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1.
Avian Pathol ; 50(2): 161-173, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33291970

ABSTRACT

Mycoplasma gallisepticum and Mycoplasma synoviae are bacterial pathogens that cause disease in poultry, adversely affecting their health and welfare, and are a financial burden on producers. This manuscript describes the results of the MycoPath project that is the first international antimicrobial susceptibility programme for mycoplasma pathogens isolated from poultry. Improved comparative analysis of minimal inhibitory concentration (MIC) results from participating countries was facilitated by using one laboratory determining all MICs. Chicken and turkey isolates were obtained from France, Germany, Great Britain, Hungary, Italy and Spain during 2014-2016. One isolate per farm was retained. The MIC of seven antimicrobial agents was determined using a broth microdilution method, with Friis Medium (M. gallisepticum) or Modified Chanock's Medium (M. synoviae). Of the 222 isolates recovered, 82 were M. gallisepticum and 130 were M. synoviae. M. gallisepticum MIC50/90 values were 0.12/0.5, 2/8, 0.5/4, 0.12/>64, 0.008/0.062, 0.008/32, 0.062/4 mg/l for doxycycline, enrofloxacin, oxytetracycline, spiramycin, tiamulin, tilmicosin and tylosin, respectively. For M. synoviae, the values were 0.5/1, 8/16, 0.5/1, 0.5/8, 0.25/0.5, 0.062/2 and 0.062/16 mg/l respectively. A bimodal MIC distribution for the fluoroquinolone (enrofloxacin) and the macrolides (spiramycin, tilmicosin and tylosin) indicate that both species have sub-populations that are less susceptible in vitro to those antimicrobials. Some differences in susceptibilities were observed according to host species, Mycoplasma species, and country of origin. This study provides a baseline of novel data for future monitoring of antimicrobial resistance in poultry Mycoplasma species. Additionally, this information will facilitate the selection of the antimicrobial agents most likely to be effective, thus ensuring their minimal use with targeted and correct therapeutic treatments.Highlights First large-scale pan-European collection of representative Mg and Ms isolates.MIC values assessed in central laboratory for Mg and Ms from chickens and turkeys.Range of MIC values for 82 Mg and 130 Ms isolates to seven licenced antibiotics shown.Data can be used to help determine Mg and Ms veterinary-specific breakpoints.


Subject(s)
Anti-Infective Agents/pharmacology , Chickens/microbiology , Mycoplasma Infections/veterinary , Mycoplasma gallisepticum/drug effects , Mycoplasma synoviae/drug effects , Poultry Diseases/microbiology , Turkeys/microbiology , Animals , Drug Resistance, Bacterial , Europe , Fluoroquinolones/pharmacology , Macrolides/pharmacology , Microbial Sensitivity Tests/veterinary , Mycoplasma Infections/microbiology , Poultry
2.
Vet J ; 259-260: 105474, 2020.
Article in English | MEDLINE | ID: mdl-32553237

ABSTRACT

Mycoplasma hyopneumoniae (M. hyopneumoniae) is the primary agent of enzootic pneumonia, a chronic and economically important respiratory disease of pigs. Control and prevention of M. hyopneumoniae infections can be accomplished by optimization of management and housing conditions, and by vaccination. The present paper summarizes the current knowledge on the main characteristics and efficacy of antimicrobials used for the treatment of clinical M. hyopneumoniae infections, the in vitro and in vivo activities of these antimicrobials and the reported resistance mechanisms against some. Potentially active antimicrobials against M. hyopneumoniae include tetracyclines, macrolides, lincosamides, pleuromutilins, amphenicols, aminoglycosides, aminocyclitols and fluoroquinolones. Antimicrobial treatment can be administered either orally or parenterally. Based on the overall results of efficacy studies performed under experimental and/or field conditions, the majority of agents belonging to these antimicrobial classes improved clinical parameters (clinical signs, lung lesions) and reduced performance losses due to M. hyopneumoniae infection. Antimicrobials may, however, not be able to prevent infection or to eradicate the bacterium from the respiratory tract. The decision to medicate should, therefore, be considered carefully. M. hyopneumoniae shows an intrinsic resistance against ß-lactam antibiotics, sulfonamides and trimethoprim. A few reports have shown acquired antimicrobial resistance against some antibiotics, along with associated resistance mechanisms. The results of antimicrobial susceptibility testing are difficult to interpret in terms of treatment outcome, as no clinical breakpoints have been defined for M. hyopneumoniae.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Mycoplasma hyopneumoniae , Pneumonia of Swine, Mycoplasmal/drug therapy , Animals , Drug Resistance, Bacterial , Microbial Sensitivity Tests/veterinary , Swine
3.
Vet Microbiol ; 237: 108422, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31585641

