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	<title>zoonotic transmission &#8211; Science</title>
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	<title>zoonotic transmission &#8211; Science</title>
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		<title>Hepatitis E Clusters in Shanghai Map to Dense Urban Neighborhoods Near Rivers</title>
		<link>https://scienmag.com/hepatitis-e-clusters-in-shanghai-map-to-dense-urban-neighborhoods-near-rivers/</link>
		
		<dc:creator><![CDATA[Kristina Jarvis]]></dc:creator>
		<pubDate>Fri, 25 Sep 2026 00:03:34 +0000</pubDate>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[dense urban hepatitis E hotspots]]></category>
		<category><![CDATA[disease cluster]]></category>
		<category><![CDATA[epidemiology]]></category>
		<category><![CDATA[geographic risk factors for hepatitis E]]></category>
		<category><![CDATA[Hepatitis E]]></category>
		<category><![CDATA[hepatitis E case distribution in Shanghai]]></category>
		<category><![CDATA[hepatitis E infection patterns in China]]></category>
		<category><![CDATA[hepatitis E outbreaks near rivers]]></category>
		<category><![CDATA[hepatitis E public health interventions]]></category>
		<category><![CDATA[hepatitis E surveillance epidemiology]]></category>
		<category><![CDATA[hepatitis E transmission in metropolitan areas]]></category>
		<category><![CDATA[Hepatitis E urban clusters]]></category>
		<category><![CDATA[hepatitis E virus]]></category>
		<category><![CDATA[logistic regression]]></category>
		<category><![CDATA[population density]]></category>
		<category><![CDATA[public health surveillance]]></category>
		<category><![CDATA[risk factors]]></category>
		<category><![CDATA[Shanghai]]></category>
		<category><![CDATA[Shanghai hepatitis E risk mapping]]></category>
		<category><![CDATA[spatial analysis of hepatitis E in Shanghai]]></category>
		<category><![CDATA[spatial-temporal analysis]]></category>
		<category><![CDATA[urban environmental factors and hepatitis E]]></category>
		<category><![CDATA[viral hepatitis]]></category>
		<category><![CDATA[zoonotic transmission]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=213595</guid>

					<description><![CDATA[A six-year surveillance study of 4,668 hepatitis E cases in Shanghai identified significant spatial-temporal clusters concentrated in dense, commercially active urban communities near rivers, with a seasonal peak from December to May.]]></description>
										<content:encoded><![CDATA[<p>Hepatitis E has long lived in the shadow of its viral hepatitis cousins, hepatitis A, B, and C, yet it remains one of the most common causes of acute viral liver infection worldwide. A new six-year analysis of surveillance data from Shanghai, one of the most densely populated metropolitan areas on Earth, now offers one of the most granular pictures yet of where and when this underappreciated pathogen strikes in an urban setting. Drawing on nearly five thousand confirmed cases reported between 2017 and 2022, a team of researchers from the Shanghai Municipal Center for Disease Control and Prevention, Shanghai Jiao Tong University, and Fudan University has mapped the disease&#8217;s spatial and temporal fingerprints at the level of individual communities, and the results point to a distinctive urban geography of risk.</p>
<p>The study, published in BMC Infectious Diseases, analyzed 4,668 hepatitis E cases drawn from China&#8217;s National Notifiable Disease Reporting System, a nationwide passive surveillance network to which clinicians and laboratories must report diagnoses of legally designated infectious diseases. Over the six-year window, Shanghai recorded an average annual notification rate of 3.14 cases per 100,000 population. That figure places hepatitis E firmly on the map of locally relevant infectious diseases in the city, even though it rarely attracts the public attention devoted to respiratory pathogens or foodborne outbreaks. Hepatitis E virus, or HEV, is transmitted primarily through the fecal-oral route, most often via contaminated water, and through zoonotic pathways, particularly the consumption of undercooked pork, game meat, and shellfish from infected animals.</p>
<p>To understand the disease&#8217;s rhythm in time, the researchers applied temporal scan statistics, a method that slides a window of variable length across the surveillance timeline and asks whether case counts within any given interval exceed what would be expected by chance. The analysis identified a statistically significant temporal cluster spanning January 1, 2017 to May 31, 2019, with a relative risk of 1.35 and a log likelihood ratio of 52.18, well beyond the threshold of statistical significance. In practical terms, cases accumulated during this early window at a rate roughly a third higher than the six-year baseline. The team also detected a recurring seasonal signature: notifications clustered in the months from December through May, a winter-to-spring peak that echoes patterns reported in other regions of China and is often linked to seasonal dietary customs, including festival-period consumption of raw or undercooked animal products.</p>
<p>The spatial dimension of the analysis proved more surprising. When the researchers ran a spatial-temporal scan across the entire six-year period, they found one statistically significant cluster with a relative risk of 1.73 and a log likelihood ratio of 135.74. Communities with the highest raw notification rates tended to sit in the southeastern parts of the city, but the most likely cluster identified by the scan statistic was not there. Instead, it was located in the urban core. When the team repeated the scan year by year, the same pattern held: the most likely cluster consistently fell in central urban districts, with secondary clusters appearing in suburban towns on the metropolitan periphery. The discrepancy between where cases are most numerous and where the statistical signal of clustering is strongest is itself informative, because scan statistics adjust for underlying population size and expected case counts rather than simply flagging the tallest bars on a map.</p>
