Monkeypox Outbreak 2022: Clinical and Virological Features of 30 Patients at the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, Bologna, Northeastern Italy
Monkeypox infection is a zoonosis first described in humans in 1970 in Congo. While previously manifesting in small, confined outbreaks, the disease is rapidly spreading globally. The aim of this study was to investigate microbiological samples (skin, rectal, and oropharyngeal swab samples and plasm...
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Veröffentlicht in: | Journal of clinical microbiology 2023-01, Vol.61 (1), p.e0136522-e0136522 |
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creator | Gaspari, Valeria Rossini, Giada Robuffo, Silvia Rapparini, Luca Scagliarini, Alessandra Mistral De Pascali, Alessandra Piraccini, Bianca Maria Lazzarotto, Tiziana |
description | Monkeypox infection is a zoonosis first described in humans in 1970 in Congo. While previously manifesting in small, confined outbreaks, the disease is rapidly spreading globally. The aim of this study was to investigate microbiological samples (skin, rectal, and oropharyngeal swab samples and plasma and urine samples) that can help in adequate diagnostic, therapeutic, and prognostic management. We present 30 laboratory-confirmed monkeypox patients with peculiar clinical and virological features admitted to the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, University of Bologna, in the period between 20 June and 10 August 2022. Demographic, anamnestic, and clinical data were obtained, and microbiological samples were collected and analyzed by real-time PCR to detect the presence of monkeypox virus (MPXV) DNA. All monkeypox patients were adult men who have sex with men (MSM) (mean age, 37.5 years). Nonskin samples were collected from 29 patients during the acute phase of the infection. The detection rates of MPXV DNA in plasma, urine, and oropharyngeal swab samples (82.3%, 64.7%, and 75.0%, respectively) were highest in samples collected 4 to 6 days after symptom onset. The presence of MPXV in plasma and urine samples was analyzed 11 to 38 days after symptom onset to monitor viral shedding duration. Interestingly, MPXV DNA was detected in a urine sample collected on day 21 in one patient. Prolonged positivity in urine after the clinical recovery suggests a potential source of infection by contamination of wastewater and sewage and transmission to possible animal reservoirs and highlights the need for further investigations on nonskin samples to extend and more adequately standardize the patient isolation period. |
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While previously manifesting in small, confined outbreaks, the disease is rapidly spreading globally. The aim of this study was to investigate microbiological samples (skin, rectal, and oropharyngeal swab samples and plasma and urine samples) that can help in adequate diagnostic, therapeutic, and prognostic management. We present 30 laboratory-confirmed monkeypox patients with peculiar clinical and virological features admitted to the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, University of Bologna, in the period between 20 June and 10 August 2022. Demographic, anamnestic, and clinical data were obtained, and microbiological samples were collected and analyzed by real-time PCR to detect the presence of monkeypox virus (MPXV) DNA. All monkeypox patients were adult men who have sex with men (MSM) (mean age, 37.5 years). Nonskin samples were collected from 29 patients during the acute phase of the infection. The detection rates of MPXV DNA in plasma, urine, and oropharyngeal swab samples (82.3%, 64.7%, and 75.0%, respectively) were highest in samples collected 4 to 6 days after symptom onset. The presence of MPXV in plasma and urine samples was analyzed 11 to 38 days after symptom onset to monitor viral shedding duration. Interestingly, MPXV DNA was detected in a urine sample collected on day 21 in one patient. Prolonged positivity in urine after the clinical recovery suggests a potential source of infection by contamination of wastewater and sewage and transmission to possible animal reservoirs and highlights the need for further investigations on nonskin samples to extend and more adequately standardize the patient isolation period.</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/jcm.01365-22</identifier><identifier>PMID: 36598196</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Adult ; Animals ; Clinical Microbiology ; Disease Outbreaks ; DNA ; Hospitals - statistics & numerical data ; Humans ; Male ; Mpox (monkeypox) - diagnosis ; Mpox (monkeypox) - epidemiology ; Sexual and Gender Minorities - statistics & numerical data ; Virology</subject><ispartof>Journal of clinical microbiology, 2023-01, Vol.61 (1), p.e0136522-e0136522</ispartof><rights>Copyright © 2023 American Society for Microbiology.