Direct Contact Transmission Research Articles

Characterization of a SARS-CoV-2 Omicron BA.5 direct-contact transmission model in hamsters

As SARS-CoV-2 continues to evolve antigenically to escape vaccine- or infection-induced immunity, suitable animal models are needed to study novel interventions against viral variants. Syrian hamsters are often used because of their high susceptibility to SARS-CoV-2 and associated tissue damage in the respiratory tract. Here, we established a direct-contact transmission model for SARS-CoV-2 Omicron BA.5 in hamsters. First, we determined whether 103 or 104 TCID50 in a low-volume inoculum led to reproducible infection and viral shedding in male and female hamsters. Next, we determined the optimal co-housing timing and duration between donor and recipient hamsters required for consistent direct-contact transmission. Finally, we compared viral loads and histopathological lesions in the respiratory tissues of donor and recipient hamsters. Intranasal inoculation of hamsters with 103 TCID50 and 104 TCID50 Omicron BA.5 in 10 µl per nostril led to reproducible infection. Viral loads in the throat measured by RT-qPCR were comparable between male and female hamsters. Notably, the shedding of infectious virus was significantly higher in male hamsters. Compared to SARS-CoV-2 D614G, Omicron BA.5 infection reached lower viral loads, had a delayed peak of virus replication, and induced limited body weight loss. To ensure consistent direct-contact transmission from inoculated donor hamsters to naïve recipients, a co-housing duration of 24 h starting 20 h post-infection of the donors was optimal. We detected mild inflammation in the respiratory tract of donor and recipient hamsters, and viral loads were higher and peaked earlier in donor hamsters compared to recipient hamsters. Taken together, we developed a robust Omicron BA.5 direct-contact transmission model in hamsters, that provides a valuable tool to study novel interventions.

Investigation of an optimal control strategy for a cholera disease transmission model with programs

Cholera is a disease of poverty affecting people with inadequate access to safe water and basic sanitation. Conflict, unplanned urbanization and climate change all increase the risk of cholera. In this article, an optimal control deterministic mathematical model of cholera disease with cost-effectiveness analysis is developed and analyzed considering both direct and indirect contact transmission pathways. The model qualitative behaviors, such as the invariant region, the existence of a positive invariant solution, the two equilibrium points (disease-free and endemic equilibrium), and their stabilities (local as well as global stability) of the model are studied. Moreover, the basic reproduction number of the model is obtained. We also performed sensitivity analysis of the basic parameters of the model. Then an optimal control problem is designed with a control functional having five controls: vaccination, treatment, environment sanitation and personal hygiene, and water quality improvement program. We examined the existence and uniqueness of the optimal controls of the system. Through the implementation of Pontryagin's maximum principle, the characterization of the optimal controls optimality system is established. The numerical simulation results the integrated control strategies demonstrated that strategy 2, 7, and 12 are effective programs to combat cholera disease from the community. Based on the local circumstances, available funds, and resources, it is recommended to the government stakeholders and policymakers to execute any one of the three integrated intervention programs.

A Copper-Based Coating for the Control of Airborne Viable Bacteria in a Prison Environment

Infections in confined environments can spread by direct contact, contaminated surfaces, and airborne transmission. This is critical in prison facilities, where cleaning and sanitary conditions are inadequate. An alternative is the development of antimicrobial surfaces. A new antimicrobial coating was developed by incorporating copper microparticles into a standard commercial paint, aiming to reduce the concentration of bacteria on surfaces by granting antimicrobial properties to surfaces. The copper additive comprised Cu2Cl(OH)3 deposited on polyhedral zeolite. The efficacy of this coating was evaluated in detention cells in a police station, which are temporary prisons and inherently dirty environments. The experiment compared a cell painted with the copper additive coating and a control cell with the standard paint. Viable coliforms were measured on different surfaces and in the air for five months under normal usage. Bacterial load was reduced by ca. 68% by the copper-amended paint on cement surfaces. Surprisingly, airborne viable coliforms were reduced by ca. 87% in the detention cell treated with the copper coating. This research highlights the potential of antimicrobial coatings in controlling the spread of infections through contact with contaminated surfaces and emphasizes the significant reduction in airborne bacterial load. It is especially relevant for controlling infections where sanitization is limited but can be extended to other built environments, such as healthcare facilities.