<p>That adjustment matters. Dense urban neighborhoods generate large numbers of cases in absolute terms simply because so many people live there, but a cluster statistic asks a subtler question: are there more cases than the local population structure would predict? The fact that the urban core repeatedly emerged as the most likely cluster suggests that something about these districts, beyond sheer headcount, elevates hepatitis E transmission or detection. Possibilities include greater reliance on food purchased from restaurants and markets, more frequent consumption of seafood and pork dishes, higher turnover of food handlers, or simply better access to healthcare and laboratory testing, which would raise the probability that infections are recognized and reported. The study&#8217;s design cannot distinguish among these mechanisms, a limitation the authors acknowledge explicitly.</p>
<p>To probe what distinguishes clustered communities from the rest, the researchers turned to binary logistic regression, a statistical technique that estimates the odds of membership in a high-risk cluster as a function of community-level characteristics. Three variables emerged as significant. Population density showed the strongest association: communities with higher density had markedly higher odds of falling into a high-risk cluster, with an odds ratio of 7.367. The count of shopping malls, used as a proxy for commercial activity and food-service intensity, was also positively associated, with an odds ratio of 1.531. Intriguingly, distance to the nearest river showed a negative association, with an odds ratio of 0.742, meaning that communities closer to rivers had higher odds of clustering. This last finding is consistent with the hypothesis that waterways and the aquatic food chains they support, including shellfish and fish harvested or sold in riverside markets, may play a role in HEV transmission, although the ecological nature of the analysis means the link remains speculative.</p>
<p>The authors are careful, and rightly so, about how far these associations can be pushed. Because the analysis operates at the level of communities rather than individuals, it is vulnerable to the ecological fallacy: a community-level correlation does not establish that the people within a cluster acquired their infections through the hypothesized route. A mall-dense neighborhood may have many cases not because its residents eat at malls but because mall density tracks with other unmeasured features of urban life. Similarly, proximity to a river may correlate with historical settlement patterns, sanitation infrastructure, or dietary traditions rather than with any direct waterborne exposure. The researchers describe their findings as ecological and hypothesis-generating, and they emphasize that confirming the actual transmission routes of hepatitis E in Shanghai will require individual-level epidemiological studies, including case-control designs that compare exposures of confirmed cases with those of matched controls.</p>
<p>Even with those caveats, the study carries practical weight for public health planning. Shanghai sits within the Yangtze River Delta, one of the most economically dynamic and densely interconnected regions in the world, and its surveillance system feeds into national and global assessments of viral hepatitis burden. The World Health Assembly has set targets for eliminating viral hepatitis as a public health threat, and hepatitis E, though often self-limiting in healthy adults, can be devastating for pregnant women, who face elevated risks of fulminant liver failure, and for people with chronic liver disease or compromised immune systems. Knowing that risk concentrates in dense, commercially active, riverside urban communities gives health authorities a concrete template for targeting interventions, whether that means food-safety inspections in high-risk districts, health education campaigns timed to the December-to-May seasonal peak, or enhanced testing of at-risk populations such as pregnant women in clustered neighborhoods.</p>
<p>The methodological approach also deserves attention from the wider infectious-disease community. Spatial-temporal scan statistics, originally developed for cancer cluster detection and later adapted for communicable disease surveillance, have become a standard tool for turning routine notification data into actionable geographic intelligence. By combining them with community-level socioeconomic and environmental covariates in a regression framework, the Shanghai team demonstrated a pipeline that other cities with robust notifiable-disease systems could replicate. The work also underscores the value of long surveillance windows: a six-year dataset made it possible to separate a one-off elevated period in 2017 through 2019 from a stable seasonal rhythm and a persistent geographic core, distinctions that shorter studies would blur.</p>
<p>What remains to be resolved is the biology behind the map. Genotyping of viral sequences from urban and suburban cases could reveal whether a single transmission chain or multiple introductions drive the clusters, and molecular epidemiology could test whether zoonotic strains from the pork supply chain dominate in commercial districts while water-associated genotypes predominate near rivers. Seroprevalence surveys could measure how much asymptomatic infection the notification data miss, since hepatitis E is frequently mild or silent in young, healthy adults. Until such studies are done, the Shanghai analysis stands as a carefully constructed hypothesis: that in a modern megacity, hepatitis E risk is written into the urban fabric itself, concentrated where people, commerce, and waterways converge. It is a hypothesis that public health officials in Shanghai, and in riverine megacities across Asia and beyond, now have both the reason and the roadmap to test.</p>
<p><strong>Subject of Research:</strong> Spatial-temporal epidemiology and community-level risk factors of hepatitis E virus infection in Shanghai, China</p>
<p><strong>Article Title:</strong> Identification of the spatial-temporal cluster and risk factors of hepatitis E from 2017 to 2022 in Shanghai, China</p>
<p><strong>Article References:</strong> Zhi-Tao, M., Ling-Xiao, Q., Kai-Yun, C., Xin, S., Di, X., Zhao-He, L., Yi-Han, L., Kang, C., Jing, L., &amp; Hong, R. (2026). Identification of the spatial-temporal cluster and risk factors of hepatitis E from 2017 to 2022 in Shanghai, China. <em>BMC Infectious Diseases</em>. <a href="https://doi.org/10.1186/s12879-026-14463-4" rel="noopener noreferrer">https://doi.org/10.1186/s12879-026-14463-4</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s12879-026-14463-4" rel="noopener noreferrer">10.1186/s12879-026-14463-4</a></p>