</rights><rights>Copyright © 2023 American Society for Microbiology. 2023 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a418t-a5b46f80b803171ed477efac2f91abcc8578ccfc87d566a96682e57408e717023</citedby><cites>FETCH-LOGICAL-a418t-a5b46f80b803171ed477efac2f91abcc8578ccfc87d566a96682e57408e717023</cites><orcidid>0000-0002-4029-941X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/jcm.01365-22$$EPDF$$P50$$Gasm2$$H</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/jcm.01365-22$$EHTML$$P50$$Gasm2$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,52751,52752,52753,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36598196$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Tang, Yi-Wei</contributor><creatorcontrib>Gaspari, Valeria</creatorcontrib><creatorcontrib>Rossini, Giada</creatorcontrib><creatorcontrib>Robuffo, Silvia</creatorcontrib><creatorcontrib>Rapparini, Luca</creatorcontrib><creatorcontrib>Scagliarini, Alessandra</creatorcontrib><creatorcontrib>Mistral De Pascali, Alessandra</creatorcontrib><creatorcontrib>Piraccini, Bianca Maria</creatorcontrib><creatorcontrib>Lazzarotto, Tiziana</creatorcontrib><title>Monkeypox Outbreak 2022: Clinical and Virological Features of 30 Patients at the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, Bologna, Northeastern Italy</title><title>Journal of clinical microbiology</title><addtitle>J Clin Microbiol</addtitle><addtitle>J Clin Microbiol</addtitle><description>Monkeypox infection is a zoonosis first described in humans in 1970 in Congo. While previously manifesting in small, confined outbreaks, the disease is rapidly spreading globally. The aim of this study was to investigate microbiological samples (skin, rectal, and oropharyngeal swab samples and plasma and urine samples) that can help in adequate diagnostic, therapeutic, and prognostic management. We present 30 laboratory-confirmed monkeypox patients with peculiar clinical and virological features admitted to the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, University of Bologna, in the period between 20 June and 10 August 2022. Demographic, anamnestic, and clinical data were obtained, and microbiological samples were collected and analyzed by real-time PCR to detect the presence of monkeypox virus (MPXV) DNA. All monkeypox patients were adult men who have sex with men (MSM) (mean age, 37.5 years). Nonskin samples were collected from 29 patients during the acute phase of the infection. The detection rates of MPXV DNA in plasma, urine, and oropharyngeal swab samples (82.3%, 64.7%, and 75.0%, respectively) were highest in samples collected 4 to 6 days after symptom onset. The presence of MPXV in plasma and urine samples was analyzed 11 to 38 days after symptom onset to monitor viral shedding duration. Interestingly, MPXV DNA was detected in a urine sample collected on day 21 in one patient. Prolonged positivity in urine after the clinical recovery suggests a potential source of infection by contamination of wastewater and sewage and transmission to possible animal reservoirs and highlights the need for further investigations on nonskin samples to extend and more adequately standardize the patient isolation period.</description><subject>Adult</subject><subject>Animals</subject><subject>Clinical Microbiology</subject><subject>Disease Outbreaks</subject><subject>DNA</subject><subject>Hospitals - statistics & numerical data</subject><subject>Humans</subject><subject>Male</subject><subject>Mpox (monkeypox) - diagnosis</subject><subject>Mpox (monkeypox) - epidemiology</subject><subject>Sexual and Gender Minorities - statistics & numerical data</subject><subject>Virology</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1v1DAQhiMEokvhxhn5BkibYjsfdjgg0YXSSoVFakHcrIl30nrr2FvbQd3fxJ8k6ZYKDpwsa555Zuw3y54zesAYl2_Wuj-grKirnPMH2YzRRuZ1TX88zGaUNlXOWCH2sicxrillZVlVj7O9kW4ka-pZ9uuzd1e43fgbshxSGxCuCKecvyULa5zRYAm4Fflugrf-4vZ-hJCGgJH4jhSUfIVk0KVIIJF0ieQMbwawdkvOA7jYm5RwRT6YiBDHnsWIBpxaz8Cll2QZordAjn3cmAR2Tg6nOQ7m5IsPow5iwuDIyVjbPs0edWAjPrs797NvRx_PF8f56fLTyeL9aQ4lkymHqi3rTtJW0oIJhqtSCOxA865h0GotKyG17rQUq6quoalrybESJZUomKC82M_e7byboe1xpaeVwapNMD2ErfJg1L8VZy7Vhf-pGikaxqtR8OpOEPz1gDGp3kSN1oJDP0TFRU0lp2UlR3S-Q3XwMQbs7scwqqZ81Zivus1X8Wm11zscYs_V2g_BjT_xP_bF38-4F_8Jv_gNoiCwwg</recordid><startdate>20230126</startdate><enddate>20230126</enddate><creator>Gaspari, Valeria</creator><creator>Rossini, Giada</creator><creator>Robuffo, Silvia</creator><creator>Rapparini, Luca</creator><creator>Scagliarini, Alessandra</creator><creator>Mistral De Pascali, Alessandra</creator><creator>Piraccini, Bianca