Trade risk transmission of global cobalt industrial chain based on multi-layer network

In order to study the potential systemic risk transmission in cobalt trade, this paper combined the infectious disease model with complex networks to build a multi-layer network trade risk transmission model for cobalt trade based on the transmission of export restrictions and bilateral friction in a single country, in order to simulate the degree of impact of risk transmission in cobalt industry chain, identify key countries and risk transmission paths. The results show that multi-layer network risk transmission of global cobalt trade based on two communication forms has the characteristics of “robust and fragile”. In addition, the risk transmission situation based on bilateral frictions is mainly transmitted by core countries and direct contacts. The risk transmission based on the export restriction of a single country is mainly through direct contact, indirect contact and regional transmission. We also find that the multi-layer trade network of global cobalt trade can resist the bilateral frictional transmission mode better than the transmission mode of single country export restriction. The results can support policy makers to optimize the cobalt trade structure and mitigate the negative impact of trade disruptions.

Transmission dynamics of avian influenza viruses in Egyptian poultry markets

Live bird markets (LBMs) are considered hotspots for Avian Influenza Viruses (AIVs). In such markets, AIVs pose threats to both poultry and public health. Within LBMs, AIVs spread through various routes, including direct contact, environmental contamination, and aerosol transmission. Unique factors in Egyptian LBMs, such as the coexistence of wild and domestic birds, increase transmission risks between birds as well as spill-overs into exposed humans. Understanding the transmission dynamics of AIVs is vital for implementing effective control measures. We conducted a study in four Egyptian LBMs located in Mediterranean coast cities from November 2021 to March 2023. In this study we tested 3,971 samples from poultry, wild birds, and the environment, out of which 692 (17.4%) were positive for AIV. Poultry exhibited a higher prevalence (42.2%) than wild birds (34.4%). Environmental samples, including water (30.8%), surfaces (17.2%), and air (18.2%), also tested positive for AIV. Diverse AIV subtypes, including H5N1, H9N2, H5/H9 co-infection, and H5N8, were detected among avian species and the environment. Temporal analysis revealed fluctuating IAV positivity rates from November 2021 to March 2023. These results emphasize the importance of continuous surveillance, resource allocation, and multisectoral collaboration to protect poultry and human health, and prevent novel influenza strains’ emergence in Egyptian LBMs.

Dynamical Analysis of Peptic Ulcer Disease Model in Nigeria with the Effect of Vaccination and Treatment Program

The study developed a non-linear deterministic mathematical model to investigate the transmission dynamics of peptic ulcer disease in human population by considering both direct and indirect contact transmission with vaccine and treatment as control. In developing the model, the population was compartmentalized into susceptible-vaccinated-exposed-infected-treated-helicobacter pylori concentration in the environment recovered. The model developed is a system of differential equations. The rate of change of the system, existence and uniqueness of solution, region of absolute stability and positivity of the solution was established. Existence of disease-free equilibrium state and basic reproduction number was also established. Mathematical analysis was determined by the basic reproduction number if , the disease-free equilibrium is locally asymptotically stable whereas if then the equilibrium is unstable whereas the numerical analysis for the estimated basic reproduction number of the model is greater than unity in perspective of Nigeria, for which the Herd Immunity Threshold indicated that vaccinating 99.47% of Nigeria population can control spreading of Peptic ulcer disease in the country. The paper recommended amongst other things that if significant changes concerning the issue of threshold target are observed to improve the rate at which peptic ulcer can be minimized from the population where Government and non-governmental organization should encourage the use of peptic ulcer drugs and vaccines among individuals.

