and in the intestinal tracts of humans, mammals, and reptiles as normal flora. (medscape.com)
  • Johnson JR, Feingold M. Case of chorioamnionitis in an immunocompetent woman caused by Morganella morganii. (medscape.com)
  • M morganii is a rare cause of severe invasive disease. (medscape.com)
  • c ) Reconstitution of SCID mice with intraperitoneal PBMCs depleted of Vδ2 T cells resulted in higher bacterial loads in the peritoneal lavages of these mice 5 days after intraperitoneal inoculation of M. morganii (3 × 10 7 CFUs). (jci.org)
  • g ) SCID mice reconstituted intraperitoneally with IBA-pretreated PBMCs (IBA) had lower numbers of bacterial CFUs than those receiving medium-pretreated PBMCs (Medium) 5 days after intravenous infection with 3 × 10 7 CFUs of M. morganii . (jci.org)
  • In 1984, McDermott reported 19 episodes of M morganii bacteremia in 18 patients during a 5.5-year period at a Veterans Administration hospital. (medscape.com)
  • Upon microbial analysis, the areas were shown to have heavy growth of M. morganii. (wikipedia.org)
  • What is the birth name of Joe Morganella? (answers.com)
  • Joe Morganella's birth name is Joseph Paul Morganella III. (answers.com)
  • Ranu SS, Valencia GB, Piecuch S. Fatal early onset infection in an extremely low birth weight infant due to Morganella morganii. (medscape.com)
  • M. morganii can produce the enzyme catalase, so it is able to convert hydrogen peroxide to water and oxygen. (wikipedia.org)
  • Methyl red tests positive in M. morganii, an indicator dye that turns red due to the bacterium's acid production during fermentation. (wikipedia.org)