Mycoplasma anserisalpingitidis sp. nov., isolated from European domestic geese (Anser anser domesticus) with reproductive pathology

Author:

Volokhov Dmitriy V.1ORCID,Grózner Dénes23ORCID,Gyuranecz Miklós32,Ferguson-Noel Naola4,Gao Yamei1,Bradbury Janet M.5ORCID,Whittaker Paul67,Chizhikov Vladimir E.61,Szathmary Susan89ORCID,Stipkovits Laszlo8ORCID

Affiliation:

1. Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, 10903 New Hampshire Avenue, Silver Spring, MD 20993, USA

2. Institute for Veterinary Medical Research, Centre for Agricultural Research, Hungária krt. 21, Budapest, 1143, Hungary

3. Department of Microbiology and Infectious Diseases, University of Veterinary Medicine, Hungária krt. 23-25, Budapest, 1143, Hungary

4. Poultry Diagnostic & Research Center, University of Georgia, 953 College Station Rd., Athens, GA 30602, USA

5. University of Liverpool, School of Veterinary Science, Leahurst Campus, Neston, CH64 7TE, UK

6. Present address: Currently retired from the US FDA, Maryland, USA

7. Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, 5001 Campus Dr., College Park, MD 20740, USA

8. RT-Europe Research Center, 9200 Var 2, Mosonmagyaróvár, Hungary

9. Galen Bio, Inc. Carlsbad, 5922 Farnsworth Ct Carlsbad, CA 92008, USA

Abstract

In 1983,Mycoplasmasp. strain 1220 was isolated in Hungary from the phallus lymph of a gander with phallus inflammation. Between 1983 and 2017,Mycoplasmasp. 1220 was also identified and isolated from the respiratory tract, liver, ovary, testis, peritoneum and cloaca of diseased geese in several countries. Seventeen studied strains produced acid from glucose and fructose but did not hydrolyse arginine or urea, and all grew under aerobic, microaerophilic and anaerobic conditions at 35 to 37 ˚C in either SP4 or pleuropneumonia-like organism medium supplemented with glucose and serum. Colonies on agar showed a typical fried-egg appearance and transmission electron microscopy revealed a typical mycoplasma cellular morphology. Molecular characterization included analysis of the following genetic loci: 16S rRNA, 23S rRNA, 16S–23S rRNA ITS,rpoB,rpoC,rpoD,uvrA,parC,topA,dnaE,fusAandpyk. The genome was sequenced for type strain 1220T. The 16S rRNA gene sequences of studied strains ofMycoplasmasp. 1220 shared 99.02–99.19 % nucleotide similarity withM. anatisstrains but demonstrated ≤95.00–96.70 % nucleotide similarity to the 16S rRNA genes of other species of the genusMycoplasma. Phylogenetic, average nucleotide and amino acid identity analyses revealed that the novel species was most closely related toMycoplasma anatis. Based on the genetic data, we propose a novel species of the genusMycoplasma, for which the nameMycoplasma anserisalpingitidissp. nov. is proposed with the type strain 1220T(=ATCC BAA-2147T=NCTC 13513T=DSM 23982T). The G+C content is 26.70 mol%, genome size is 959110 bp.

Publisher

Microbiology Society

Subject

General Medicine,Ecology, Evolution, Behavior and Systematics,Microbiology

Reference68 articles.

1. Molecular Biology and Pathogenicity of Mycoplasmas

2. Mycoplasma infection of geese. I. incidence of mycoplasmas and acholeplasmas in geese;Stipkovits;Avian Pathol,1975

3. Mycoplasma infection of geese II. Studies on pathogenicity of mycoplasmas in goslings and goose and chicken embryos

4. The pathogenicity of avian mycoplasmas;Stipkovits;Zentralbl Bakteriol Orig A,1979

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