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Molecular Survey of Bacterial Zoonotic Agents in Bats from the Country of Georgia (Caucasus)

https://doi.org/10.1371/journal.pone.0171175
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-60327-353-4_17openalex-snapshot
Detection of Pathogenic Leptospira spp. Through Real-Time PCR (qPCR) Targeting the LipL32 Gene
inferredcites →https://doi.org/10.1016/0378-1119(93)90236-vopenalex-snapshot
Sequence and characterization of an insertion sequence, IS711, from Brucella ovis
inferredcites →https://doi.org/10.1016/j.meegid.2012.06.009openalex-snapshot
Global distribution and genetic diversity of Bartonella in bat flies (Hippoboscoidea, Streblidae, Nycteribiidae)
inferredcites →https://doi.org/10.1016/j.meegid.2016.07.033openalex-snapshot
Phylogenetic and geographic patterns of bartonella host shifts among bat species
inferredcites →https://doi.org/10.1016/j.pt.2016.04.007openalex-snapshot
Global Patterns of Zoonotic Disease in Mammals
inferredcites →https://doi.org/10.1016/j.vetmic.2009.03.012openalex-snapshot
Leptospira and leptospirosis
inferredcites →https://doi.org/10.1016/j.vetmic.2014.02.021openalex-snapshot
Novel Bartonella infection in northern and southern sea otters (Enhydra lutris kenyoni and Enhydra lutris nereis)
inferredcites →https://doi.org/10.1051/vetres:2007023openalex-snapshot
Canine bartonellosis: serological and molecular prevalence in Brazil and evidence of co-infection with Bartonella henselae and Bartonella vinsonii subsp. berkhoffii
inferredcites →https://doi.org/10.1089/vbz.2007.0143openalex-snapshot
Brucellosis of the Common Vole ( Microtus arvalis )
inferredcites →https://doi.org/10.1089/vbz.2008.0036openalex-snapshot
Isolation of Brucella microti from Mandibular Lymph Nodes of Red Foxes, Vulpes vulpes , in Lower Austria
inferredcites →https://doi.org/10.1099/jmm.0.45860-0openalex-snapshot
Detection of pathogenic leptospires by real-time quantitative PCR
inferredcites →https://doi.org/10.1111/j.1096-3642.2011.00696.xopenalex-snapshot
Ecological and Behavioral Methods for the Study of Bats
inferredcites →https://doi.org/10.1111/j.1863-2378.2012.01536.xopenalex-snapshot
Bats and Bacterial Pathogens: A Review
inferredcites →https://doi.org/10.1128/aem.00620-10openalex-snapshot
Characterization of Novel Brucella Strains Originating from Wild Native Rodent Species in North Queensland, Australia
inferredcites →https://doi.org/10.1128/aem.02203-10openalex-snapshot
Persistent Infection or Successive Reinfection of Deer Mice withBartonella vinsoniisubsp.arupensis
inferredcites →https://doi.org/10.1128/cmr.00017-06openalex-snapshot
Bats: Important Reservoir Hosts of Emerging Viruses
inferredcites →https://doi.org/10.1128/cmr.14.2.296-326.2001openalex-snapshot
Leptospirosis
inferredcites →https://doi.org/10.1177/0300985814540545openalex-snapshot
Advancement of Knowledge of Brucella Over the Past 50 Years
inferredcites →https://doi.org/10.1177/104063879400600408openalex-snapshot
Characteristics of a Brucella Species from a Bottlenose Dolphin ( Tursiops Truncatus )
inferredcites →https://doi.org/10.1186/s12889-015-1761-yopenalex-snapshot
Expansion of brucellosis detection in the country of Georgia by screening household members of cases and neighboring community members
inferredcites →https://doi.org/10.1371/journal.pntd.0002902openalex-snapshot
Epidemiology of Leptospira Transmitted by Rodents in Southeast Asia
inferredcites →https://doi.org/10.1371/journal.pone.0080894openalex-snapshot
Global Distribution of Bartonella Infections in Domestic Bovine and Characterization of Bartonella bovis Strains Using Multi-Locus Sequence Typing
inferredcites →https://doi.org/10.1371/journal.ppat.1005176openalex-snapshot
Leptospira and Bats: Story of an Emerging Friendship
inferredcites →https://doi.org/10.1590/s1135-57272001000300009openalex-snapshot
Zoonosis y enfermedades transmisibles comunes al hombre y a los animales. Volumen I: Bacteriosis y micosis
inferredcites →https://doi.org/10.1638/2007-0033.1openalex-snapshot
Yersinia pseudotuberculosis in a Closed Colony of Egyptian Fruit Bats (Rousettus aegyptiacus)
inferredcites →https://doi.org/10.3201/eid0902.020083openalex-snapshot
Emerging Pattern of Rabies Deaths and Increased Viral Infectivity
inferredcites →https://doi.org/10.3201/eid1603.081673openalex-snapshot
CandidatusBartonella mayotimonensis and Endocarditis
inferredcites →https://doi.org/10.3201/eid1603.091035openalex-snapshot
YersiniaSpecies Isolated from Bats, Germany
inferredcites →https://doi.org/10.3201/eid1612.100601openalex-snapshot
Bartonellaspp. in Bats, Kenya
inferredcites →https://doi.org/10.3201/eid1707.101867openalex-snapshot
Bartonella spp. in Bats, Guatemala
inferredcites →https://doi.org/10.3201/eid2006.130956openalex-snapshot
Bats as Reservoir Hosts of Human Bacterial Pathogen,Bartonella mayotimonensis
inferredcites →https://doi.org/10.3201/eid2203.151823openalex-snapshot
Human Lymphadenopathy Caused by RatborneBartonella, Tbilisi, Georgia
