key: cord-0746735-n51qv9pp authors: Wacharapluesadee, Supaporn; Sintunawa, Chirapol; Kaewpom, Thongchai; Khongnomnan, Kritsada; Olival, Kevin J.; Epstein, Jonathan H.; Rodpan, Apaporn; Sangsri, Paiboon; Intarut, Nirun; Chindamporn, Ariya; Suksawa, Kanyarat; Hemachudha, Thiravat title: Group C Betacoronavirus in Bat Guano Fertilizer, Thailand date: 2013-08-03 journal: Emerg Infect Dis DOI: 10.3201/eid1908.130119 sha: c16fecd2784f334dbf3265085fa2fc4d20ea19ae doc_id: 746735 cord_uid: n51qv9pp nan To the Editor: Bats play a critical role in the transmission and origin of zoonotic diseases, primarily viral zoonoses associated with high casefatality rates, including those caused by Nipah virus (NiV) and severe acute respiratory syndrome (SARS)-like coronavirus (CoV) infections (1) . Recently, the World Health Organization (WHO) reported 44 confirmed cases of human infection with Middle East respiratory syndrome CoV, resulting in 22 deaths. Full-genome and phylogenetic analyses of these Middle East respiratory syndrome CoVs have been published elsewhere (2) . The identified viruses from 2 patients (previously referred to as England/ Qatar/2012 and EMC/2012) are genetically related and belong to group C betacoronavirus, which is most related to CoVs from Nycteris bats in Ghana and Pipistrellus bats in Europe (2, 3) . In addition, bat CoVs HKU4 and HKU5 originated from Tylonycteris pachypus and Pipistrellus abramus bats, respectively, in the People's Republic of China (4) . Bats are also known to harbor and transmit nonviral zoonotic pathogens, including the fungal pathogen Histoplasma capsulatum, which causes histoplasmosis in humans (5) . Bat guano is sold for use as a fertilizer in several countries, including Thailand, Indonesia, Mexico, Cuba, and Jamaica. The practice of collecting and harvesting bat guano may pose a considerable health risk because guano miners have a high level of contact and potential exposure to bat-borne pathogens. To assess pathogens in bat guano, we examined bat guano from a cave in the Khao Chong Phran Non-hunting Area (KCP-NHA) in Ratchaburi Province, Thailand, where bat guano was sold as agricultural fertilizer, for the presence of NiV, CoV, and H. capsulatum fungi. Bats from 14 species in 7 families have been found roosting within this area. Tadarida plicata bats are the most abundant species (2,500,000 bats), and 3 other species of bats found at the site each had thousands of members: Taphozous melanopogon, Taphozous theobaldi, and Hipposideros larvatus. A random sample of dry bat guano, ≈100 g, was collected in a sterile plastic bag weekly from the main cave at KCP-NHA from September 2006 through August 2007. The specimens were sent for analysis by express mail (at room temperature within 2-3 days) to the WHO Collaborating Centre for Research and Training in the Viral Zoonoses Laboratory at Chulalongkorn University. Samples were frozen immediately at -80°C until nucleic acids were extracted and PCR assays were run. A total of 52 collected bat guano specimens were examined in this study. Two aliquots of feces from each weekly specimen (104 samples total) were screened for CoV, NiV, and H. capsulatum by PCR. RNA was extracted from 10 mg of fecal pellet by using the QIAamp Viral RNA Mini Kit (QIA-GEN, Hilden, Germany). CoV RNA was detected by using nested reverse transcription PCR with the degenerated primers to amplify the RNA-dependent RNA polymerase (RdRp) gene (6) . NiV RNA was detected by duplex nested reverse transcription PCR (7). To detect H. capsulatum and other fungi, we extracted genomic DNA directly from bat guano by using the silica-guanidine thiocyanate protocol, NucliSense Isolation Reagent (bioMérieux, Boxtel, the Netherlands), according to the manufacturer's protocol. We tested for fungal ribosomal DNA (rDNA) in extracted total nucleic acid specimens by using the PCR protocol designed to amplify all rDNA from 4 major fungus phyla at the internal