scholarly journals INVESTIGATE OF VIRULENCE- GENES OF PASTEURELLA MULTOCIDA TYPES AND ANTIBIOTIC SUSCEPTIBILITY IN BUFFALOES IN MARSHES OF SOUTH OF IRAQ

2020 ◽  
pp. 24-37
Keyword(s):  
Antibiotic Susceptibility ◽  
Pasteurella Multocida ◽  
Virulence Genes ◽  
South Of Iraq

scholarly journals Burden, Antibiotic Resistance, and Clonality of Shigella spp. Implicated in Community-Acquired Acute Diarrhoea in Lilongwe, Malawi

2021 ◽  
Vol 6 (2) ◽  
pp. 63
Author(s):  
Abel F.N.D. Phiri ◽  
Akebe Luther King Abia ◽  
Daniel Gyamfi Amoako ◽  
Rajab Mkakosya ◽  
Arnfinn Sundsfjord ◽  
...  
Keyword(s):  
Real Time ◽  
Antibiotic Susceptibility ◽  
Virulence Genes ◽  
Shigella Flexneri ◽  
Acute Diarrhoea ◽  
Virulence Determinants ◽  
African Countries ◽  
Shigella Species ◽  
Shigella Spp ◽  
Sub Saharan

Although numerous studies have investigated diarrhoea aetiology in many sub-Saharan African countries, recent data on Shigella species’ involvement in community-acquired acute diarrhoea (CA-AD) in Malawi are scarce. This study investigated the incidence, antibiotic susceptibility profile, genotypic characteristics, and clonal relationships of Shigella flexneri among 243 patients presenting with acute diarrhoea at a District Hospital in Lilongwe, Malawi. Shigella spp. were isolated and identified using standard microbiological and serological methods and confirmed by identifying the ipaH gene using real-time polymerase chain reaction. The isolates’ antibiotic susceptibility to 20 antibiotics was determined using the VITEK 2 system according to EUCAST guidelines. Genes conferring resistance to sulfamethoxazole (sul1, sul2 and sul3), trimethoprim (dfrA1, dfrA12 and dfrA17) and ampicillin (oxa-1 and oxa-2), and virulence genes (ipaBCD, sat, ial, virA, sen, set1A and set1B) were detected by real-time PCR. Clonal relatedness was assessed using ERIC-PCR. Thirty-four Shigella flexneri isolates were isolated (an overall incidence of 14.0%). All the isolates were fully resistant to sulfamethoxazole/trimethoprim (100%) and ampicillin (100%) but susceptible to the other antibiotics tested. The sul1 (79%), sul2 (79%), sul3 (47%), dfrA12 (71%) and dfrA17 (56%) sulfonamide and trimethoprim resistance genes were identified; Oxa-1, oxa-2 and dfrA1 were not detected. The virulence genes ipaBCD (85%), sat (85%), ial (82%), virA (76%), sen (71%), stx (71%), set1A (26%) and set1B (18%) were detected. ERIC-PCR profiling revealed that the Shigella isolates were genetically distinct and clonally unrelated, indicating the potential involvement of genetically distinct S. flexneri in CA-AD in Malawi. The high percentage resistance to ampicillin and sulfamethoxazole/trimethoprim and the presence of several virulence determinants in these isolates emphasises a need for continuous molecular surveillance studies to inform preventive measures and management of Shigella-associated diarrhoeal infections in Malawi.

scholarly journals Prevalence of virulence genes and antibiotic susceptibility of Bacillus used in commercial aquaculture probiotics in China

2021 ◽  
Vol 21 ◽  
pp. 100784
Author(s):  
Melody Abena Anokyewaa ◽  
Kwaku Amoah ◽  
Yuan Li ◽  
Yishan Lu ◽  
Felix K.A. Kuebutornye ◽  
...  
Keyword(s):  
Antibiotic Susceptibility ◽  
Virulence Genes

Virulence Genes Profile and Typing of Ovine Pasteurella multocida

2008 ◽  
Vol 3 (4) ◽  
pp. 206-213 ◽  
Author(s):  
J. Shayegh ◽  
S. Atashpaz ◽  
M.S. Hejazi
Keyword(s):  
Pasteurella Multocida ◽  
Virulence Genes

scholarly journals Assessment of Pathogenic Potential, Virulent Genes Profile, and Antibiotic Susceptibility of Proteus mirabilis from Urinary Tract Infection