inferredcites →https://doi.org/10.4269/ajtmh.16-0041openalex-snapshot
Prevalence and Diversity of Bartonella Species in Rodents from Georgia (Caucasus)
inferredcites →https://doi.org/10.4269/ajtmh.2005.73.964openalex-snapshot
DIVERSITY OF BAT-ASSOCIATED LEPTOSPIRA IN THE PERUVIAN AMAZON INFERRED BY BAYESIAN PHYLOGENETIC ANALYSIS OF 16S RIBOSOMAL DNA SEQUENCES
inferredcites →https://doi.org/10.4269/ajtmh.2010.09-0227openalex-snapshot
The Contribution of Bats to Leptospirosis Transmission in São Paulo City, Brazil
inferredcites →https://doi.org/10.5860/choice.47-4417openalex-snapshot
Ecological and behavioral methods for the study of bats
inferredcites →https://doi.org/10.7589/0090-3558-12.1.52openalex-snapshot
ANTI-BRUCELLA AGGLUTININS IN BATS AND “CALUTHRIX” MONKEYS
inferredcites →https://doi.org/10.7589/0090-3558-19.3.192openalex-snapshot
LEPTOSPIRES IN WILDLIFE FROM TRINIDAD AND GRENADA
inferredcites →https://doi.org/10.7589/0090-3558-41.4.753openalex-snapshot
FLYING FOXES AS CARRIERS OF PATHOGENIC LEPTOSPIRA SPECIES
inferredcites →https://doi.org/10.7589/0090-3558-8.4.343openalex-snapshot
LEPTOSPIROSIS IN DANISH WILD MAMMALS
inferredcites →https://doi.org/10.7589/0090-3558-9.1.64openalex-snapshot
YERSINIOSIS IN WILDLIFE AND ITS PUBLIC HEALTH IMPLICATIONS

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Zoonotic Bacterial Pathogens in Bats Samples Around the World: A Scoping Review
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Mediterranean Horseshoe Bat Rhinolophus euryale Blasius, 1853
inferred← citeshttps://doi.org/10.1007/978-3-030-44029-9_44openalex-snapshot
Serotine Eptesicus serotinus (Schreber, 1774)
inferred← citeshttps://doi.org/10.1007/978-3-030-85877-3_28-1openalex-snapshot
Bat-Related Zoonoses
inferred← citeshttps://doi.org/10.1007/978-3-031-27164-9_28openalex-snapshot
Bat-Related Zoonoses
inferred← citeshttps://doi.org/10.1007/978-3-319-65038-8_40-1openalex-snapshot
Mediterranean Horseshoe Bat Rhinolophus euryale Blasius, 1853
inferred← citeshttps://doi.org/10.1007/978-3-319-65038-8_44-1openalex-snapshot
Serotine Eptesicus serotinus (Schreber, 1774)
inferred← citeshttps://doi.org/10.1007/s00436-022-07668-4openalex-snapshot
First detection of Bartonella spp. in bat bugs Cimex pipistrelli (Hemiptera: Cimicidae), Central Europe
inferred← citeshttps://doi.org/10.1007/s10344-026-02169-6openalex-snapshot
Review of bat research in Georgia (Sakartvelo): historical trends, knowledge gaps, and conservation needs
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Differences in gut microbiota composition, diversity, and predicted functional activity between wild and captive zoo Carollia perspicillata in a One Health perspective
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Wildlife as reservoirs of brucellosis and their transmission
inferred← citeshttps://doi.org/10.1016/j.actatropica.2024.107298openalex-snapshot
Leptospira infection in bats in Vietnam
inferred← citeshttps://doi.org/10.1016/j.actatropica.2024.107506openalex-snapshot
In search of pathogenic Leptospira species in Myotis and other vesper bats, Russia
inferred← citeshttps://doi.org/10.1016/j.cimid.2017.09.001openalex-snapshot
Bartonella , bats and bugs: A review
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The heart microbiome of insectivorous bats from Central and South Eastern Europe
inferred← citeshttps://doi.org/10.1016/j.cimid.2021.101692openalex-snapshot
Cross-sectional study on Brucella spp., Leptospira spp. and Salmonella spp. in bats from Montes Claros, Minas Gerais, Brazil
inferred← citeshttps://doi.org/10.1016/j.eas.2023.100033openalex-snapshot
Serological and molecular investigations on Toxoplasma gondii and Leptospira spp. in bats captured in urban areas from Brazil
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Emerging diversity and ongoing expansion of the genus Brucella
inferred← citeshttps://doi.org/10.1016/j.prevetmed.2024.106135openalex-snapshot
Zoonotic bacterial pathogens in bats samples around the world: a scoping review
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2023.102283openalex-snapshot
Molecular detection of Babesia vesperuginis in bats from Lithuania
inferred← citeshttps://doi.org/10.1080/22221751.2022.2117095openalex-snapshot
Detection of Leptospira species in bat cadavers, Czech and Slovak Republics
inferred← citeshttps://doi.org/10.1088/1755-1315/1425/1/012022openalex-snapshot
New Report: An Overview of Bats Bacteria And Its Implication For Tourism In KEK Mandalika, Lombok Island West Nusa Tenggara - Indonesia
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Longitudinal Study of Bacterial Infectious Agents in a Community of Small Mammals in New Mexico
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Species identity and capture locality strongly shape the bat organ microbiome: a 16S rRNA survey across internal tissues
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Survey of Parasitic Bacteria in Bat Bugs, Colorado
inferred← citeshttps://doi.org/10.1101/2020.04.30.069815openalex-snapshot