ABSTRACT

Mycoplasma flocculare is genetically closely related to M. hyopneumoniae, the etiologic agent of porcine enzootic pneumonia, and is frequently isolated with this second species. In this article, we report on the development of the first multilocus sequence typing (MLST) scheme for M. flocculare, based on three genes (adk, rpoB and tpiA). In total, 5022 bp of sequence were analyzed. MLST was used to characterize seven M. flocculare isolates and the reference strain. Eight distinct sequence types were defined, showing the great intraspecies variability of M. flocculare, and the high discriminatory power of the new typing method. The relative contribution of recombinations to the genomic evolution of M. flocculare was revealed by calculating the index of association (IA: 0.0185). This MLST scheme is now available for the acquisition of new knowledge on M. flocculare epidemiology via an online database comprising the DNA sequences of each allele, available at http://pubmlst.org/mflocculare/.


Subject(s)
Multilocus Sequence Typing/methods , Mycoplasma/genetics , Polymorphism, Genetic/genetics , Phylogeny
4.
Microbiol Spectr ; 6(4)2018 07.
Article in English | MEDLINE | ID: mdl-30003864

ABSTRACT

Mycoplasmas are intrinsically resistant to antimicrobials targeting the cell wall (fosfomycin, glycopeptides, or ß-lactam antibiotics) and to sulfonamides, first-generation quinolones, trimethoprim, polymixins, and rifampicin. The antibiotics most frequently used to control mycoplasmal infections in animals are macrolides and tetracyclines. Lincosamides, fluoroquinolones, pleuromutilins, phenicols, and aminoglycosides can also be active. Standardization of methods used for determination of susceptibility levels is difficult since no quality control strains are available and because of species-specific growth requirements. Reduced susceptibility levels or resistances to several families of antimicrobials have been reported in field isolates of pathogenic Mycoplasma species of major veterinary interest: M. gallisepticum and M. synoviae in poultry; M. hyopneumoniae, M. hyorhinis, and M. hyosynoviae in swine; M. bovis in cattle; and M. agalactiae in small ruminants. The highest resistances are observed for macrolides, followed by tetracyclines. Most strains remain susceptible to fluoroquinolones. Pleuromutilins are the most effective antibiotics in vitro. Resistance frequencies vary according to the Mycoplasma species but also according to the countries or groups of animals from which the samples were taken. Point mutations in the target genes of different antimicrobials have been identified in resistant field isolates, in vitro-selected mutants, or strains reisolated after an experimental infection followed by one or several treatments: DNA-gyrase and topoisomerase IV for fluoroquinolones; 23S rRNA for macrolides, lincosamides, pleuromutilins, and amphenicols; 16S rRNAs for tetracyclines and aminoglycosides. Further work should be carried out to determine and harmonize specific breakpoints for animal mycoplasmas so that in vitro information can be used to provide advice on selection of in vivo treatments.


Subject(s)
Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial/drug effects , Mycoplasma Infections/drug therapy , Mycoplasma Infections/veterinary , Mycoplasma/drug effects , Animals , Anti-Bacterial Agents/classification , Anti-Bacterial Agents/standards , Anti-Bacterial Agents/therapeutic use , Cattle , DNA Gyrase/drug effects , DNA Topoisomerase IV/drug effects , Drug Resistance, Bacterial/genetics , Microbial Sensitivity Tests/methods , Mycoplasma/genetics , Mycoplasma/pathogenicity , Mycoplasma Infections/microbiology , Point Mutation , Poultry , RNA, Ribosomal, 16S/drug effects , RNA, Ribosomal, 23S/drug effects , Ruminants , Species Specificity , Swine
5.
Vet Microbiol ; 106(1-2): 129-37, 2005 Mar 20.
Article in English | MEDLINE | ID: mdl-15737482