<p><strong>Keywords:</strong> hepatitis E, hepatitis E virus, spatial-temporal analysis, disease cluster, Shanghai, epidemiology, public health surveillance, risk factors, population density, zoonotic transmission, viral hepatitis, logistic regression</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">213595</post-id>	</item>
		<item>
		<title>Weasel Bite Linked to Deadly Tick-Borne Virus in Rare Chinese Case</title>
		<link>https://scienmag.com/weasel-bite-linked-to-deadly-tick-borne-virus-in-rare-chinese-case/</link>
		
		<dc:creator><![CDATA[Kristina Jarvis]]></dc:creator>
		<pubDate>Thu, 24 Sep 2026 02:06:08 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[Animal bite and viral illness]]></category>
		<category><![CDATA[case report]]></category>
		<category><![CDATA[China]]></category>
		<category><![CDATA[Emerging infectious diseases China]]></category>
		<category><![CDATA[Infectious disease diagnosis challenges]]></category>
		<category><![CDATA[metagenomic next-generation sequencing]]></category>
		<category><![CDATA[Mustela sibirica]]></category>
		<category><![CDATA[Rare zoonotic disease cases]]></category>
		<category><![CDATA[Role of small mammals in virus spread]]></category>
		<category><![CDATA[Severe Fever with Thrombocytopenia Syndrome]]></category>
		<category><![CDATA[SFTS]]></category>
		<category><![CDATA[SFTSV]]></category>
		<category><![CDATA[SFTSV infection]]></category>
		<category><![CDATA[Siberian weasel]]></category>
		<category><![CDATA[thrombocytopenia]]></category>
		<category><![CDATA[tick-borne virus]]></category>
		<category><![CDATA[tick-borne virus transmission]]></category>
		<category><![CDATA[Underrecognized transmission routes]]></category>
		<category><![CDATA[viral hemorrhagic fever]]></category>
		<category><![CDATA[Viral illness from carnivorous animals]]></category>
		<category><![CDATA[Viral pathogen transmission pathways]]></category>
		<category><![CDATA[Weasel bite]]></category>
		<category><![CDATA[wildlife surveillance]]></category>
		<category><![CDATA[zoonotic transmission]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=212114</guid>

					<description><![CDATA[A confirmed case of severe fever with thrombocytopenia syndrome in a Chinese woman bitten by a Siberian weasel suggests a possible new zoonotic transmission route for the normally tick-borne virus.]]></description>
										<content:encoded><![CDATA[<p>A 55-year-old woman in northeastern China developed a life-threatening viral illness after being bitten by a Siberian weasel, and clinicians now suspect the animal bite—not a tick—was the source of her infection. The case, reported in Virology Journal by a team of critical care physicians at Beijing Ditan Hospital, Capital Medical University, describes a confirmed infection with severe fever with thrombocytopenia syndrome virus, or SFTSV, a pathogen that has long been considered almost exclusively tick-borne. Because the patient reported no contact with ticks or any other animals, the weasel bite stands out as the only plausible exposure, raising the possibility that small carnivorous mammals may play a previously underappreciated role in the chain of transmission that delivers this virus to humans.</p>
<p>The patient, who lived in Dalian in Liaoning Province, first noticed the bite and then, five days later, developed high fever, profound malaise and diarrhea. These early symptoms are deceptively nonspecific and mimic many common febrile illnesses circulating in the region, which is precisely what makes SFTS so dangerous in its initial phase. By the time she reached specialized care, laboratory testing revealed the two biochemical hallmarks that give the disease its name: a sharply reduced platelet count, known as thrombocytopenia, and evidence of multi-organ stress. Platelets are the cellular fragments that allow blood to clot, and their depletion can turn a routine fever into a hemorrhagic emergency. The clinical team faced a rapidly deteriorating patient whose blood was losing its ability to coagulate while her organs began to fail.</p>
<p>Diagnosis came on the twelfth day of illness, when metagenomic next-generation sequencing detected SFTSV genetic material in the patient&#8217;s peripheral blood. This technology represents a fundamental shift in how unexplained severe infections are identified. Rather than testing for a preselected list of suspected pathogens, metagenomic sequencing extracts all genetic material from a clinical sample and matches it against comprehensive databases, allowing previously unconsidered viruses to surface. In this case, the approach was decisive: SFTSV was not among the leading clinical suspicions when the woman was admitted, and conventional targeted tests might have missed it or delayed confirmation until it was too late to guide management. The sequencing result converted a puzzling febrile illness into a defined viral hemorrhagic syndrome with a known epidemiology.</p>
<p>SFTSV belongs to the genus Bandavirus within the family Phenuiviridae and was first identified in China in 2009 following outbreaks of a mysterious and often fatal febrile illness in rural communities. Since then, the virus has been documented across China and in South Korea, Japan and Vietnam, with reported case-fatality rates that range from roughly five percent to well above twenty percent in some series, depending on the population and the quality of supportive care. The principal vector is the tick, particularly Haemaphysalis longicornis, an aggressive biter that feeds on a wide range of mammals. Human infections typically occur during spring and summer, when ticks are most active and agricultural work brings people into contact with tick habitat. The virus replicates in the tick and can be transmitted through the bite, but the epidemiology has always contained puzzles that a purely tick-centered model struggles to explain.</p>
