• 1.

    Neimark H, Johansson KE, Rikihisa Y, et al. Proposal to transfer some members of the genera Haemobartonella and Eperythrozoon to the genus Mycoplasma with descriptions of ‘Candidatus Mycoplasma haemofelis’, ‘Candidatus Mycoplasma haemomuris’, ‘Candidatus Mycoplasma haemosuis’ and ‘Candidatus Mycoplasma wenyonii. Int J Syst Evol Microbiol 2001;51:891899.

    • Search Google Scholar
    • Export Citation
  • 2.

    Neimark H, Hoff B, Ganter M. Mycoplasma ovis comb. nov. (formerly Eperythrozoon ovis), an epierythrocytic agent of haemolytic anaemia in sheep and goats. Int J Syst Evol Microbiol 2004;54:365371.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3.

    Uilenberg G, Thiaucourt F, Jongejan F. On molecular taxonomy: what is in a name? Exp Appl Acarol 2004;32:301312.

  • 4.

    Messick JB. Hemotrophic mycoplasmas (hemoplasmas): a review and new insights into pathogenic potential. Vet Clin Pathol 2004;33:213.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5.

    Büttner M, Plank G, Heinritzi K. Effect of immunosuppressive treatment on Eperythrozoon suis infection and porcine peripheral-blood natural-killer-(NK) cell activity. Zentralbl Veterinarmed [B] 1995;42:301310.

    • Search Google Scholar
    • Export Citation
  • 6.

    Yuan CL, Yang ZB, Zhu JG, et al. Effect of an immunosuppressor (dexamethosone) on Eperythrozoon infection. Vet Res Commun 2007;31:661664.

  • 7.

    Cox HW, Calaf-Iturri G. Autoimmune factors associated with anaemia in acute Haemobartonella and Eperythrozoon infections of rodents. Ann Trop Med Parasitol 1976;70:7379.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 8.

    Heinritzi K, Plank G. The effect of Eperythrozoon suis infection on the osmotic fragility of erythrocytes. Berl Munch Tierarztl Wochenschr 1992;105:380383.

    • Search Google Scholar
    • Export Citation
  • 9.

    Heinritzi K. Eperythrozoon infection in swine as a disease factor. Berl Munch Tierarztl Wochenschr 1989;102:337342.

  • 10.

    Puntaric V, Borciü D, Vukeliü D, et al. Eperythrozoonosis in man. Lancet 1986;11:868869.

  • 11.

    Yang D, Tai X, Qiu Y, et al. Prevalence of Eperythrozoon spp. infection and congenital eperythrozoonosis in humans in Inner Mongolia, China. Epidemiol Infect 2000;125:421426.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 12.

    Sambrook J, Russell DW. Molecular cloning: a laboratory manual. 3rd ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 2001.

    • Search Google Scholar
    • Export Citation
  • 13.

    Kenny MJ, Shaw SE, Beugnet F, et al. Demonstration of two distinct hemotropic mycoplasmas in French dogs. J Clin Microbiol 2004;42:53975399.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 14.

    Tasker S, Binns SH, Day MJ, et al. Use of a PCR assay to assess the prevalence and risk factors for Mycoplasma haemofelis and ‘Candidatus Mycoplasma haemominutum’ in cats in the United Kingdom. Vet Rec 2003;152:193198.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 15.

    Willi B, Boretti FS, Baumgartner C, et al. Prevalence, risk factor analysis, and follow-up of infections caused by three feline hemoplasma species in cats in Switzerland. J Clin Microbiol 2006;44:961969.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 16.

    Guimaraes AM, Biondo AW, Lara AC, et al. Exploratory study of Mycoplasma suis (Eperythrozoon suis) on four commercial pig farms in southern Brazil. Vet Rec 2007;160:5053.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 17.

    Prullage JB, Williams RE, Gaafar SM. On the transmissibility of Eperythrozoon suis by Stomoxys calcitrans and Aedes aegypti. Vet Parasitol 1993;50:125135.

    • Crossref
    • Search Google Scholar
    • Export Citation

Advertisement

Prevalence of Mycoplasma suis (Eperythrozoon suis) infection in swine and swine-farm workers in Shanghai, China

Cong L. YuanSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.

Search for other papers by Cong L. Yuan in
Current site
Google Scholar
PubMed
Close
 DVM
,
Ai B. LiangHematology Department, Tongji Hospital, Tongji University, Shanghai, 200092, People's Republic of China.