2020 ◽  
Vol 2020 ◽  
pp. 1-5 ◽  
Author(s):  
Emad I. Hussein ◽  
Khalid Al-Batayneh ◽  
Majed M. Masadeh ◽  
Fatina W. Dahadhah ◽  
Mazhar Salim Al Zoubi ◽  
...  
Keyword(s):  
Urinary Tract Infection ◽  
Urinary Tract ◽  
Antimicrobial Susceptibility ◽  
Proteus Mirabilis ◽  
Antibiotic Susceptibility ◽  
Virulence Genes ◽  
Detection Method ◽  
Pathogenic Potential ◽  
The Third ◽  
Urine Specimens

Proteus mirabilis is the third most common bacterium that can cause complicated UTI, especially in catheterized patients. Urovirulence genes of P. mirabilis strains are poorly identified among UTI patients. The aims of the present study were to determine the prevalence of the uropathogenic P. mirabilis strains isolated from UTI patients by the detection of several P. mirabilis virulence genes and to characterize the antibiotic susceptibility profile of P. mirabilis isolates. P. mirabilis isolates were collected from urine specimens of patients suffering from UTI. Virulence genes in P. mirabilis, namely, hpmA, hpmB, rsbA, luxS, ureC1, hlyA, rpoA, atfA, atfC, mrpA, and pm1 were detected in the isolates via PCR detection method. All P. mirabilis virulence genes were detected in more than 90% of the isolates except hlyA gene, which was detected in only 23.8% of the isolates. The rate of susceptibility for ceftriaxone was 96.8%, followed by norfloxacin (82.5%), gentamicin (71.4%), ciprofloxacin (69.8%), cephalexin (52.4%), nalidixic acid (42.9%), sulfamethoxazole (39.7%), ampicillin (36.5%), and nitrofurantoin (3.2%). Significant associations (P<0.05) were detected between antimicrobial susceptibility of each of the following antibiotics and the presence virulence genes. Cephalexin antimicrobial susceptibility was significantly associated with the presence each of ureC1 and atfC. Sulfamethoxazole antimicrobial susceptibility was significantly associated with the presence atfA. Ceftriaxone antimicrobial susceptibility was significantly associated with the presence each of hpmA, ureC1, rpoA, atfC, mrpA, and pm1. Nitrofurantoin antimicrobial susceptibility was significantly associated with the presence each of hpmA, ureC1, rpoA, atfA, atfC, mrpA, and pm1. In conclusion, an association between the presence of urovirulence genes of P. mirabilis and increasing P. mirabilis resistance to antimicrobials has been demonstrated.

Virulence Gene Pattern of Pasteurella multocida Isolates of Buffalo in Association to Capsule Biosynthesis Genes

2020 ◽  
Author(s):  
N. Sujatha ◽  
K. Lakshmi Kavitha ◽  
K.V. Subramanyam ◽  
T. Srinivasa Rao ◽  
R.N. Ramani Pushpa
Keyword(s):  
Virulence Factors ◽  
Pasteurella Multocida ◽  
Virulence Genes ◽  
Systemic Disease ◽  
Virulence Gene ◽  
Disease Status ◽  
Host Cells ◽  
Wide Range ◽  
Serotype B ◽  
Apparently Healthy

Background: Pasteurella multocida is the causative agent of many economically important diseases in a wide range of hosts. The mechanisms by which these bacteria can invade the mucosa, evade innate immunity and cause systemic disease are slowly being elucidated. Many key virulence factors are yet to be identified, including those required for initial attachment and invasion of host cells and for persistence in a relatively nutrient poor and hostile environment. This has led to intensive research to understand host adaptation mechanisms and virulence factors in order to develop effective vaccines. Methods: The present study was carried out to know the distribution of virulence genes viz., haemoglobin binding proteins (hgbA and hgbB), outer membrane protein (ompH), fimbrial antigen (ptfA), filamentous haemagglutinin (pfhA) and transferrin binding protein (tbpA) by PCR in P. multocida CapA isolates from apparently healthy or carrier animals and CapB isolates from field Haemorrhagic septicemia (HS) cases to monitor the epidemiological associations of virulence genes in Cap A and Cap B isolates.Result: The study revealed that all the six virulence associated genes were present in Cap B isolates. None of the Cap A isolates harboured tbpA and pfhA genes. These two genes were closely related to serotype B causing Haemorrhagic septicemia and were epidemiologically associated with disease status.