<p>Those puzzles center on the animal reservoir. Ticks are vectors, but the virus must circulate in vertebrate hosts for the system to persist in nature. Surveys have detected SFTSV antibodies or viral RNA in a striking variety of animals, including cattle, goats, sheep, dogs, cats, wild rodents, hedgehogs and various wild carnivores. Domestic livestock can sustain high-level viremia and are thought to amplify the virus, with ticks acquiring infection while feeding on them. Direct transmission from animals to humans has also been documented through contact with the blood or secretions of infected livestock, and person-to-person spread through contact with infected blood has occurred in hospital and funeral settings. What had not been convincingly described before this report was a scenario in which a wild mammal itself, rather than a tick feeding on it, appeared to transmit the virus directly to a human through a bite.</p>
<p>The Siberian weasel, Mustela sibirica, is a small, agile carnivore widespread across East and Southeast Asia, inhabiting forests, grasslands, agricultural landscapes and even the edges of towns. It is a capable hunter of rodents, which are themselves among the animals in which SFTSV has been detected, so a weasel could plausibly acquire the virus either from infected prey or from ticks carried by that prey. Weasels do bite humans, particularly when cornered, displaced from dens or drawn into conflict around poultry and livestock. In rural and semi-rural parts of northeastern China, encounters between people and these animals are not rare. If a weasel can carry SFTSV in its saliva or blood at infectious levels, a bite would provide a direct inoculation route that bypasses the tick entirely, and the five-day interval between the bite and the onset of fever in this patient is consistent with the incubation period typically observed for SFTSV.</p>
<p>The clinical course in this case underscores how little clinicians can currently offer once severe disease takes hold. Despite timely antiviral and supportive treatment, the patient progressed rapidly to multiple organ dysfunction and had a poor prognosis. There is no approved vaccine and no licensed specific antiviral therapy for SFTS; management rests on intensive supportive care, including fluid management, transfusion of platelets and other blood products, and organ support in critical cases. The antiviral drug ribavirin has been used, but evidence for its benefit is limited. Several candidate vaccines are in development, and experimental monoclonal antibody therapies have shown promise in early studies, but none of these tools has yet reached routine clinical practice in endemic regions. Prevention therefore depends overwhelmingly on avoiding exposure, which in turn depends on knowing exactly what the exposures are.</p>
<p>That is where this case report carries its greatest weight. If the weasel bite was indeed the route of infection, public health advice in endemic areas may need to expand beyond the standard warnings about tick avoidance to include caution around wild mammals, particularly small carnivores that can inflict bites. The authors of the report emphasize that the association remains unconfirmed: no animal was available for testing, so the weasel was never shown to carry the virus, and the possibility of an unrecognized tick exposure or another cryptic route cannot be entirely excluded. A single case can establish plausibility but not proof. What it does establish is a testable hypothesis, and the authors call for urgent surveillance of animal hosts in endemic regions to determine whether Mustela sibirica and other wild carnivores harbor SFTSV and whether they contribute measurably to human infections.</p>
<p>Surveillance of that kind would involve sampling wild and domestic animals in areas where human cases occur, testing blood and tissues for viral RNA and antibodies, and mapping the ecological relationships among ticks, reservoir mammals and human populations. Modern tools make this more feasible than it once was: metagenomic sequencing, the same technology that diagnosed this patient, can be applied to wildlife samples to reveal the full spectrum of viruses circulating in a given ecosystem. Combining that molecular surveillance with epidemiological interviews of human patients—asking systematically about animal encounters as well as tick exposure—could reveal whether bite-associated transmission is a rare curiosity or a recurring and undercounted pathway. Given the high mortality of SFTS and its expanding geographic footprint, even a modest additional transmission route would be worth detecting.</p>
<p>For now, the Dalian case stands as a cautionary data point at the intersection of virology, ecology and clinical medicine. It demonstrates the diagnostic power of unbiased sequencing in severe unexplained fevers, it documents the fulminant course that SFTS can take even under modern intensive care, and it widens the circle of suspected hosts to include a wild carnivore that lives in close proximity to people across much of Asia. The physicians who treated the patient, who consented to the publication of her case, frame the finding as a signal rather than a conclusion: a possible zoonotic route that demands investigation before it can be confirmed or dismissed. As climate change, land-use change and expanding human activity continue to redraw the boundaries between people, wildlife and the arthropods that connect them, cases like this one suggest that the transmission map of SFTSV may be more complicated—and the list of animals capable of passing it to humans potentially longer—than the tick-borne textbook model has assumed.</p>
<p><strong>Subject of Research:</strong> A suspected zoonotic transmission of severe fever with thrombocytopenia syndrome virus via a Siberian weasel bite in China</p>
<p><strong>Article Title:</strong> Severe fever with thrombocytopenia syndrome (SFTS) likely associated with a bite from a Siberian weasel (Mustela sibirica): a case report from China</p>
<p><strong>Article References:</strong> Severe fever with thrombocytopenia syndrome (SFTS) likely associated with a bite from a Siberian weasel (Mustela sibirica): a case report from China. (n.d.). <a href="https://doi.org/10.1186/s12985-026-03286-z" rel="noopener noreferrer">https://doi.org/10.1186/s12985-026-03286-z</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s12985-026-03286-z" rel="noopener noreferrer">10.1186/s12985-026-03286-z</a></p>
<p><strong>Keywords:</strong> SFTS, SFTSV, Siberian weasel, Mustela sibirica, zoonotic transmission, tick-borne virus, metagenomic next-generation sequencing, viral hemorrhagic fever, thrombocytopenia, China, wildlife surveillance, case report</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">212114</post-id>	</item>
		<item>
		<title>Gut Parasites in Captive Macaques Reveal Close Genetic Ties to Human Infections</title>
