Background: Dairy sector is a leading industry in our country. Mastitis being most concerned and frightful disease, not only affecting health of animals but also the economy of the livestock owner. Prevailing status of the antimicrobial resistance makes the treatment of mastitis much more difficult. Biofilm formation in mastitis milk could place difficulty in the treatment of animals as it further increases the possibility of antimicrobial resistance. Essential oils generally being less toxic, could be optimal alternatives to conventional antibiotics, most of these essential oils higher MIC values than antibiotics, needed to be given in increased concentration in feed/water. 
 
Methods: Different dairy farms were screened for mastitis (164 dairy cattle and buffalo) Staphylococcus aureus isolates were identified and characterized phenotypically by standard biochemical tests. The biofilm formation ability was studied by different methods along with the quantitative analysis and MIC of standard drug cefoperazone. 
 
Result: Out of total milk samples 17 samples were identified Staphylococcus aureus positive with Congo red agar (70% positive), Light Microscopy method (52% positive) and Microtiter plate (Crystal Violet) method. (100% sensitivity). The antimicrobial and antibiofilm effect of Cinnamon oil were studied by Microtiter plate method, SEM analysis and confocal techniques. Cinnamon oil gave antibiofilm activity in all the concentration used (1%, 2%, 3%). The MIC of Cefoperazone was in the range of 64 &mu;g/to 16 &mu;g/ml. No significant changes were observed on biofilm production at sub-MIC of cefoperazone.

Antimicrobial and Antibiofilm Activity of Cinnamon Oil on Staphylococcus aureus Isolated from Cattle Milk with Mastitis

In this study, the isolation, identification and antibiotic susceptibility of bacterial agents taken from urine and sediment samples of 10 cats and 10 dogs, which were diagnosed with urinary tract infection was aimed. Each urine and sediment samples were streaked onto blood agar which contains 5 % sheep blood, Eosin Methylene Blue agar and MacConkey agar for bacterial examination. In conclusion, Staphylococcus aureus from 4 dogs, Staphylococcus epidermidis from 2 dogs, Serratia liquefaciens from 1 dog, Plesiomonas shigelloides from 1 dog, Yersinia enterocolitica from 1 cat, were isolated and identified. In conclusion of antibiogram test, 78 % of the isolates were susceptible to Amoxicillin-Clavulanic acid, 67 % of the isolates were susceptible to Ceftriaxone and Cefoperazone, 55.5 % of the isolates were susceptible to Enrofloxacin, 22.5 % of the isolates were susceptible to Lincomycin and 22 % of the isolates were susceptible to Erythromycin. The isolates were resistant to Sulfamethoxazole-Trimethoprime and Oxacillin in the ratio of 78 % and 67 % respectively. Consequently, it is concluded that the isolates obtained from dogs highlight the resistancy to antibiotics, bacterial agents play a less role in feline urinary tract infections and the appropriate antibiotic application procedure will enhance the success of therapy.

Identification of bacterial pathogens that cause urinary tract&nbsp;infections and detection of their antibiotic susceptibility

A bacterium was isolated from benzalkonium chloride solution (5%) stored in an uncovered bottle. The strain was identified as Staphylococcus aureas named SA-RBC through the test of its morphology, biochemical and physiological characterization. The isolated strain SA-RBC has important symbol of pathogenic Staphylococcus by producing coagulase, phosphatase and thermonuclease. Resistance of SA-RBC to disinfectants or antibiotics was tested. The results showed that the strain was highly resistant to benzalkonium chloride, benzalkonium bromide, glutaraldehyde and sodium hypochlorite, but susceptive to phenylic acid. SA-RBC was highly resistant to oxacillin, cefoperazone, cefoxitin, gentamicin, ciprofloxacin, and tetracycline. The tolerable growth concentration of SA-RBC on various surfactants was examined. The results indicated that the strain SA-RBC could grow in a higher concentration of cationic surfactants up to 5%, compared with the control strains (Escherichia coli ATCC 25922, S.epidermidis ATCC12228 and S.aureus ATCC 29213) which were unable to grow in 0.1% cationic surfactants. The strain SA-RBC could not utilize benzalkonium chloride as the sole source of carbon and/or nitrogen. The findings in this study suggested that Staphylococcus aureas might be an original contaminant in the quaternary ammonium disinfectant and has potential risk for public health.