ABSTRACT

The ability of the avian pathogen Mycoplasma gallisepticum to persist despite fluoroquinolone treatment was investigated in chickens. Groups of specific pathogen free chickens were experimentally infected with M. gallisepticum and treated with enrofloxacin at increasing concentrations up to the therapeutic dose. When M. gallisepticum could no longer be re-isolated from chickens, birds were stressed by inoculation of infectious bronchitis virus or avian pneumovirus. Although M. gallisepticum could not be cultured from tracheal swabs collected on several consecutive sampling days after the end of the enrofloxacin treatments, the infection was not eradicated. Viral infections reactivated the mycoplasma infection. Mycoplasmas were isolated from tracheal rings cultured for several days, suggesting that M. gallisepticum persisted in the trachea despite the enrofloxacin treatment. The minimal inhibitory concentration (MIC) of enrofloxacin for most of the re-isolated mycoplasmas was the same as that of the strain with which the birds were inoculated. Furthermore, no mutation could be detected in the fluoroquinolone target genes. These results suggest that M. gallisepticum can persist in chickens without development of resistance despite several treatments with enrofloxacin.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Chickens , Fluoroquinolones/therapeutic use , Mycoplasma Infections/veterinary , Mycoplasma gallisepticum/growth & development , Poultry Diseases/drug therapy , Poultry Diseases/microbiology , Quinolones/therapeutic use , Animals , Anti-Bacterial Agents/blood , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Enrofloxacin , Fluoroquinolones/blood , Infectious bronchitis virus/isolation & purification , Metapneumovirus/isolation & purification , Microbial Sensitivity Tests/veterinary , Mycoplasma Infections/blood , Mycoplasma Infections/drug therapy , Mycoplasma Infections/microbiology , Mycoplasma gallisepticum/genetics , Polymerase Chain Reaction/veterinary , Poultry Diseases/blood , Quinolones/blood , Random Allocation , Respiratory Tract Diseases/blood , Respiratory Tract Diseases/drug therapy , Respiratory Tract Diseases/microbiology , Respiratory Tract Diseases/veterinary , Specific Pathogen-Free Organisms , Trachea/microbiology
6.
PLoS One ; 9(8): e104605, 2014.
Article in English | MEDLINE | ID: mdl-25101681

ABSTRACT

As nutritional status and inflammation are strongly connected, feeding and nutritional strategies could be effective to improve the ability of pigs to cope with disease. The aims of this study were to investigate the impact of a feed restriction on the ability of pigs to resist and be tolerant to a coinfection with Mycoplasma hyopneumoniae (Mhp) and the European H1N1 swine influenza virus, and the consequences for nutrient metabolism, with a focus on amino acids. Two groups of specific pathogen-free pigs were inoculated with Mhp and H1N1 21 days apart. One group was fed ad libitum, the other group was subjected to a two-week 40% feed restriction starting one week before H1N1 infection. The two respective mock control groups were included. Three days post-H1N1 infection, 200 g of feed was given to pigs previously fasted overnight and serial blood samples were taken over 4 hours to measure plasma nutrient concentrations. Throughout the study, clinical signs were observed and pathogens were detected in nasal swabs and lung tissues. Feed-restricted pigs presented shorter hyperthermia and a positive mean weight gain over the 3 days post-H1N1 infection whereas animals fed ad libitum lost weight. Both infection and feed restriction reduced postprandial glucose concentrations, indicating changes in glucose metabolism. Post-prandial plasma concentrations of the essential amino acids histidine, arginine and threonine were lower in co-infected pigs suggesting a greater use of those amino acids for metabolic purposes associated with the immune response. Altogether, these results indicate that modifying feeding practices could help to prepare animals to overcome an influenza infection. Connections with metabolism changes are discussed.


Subject(s)
Caloric Restriction , Coinfection , Influenza A Virus, H1N1 Subtype , Mycoplasma hyopneumoniae , Orthomyxoviridae Infections/metabolism , Pneumonia of Swine, Mycoplasmal/metabolism , Animals , Swine
7.
PLoS One ; 9(2): e87672, 2014.
Article in English | MEDLINE | ID: mdl-24503775

ABSTRACT

Mycoplasma (M.) bovis is frequently implicated in respiratory diseases of young cattle worldwide. Today, to combat M. bovis in Europe, only antimicrobial therapy is available, but often fails, leading to important economical losses. The antimicrobial susceptibility of M. bovis is not covered by antimicrobial resistance surveillance networks. The objectives of this study were to identify resistances that were acquired over the last 30 years in France and to determine their prevalence within contemporary strains. The minimum inhibition concentration (MIC) values of 12 antimicrobials, considered active on M. bovis, were compared, using an agar dilution method, between 27 and 46 M. bovis isolates respectively obtained in 1978-1979 and in 2010-2012 from 73 distinct respiratory disease outbreaks in young cattle all over France. For eight antimicrobials, resistances were proven to be acquired over the period and expressed by all contemporary strains. The increase of the MIC value that inhibited 50% of the isolates (MIC50) was: i) substantial for tylosin, tilmicosin, tulathromycin and spectinomycin, from 2 to >64, 2 to >128, 16 to 128 and 4 to >64 µg/mL, respectively, ii) moderate for enrofloxacin, danofloxacin, marbofloxacin and oxytetracycline, from 0.25 to 0.5, 0.25 to 0.5, 0.5 to 1, 32 to >32 µg/mL, respectively. No differences were observed for gamithromycin, tildipirosin, florfenicol and valnemulin with MIC50 of 128, 128, 8, <0.03 µg/mL, respectively. If referring to breakpoint MIC values published for respiratory bovine pathogens, all contemporary isolates would be intermediate in vivo for fluoroquinolones and resistant to macrolides, oxytetracycline, spectinomycin and florfenicol.