Maria</creator><creator>Lazzarotto, Tiziana</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4029-941X</orcidid></search><sort><creationdate>20230126</creationdate><title>Monkeypox Outbreak 2022: Clinical and Virological Features of 30 Patients at the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, Bologna, Northeastern Italy</title><author>Gaspari, Valeria ; Rossini, Giada ; Robuffo, Silvia ; Rapparini, Luca ; Scagliarini, Alessandra ; Mistral De Pascali, Alessandra ; Piraccini, Bianca Maria ; Lazzarotto, Tiziana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a418t-a5b46f80b803171ed477efac2f91abcc8578ccfc87d566a96682e57408e717023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Clinical Microbiology</topic><topic>Disease Outbreaks</topic><topic>DNA</topic><topic>Hospitals - statistics & numerical data</topic><topic>Humans</topic><topic>Male</topic><topic>Mpox (monkeypox) - diagnosis</topic><topic>Mpox (monkeypox) - epidemiology</topic><topic>Sexual and Gender Minorities - statistics & numerical data</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gaspari, Valeria</creatorcontrib><creatorcontrib>Rossini, Giada</creatorcontrib><creatorcontrib>Robuffo, Silvia</creatorcontrib><creatorcontrib>Rapparini, Luca</creatorcontrib><creatorcontrib>Scagliarini, Alessandra</creatorcontrib><creatorcontrib>Mistral De Pascali, Alessandra</creatorcontrib><creatorcontrib>Piraccini, Bianca Maria</creatorcontrib><creatorcontrib>Lazzarotto, Tiziana</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gaspari, Valeria</au><au>Rossini, Giada</au><au>Robuffo, Silvia</au><au>Rapparini, Luca</au><au>Scagliarini, Alessandra</au><au>Mistral De Pascali, Alessandra</au><au>Piraccini, Bianca Maria</au><au>Lazzarotto, Tiziana</au><au>Tang, Yi-Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monkeypox Outbreak 2022: Clinical and Virological Features of 30 Patients at the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, Bologna, Northeastern Italy</atitle><jtitle>Journal of clinical microbiology</jtitle><stitle>J Clin Microbiol</stitle><addtitle>J Clin Microbiol</addtitle><date>2023-01-26</date><risdate>2023</risdate><volume>61</volume><issue>1</issue><spage>e0136522</spage><epage>e0136522</epage><pages>e0136522-e0136522</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><abstract>Monkeypox infection is a zoonosis first described in humans in 1970 in Congo. While previously manifesting in small, confined outbreaks, the disease is rapidly spreading globally. The aim of this study was to investigate microbiological samples (skin, rectal, and oropharyngeal swab samples and plasma and urine samples) that can help in adequate diagnostic, therapeutic, and prognostic management. We present 30 laboratory-confirmed monkeypox patients with peculiar clinical and virological features admitted to the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, University of Bologna, in the period between 20 June and 10 August 2022. Demographic, anamnestic, and clinical data were obtained, and microbiological samples were collected and analyzed by real-time PCR to detect the presence of monkeypox virus (MPXV) DNA. All monkeypox patients were adult men who have sex with men (MSM) (mean age, 37.5 years). Nonskin samples were collected from 29 patients during the acute phase of the infection. The detection rates of MPXV DNA in plasma, urine, and oropharyngeal swab samples (82.3%, 64.7%, and 75.0%, respectively) were highest in samples collected 4 to 6 days after symptom onset. The presence of MPXV in plasma and urine samples was analyzed 11 to 38 days after symptom onset to monitor viral shedding duration. Interestingly, MPXV DNA was detected in a urine sample collected on day 21 in one patient. Prolonged positivity in urine after the clinical recovery suggests a potential source of infection by contamination of wastewater and sewage and transmission to possible animal reservoirs and highlights the need for further investigations on nonskin samples to extend and more adequately standardize the patient isolation period.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>36598196</pmid><doi>10.1128/jcm.01365-22</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4029-941X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Animals Clinical Microbiology Disease Outbreaks DNA Hospitals - statistics & numerical data Humans Male Mpox (monkeypox) - diagnosis Mpox (monkeypox) - epidemiology Sexual and Gender Minorities - statistics & numerical data Virology |
title | Monkeypox Outbreak 2022: Clinical and Virological Features of 30 Patients at the Sexually Transmitted Diseases Centre of Sant' Orsola Hospital, Bologna, Northeastern Italy |
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