scholarly journals Transmission of Novel Bacterial Pathogens through Pigs Transported from Myanmar to Mizoram

2021 ◽  
Author(s):  
C. Lalremruata ◽  
T.K. Dutta ◽  
P. Roychoudhury ◽  
Sanjeev Kumar ◽  
A. Sen ◽  
...  
Keyword(s):  
Pasteurella Multocida ◽  
Virulence Genes ◽  
Bacterial Pathogens ◽  
Bacterial Species ◽  
Microbial Pathogens ◽  
Identification System ◽  
Bacterial Strains ◽  
Illegal Migration ◽  
Isolation And Identification ◽  
Specific Pcr

Background: Illegal migration of pigs/piglets from Myanmar to Mizoram is a common practice to meet the local demands. The migrated animals are suspected as potential carrier of various microbial pathogens. The present study was conducted on isolation, identification and molecular characterization of major bacterial pathogens (Actinobacillus pleuropneumoniae, Bordetella bronchiseptica, Haemophilus parasuis, Mycoplasma hyopneumoniae and Pasteurella multocida) in pigs illegally migrated from Myanmar to Mizoram. Methods: A total of 209 rectal swabs and 209 nasal swabs were collected from apparently healthy migrated pigs during October 2018 to April, 2019. All the samples were processed for PCR based detection of target bacterial species followed by isolation and identification by bacteriological techniques. The bacterial species were further confirmed by BD Phoenix automated bacterial identification system and selected virulence genes of the bacterial species were determined by specific PCR assay. Result: By species specific PCR, 110 samples were found to be positive for selected bacterial species, of which 20 (9.57%), 1 (0.478%), 86 (41.15%), 2 (0.956%) and 1 (0.478%) were A. pleuropneumoniae, B. bronchiseptica, H. parasuis, M. hyopneumoniae and P. multocida, respectively. A total of 52 bacterial strains were isolated and identified, of which 11, 1, 39 and 1 were A. pleuropneumoniae, B. bronchiseptica, H. parasuis, M. hyopneumoniae and P. multocida, respectively. Virulence genes were detected in A. pleuropneumoniae and H. parasuis isolates. Based upon the published literatures, this is the first ever report of isolation and identification of pathogenic A. pleuropneumoniae and H. parasuis in pigs in India.

scholarly journals Comparison of Pasteurella spp. Simultaneously Isolated from Nasal and Transtracheal Swabs from Cattle with Clinical Signs of Bovine Respiratory Disease

2000 ◽  
Vol 38 (1) ◽  
pp. 327-332
Author(s):  
D. C. DeRosa ◽  
G. D. Mechor ◽  
J. J. Staats ◽  
M. M. Chengappa ◽  
T. R. Shryock
Keyword(s):  
Respiratory Disease ◽  
Antibiotic Susceptibility ◽  
Pasteurella Multocida ◽  
Nasal Swab ◽  
Bacterial Species ◽  
Bovine Respiratory Disease ◽  
Clinical Signs ◽  
Bacterial Pathogen ◽  
Matched Pair ◽  
Matched Pairs

ABSTRACT Twenty-four matched pairs of isolates of Pasteurella haemolytica and three matched pairs of isolates of Pasteurella multocida were isolated by using a nasal swab and a transtracheal swab from individual calves with clinical signs of bovine respiratory disease. The identity of each matched pair was confirmed biochemically and serologically. The similarity of the isolates obtained from a nasal swab and from a transtracheal swab was compared by using ribotyping and antibiotic susceptibility analyses. Although the calves were sampled only once with a nasal and a transtracheal swab, when both samples were bacteriologically positive the nasal swab identified the same bacterial species as the transtracheal swab 96% of the time. The nasal swab isolate was genetically identical to the transtracheal isolate in 70% of the matched pairs. Six different ribotypes were observed for the P. haemolytica isolates, while only one ribotype was observed for the limited number of P. multocida isolates. Of the six P. haemolytica ribotypes, two ribotypes predominated. All the paired isolates displayed similar susceptibility to ceftiofur, erythromycin, tilmicosin, trimethoprim-sulfamethoxazole, and florfenicol, with some minor variations for ampicillin and spectinomycin. These results suggest that a nasal swab culture can be predictive of the bacterial pathogen within the lung when the isolates are from an acutely ill animal and can be used to determine antibiotic susceptibility.

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