Cross-species spill-over potential of the H9N2 bat influenza A virus

In 2017, a novel influenza A virus (IAV) was isolated from an Egyptian fruit bat. In contrast to other bat influenza viruses, the virus was related to avian A(H9N2) viruses and was probably the result of a bird-to-bat transmission event. To determine the cross-species spill-over potential, we biologically characterize features of A/bat/Egypt/381OP/2017(H9N2). The virus has a pH inactivation profile and neuraminidase activity similar to those of human-adapted IAVs. Despite the virus having an avian virus–like preference for α2,3 sialic acid receptors, it is unable to replicate in male mallard ducks; however, it readily infects ex-vivo human respiratory cell cultures and replicates in the lungs of female mice. A/bat/Egypt/381OP/2017 replicates in the upper respiratory tract of experimentally-infected male ferrets featuring direct-contact and airborne transmission. These data suggest that the bat A(H9N2) virus has features associated with increased risk to humans without a shift to a preference for α2,6 sialic acid receptors.

A SIR-UC EPIDEMIC MODEL: THE ANALYSIS OF SUSCEPTIBLE-INFECTED-REMOVED (SIR) EPIDEMIC MODEL WITH THE COVERAGE OF HEALTH INSURANCE (UNCOVERED AND COVERED INDIVIDUALS)

Susceptible-Infected-Removed (SIR) model is a widely used epidemic model that simulates the spread of infectious diseases within a population. It classifies individuals into susceptible, infected, and removed states, with the number of individuals in each state being time-dependent variables denoted by S(t), I(t), and R(t), respectively. The model considers direct contact transmission between infected and susceptible individuals. In developed countries, some people cannot afford medical treatment. In contrary, the recovery rate of infected individual in the population is directly proportional to the number of people receiving medical treatment. Affordable health insurance increases the number of people receiving medical treatment thus insurance should be considered aspect in epidemic model. The main purpose of this research is to analyze the effect of insurance on the SIR epidemic model. This research classifies individuals in both S(t) and I(t) based on their insurance coverage status. This model assumes permanent immunity for R(t), thus it is unnecessary to classify individuals in this state based on their insurance coverage status because they do not spread the disease nor have potential to be re-infected. Numerical simulation is organized to find the effect of insurance in SIR model by analyzing the equilibrium point. The result based on the equilibrium point suggests that the insurance in SIR epidemic model: (1) decrease the I(t) because it accelerate the recovery rate; (2) decrease theR(t) because there is less infected people for recovery; (3) increase the S(t) because there is less infected people to transmit the disease, compared to the SIR model without the insurance.

Multidrug-Resistant Bacteria Contaminating Plumbing Components and Sanitary Installations of Hospital Restrooms.

Antimicrobial resistance (AMR) poses several issues concerning the management of hospital-acquired infections, leading to increasing morbidity and mortality rates and higher costs of care. Multidrug-resistant (MDR) bacteria can spread in the healthcare setting by different ways. The most important are direct contact transmission occurring when an individual comes into physical contact with an infected or colonized patient (which can involve healthcare workers, patients, or visitors) and indirect contact transmission occurring when a person touches contaminated objects or surfaces in the hospital environment. Furthermore, in recent years, toilets in hospital settings have been increasingly recognised as a hidden source of MDR bacteria. Different sites in restrooms, from toilets and hoppers to drains and siphons, can become contaminated with MDR bacteria that can persist there for long time periods. Therefore, shared toilets may play an important role in the transmission of nosocomial infections since they could represent a reservoir for MDR bacteria. Such pathogens can be further disseminated by bioaerosol and/or droplets potentially produced during toilet use or flushing and be transmitted by inhalation and contact with contaminated fomites. In this review, we summarize available evidence regarding the molecular features of MDR bacteria contaminating toilets of healthcare environments, with a particular focus on plumbing components and sanitary installation. The presence of bacteria with specific molecular traits in different toilet sites should be considered when adopting effective managing and containing interventions against nosocomial infections potentially due to environmental contamination. Finally, here we provide an overview of traditional and new approaches to reduce the spreading of such infections.

