2018
DOI: 10.1371/journal.pone.0201295
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Surveillance for respiratory and diarrheal pathogens at the human-pig interface in Sarawak, Malaysia

Abstract: BackgroundThe large livestock operations and dense human population of Southeast Asia are considered a hot-spot for emerging viruses.ObjectivesTo determine if the pathogens adenovirus (ADV), coronavirus (CoV), encephalomyocarditis virus (EMCV), enterovirus (EV), influenza A-D (IAV, IBV, ICV, and IDV), porcine circovirus 2 (PCV2), and porcine rotaviruses A and C (RVA and RVC), are aerosolized at the animal-interface, and if humans working in these environments are carrying these viruses in their nasal airways.S… Show more

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Cited by 50 publications
(55 citation statements)
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References 35 publications
(35 reference statements)
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“…Another study also identified the existence of PCV2 in bioaerosol samples from pig farms and abattoirs. In addition, PCV2 was detected in nasal washes of workers (4/78) from pig farms (65). This revealed that PCV2 was a potential airborne virus.…”
Section: Pcvs In Environmental Samplesmentioning
confidence: 94%
See 1 more Smart Citation
“…Another study also identified the existence of PCV2 in bioaerosol samples from pig farms and abattoirs. In addition, PCV2 was detected in nasal washes of workers (4/78) from pig farms (65). This revealed that PCV2 was a potential airborne virus.…”
Section: Pcvs In Environmental Samplesmentioning
confidence: 94%
“…Interestingly, scientists from Northern Ireland, the United States, and Germany could not detect antibodies or antigens of PCV2 in human samples (56)(57)(58)(59). However, in other studies, antibody of PCV1 or antigen of PCV2 was detected in human sera, digestive tract samples and respiratory tract samples (60)(61)(62)(63)(64)(65). Although there is serological and molecular proof of PCV presence in humans, the detection rate is very low.…”
Section: Pcvs In Human Samplesmentioning
confidence: 98%
“…DNA/RNA was extracted from 0.5 mL of each aerosol sample and negative control sample solution using the QIAamp Viral RNA kit and QIAamp DNA Blood kit (Qiagen) following the manufacturer's instructions. Using previously validated probe-based molecular assays [38][39][40][41][42] adapted to the Duke-NUS Laboratory of One Health Research, extracted RNA was tested for the presence/absence of influenza A and B viruses, enteroviruses, coronaviruses, and RSV subtypes A and B using superscript III One-step real-time RT-PCR with Platinum Taq Polymerase. RSV-A and RSV-B assays were not adapted to our laboratory during the time of sampling and therefore were performed 3 months after the last aerosol sample was collected.…”
Section: Sample Processingmentioning
confidence: 99%
“…Additionally, high concordance was noted between A(H1N1)pdm09-like H1N1 viruses isolated from workers with ILI and IAV circulating among swine, indicating species crossover. A second study, led by Borkenhagen et al identified influenza B and influenza D viruses in swine worker nasal passages during a surveillance study in Malaysia [44]. The authors also recovered porcine circovirus 2 in worker nasal specimen as well as in pig specimen, indicating zoonotic concern associated with this viral pathogen of growing concern in Asia.…”
Section: Influenza Virusesmentioning
confidence: 97%