		<link>https://scienmag.com/gut-parasites-in-captive-macaques-reveal-close-genetic-ties-to-human-infections/</link>
		
		<dc:creator><![CDATA[Juliet Wilcox]]></dc:creator>
		<pubDate>Tue, 22 Sep 2026 21:50:18 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[captive macaques parasite diversity]]></category>
		<category><![CDATA[China]]></category>
		<category><![CDATA[crab-eating macaques]]></category>
		<category><![CDATA[cross-species infection of Entamoeba]]></category>
		<category><![CDATA[E. coli]]></category>
		<category><![CDATA[E. dispar]]></category>
		<category><![CDATA[E. histolytica]]></category>
		<category><![CDATA[Entamoeba]]></category>
		<category><![CDATA[Entamoeba species]]></category>
		<category><![CDATA[fecal-oral parasite transmission]]></category>
		<category><![CDATA[genetic similarity of Entamoeba strains]]></category>
		<category><![CDATA[Gut parasites]]></category>
		<category><![CDATA[intestinal protozoa in non-human primates]]></category>
		<category><![CDATA[molecular epidemiology]]></category>
		<category><![CDATA[non-human primates]]></category>
		<category><![CDATA[One Health]]></category>
		<category><![CDATA[parasite reservoirs in primate populations]]></category>
		<category><![CDATA[phylogenetics]]></category>
		<category><![CDATA[primate-human disease transmission]]></category>
		<category><![CDATA[public health implications of primate parasites]]></category>
		<category><![CDATA[SSU rRNA]]></category>
		<category><![CDATA[zoonotic disease risk in captive animals]]></category>
		<category><![CDATA[zoonotic parasites]]></category>
		<category><![CDATA[zoonotic transmission]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=208047</guid>

					<description><![CDATA[A molecular survey of 504 captive crab-eating macaques in China found six Entamoeba species, with macaque-derived strains showing close genetic ties to human isolates.]]></description>
										<content:encoded><![CDATA[<p>A large molecular survey of captive crab-eating macaques in China has revealed that these primates carry a strikingly diverse array of Entamoeba parasites, including species capable of infecting humans, and that the strains they harbor are genetically close to isolates recovered from people. The study, published in Acta Parasitologica, analyzed more than five hundred fecal samples from commercial breeding facilities in Beijing and Suzhou and offers one of the most detailed pictures yet of how these single-celled parasites circulate within non-human primate populations under managed care. For researchers tracking zoonotic disease, the findings carry a clear message: macaques living in close proximity to human caretakers may serve as reservoirs for parasites that are only a genetic step away from causing human disease.</p>
<p>Entamoeba species are intestinal protozoa with a worldwide distribution, infecting humans and a broad range of animals. While some members of the genus, most famously Entamoeba histolytica, are responsible for amoebic dysentery and liver abscesses in people, others colonize the gut without causing obvious harm. Because these organisms are transmitted through fecally contaminated food and water, environments where humans and animals share space create ideal conditions for cross-species transmission. Non-human primates are of particular concern in this regard, since their physiological and genetic similarity to humans means that many of their parasites face relatively few barriers when jumping between hosts.</p>
<p>The research team, led by scientists at Anhui Science and Technology University, collected a total of 504 fecal samples from crab-eating macaques, also known as long-tailed macaques (Macaca fascicularis), housed at commercial breeding farms in two geographically distinct Chinese cities. Rather than relying on microscopy, which can confuse morphologically identical Entamoeba species, the researchers used polymerase chain reaction amplification and sequencing of the small subunit ribosomal RNA gene, a genetic marker that allows precise differentiation among six distinct Entamoeba species. This molecular approach is essential because species such as E. histolytica, E. dispar, and E. moshkovskii look identical under the microscope yet differ dramatically in their clinical significance.</p>
<p>The results revealed a layered picture of infection. Entamoeba coli was by far the most prevalent species, detected in 49.01 percent of samples, or 247 of the 504 specimens tested, with a 95 percent confidence interval spanning 44.6 to 53.4 percent. E. dispar followed at 36.51 percent, while E. histolytica, the most medically consequential species, was found in 8.13 percent of samples. The remaining species appeared at lower frequencies: E. chattoni at 5.95 percent, E. moshkovskii at 0.79 percent, and E. nuttalli at just 0.6 percent. The detection of E. histolytica in more than one in twelve animals is noteworthy, as this species remains a leading cause of parasitic death in humans globally.</p>
<p>Statistical analysis of the infection data uncovered a significant relationship between host age and the risk of carrying E. coli, with the association reaching a p-value below 0.0001. This strong age dependence suggests that older macaques accumulate infections over time, possibly through prolonged exposure to contaminated enclosures, changes in immune competence, or altered grooming and foraging behaviors. Understanding such risk factors is critical for breeding facilities, where managing parasite burden can affect animal welfare, the validity of biomedical research using these animals, and the safety of staff who work in close contact with the colonies.</p>
<p>The most striking findings emerged from the phylogenetic analysis. When the researchers reconstructed evolutionary relationships among the 247 E. coli isolates recovered from the macaques, they identified two distinct genotypes, designated SZ E. coli CEMs1 and SZ E. coli CEMs2. Both genotypes clustered firmly within the major E. coli clade and showed close genetic affinity with strains previously recovered from humans and other primate species. This pattern of shared lineages across host species is precisely what would be expected if the parasites are moving between humans and macaques, rather than evolving in isolated host-specific populations.</p>