A novel goose-origin Tembusu virus exhibits pathogenicity in day-old chicks with evidence of direct contact transmission

In late 2020, an outbreak of Tembusu virus (TMUV)-associated disease occurred in a 45-day-old white Roman geese flock in Taiwan. Here, we present the identification and isolation of a novel goose-origin TMUV strain designated as NTU/C225/2020. The virus was successfully isolated using minimal-pathogen-free duck embryos. Phylogenetic analysis of the polyprotein gene showed that NTU/C225/2020 clustered together with the earliest isolates from Malaysia and was most closely related to the first Taiwanese TMUV strain, TP1906. Genomic analysis revealed significant amino acid variations among TMUV isolates in NS1 and NS2A protein regions. In the present study, we characterized the NTU/C225/2020 culture in duck embryos, chicken embryos, primary duck embryonated fibroblasts, and DF-1 cells. All host systems were susceptible to NTU/C225/2020 infection, with observable lesions. In addition, animal experiments showed that the intramuscular inoculation of NTU/C225/2020 resulted in growth retardation and hyperthermia in day-old chicks. Gross lesions in the infected chicks included hepatomegaly, hyperemic thymus, and splenomegaly. Viral loads and histopathological damage were displayed in various tissues of both inoculated and naïve co-housed chicks, confirming the direct chick-to-chick contact transmission of TMUV. This is the first in vivo study of a local TMUV strain in Taiwan. Our findings provide essential information for TMUV propagation and suggest a potential risk of disease outbreak in chicken populations.

Mutations in HA and PA affect the transmissibility of H7N9 avian influenza virus in chickens

Low pathogenic (LP) H7N9 avian influenza virus (AIV) emerged in 2013 and had spread widely over several months in China, experienced a noteworthy reduction in isolation rate in poultry and human since 2017. Here, we examined the transmission of H7N9 viruses to better understand viral spread and dissemination mechanisms. Three out of four viruses (2013–2016) could transmit in chickens through direct contact, and airborne transmission was confirmed in the JT157 (2016) virus. However, we did not detect the transmission of the two 2017 viruses, WF69 and AH395, through either direct or airborne exposure. Molecular analysis of genome sequence of two viruses identified eleven mutations located in viral proteins (except for matrix protein), such as PA (K362R and S364N) and HA (D167N, H7 numbering), etc. We explored the genetic determinants that contributed to the difference in transmissibility of the viruses in chickens by generating a series of reassortants in the JT157 background. We found that the replacement of HA gene in JT157 by that of WF69 abrogated the airborne transmission in recipient chickens, whereas the combination of HA and PA replacement led to the loss of airborne and direct contact transmission. Failure with contact transmission of the viruses has been associated with the emergence of the mutations D167N in HA and K362R and S364N in PA. Furthermore, the HA D167N mutation significantly reduced viral attachment to chicken lung and trachea tissues, while mutations K362R and S364N in PA reduced the nuclear transport efficiency and the PA protein expression levels in both cytoplasm and nucleus of CEF cells. The D167N substitution in HA reduced the H7N9 viral acid stability and avian-like receptor binding, while enhanced human-like receptor binding. Further analysis revealed these mutants grew poorly in vitro and in vivo. To conclude, H7N9 AIVs that contain mutations in the HA and PA protein reduced the viral transmissibility in chicken, and may pose a reduced threat for poultry but remain a heightened public health risk.

Design and validation of an exposure system for efficient inter-animal SARS-CoV-2 airborne transmission in Syrian hamsters.

The main route of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) transmission is airborne. However, there are few experimental systems that can assess the airborne transmission dynamics of SARS-CoV-2 in vivo. Here, we designed, built, and characterized a hamster transmission caging and exposure system that allows for efficient SARS-CoV-2 airborne transmission in Syrian hamsters without contributions from fomite or direct contact transmission. We successfully measured SARS-CoV-2 viral RNA in aerosols and demonstrated that SARS-CoV-2 is transmitted efficiently at either a 1:1 or 1:4 infected index to naïve recipient hamster ratio. This is meaningful as a 1:4 infected index to naïve hamster ratio would allow for simultaneous comparisons of various interventions in naïve animals to determine their susceptibility to infection by aerosol transmission of SARS-CoV-2. Our SARS-CoV-2 exposure system allows for testing viral airborne transmission dynamics and transmission-blocking therapeutic strategies against SARS-CoV-2 in Syrian hamsters.

