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Reverse Zoonotic Transmission of SARS-CoV-2 and Monkeypox Virus: A Comprehensive Review
Chiranjib Chakraborty, Manojit Bhattacharya, Md Aminul Islam, Hatem Zayed, Elijah Ige Ohimain, Sang-Soo Lee, Prosun Bhattacharya, Kuldeep Dhama
J. Microbiol. 2024;62(5):337-354.   Published online May 23, 2024
DOI: https://doi.org/10.1007/s12275-024-00138-9
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  • 3 Web of Science
  • 1 Crossref
AbstractAbstract
Reverse zoonosis reveals the process of transmission of a pathogen through the human-animal interface and the spillback of the zoonotic pathogen. In this article, we methodically demonstrate various aspects of reverse zoonosis, with a comprehensive discussion of SARS-CoV-2 and MPXV reverse zoonosis. First, different components of reverse zoonosis, such as humans, different pathogens, and numerous animals (poultry, livestock, pets, wild animals, and zoo animals), have been demonstrated. Second, it explains the present status of reverse zoonosis with different pathogens during previous occurrences of various outbreaks, epidemics, and pandemics. Here, we present 25 examples from literature. Third, using several examples, we comprehensively illustrate the present status of the reverse zoonosis of SARS-CoV-2 and MPXV. Here, we have provided 17 examples of SARS-CoV-2 reverse zoonosis and two examples of MPXV reverse zoonosis. Fourth, we have described two significant aspects of reverse zoonosis: understanding the fundamental aspects of spillback and awareness. These two aspects are required to prevent reverse zoonosis from the current infection with two significant viruses. Finally, the One Health approach was discussed vividly, where we urge scientists from different areas to work collaboratively to solve the issue of reverse zoonosis.

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Citations to this article as recorded by  
  • Development of a multiplex real-time PCR for the simultaneous detection of monkeypox virus clades I, II, and goatpox virus
    Yongqiang Lin, Zijing Guo, Jinsong Chen, Xianwen Zhang, Long Zhou, Yanmin Li, Zhidong Zhang
    Frontiers in Veterinary Science.2024;[Epub]     CrossRef
Minireveiw] Urban Microbiomes and Urban Ecology: How Do Microbes in the Built Environment Affect Human Sustainability in Cities?
Gary M. King
J. Microbiol. 2014;52(9):721-728.   Published online September 2, 2014
DOI: https://doi.org/10.1007/s12275-014-4364-x
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  • 34 Crossref
AbstractAbstract
Humans increasingly occupy cities. Globally, about 50% of the total human population lives in urban environments, and in spite of some trends for deurbanization, the transition from rural to urban life is expected to accelerate in the future, especially in developing nations and regions. The Republic of Korea, for example, has witnessed a dramatic rise in its urban population, which now accounts for nearly 90% of all residents; the increase from about 29% in 1955 has been attributed to multiple factors, but has clearly been driven by extraordinary growth in the gross domestic product accompanying industrialization. While industrialization and urbanization have unarguably led to major improvements in quality of life indices in Korea and elsewhere, numerous serious problems have also been acknowledged, including concerns about resource availability, water quality, amplification of global warming and new threats to health. Questions about sustainability have therefore led Koreans and others to consider deurbanization as a management policy. Whether this offers any realistic prospects for a sustainable future remains to be seen. In the interim, it has become increasingly clear that built environments are no less complex than natural environments, and that they depend on a variety of internal and external connections involving microbes and the processes for which microbes are responsible. I provide here a definition of the urban microbiome, and through examples indicate its centrality to human function and wellbeing in urban systems. I also identify important knowledge gaps and unanswered questions about urban microbiomes that must be addressed to develop a robust, predictive and general understanding of urban biology and ecology that can be used to inform policy-making for sustainable systems.