<p>The presence of E. nuttalli, although rare in this cohort, adds another dimension to the zoonotic picture. This species, once confused with E. histolytica, is known to infect rhesus macaques and can cause liver abscesses in experimental animals, and previous studies have documented its genetic differentiation across macaque populations in Nepal, Myanmar, and China. Similarly, the detection of E. moshkovskii, an organism long considered a free-living amoeba but increasingly reported in human patients with diarrhea, underscores how fluid the boundaries between environmental, animal, and human Entamoeba lineages can be. The low prevalence of these species in the sampled colonies does not diminish their significance; rather, it highlights the value of sensitive molecular surveillance in detecting rare but potentially important infections.</p>
<p>From a practical standpoint, the findings carry implications for multiple stakeholders. For breeding facilities that supply macaques for biomedical research, high parasite prevalence complicates efforts to produce animals of defined health status, since subclinical infections can confound immunological and gastrointestinal studies. For public health authorities, the phylogenetic proximity of macaque-derived E. coli strains to human isolates argues for treating captive macaque colonies as potential zoonotic reservoirs warranting routine monitoring. And for the growing field of One Health, which examines the interconnected health of humans, animals, and environments, the study provides a concrete example of how intensively managed animal populations can harbor parasites with demonstrated potential for cross-host transmission.</p>
<p>The authors emphasize that enhanced surveillance is needed, both within breeding facilities and in contexts where macaques and humans interact more loosely, such as zoological gardens and areas where free-ranging macaques contact tourists. Prior studies of captive primates and their handlers in European zoos have already documented shared intestinal protists, suggesting that occupational exposure is a realistic concern. The Chinese breeding farms surveyed here represent a controlled setting, yet even under such conditions, nearly half the animals carried E. coli and a meaningful fraction harbored potentially pathogenic species, indicating that standard husbandry practices may not be sufficient to interrupt transmission cycles.</p>
<p>Looking forward, the genetic characterization of the two macaque E. coli genotypes opens avenues for finer-scale epidemiological work. Comparing these lineages with sequence data from human patients, livestock, and wild primates across Asia could clarify the directionality of transmission events and identify which host populations act as sources and which as sinks. Such work would build on a growing body of molecular epidemiology that has transformed Entamoeba from a morphologically defined genus into a genetically structured assemblage of species with distinct host associations and virulence potentials. As the new study demonstrates, even a parasite long regarded as a harmless commensal can reveal important truths about the porous boundaries between animal and human health, and about the responsibility that comes with keeping our closest relatives in close quarters.</p>
<p><strong>Subject of Research:</strong> Zoonotic Entamoeba parasite prevalence and genetic diversity in captive crab-eating macaques in China</p>
<p><strong>Article Title:</strong> Distribution of Zoonotic Entamoeba spp. in Crab-Eating Macaques Across China</p>
<p><strong>Article References:</strong> Guo, Q., Gong, R., Ge, X., Li, M., Ma, J., Liu, X., &amp; Li, W. (2026). Distribution of Zoonotic Entamoeba spp. in Crab-Eating Macaques Across China. <em>Acta Parasitologica, 71</em>(5), Article 216. <a href="https://doi.org/10.1007/s11686-026-01399-7" rel="noopener noreferrer">https://doi.org/10.1007/s11686-026-01399-7</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s11686-026-01399-7" rel="noopener noreferrer">10.1007/s11686-026-01399-7</a></p>
<p><strong>Keywords:</strong> Entamoeba, crab-eating macaques, zoonotic parasites, E. histolytica, E. coli, E. dispar, SSU rRNA, phylogenetics, China, non-human primates, One Health, molecular epidemiology</p>
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		<title>Pig farming reshapes farmers&#8217; gut microbiome and antibiotic resistance genes, study finds</title>
		<link>https://scienmag.com/pig-farming-reshapes-farmers-gut-microbiome-and-antibiotic-resistance-genes-study-finds/</link>
		
		<dc:creator><![CDATA[Morgan Morrow]]></dc:creator>
		<pubDate>Sun, 30 Aug 2026 02:16:36 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[antibiotic resistance gene transfer]]></category>
		<category><![CDATA[antibiotic resistance gene transfer mechanisms]]></category>
		<category><![CDATA[antibiotic resistance genes]]></category>
		<category><![CDATA[antimicrobial resistance in agriculture]]></category>
		<category><![CDATA[effects of livestock exposure on human microbiota]]></category>
		<category><![CDATA[Escherichia coli sequencing]]></category>
		<category><![CDATA[Gut microbiome]]></category>
		<category><![CDATA[impact of livestock environment on human health]]></category>
		<category><![CDATA[livestock-human microbial interface]]></category>
		<category><![CDATA[metagenomics in agriculture]]></category>
		<category><![CDATA[metagenomics in livestock]]></category>
		<category><![CDATA[microbial communities in pig farmers]]></category>
		<category><![CDATA[microbial diversity in farmers]]></category>
		<category><![CDATA[microbiome diversity in farm workers]]></category>
		<category><![CDATA[microbiome health impact]]></category>
		<category><![CDATA[occupational exposure to livestock]]></category>
		<category><![CDATA[occupational health in pig farming]]></category>
		<category><![CDATA[Pig farming]]></category>
		<category><![CDATA[transfer of antibiotic resistance from animals to humans]]></category>
		<category><![CDATA[zoonotic transmission]]></category>
		<guid isPermaLink="false">https://scienmag.com/pig-farming-reshapes-farmers-gut-microbiome-and-antibiotic-resistance-genes-study-finds/</guid>