An Exemplary Computational Approach to Investigate Lumpy Skin Disease in Indian Cattle

Lumpy Skin Disease (LSD) is a highly consequential infectious ailment that affects cattle caused by the Lumpy Skin Disease Virus (LSDV), which is a DNA virus classified under the Capripoxvirus genus of the Poxviridae family. This affliction presents a significant obstacle in the cattle industries of several Asian and African countries. Although the virus may be found in many physiological fluids and excretions, such as sperm, skin lesions are the primary source of infection. Hematophagous arthropods, such as biting flies, mosquitoes, and ticks, act as mechanical vectors for transmission. The geographical expansion of LSDV is believed to have been assisted by vector-borne transmission. However, a lack of quantitative understanding of the transmission of LSDV hinders the implementation of efficient disease control measures. Obstacles as mentioned earlier, this work focuses on developing a mathematical model to analyze the phenomenon of Lumpy Skin Disease, with a specific emphasis on its implications for the cattle sectors in African and Asian countries. The model encompasses a set of differential equations incorporating the influences of infection forces originating from sick and asymptomatic cattle, along with infected vectors. The research demonstrates a plausible correlation between Lumpy Skin Disease and increased death rates in cattle. Employing rigorous examination and computational modelling, a valuable understanding of the fundamental dynamics of disease outbreaks is obtained. The mathematical model shows potential for predicting the future transmission of Lumpy Skin Disease. This presents a prospective opportunity for understanding and alleviating the disease's effects on bovine populations. Moreover, the analysis reveals that the impact of direct contact transmission on the spread of LSDV during documented outbreaks was negligible, therefore providing valuable insights into the dynamics of disease transmission. As the model is rigorously analyzed to gain insights into its qualitative dynamics of epidemics, which are present in the numerical simulations, this mathematical model can be allowed to estimate the future spread of the disease.

Characterization of the SARS-CoV-2 BA.5.5 and BQ.1.1 Omicron variants in mice and hamsters.

The continued evolution and emergence of novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants have resulted in challenges to vaccine and antibody efficacy. The emergence of each new variant necessitates the need to re-evaluate and refine animal models used for countermeasure testing. Here, we tested a recently circulating SARS-CoV-2 Omicron lineage variant, BQ.1.1, in multiple rodent models including K18-human ACE2 (hACE2) transgenic, C57BL/6J, and 129S2 mice, and Syrian golden hamsters. In contrast to a previously dominant BA.5.5 Omicron variant, inoculation of K18-hACE2 mice with BQ.1.1 resulted in substantial weight loss, a characteristic seen in pre-Omicron variants. BQ.1.1 also replicated to higher levels in the lungs of K18-hACE2 mice and caused greater lung pathology than the BA.5.5 variant. However, in C57BL/6J mice, 129S2 mice, and Syrian hamsters, BQ.1.1 did not cause increased respiratory tract infection or disease compared to animals administered BA.5.5. Moreover, the rates of direct contact or airborne transmission in hamsters were not significantly different after BQ.1.1 and BA.5.5 infections. Taken together, these data suggest that the BQ.1.1 Omicron variant has increased virulence in rodent species that express hACE2, possibly due to the acquisition of unique spike mutations relative to earlier Omicron variants. IMPORTANCE As severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to evolve, there is a need to rapidly assess the efficacy of vaccines and antiviral therapeutics against newly emergent variants. To do so, the commonly used animal models must also be re-evaluated. Here, we determined the pathogenicity of the BQ.1.1 SARS-CoV-2 variant in multiple SARS-CoV-2 animal models including transgenic mice expressing human ACE2 (hACE2), two strains of conventional laboratory mice, and Syrian hamsters. While BQ.1.1 and BA.5.5 infection resulted in similar levels of viral burden and clinical disease in hamsters and the conventional strains of laboratory mice tested, increases in lung infection were detected in hACE2-expressing transgenic mice, which corresponded with greater levels of pro-inflammatory cytokines and lung pathology. Taken together, our data highlight important differences in two closely related Omicron SARS-CoV-2 variant strains and provide a foundation for evaluating countermeasures.