Isolation and identification of a novel Staphylococcus from benzalkonium chloride solution

<div style="text-align: justify;">The objective of the present study was to determine the bacterial and fungal agents accompanying with cutaneous lesions of dogs suffering from Canine Visceral Leishmaniasis (CVL). Sterile swap samples were taken from cutaneous lesions inspected of ears, dorsal, collar, pectoral, inguinal and interdigital spaces of 20 dogs, &nbsp;in which diagnosis were based on a combination of clinical symptoms, anti-leishmania antibody titers by use of Immunofluorescence antibody test (IFAT), and dogs were further classified according to the Leishvet Guidelines involving serological, hematological, serum biochemical, and urinalysis. Swap samples were inoculated to culture media for isolation and identification of bacterial and mycotic agents. 48 Staphylococcus aureus, 4 Bacillus cereus, 8 Staphylococcus epidermidis, 24 Candida albicans, 24 Microsporium canis and 4 Aspergillus niger were isolated and identified in both group of dogs. Regarding antibiotic susceptibility test, the isolates were found 100% susceptible to cefoperazone and amoxicillin-clavulanic acid, 53% &nbsp;to danofloxacin, 46% of the isolates were susceptible to enrofloxacin, and all of the isolates were &nbsp;resistant (100%) to penicillin G and gentamicin. In conclusion, the antibacterial and antifungal therapy should be provided in accordance with antibiotic susceptibility tests in skin lesions of dogs suffering with CVL.</div>

<div style="text-align: justify;">Investigation of bacterial and fungal agents from cutaneous lesions in canine Leishmaniasis</div>

<div style="text-align:justify">Background: Campylobacter species are a leading cause of most important food-borne diarrhoeal illness worldwide while, poultry has been identified as a significant cause of Campylobacter infection in humans. C. jejuni is highly effective in colonizing chicken intestinal mucosa without causing any clinical manifestations and the consumption of poultry meat is the major source of transmission of bacteria to humans. 
 
Methods: The total of 19 chicken meat samples collected from retail markets in Chennai were screened by cultural examination, further subjected to phenotypic characterization using biochemical test and genotypic characterization using polymerase chain reaction assay targeting hip O and map A genes. 
 
Result: All the isolates showed growth on modified blood free charcoal cefoperazone deoxycholate agar media (mCCDA) and 18 (94.73%) samples showed typical morphological characteristics. The 12 (63.15%) isolates showed biochemical reactions positive. The results from polymerase chain reaction showed that 10 (83.33%) isolates were positive for C. jejuni. This study suggested that, it is essential to investigate the incidence of Campylobacter jejuni infection in poultry and the risk factors at all production stages of meat production to help reducing the disease in humans in terms of food safety.</div>

Morphological, Biochemical and Genotypic Analysis of Zoonotic Campylobacter jejuni Isolated from Chicken Meat Samples

<div>Background: Campylobacter has emerged as an important zoonotic food borne pathogen of human and animals worldwide. Campylobacter is one of the most common bacterial enteropathogens of food borne origin in industrialized countries with C. jejuni being the most common species followed by C. coli. There are very few cases reported from mastitis therefore this study was aimed to determine the incidence of Campylobacter jejuni from from mastitis milk and raw milk samples.&nbsp;&nbsp; 
 
Methods: Total of 72 milk samples comprising mastitis milk (20) and raw milk (52) were collected. The samples were subjected to cultural examination, biochemical as well as molecular identification.&nbsp;The isolates were further subjected to phenotypic characterization by biochemical test and genotypic characterization by Polymerase Chain Reaction. The isolates were subjected to PCR targeting hip O and MAP A genes. 
 
Result: The 52 samples showed growth on modified Blood Free Charcoal Cefoperazone Deoxycholate agar media and 18 (34.61%) samples showed typical morphological characteristics. The result revealed that 10 (19.23%) isolates were positive by phenotypic characteristic and 7(70%) by Polymerase chain reaction for C. jejuni. The outcome result showed that importance of Campylobacter jejuni in cattle, especially raw milk and milk from mastitis cows, as a potential source for transmission of Campylobacteriosis in human and dairy farm environment. This can cause acute bacterial gastroenteritis in humans and associated with foodborn infection, food safety and a serious public health threat.</div>

