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In an earlier study we showed that Japanese sika deer (\n                      <jats:italic>Cervus nippon<\/jats:italic>\n                      ) harbor three\n                      <jats:italic>Bartonella<\/jats:italic>\n                      species, namely\n                      <jats:italic>B. capreoli<\/jats:italic>\n                      (lineage A) and two novel\n                      <jats:italic>Bartonella<\/jats:italic>\n                      species (lineages B and C); however, there is currently no information on the vector of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      bacteria in sika deer. The aim of this study was to clarify potential vectors of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      in Japanese sika deer.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Thirty-eight wingless deer keds (\n                      <jats:italic>L. fortisetosa<\/jats:italic>\n                      ) and 36 ticks (\n                      <jats:italic>Haemaphysalis<\/jats:italic>\n                      and\n                      <jats:italic>Ixodes<\/jats:italic>\n                      species) were collected from sika deer. The prevalence of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      in the arthropods was evaluated by real-time PCR targeting the 16S\u221223S internal transcribed spacer (ITS) and by culture of the organisms. The total number of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      bacteria were quantified using real-time PCR. The distribution of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      bacteria in deer ked organs was examined by immunofluorescence analysis. The relationship of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      strains isolated from sika deer and arthropods were examined by a phylogenetic analysis based on concatenated sequences of the\n                      <jats:italic>gltA<\/jats:italic>\n                      ,\n                      <jats:italic>rpoB<\/jats:italic>\n                      ,\n                      <jats:italic>ftsZ<\/jats:italic>\n                      , and\n                      <jats:italic>ribC<\/jats:italic>\n                      genes, followed by a BLAST search for\n                      <jats:italic>gltA<\/jats:italic>\n                      and\n                      <jats:italic>rpoB<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      <jats:italic>Bartonella<\/jats:italic>\n                      prevalence in deer keds was 87.9% by real-time PCR and 51.5% in culture and that in the ticks was 8.3% by real-time PCR and 2.8% in culture. The mean number of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      bacteria per ked was calculated to be 9.2 \u00d7 10\n                      <jats:sup>5<\/jats:sup>\n                      cells.\n                      <jats:italic>Bartonella<\/jats:italic>\n                      aggregates were localized in the midgut of the keds. The phylogenetic analysis and BLAST search showed that\u00a0both the host deer and the keds harbored two\n                      <jats:italic>Bartonella<\/jats:italic>\n                      species (lineages B and C), while\n                      <jats:italic>B. capreoli<\/jats:italic>\n                      (lineage A) was not detected in the keds. Two novel\n                      <jats:italic>Bartonella<\/jats:italic>\n                      species (lineages D and E) were isolated from one ked.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      <jats:italic>Lipoptena fortisetosa<\/jats:italic>\n                      likely serves as a vector of at least two\n                      <jats:italic>Bartonella<\/jats:italic>\n                      species (lineages B and C), whereas ticks do not seem to play a significant role in the transmission of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      between sika deer based on the lower detection rates of\n                      <jats:italic>Bartonella<\/jats:italic>\n                      in ticks compared to keds.\n                      <jats:italic>Bartonella<\/jats:italic>\n                      species in lineages D and E appear to be\n                      <jats:italic>L. fortisetosa<\/jats:italic>\n                      -specific strains.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Graphical Abstract<\/jats:title>\n                  <\/jats:sec>","DOI":"10.1186\/s13071-021-04585-w","type":"journal-article","created":{"date-parts":[[2021,1,22]],"date-time":"2021-01-22T02:03:21Z","timestamp":1611281001000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":24,"title":["Lipoptena fortisetosa as a vector of Bartonella bacteria in Japanese sika deer (Cervus nippon)"],"prefix":"10.1186","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6837-977X","authenticated-orcid":false,"given":"Shingo","family":"Sato","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hidenori","family":"Kabeya","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sayuri","family":"Ishiguro","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasuhiro","family":"Shibasaki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Soichi","family":"Maruyama","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2021,1,22]]},"reference":[{"key":"4585_CR1","doi-asserted-by":"publisher","first-page":"894","DOI":"10.1016\/j.meegid.2012.03.005","volume":"12","author":"M Kosoy","year":"2012","unstructured":"Kosoy M, Hayman DT, Chan KS. 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