Evaluation of Protein C and Protein S Levels in Covid Patients Compared to Normal Population and Their Relation to Disease Severity

Abstract Background The novel coronavirus, SARS-CoV-2, has caused a global outbreak starting December 2019 in China. Since then, it caused a global pandemic infecting more than 140 million patients worldwide. The viral transmission happens primarily through direct contact or droplet transmission. However airborne transmission in certain circumstances was demonstrated in multiple studies. Aim of the Work Primary Objective: Comparing Protein C & S levels in normal population to patients infected with COVID 19. Secondary Objective: Measuring the correlation of protein C & S levels in plasma & it’s relation to COVID 19 infection severity. Patients and Methods This is a case control study measuring Protein C & S levels in patients infected with COVID 19 compared to normal population over a period of six months, to assess their consumption as an anti-thrombotic protein against COVID 19 infection associated state of hypercoagulability. The study included a hundred participant divided into two groups. The first group had sixty patients infected with COVID 19 and the second group had forty normal healthy Egyptian adults. Results Our study showed that when comparing the patients blood indices to the controls there was a significant increase in TLC. Regarding the serum chemistry, our study showed that in the patients group the serum creatinine and blood urea nitrogen. For liver enzymes and liver function tests, our study showed that AST, ALT, Alkaline phosphatase, and gamma G. T. all of them are elevated in the Covid 19 patients when compared to the control group. Conclusion This study concluded that the level of protein C activity and the level of Protein S activity are both decreased in patients of the Covid 19 when compared to normal population. It also, concluded that the decrease in their levels is in statistical significance relation to the disease severity in the Covid 19 patients. Also, their levels were lower in patients who developed DVT or thrombosis in the Covid 19 infected group. Finally in chronic kidney disease patients only protein C was related to the disease severity not protein S nor D-dimer.

Comparing molnupiravir and nirmatrelvir/ritonavir efficacy and the effects on SARS-CoV-2 transmission in animal models

Therapeutic options against SARS-CoV-2 are underutilized. Two oral drugs, molnupiravir and paxlovid (nirmatrelvir/ritonavir), have received emergency use authorization. Initial trials suggested greater efficacy of paxlovid, but recent studies indicated comparable potency in older adults. Here, we compare both drugs in two animal models; the Roborovski dwarf hamster model for severe COVID-19-like lung infection and the ferret SARS-CoV-2 transmission model. Dwarf hamsters treated with either drug survive VOC omicron infection with equivalent lung titer reduction. Viral RNA copies in the upper respiratory tract of female ferrets receiving 1.25 mg/kg molnupiravir twice-daily are not significantly reduced, but infectious titers are lowered by >2 log orders and direct-contact transmission is stopped. Female ferrets dosed with 20 or 100 mg/kg nirmatrelvir/ritonavir twice-daily show 1–2 log order reduction of viral RNA copies and infectious titers, which correlates with low nirmatrelvir exposure in nasal turbinates. Virus replication resurges towards nirmatrelvir/ritonavir treatment end and virus transmits efficiently (20 mg/kg group) or partially (100 mg/kg group). Prophylactic treatment with 20 mg/kg nirmatrelvir/ritonavir does not prevent spread from infected ferrets, but prophylactic 5 mg/kg molnupiravir or 100 mg/kg nirmatrelvir/ritonavir block productive transmission. These data confirm reports of similar efficacy in older adults and inform on possible epidemiologic benefit of antiviral treatment.

Characterization of an Emergent Chicken H3N8 Influenza Virus in Southern China: a Potential Threat to Public Health.