Characterization of Campylobacter jejuni An Important Zoonotic Food Borne Pathogen from Mastitis Milk and Raw Milk Samples

<div>Background: Mammaliicoccus sciuri is a multidrug resistant human pathogen. Literature on its role causing bovine mastitis is scarce. Detection of M. sciuri from a cow with clinical mastitis in Malkangiri district of Odisha stimulated to ascertain its status in a larger population and to study its characteristics in genotypic and phenotypic levels.&nbsp; 
 
Methods:&nbsp;520 lactating cows from various herds of Malkangiri district of Odisha, India were screened for presence of clinical mastitis. Milk samples were collected aseptically from 15 cows with clinical mastitis. 16S rRNA amplification was performed to know presence of bacterial pathogen (s). Conventional PCR was carried out to detect resistance genes against &beta;-lactam (blaZ), aminoglycoside (aacA-aphD) and tetracycline (tetK, tetM). In vitro sensitivity test was studied against M. sciuri isolates using nine antibiotic discs. Phylogenetic analysis was performed to compare its origin.&nbsp; 
 
Result: M. sciuri was isolated in 6 (40.0%) mastitis positive milk samples. In vitro antibiotic sensitivity test against M. sciuri isolates showed highest degree of resistant to penicillin (100%) followed by, cefoperazone (33.3%), streptomycin (33.3%), tetracycline (16.0%). One isolate of M. sciuri had tetK, tetM resistance gene. Phylogenetic analysis showed (75-100%) similarity with other isolates obtained from GeneBank. Present study highlights tetK gene in M. sciuri.&nbsp;</div>

Genotypic and Phenotypic Characterization of Mammaliicoccus sciuri - A MDR Strain causing Clinical Mastitis in Cows of Odisha, India

<div style="text-align: justify;">Sub-clinical Mastitis is one of the major problems in India which is among the largest milk producing countries in the world, hampering national economy. Among 422 bovine milk samples screened from different cattle farms of West Bengal with history of infection and drop in milk yield by on-spot bromothymol blue (BTB) test, 371 samples were considered for collection and secondary screening by somatic cell count study. The collected milk samples showed significantly high average SCC value of 3.26-4.88 lakh cells/ml of milk which was indicative of infection. Samples (23, 6.53%) were found to be positive for Pseudomonas sp. showing distinct bluish-green pigmentation on cetrimide agar, typical results on morphological and in biochemical characterization. Presence of 19 (5.39%) Pseudomonas aeruginosa isolates were confirmed by fluorescent technique for detection of characteristic blue-green fluorescence by the pigment pyoverdin. PCR of these positive isolates revealed that 11 isolates were positive for toxA and 6 isolates for exoS genes with 2 isolates possessing both the genes. In Mice pathogenicity test, highest fatality (100%) was shown by the isolates with both the genes followed by isolates with toxA (66.67%) and exoS (41.67%) respectively with successful re-isolation of P. aeruginosa from the dead mice. Post-mortem examination of the dead mice showed marked haemorrhages on liver, blackish discoloration of intestines and haemorrhages on lungs. Antibiogram revealed that the isolates were highly sensitive to drugs like amikacin (89.47%), imipenem (84.21%), meropenem (78.95%) and cefoperazone-sulbactam (84.21%) but resistant to tetracycline (68.42%), piperacillin (63.16%), oxacillin (52.63%), mecilinam (47.37%) and others.</div>

<div style="text-align: justify;">Mice pathology study of toxA and exoS genes bearing Pseudomonas aeruginosa isolated from bovine Sub-clinical mastitis in West Bengal with their Antibiogram</div>

Background: Escherichia coli cause mammary gland inflammation in dairy cows with striking local and sometimes severe systemic clinical symptoms. This disease affects many high producing cows in dairy herds and may cause several cases of death per year in the most severe cases. The present study was planned to evaluate the antibiogram and virulence factors of the isolated bacteria responsible for mastitis.&nbsp; 
 
Methods: In this study, 300 milk samples were collected and subjected to identify clinical mastitis (based on clinical symptoms) and sub clinical mastitis (using California mastitis test). E. coli was isolated and identified from mastitis positive samples and further tested for antibiogram and virulence factors such as haemolysis, biofilm formation and fimH and pap genes presence. 
 