Search for other papers by Ai B. Liang in
Current site
Google Scholar
PubMed
Close
 PhD
,
Cong B. YaoSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.
Hematology Department, Tongji Hospital, Tongji University, Shanghai, 200092, People's Republic of China.

Search for other papers by Cong B. Yao in
Current site
Google Scholar
PubMed
Close
 DVM
,
Zhi B. YangSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.

Search for other papers by Zhi B. Yang in
Current site
Google Scholar
PubMed
Close
 DVM
,
Jian G. ZhuSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.

Search for other papers by Jian G. Zhu in
Current site
Google Scholar
PubMed
Close
 DVM
,
Li CuiSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.

Search for other papers by Li Cui in
Current site
Google Scholar
PubMed
Close
 DVM
,
Fei YuSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.

Search for other papers by Fei Yu in
Current site
Google Scholar
PubMed
Close
 MS
,
Ning Y. ZhuSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.

Search for other papers by Ning Y. Zhu in
Current site
Google Scholar
PubMed
Close
 MS
,
Xiao W. YangAnimal Science College, Guizhou University, Guizhou Province, 550025, People's Republic of China.

Search for other papers by Xiao W. Yang in
Current site
Google Scholar
PubMed
Close
 MS
, and
Xiu G. HuaSchool of Agriculture and Biology, Shanghai Key Laboratory of Veterinary Medicine, Shanghai Jiaotong University, Shanghai, 200240, People's Republic of China.

Search for other papers by Xiu G. Hua in
Current site
Google Scholar
PubMed
Close
 DVM
View More View Less

Abstract

Objective—To determine the prevalence of Mycoplasma suis infection in swine, swine-farm workers, and swine veterinarians in Shanghai, China.

Sample Population—172 swine and 65 workers and veterinarians from 19 commercial swine farms.

Procedures—Blood samples were collected from all study subjects. Blood samples were examined for the presence of M suis by means of compound and scanning electron microscopy. A species-specific PCR assay was developed for detection of M suis DNA extracted from blood samples. Relationships between infection status of swine and sex, age, geographic location, and clinical signs of disease were evaluated by use of a C2 test. The phylogenetic relationship between partial 16S ribosomal RNA (rRNA) sequences from swine and human isolates of M suis was determined.

Results—86% (148/172) of swine and 49% (32/65) of humans had positive PCR assay results for M suis infection. Swine infection status was not associated with any variable, with the exception of pyrexia and subcutaneous bleeding. The partial 16S rRNA sequences from human and swine isolates of M suis were 98% homologous and in the same phylogenetic cluster as a previously identified swine isolate of M suis.

Conclusions and Clinical Relevance—A large proportion of swine and humans in close contact with those swine were infected with M suis in Shanghai, China. The close phylogenetic relationship between swine and human isolates of M suis suggested possible interspecies transmission; however, additional research is required to better assess that possibility.

Abstract

Objective—To determine the prevalence of Mycoplasma suis infection in swine, swine-farm workers, and swine veterinarians in Shanghai, China.

Sample Population—172 swine and 65 workers and veterinarians from 19 commercial swine farms.

Procedures—Blood samples were collected from all study subjects. Blood samples were examined for the presence of M suis by means of compound and scanning electron microscopy. A species-specific PCR assay was developed for detection of M suis DNA extracted from blood samples. Relationships between infection status of swine and sex, age, geographic location, and clinical signs of disease were evaluated by use of a C2 test. The phylogenetic relationship between partial 16S ribosomal RNA (rRNA) sequences from swine and human isolates of M suis was determined.

Results—86% (148/172) of swine and 49% (32/65) of humans had positive PCR assay results for M suis infection. Swine infection status was not associated with any variable, with the exception of pyrexia and subcutaneous bleeding. The partial 16S rRNA sequences from human and swine isolates of M suis were 98% homologous and in the same phylogenetic cluster as a previously identified swine isolate of M suis.

Conclusions and Clinical Relevance—A large proportion of swine and humans in close contact with those swine were infected with M suis in Shanghai, China. The close phylogenetic relationship between swine and human isolates of M suis suggested possible interspecies transmission; however, additional research is required to better assess that possibility.

Contributor Notes

Supported by the Ministry of Science and Technology of the People's Republic of China (863 grant No. 2006AA02Z454).

Address correspondence to Dr. Hua.