					<description><![CDATA[The people who raise the world&#8217;s pigs spend their working lives inside one of the most microbially concentrated environments modern society has created, and new research suggests their bodies keep a detailed record of it. In a study published on 30 August 2026 in the journal Microbiome, researchers based at Sichuan University, working with collaborators [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>The people who raise the world&#8217;s pigs spend their working lives inside one of the most microbially concentrated environments modern society has created, and new research suggests their bodies keep a detailed record of it. In a study published on 30 August 2026 in the journal <em>Microbiome</em>, researchers based at Sichuan University, working with collaborators at the Sichuan Animal Science Academy, report that pig farm workers carry gut microbial communities that are measurably different from those of their non-farming neighbors: poorer in health-associated species, skewed toward mucus-scavenging metabolisms, and substantially richer in antibiotic resistance genes that trace back to veterinary medicine. The investigation, one of the most exhaustive portraits yet of the livestock–human microbial interface, combined shotgun metagenomics of 431 fecal samples with whole-genome sequencing of 833 <em>Escherichia coli</em> isolates gathered across 103 swine farms in Sichuan Province, China. Its central message is subtle but consequential. Whole bacteria rarely appeared to jump from pig to person. The mobile DNA that carries resistance genes, by contrast, seemed to cross the species boundary with unsettling ease.</p>
<p>To quantify occupational exposure with real statistical power, the team recruited 96 pig farmers and 97 residents drawn from the same rural communities. The residents shared the farmers&#8217; geography, water systems and broadly similar diets but had no direct contact with swine, which made them an unusually clean control group: direct animal exposure became the variable of interest. The researchers also sampled 238 pigs from the same farms, yielding a three-way comparison of pigs, farmers and residents. Each human volunteer provided fecal samples and completed questionnaires covering age, sex, antibiotic use and health status, under protocols approved by the Medical Ethics Committee of Sichuan University. Shotgun metagenomics — the sequencing of all of the DNA in a sample rather than a single marker gene — allowed the researchers to inventory not only which microbial species were present but which functional genes they carried, including the complete collection of antibiotic resistance genes known as the resistome. In parallel, the team cultured <em>E. coli</em> from all three groups: 665 pig isolates, 80 from farmers and 88 from residents.</p>
<p>The compositional differences between farmers and residents were unambiguous. Farmers showed reduced gut alpha-diversity, meaning their intestinal ecosystems contained fewer distinct species and were less evenly balanced, and they scored lower on the Gut Microbiome Health Index, a species-based metric that associates community composition with overall health status. A multivariate dispersion analysis indicated that farmers and residents differed in composition rather than merely in variability, and supplementary analyses accounted for age and sex. The functional shifts were equally telling. Farmers were depleted of several taxa that degrade dietary fiber and produce short-chain fatty acids — acetate, propionate and, above all, butyrate, the preferred fuel of the cells lining the colon and a key regulator of inflammation and immune tone. In their place, the researchers found organisms and metabolic pathways geared toward exploiting mucin-derived glycans, the complex sugars that make up the gut&#8217;s protective mucus layer. Carbohydrate-active enzyme profiling captured this pivot: instead of harvesting energy from plant fiber, the farmer microbiome appeared increasingly specialized in grazing the host&#8217;s own mucus, a pattern that earlier studies have linked to diminished gut resilience.</p>
<p>The resistome followed an exposure gradient so clean it looked almost schematic: resistance gene abundance was highest in pigs, intermediate in farmers and lowest in residents, a pattern established through differential abundance testing with correction for false discovery. Farmers carried elevated levels of determinants conferring resistance to drug classes that dominate veterinary formularies — florfenicol, a phenicol antibiotic used extensively in swine production; quinolones; macrolide–lincosamide–streptogramin combinations; and aminoglycosides. Strikingly, genes conferring resistance to β-lactams, the antibiotic family that anchors human clinical medicine, were proportionally underrepresented in farmers. The resistome of a pig farmer, in other words, mirrors the drug cabinet of the barn rather than the pharmacy of the clinic. That pharmacological fingerprint matters epidemiologically, because the resistance genes a person carries shape the raw material available to their own future infections, and to the bacteria that circulate through their households and communities.</p>
<p>The study&#8217;s most consequential findings concerned not the resistance genes themselves but the vehicles that carry them. Bacteria trade DNA through mobile genetic elements, chief among them plasmids: self-replicating circles of DNA that can pass from cell to cell by conjugation and haul cargo genes, including resistance determinants, across species lines. When the team assembled and dereplicated plasmid sequences from the metagenomes, they recovered 157,298 nonredundant plasmid contigs, of which 1,415 carried antibiotic resistance genes. The distribution was stark: 83.1 percent of the ARG-bearing plasmid contigs were enriched in pigs, 18.3 percent in farmers and just 3.9 percent in residents. Most striking of all, 88.8 percent of the farmer-enriched plasmid contigs were also enriched in pigs, and they harbored genes of genuine clinical concern. Among them were <em>optrA</em>, the first transferable gene known to confer resistance to oxazolidinones such as linezolid, a last-resort antibiotic against multidrug-resistant Gram-positive infections; <em>cfr</em>, which compromises several antibiotic classes at once, including linezolid and pleuromutilins; and <em>mcr-10.1</em>, a member of the mobilized colistin resistance family, colistin being a polymyxin of last resort in human medicine. The picture that emerges is of a pig-centered plasmid reservoir, with farmer guts sitting directly in its shadow.</p>