Result: Out of 300 milk samples collected, 121 (40.33%) were positive for mastitis. E. coli was isolated from only 30 (24.79%) out of 121 mastitis positive samples. On Serotyping for somatic antigen, 13 E. coli isolates belonged to somatic serogroup O83, 2 to O157 and one each to O8, O20, O49, O119, O128 and O145. The highest sensitivity of E. coli isolates was recorded for ciprofloxacin, followed by gentamicin, tetracycline, nitrofurantoin, chloramphenicol, amikacin, cefixime, trimethoprim, ampicillin/sulbactam, ceftriaxone, cefoperazone, cefotaxime, kanamycin, cefotaxime/clavulanic acid and amoxycillin in the decreasing order. Multidrug resistance (MDR) was recorded in 96.66% of isolates.&nbsp;Out of 30 E. coli isolates, 46.66% were haemolytic and 40.0% positive for Congo red dye binding. Biofilm production was shown by 76.66% isolates. Molecular characterization revealed presence of fimH gene in 9 isolates, but pap gene was not detected in any of the strain. It may be concluded that E. coli is an emerging environmental mastitogen in cows and isolation of MDR strains with virulence factors is of serious concern.

Antibiogram, Haemolysis and Biofilm Properties of Escherichia coli from Bovine Mastitis

<div>Background: Pathomicrobial and molecular investigations of respiratory system diseases was undertaken on twelve adult buffalo carcasses received for necropsy examination at post mortem facility of Department of Veterinary Pathology, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar, Haryana during the period from August, 2018 to February, 2019.&nbsp; 
 
Methods: After collection of the samples, laboratory work was undertaken in the laboratories of Department of Veterinary Pathology, Department of Animal Biotechnology and Central Laboratory of the College, LUVAS, Hisar, Haryana (India) in the year 2018-2019 regarding the examination of the clinical history, pathological, microbiological and molecular investigations. 
 
Result: The gross pathological changes observed in lungs were variable degree of vascular changes, mild to severe consolidation, fibrin deposition along with adhesions to the thoracic wall. Histopathological findings revealed abnormalities of inflation such as pulmonary emphysema, atelectasis, pulmonary congestion and haemorrhages which was associated with different types of pneumonia viz. fibrinous bronchopneumonia, suppurative giant cell pneumonia, interstitial pneumonia and serous pneumonia. Lung, heart blood and tracheal swab samples collected from the buffalo carcasses revealed eighteen bacterial isolates which were identified by Vitek 2 system. These include E. coli (11 isolates), Salmonella enteric enterica (2 isolates), Acinetobacter ursingii (1 isolate), Staphylococcus haemolyticus (1 isolate), Staphylococcus sciuri (1 isolate), Staphylococcus warneri (1 isolate) and Staphylococcus hominis (1 isolate) mostly belonging to opportunistic pathogen category. E. coli serotypes confirmed from these cases were O83, O149 and O8. The results of in vitro drug sensitivity testing revealed that most of bacterial strains were found sensitive to cefoperazone/sulbactum and co-trimoxazole. Molecular studies confirmed Bovine Herpes Virus-1 (BHV-1) infection in one case with Fibrinous bronchopneumonia through real-time quantitative PCR indicating the prevalence of the infection in the state.</div>

Antimicrobial and Antibiofilm Activity of Cinnamon Oil on Staphylococcus aureus Isolated from Cattle Milk with Mastitis

Identification of bacterial pathogens that cause urinary tract infections and detection of their antibiotic susceptibility

Isolation and identification of a novel Staphylococcus from benzalkonium chloride solution

Investigation of bacterial and fungal agents from cutaneous lesions in canine Leishmaniasis

Morphological, Biochemical and Genotypic Analysis of Zoonotic Campylobacter jejuni Isolated from Chicken Meat Samples

Characterization of Campylobacter jejuni An Important Zoonotic Food Borne Pathogen from Mastitis Milk and Raw Milk Samples

Genotypic and Phenotypic Characterization of Mammaliicoccus sciuri - A MDR Strain causing Clinical Mastitis in Cows of Odisha, India

Mice pathology study of toxA and exoS genes bearing Pseudomonas aeruginosa isolated from bovine Sub-clinical mastitis in West Bengal with their Antibiogram

Antibiogram, Haemolysis and Biofilm Properties of Escherichia coli from Bovine Mastitis

Pathomicrobial and Molecular Investigations of Respiratory System Diseases Affecting Buffaloes