Citations

Citations to this article as recorded by  
  • Forest management impacts on soil phosphorus cycling: Insights from metagenomics in Moso bamboo plantations
    Xiaoping Zhang, Zhiyuan Huang, Zheke Zhong, Qiaoling Li, Fangyuan Bian
    Journal of Environmental Management.2025; 373: 123735.     CrossRef
  • How can plant-enriched natural environments benefit human health: a narrative review of relevant theories
    Hansen Li, Guodong Zhang
    International Journal of Environmental Health Research.2024; 34(3): 1241.     CrossRef
  • Who inhabits the built environment? A microbiological point of view on the principal bacteria colonizing our urban areas
    Jessica Zampolli, Alessandra De Giani, Massimiliano Rossi, Margherita Finazzi, Patrizia Di Gennaro
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • Urban air quality affects the apple microbiome assembly
    Matthias Schweitzer, Isabella Kögl, Birgit Wassermann, Ahmed Abdelfattah, Wisnu Adi Wicaksono, Gabriele Berg
    Environmental Research.2024; 262: 119858.     CrossRef
  • Characterizing suburban soil and microbial properties along a soil age chronosequence
    Andie Suratt, Kavisha Behl, Wai Lam Hong, Yae Eun Yoon, Steven D. Allison
    Ecosphere.2024;[Epub]     CrossRef
  • Unlocking resilience and sustainability with earth-based materials: a principled framework for urban transformation
    Michael Bühler, Pia Hollenbach, Lothar Köhler, Rachel Armstrong
    Frontiers in Built Environment.2024;[Epub]     CrossRef
  • Mixing with native broadleaf trees modified soil microbial communities of Cunninghamia lanceolata monocultures in South China
    Fenglin Zheng, Jiawei Gu, Dehao Lu, Jiaman Yang, Xiaomai Shuai, Cheng Li, Hongyue Chen
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • Abundance and absence: Human-microbial co-evolution in the Anthropocene
    Aaron Bradshaw
    The Anthropocene Review.2024; 11(1): 26.     CrossRef
  • Faecal indicator bacteria on indoor floors linked to exterior sidewalk contamination in New York City
    Alessandra C Leri, Marjan Khan
    Indoor and Built Environment.2023; 32(6): 1187.     CrossRef
  • Mapping bark bacteria: initial insights of stemflow-induced changes in bark surface phyla
    J. E. Hudson, D. F. Levia, K. M. Yoshimura, N. R. Gottel, S. A. Hudson, J. F. Biddle, Blaire Steven
    Microbiology Spectrum.2023;[Epub]     CrossRef
  • Towards the microbial home: An overview of developments in next‐generation sustainable architecture
    Rachel Armstrong
    Microbial Biotechnology.2023; 16(6): 1112.     CrossRef
  • Chitinophaga pendula, sp. nov., from an air conditioner condensate drain line
    T. Chiyoko Onouye, Hans-Jürgen Busse, Rebecca D. Prescott, Maxwell K. Darris, Stuart P. Donachie
    International Journal of Systematic and Evolutionary Microbiology .2023;[Epub]     CrossRef
  • Deciphering Bacterial Community of the Fallow and Paddy Soil Focusing on Possible Biocontrol Agents
    Aqleem Abbas, Jie Duan, Assane Hamidou Abdoulaye, Yanping Fu, Yang Lin, Jiatao Xie, Jiasen Cheng, Daohong Jiang
    Agronomy.2022; 12(2): 431.     CrossRef
  • Plant beneficial rhizobacteria community structure changes through developmental stages of peanut and maize
    María Soledad Anzuay, Natalia Pin Viso, Liliana Mercedes Ludueña, Federico Daniel Morla, Jorge Guillermo Angelini, Tania Taurian
    Rhizosphere.2021; 19: 100407.     CrossRef
  • Wastewater treatment works change the intestinal microbiomes of insectivorous bats
    Calvin Mehl, M. Corrie Schoeman, Tomasz J. Sanko, Carlos Bezuidenhout, Charlotte M. S. Mienie, Wolfgang Preiser, Dalene Vosloo, Jun Sun
    PLOS ONE.2021; 16(3): e0247475.     CrossRef
  • Microbiomes for All
    Theodore R. Muth, Avrom J. Caplan
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Analysis of the Soil Microbiome of a Los Angeles Urban Farm