Although influenza A viruses of several subtypes have occasionally infected humans, to date only those of the H1, H2, and H3 subtypes have led to pandemics and become established in humans. The detection of two human infections by avian H3N8 viruses in April and May of 2022 raised pandemic concerns. Recent studies have shown the H3N8 viruses were introduced into humans from poultry, although their genesis, prevalence, and transmissibility in mammals have not been fully elucidated. Findings generated from our systematic influenza surveillance showed that this H3N8 influenza virus was first detected in chickens in July 2021 and then disseminated and became established in chickens over wider regions of China. Phylogenetic analyses revealed that the H3 HA and N8 NA were derived from avian viruses prevalent in domestic ducks in the Guangxi-Guangdong region, while all internal genes were from enzootic poultry H9N2 viruses. The novel H3N8 viruses form independent lineages in the glycoprotein gene trees, but their internal genes are mixed with those of H9N2 viruses, indicating continuous gene exchange among these viruses. Experimental infection of ferrets with three chicken H3N8 viruses showed transmission through direct contact and inefficient transmission by airborne exposure. Examination of contemporary human sera detected only very limited antibody cross-reaction to these viruses. The continuing evolution of these viruses in poultry could pose an ongoing pandemic threat. IMPORTANCE A novel H3N8 virus with demonstrated zoonotic potential has emerged and disseminated in chickens in China. It was generated by reassortment between avian H3 and N8 virus(es) and long-term enzootic H9N2 viruses present in southern China. This H3N8 virus has maintained independent H3 and N8 gene lineages but continues to exchange internal genes with other H9N2 viruses to form novel variants. Our experimental studies showed that these H3N8 viruses were transmissible in ferrets, and serological data suggest that the human population lacks effective immunological protection against it. With its wide geographical distribution and continuing evolution in chickens, other spillovers to humans can be expected and might lead to more efficient transmission in humans.

Detection of Babesia conradae in Coyotes (Canis latrans) and Coyote-Hunting Greyhound Dogs (Canis familiaris).

Babesia conradae is a small piroplasm previously detected in coyote-hunting Greyhound dogs in California and Oklahoma. In dogs, B. conradae causes clinical signs similar to other tick-borne illnesses, and if not treated it can lead to acute kidney injury and other life-threating complications. To date, the life cycle of this apicomplexan parasite has not been fully described, but suggestions of direct contact or tick transmission have been proposed. The purpose of this study was to test coyote tissue samples from coyotes hunted by Greyhound dogs with a history of B. conradae infection to determine if this parasite is present in the coyote population in Northwestern Oklahoma. The analyzed tissue samples included liver, lung and tongue samples collected by hunters. DNA was isolated from these tissues and assessed by RT-PCR of the 18S rRNA and PCR of the COX1 genes for B. conradae. A total of 66 dogs and 38 coyotes were tested, and the results demonstrated the presence of B. conradae DNA in 21 dogs (31.8%) and 4 coyotes (10.5%). These results indicate that B. conradae is present in the dog and coyote population from the same area and that direct contact with coyotes may increase the risk of infection in dogs. Further studies are required to test possible modes of transmission, including direct bite, tick or vertical transmission.

Epidemiology, symptoms, transmission, prevention, treatment, and future prospects of the Lassa fever outbreak: a potential study.

Epidemiology, symptoms, transmission, prevention, treatment, and future prospects of the Lassa fever outbreak: a potential study.

Oral Sampling of Little Brown Bat (Myotis lucifugus) Maternity Colonies for SARS-CoV-2 in the Northeast and Mid-Atlantic, USA.

The potential introduction of SARS-CoV-2, the virus responsible for the COVID-19 pandemic, into North American bat populations is of interest to wildlife managers due to recent disease-mediated declines of several species. Populations of little brown bats (Myotis lucifugus) have collapsed due to white-nose syndrome (WNS), a disease caused by the introduction and spread of the fungal pathogen Pseudogymnoascus destructans (Pd). Throughout much of the United States and southern Canada, large colonies of the species routinely established diurnal roosts in anthropogenic structures, thereby creating the potential for direct human contact and cross-species disease transmission. Given recent declines and the potential for further disease impacts, we collected oral swabs from eight little brown bat maternity colonies to assess the presence and prevalence of SARS-CoV-2 by RT-qPCR analysis. Little brown bat colonies in Maryland (n = 1), New Hampshire (n = 1), New Jersey (n = 2), New York (n = 1), Rhode Island (n = 2), and Virginia (n = 1) were taken during May-August, 2022. From 235 assayed individuals, no bat tested positive for SARS-CoV-2. Our results indicate that little brown bats may not contract SARS-CoV-2 or that the virus persists at undetectable levels in populations of the Mid-Atlantic and Northeast during summer months. Nonetheless, continued monitoring and future work addressing other seasons may still be warranted to conclusively determine infection status.