The heart microbiome of insectivorous bats from Central and South Eastern Europe
inferred← citeshttps://doi.org/10.1111/tbed.12802openalex-snapshot
Detection of pathogenicLeptospiraspecies associated with phyllostomid bats (Mammalia: Chiroptera) from Veracruz, Mexico
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Urinary shedding of leptospires in palearctic bats
inferred← citeshttps://doi.org/10.1111/tbed.14589openalex-snapshot
Leptospira sp. infection in bats: A systematic review and meta‐analysis
inferred← citeshttps://doi.org/10.1111/zph.12880openalex-snapshot
Molecular detection and characterization of pathogenic Leptospira species in bats (Chiroptera) roosting in human habitats in Nigeria, West Africa
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Brucella microti and Rodent‐Borne Brucellosis: A Neglected Public Health Threat
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Evaluación de la respuesta de los linfocitos T durante la infección crónica por Trypanosoma cruzi y su relación con el control de la infección
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Virulent Brucella nosferati infecting Desmodus rotundus has emerging potential due to the broad foraging range of its bat host for humans and wild and domestic animals
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Detection of bacterial and protozoan pathogens in individual bats and their ectoparasites using high-throughput microfluidic real-time PCR
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Trends in Bacterial Pathogens of Bats: Global Distribution and Knowledge Gaps
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>b i /i< spp. e >i /i< em morcegos (Chiroptera, Mammalia) da região urbana de São Paulo, SP, Brasil>/b<
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Molecular detection of Bartonella spp. in deer ked (Lipoptena cervi) in Poland
inferred← citeshttps://doi.org/10.1186/s13071-017-2536-3openalex-snapshot
Babesia vesperuginis, a neglected piroplasmid: new host and geographical records, and phylogenetic relations
inferred← citeshttps://doi.org/10.1186/s13071-018-3070-7openalex-snapshot
Bartonella DNA in heart tissues of bats in central and eastern Europe and a review of phylogenetic relations of bat-associated bartonellae
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inferred← citeshttps://doi.org/10.1515/ovs-2022-0113openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-10768697/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-10809117/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-932107/v1openalex-snapshot
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Antigenic and molecular evidence of Brucella sp.-associated epididymo-orchitis in frugivorous (Artibeus lituratus) and nectarivorous (Glossophaga soricina) bats in Brazil
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Cultivable Bacteria Associated with the Microbiota of Troglophile Bats
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Bats Are Carriers of Antimicrobial-Resistant Staphylococcaceae in Their Skin
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High-Resolution Melting PCR as Rapid Genotyping Tool for Brucella Species
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Identification of a Novel Yersinia enterocolitica Strain from Bats in Association with a Bat Die-Off That Occurred in Georgia (Caucasus)
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Brucella: Reservoirs and Niches in Animals and Humans
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A Cross Sectional Sampling Reveals Novel Coronaviruses in Bat Populations of Georgia
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Bats as Hosts of Antimicrobial-Resistant Mammaliicoccus lentus and Staphylococcus epidermidis with Zoonotic Relevance
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Comparative Evaluation of Diagnostic Tests for Brucellosis in Humans and Animals: A Meta-Analytical Approach
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Bats are a potential reservoir of pathogenic Leptospira species in Colombia
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Antimicrobial resistance including extended spectrum beta lactamases (ESBL) and carbapenemase in feacal E. coli isolates from bats
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İklim Değişikliğinin Yarasalar Üzerine Olası Etkileri
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HUMAN PATHOGENS AMONG BATS
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Molecular investigation of pathogenic Leptospira in bat species in Abidjan, Cte dIvoire
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Brucellosis – A threat to one health
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The role of peritoneal myeloid cells in a mouse model of Brucella infection : identification of the omentum as a novel target organ
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Diagnosis of Caprine Brucellosis by Serology and Multiple PCR
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