    Savanah St. Clair, Maryam Saraylou, Daila Melendez, Norman Senn, Serina Reitz, Destini Kananipour, Angelo Alvarez, Rafael Clemente
    Applied and Environmental Soil Science.2020; 2020: 1.     CrossRef
  • Microbial Composition and Functional Diversity Differ Across Urban Green Infrastructure Types
    Aman S. Gill, Kai Purnell, Matthew I. Palmer, Jaime Stein, Krista L. McGuire
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Hiệu quả của phân bón urea humate kết hợp phân bón vi sinh lên sinh trưởng và năng suất lúa tại huyện Châu Thành A, tỉnh Hậu Giang
    Tất Anh Thư, Bùi Triệu Thương, Nguyễn Khởi Nghĩa
    Can Tho University Journal of Science.2020; 56(SoilSci: 191.     CrossRef
  • Exotic airborne bacteria identified in urban resuspended dust by next generation sequencing
    Nora Kováts, Eszter Horváth, Katalin Hubai, András Hoffer, Beatrix Jancsek-Turóczi, Csaba Fekete, D. Altausen, S. Abdullaev, J. Hofer
    E3S Web of Conferences.2019; 99: 04009.     CrossRef
  • Influence of Urbanization on Epiphytic Bacterial Communities of the Platanus × hispanica Tree Leaves in a Biennial Study
    Jordan Espenshade, Sofie Thijs, Stanislaw Gawronski, Hannelore Bové, Nele Weyens, Jaco Vangronsveld
    Frontiers in Microbiology.2019;[Epub]     CrossRef
  • World’s Largest Mass Bathing Event Influences the Bacterial Communities of Godavari, a Holy River of India
    Kunal Jani, Dhiraj Dhotre, Jayashree Bandal, Yogesh Shouche, Mangesh Suryavanshi, Vinay Rale, Avinash Sharma
    Microbial Ecology.2018; 76(3): 706.     CrossRef
  • Toward the Drug Factory Microbiome: Microbial Community Variations in Antibiotic-Producing Clean Rooms
    Amal M. Hamdy, Moamen El-massry, Mona T. Kashef, Magdy A. Amin, Ramy K. Aziz
    OMICS: A Journal of Integrative Biology.2018; 22(2): 133.     CrossRef
  • Assessment of urban microbiome assemblies with the help of targeted in silico gold standards
    Samuel M. Gerner, Thomas Rattei, Alexandra B. Graf
    Biology Direct.2018;[Epub]     CrossRef
  • Profiling microbial strains in urban environments using metagenomic sequencing data
    Moreno Zolfo, Francesco Asnicar, Paolo Manghi, Edoardo Pasolli, Adrian Tett, Nicola Segata
    Biology Direct.2018;[Epub]     CrossRef
  • Soil Bacterial Diversity Is Associated with Human Population Density in Urban Greenspaces
    Haitao Wang, Minying Cheng, Melissa Dsouza, Pamela Weisenhorn, Tianling Zheng, Jack A. Gilbert
    Environmental Science & Technology.2018; 52(9): 5115.     CrossRef
  • Whole metagenome profiles of particulates collected from the International Space Station
    Nicholas A. Be, Aram Avila-Herrera, Jonathan E. Allen, Nitin Singh, Aleksandra Checinska Sielaff, Crystal Jaing, Kasthuri Venkateswaran
    Microbiome.2017;[Epub]     CrossRef
  • Long-term Fertilization Structures Bacterial and Archaeal Communities along Soil Depth Gradient in a Paddy Soil
    Yunfu Gu, Yingyan Wang, Sheng’e Lu, Quanju Xiang, Xiumei Yu, Ke Zhao, Likou Zou, Qiang Chen, Shihua Tu, Xiaoping Zhang
    Frontiers in Microbiology.2017;[Epub]     CrossRef
  • Tree Leaf Bacterial Community Structure and Diversity Differ along a Gradient of Urban Intensity
    Isabelle Laforest-Lapointe, Christian Messier, Steven W. Kembel, Eoin L. Brodie
    mSystems.2017;[Epub]     CrossRef
  • Patients as Patches: Ecology and Epidemiology in Healthcare Environments
    Eric T. Lofgren, Andrea M. Egizi, Nina H. Fefferman
    Infection Control & Hospital Epidemiology.2016; 37(12): 1507.     CrossRef
  • A vision for ubiquitous sequencing
    Yaniv Erlich
    Genome Research.2015; 25(10): 1411.     CrossRef
  • Urban microbial ecology of a freshwater estuary of Lake Michigan
    Jenny C. Fisher, Ryan J. Newton, Deborah K. Dila, Sandra L. McLellan, Donald R. Zak, Julian D. Olden
    Elementa: Science of the Anthropocene.2015;[Epub]     CrossRef
  • Grand challenges in urban ecology
    Diane E. Pataki
    Frontiers in Ecology and Evolution.2015;[Epub]     CrossRef