<p>Plasmids were not the only mobile elements under scrutiny. The researchers also screened 227,476 phage contigs — the genomic signatures of bacteriophages, the viruses that infect bacteria — for resistance genes. Only 106 carried any, confirming that transduction, the viral route of gene transfer, is rare in this system. Yet the ARG-bearing phages that did surface were predominantly pig-associated, a small but pointed echo of the plasmid findings. Most gut phages are temperate, slipping into bacterial chromosomes and copying their hosts rather than killing them, which in principle lets them shuttle genes between lineages — but the numbers here show that route is a trickle, not a flood. The contrast between the two analyses is informative. Conjugative plasmids require only a local handshake between microbes that happen to share an intestine, whereas phage-mediated transfer depends on infection dynamics and host ranges. At the livestock–human interface, at least, plasmids appear to be the dominant conduit through which the animal resistome reaches human hosts.</p>
<p>To test whether whole bacteria were crossing hosts as well, the team sequenced the genomes of all 833 <em>E. coli</em> isolates and compared their multilocus sequence types and core-genome relationships, visualizing the population structure in a minimum spanning tree colored by host. The verdict on clonal transmission — the passage of an identical bacterial strain between hosts — was emphatically limited: across the entire cohort, the researchers identified just five pig-to-farmer and one pig-to-resident transmission events. <em>E. coli</em> populations were largely host-segregated, with pigs, farmers and residents each harboring distinct strain assemblages, and the isolates&#8217; resistance phenotypes had been profiled across a panel of antibiotics. The isolates nonetheless told a consistent story about genes: pig and farmer isolates carried heavier genomic burdens of resistance determinants than resident isolates. The researchers also compared the genetic surroundings of <em>tet</em>(X4)-positive plasmids, which carry resistance to the last-line antibiotic tigecycline, in pigs and farmers, probing whether shared plasmid backbones underpinned the overlap. Taken together, the data support a model in which the bacteria themselves mostly stay put while their resistance cargo migrates — horizontal gene transfer, not microbial migration, is the engine of exchange at this interface.</p>
<p>The microbial signature of farm work is distinct enough that an algorithm can read it. Using a random-forest classifier — an ensemble of decision trees that vote on a category — trained on metagenomic taxonomic profiles alone, the team distinguished farmers from residents with an area under the curve of 0.921, a specificity of 0.90 and a sensitivity of 0.775. An AUC of 0.921 means the model ranked a randomly chosen farmer above a randomly chosen resident more than nine times out of ten, and it achieved this without any resistance gene data, implying that exposure leaves its mark on community structure itself. Two organisms emerged as candidate exposure biomarkers: <em>Schaalia odontolytica</em>, an actinobacterial species better known from the oral cavity, and <em>Acinetobacter lwoffii</em>, a hardy environmental bacterium often found in animal-associated settings. Neither is by itself a pathogen of alarm; their significance is diagnostic. If validated in independent cohorts, such microbial fingerprints could serve as inexpensive, noninvasive measures of occupational exposure, complementing workplace surveys and environmental monitoring.</p>
<p>The authors are careful about what their data can and cannot show. The study is cross-sectional — a snapshot rather than a film — so it demonstrates association, not direction. Whether farmers&#8217; resistomes were seeded by the barn, continuously reinforced by it, or shaped by antibiotic use patterns that correlate with farm work cannot be resolved without the longitudinal, environment-integrated and strain-resolved follow-up studies the researchers themselves call for. Nor can metagenomic assemblies alone prove which direction a given plasmid traveled; shared enrichment in pigs and farmers is a strong clue, not a time-stamped itinerary. Whether resistance genes acquired at work persist after workers leave the industry, or ever reach their families and hospitals, likewise remains open. Even so, the implications reach well beyond Sichuan. Antimicrobial resistance is a One Health problem, and this study supplies some of the clearest evidence yet that the human gut operates as a downstream node of livestock microbial ecology — not by acquiring pig bacteria wholesale, but by quietly inheriting their genes. Funded by China&#8217;s National Key Research and Development Program and the National Natural Science Foundation of China and published open access, the work argues for veterinary antimicrobial stewardship, hygiene and exposure reduction not as abstractions but as protections for an invisible organ that, the data suggest, remembers where its owner works.</p>
<div class="scienmag-article-metadata"><strong>Subject of Research:</strong> The impact of occupational pig farming exposure on the human gut microbiome and resistome, and the role of mobile genetic elements in antimicrobial resistance gene sharing at the livestock–human interface.</p>
<p><strong>Article Title:</strong> Impact of pig farming activities on the gut microbiome and resistome of farmers: insights from metagenomics and <i>Escherichia coli</i> genomics</p>
<p><strong>Article References:</strong> Zhang, T., Wang, Q., Lin, H., Liu, L., Wang, X., Kang, R., Yang, X., Wang, H., &amp; Lei, C. (2026). Impact of pig farming activities on the gut microbiome and resistome of farmers: insights from metagenomics and Escherichia coli genomics. <em>Microbiome</em>. <a href="https://doi.org/10.1186/s40168-026-02522-6" target="_blank" rel="noopener noreferrer">https://doi.org/10.1186/s40168-026-02522-6</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s40168-026-02522-6" target="_blank" rel="noopener noreferrer">10.1186/s40168-026-02522-6</a></p>
<p><strong>Keywords:</strong> gut microbiome, resistome, antimicrobial resistance, pig farming, metagenomics, <i>Escherichia coli</i> genomics, plasmids, mobile genetic elements, optrA, One Health, occupational exposure, livestock–human interface</p>
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