Subject(s)
Anti-Infective Agents/pharmacology , Cattle Diseases/epidemiology , Cattle Diseases/microbiology , Drug Resistance, Bacterial , Mycoplasma Infections/veterinary , Mycoplasma bovis/drug effects , Animals , Cattle , France/epidemiology , Microbial Sensitivity Tests , Prevalence , Reproducibility of Results
8.
Vet Res ; 37(1): 145-54, 2006.
Article in English | MEDLINE | ID: mdl-16336931

ABSTRACT

The ability of Mycoplasma synoviae, an avian pathogen, to persist despite fluoroquinolone treatments was investigated in hens. Groups of Mycoplasma-free hens were experimentally infected with the M. synoviae 317 strain and treated twice with enrofloxacin at the therapeutic dose. The results show that the two treatments did not have any influence on this strain of M. synoviae recovery from tracheal swabs. Mycoplasmas were isolated from tracheal swab cultures, but not from inner organs such as the liver or spleen, suggesting that this strain of M. synoviae was not able to cross the mucosal barrier to disseminate throughout the host. A significant increase of the resistance level to enrofloxacin of five re-isolated mycoplasma clones, was observed after the second treatment. This increase was associated in two clones to a Ser81-->Pro substitution, found in the ParC quinolone-resistance determining region (QRDR) of DNA topoisomerase IV. This is the first time that a mutation in a gene coding for topoisomerase IV is described in M. synoviae after in vivo enrofloxacin treatments in experimentally infected hens.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Chickens , Fluoroquinolones/therapeutic use , Mycoplasma Infections/veterinary , Mycoplasma synoviae/isolation & purification , Poultry Diseases/microbiology , Animals , Anti-Bacterial Agents/pharmacology , Base Sequence , DNA Topoisomerase IV/genetics , DNA, Bacterial/analysis , Drug Resistance, Bacterial/genetics , Enrofloxacin , Female , Fluoroquinolones/pharmacology , Microbial Sensitivity Tests/veterinary , Mutation , Mycoplasma Infections/drug therapy , Mycoplasma Infections/microbiology , Mycoplasma synoviae/drug effects , Mycoplasma synoviae/genetics , Polymerase Chain Reaction/veterinary , Poultry Diseases/drug therapy , Random Allocation , Trachea/microbiology
9.
Genet Sel Evol ; 35(2): 199-217, 2003.
Article in English | MEDLINE | ID: mdl-12633533

ABSTRACT

An experimental population (1216 lambs from 30 sires) of the Inra401 sheep was created in an Inra flock to allow QTL detection for susceptibility to Salmonella infection, wool and carcass traits. The Inra401 is a sheep composite line developed from two breeds: Berrichon du Cher and Romanov. At 113 days of age on average, the lambs were inoculated intravenously with 10(8) Salmonella abortusovis Rv6 (vaccinal strain). They were slaughtered 10 days after the inoculation. Several traits were measured at inoculation and/or slaughtering to estimate the genetic resistance of the lambs to Salmonella infection: specific IgM and IgG1 antibody titres, body weight loss, spleen and pre-scapular node weights and counts of viable Salmonella persisting in these organs. This paper presents a quantitative analysis of the genetic variability of the traits related to salmonellosis susceptibility. The heritabilities of the traits varied between 0.10 and 0.64 (significantly different from zero). Thus, in sheep as well as in other species, the determinism of resistance to Salmonella infection is under genetic control. Moreover, the correlations between the traits are in agreement with the known immune mechanisms. The genetic variability observed should help QTL detection.


Subject(s)
Salmonella Infections, Animal/immunology , Salmonella Vaccines/immunology , Sheep Diseases/genetics , Animals , Antibodies, Bacterial/blood , Body Weights and Measures , Colony Count, Microbial , Genetic Variation/genetics , Models, Genetic , Quantitative Trait Loci/genetics , Sheep , Sheep Diseases/immunology
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