  • A unique assemblage of cosmopolitan freshwater bacteria and higher community diversity differentiate an urbanized estuary from oligotrophic Lake Michigan
    Ryan J. Newton, Sandra L. McLellan
    Frontiers in Microbiology.2015;[Epub]     CrossRef
MINIREVIEW] Toxin-producing Cyanobacteria in Freshwater: A Review of the Problems, Impact on Drinking Water Safety, and Efforts for Protecting Public Health
Melissa Y. Cheung , Song Liang , Jiyoung Lee
J. Microbiol. 2013;51(1):1-10.   Published online March 2, 2013
DOI: https://doi.org/10.1007/s12275-013-2549-3
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  • 181 Scopus
AbstractAbstract
Cyanobacteria have adapted to survive in a variety of environments and have been found globally. Toxin-producing cyanobacterial harmful algal blooms (CHABs) have been increasing in frequency worldwide and pose a threat to drinking and recreational water. In this study, the prevalence, impact of CHABs and mitigation efforts were reviewed, focusing on the Lake Erie region and Ohio’s inland lakes that have been impacted heavily as an example so that the findings can be transferrable to other parts of the world that face the similar problems due to the CHABs in their freshwater environments. This paper provides a basic introduction to CHABs and their toxins as well as an overview of public health implications including exposure routes, health effects, and drinking water issues, algal bloom advisory practices in Ohio, toxin measurements results in Ohio public water supplies, and mitigation efforts.
Research Support, Non-U.S. Gov't
Seasonal Abundance and Distribution of Vibrio Species in the Treated Effluents of Wastewater Treatment Facilities in Suburban and Urban Communities of Eastern Cape Province, South Africa
Etinosa O. Igbinosa , Chikwelu L. Obi , Anthony I. Okoh
J. Microbiol. 2011;49(2):224-232.   Published online May 3, 2011
DOI: https://doi.org/10.1007/s12275-011-0227-x
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  • 20 Scopus
AbstractAbstract
We assessed the seasonal abundance and distribution of Vibrio species as well as some selected environmental parameters in the treated effluents of two wastewater treatment plants (WWTP), one each located in a suburban and urban community of Eastern Cape Province, South Africa. Vibrio population density ranged from 2.1×101 to 4.36×104 CFU/ml in the suburban community and from 2.80×101 to 1.80×105 CFU/ml in the urban community. Vibrio species associated with 180 μm, 60 μm, and 20 μm plankton sizes were observed at densities of 0-1.36×103 CFU/ml, 0-8.40×102 CFU/ml, and 0-6.80×102 CFU/ml, respectively at the suburban community’s WWTP. In the urban community, observed densities of culturable Vibrio were 0-2.80×102 CFU/ml (180 μm), 0-6.60×102 CFU/ml (60 μm), and 0-1.80×103 CFU/ml (20 μm). The abundance of free-living Vibrio species ranged from 0 to 1.0×102 and 1.0×103 CFU/ml in the suburban and urban communities’ WWTPs, respectively. Molecular confirmation of the presumptive Vibrio isolates revealed the presence of V. fluvialis (41.38%), V. vulnificus (34.48%), and V. parahaemolyticus (24.14%) in the suburban community effluents. In the urban community molecular confirmation revealed that the same species were present at slightly different percentages, V. fluvialis (40%), V. vulnificus (36%), and V. parahaemolyticus (24%). There was no significant correlation between Vibrio abundance and season, either as free-living or planktonassociated entities, but Vibrio species abundance was positively correlated with temperature (r=0.565; p<0.01), salinity, and dissolved oxygen (p<0.05). Turbidity and pH showed significant seasonal variation (p<0.05) across the seasons in both locations. This study underscores the potential of WWTPs to be sources of Vibrio pathogens in the watershed of suburban and urban communities in South Africa.

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