transcribed spacer 1 and 2 regions (8) . Four ( and phylogenetically clustered with the group C betacoronavirus (Figure) , with 76%, 80%, and 77% nt identity to bat CoV HKU4, bat CoV HKU5, and human CoV EMC and England1_CoV, respectively. The other CoV sequence (KCP31: showed 82% nt identity with bat CoV HKU8, an alphacoronavirus. Although we recognize that longer sequences or full genomes may alter the topology of the phylogeny slightly and give stronger branch support, we expect that the overall topology and placement of these CoVs would remain consistent. Samples from particular bat species could not be identified because bats of different species roost in this cave, and samples were pooled during collection for bat guano fertilizer. The detection of CoVs in bat guano from the KCP-NHA cave in Ratchaburi was consistent with the previous finding of alphacoronavirus from Hipposideros armiger bats from the same province in 2007, but those researchers tested fresh bat feces (9) . All bat guano samples screened by PCR were negative for NiV and Histoplasma spp. but were positive for group C betacoronavirus. The natural reservoir and complete geographic distribution of this CoV are currently unknown. Although we did not isolate live virus from these samples, the detection of nucleic acid and previous isolation of viruses from bat feces and urine (10) warrants some concern that guano miners might be exposed to bat pathogens in fresh excreta as well as in soil substances. We suggest that guano miners use preventive measures of personal hygiene and improved barrier protection to reduce the possibility of exposure to zoonotic pathogens. Fields virology Proposal for a unified norovirus nomenclature and genotyping Evolutionary dynamics of GII.4 noroviruses over a 34-year period Epochal evolution of GGII.4 norovirus capsid proteins from 1996 to Indications for worldwide increased norovirus activity associated with emergence of a new variant of genotype II.4, late 2012 Molecular detection and epidemiology of astrovirus, bocavirus, and sapovirus in Italian children admitted to hospital with acute gastroenteritis Recombinant norovirus GII.g/GII.12 gastroenteritis in children Nationwide surveillance study of human astrovirus infections in an Italian paediatric population An automated genotyping tool for enteroviruses and noroviruses Rapid emergence and antigenic diversification of the norovirus 2012 Sydney variant in Denmark New directions in conservation medicine: applied cases of ecological health Full-genome deep sequencing and phylogenetic analysis of novel human betacoronavirus Human betacoronavirus 2c EMC/2012-related viruses in bats, Ghana and Europe Molecular diversity of coronaviruses in bats. Virology Histoplasmosis associated with exploring a batinhabited cave in Costa Rica Detection of novel SARS-like and other coronaviruses in bats from Kenya Duplex nested RT-PCR for detection of Nipah virus RNA from urine specimens of bats Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics SARS-coronavirus ancestor's foot-prints in South-East Asian bat colonies and the refuge theory Isolation of Nipah virus from Malaysian Island flying-foxes Address for correspondence: Supaporn Wacharapluesadee, WHO Collaborating Centre for Research and Training on Viral Zoonoses KCP12, and KCP15); 19 additional human and animal CoVs from the National Center for Biotechnology Information database are included. Construction of the tree was based on 152 nt of the RNA-dependent RNA polymerase gene region by maximum-likelihood method and GTR+I model with the 1,000 bootstrap resampling method MHV, murine hepatitis virus (NC001846) Rousettus bat CoV HKU9 Tylonycteris bat CoV HKU4 (NC009019) Pipistrellus bat CoV HKU5 SARS_BatCoV HKU3, severe acute respiratory syndrome (SARS)-related Rhinolophus bat CoV HKU3 (DQ022305) SARS-related Chinese ferret badger CoV SARS-related palm civet CoV An expanded version is online at wwwnc