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142 results for “coinfections”
Supplemented material to "Mycobacteriosis in various pet and wild birds from Germany: pathological findings, coinfections, and characterisation of causative Mycobacteria."
<p>This is the supplemented material to the publication "Mycobacteriosis in Various Pet and Wild Birds from Germany: Pathological Findings, Coinfections, and Characterization of Causative Mycobacteria". <br>The causative agents and confounding factors of mycobacteriosis in a set of pet (n=45) and some wild birds (n=5) from Germany were examined in this study. Not only Mycobacterium genavense (Mg), but also M. avium subsp. avium (Maa) and M. avium subsp. hominissuis (Mah), contributed to mycobacteriosis in these birds. The isolates were characterized by a combination of different typing methods. The genetic diversity of isolates belonging to Mg, Maa and Mah differed. Various coinfections by viruses, endoparasites, fungi and other bacterial species did not affect the manifestation of mycobacteriosis. Cross pathological fidings were more often seen in mycobacteriosis caused by Ma compared to Mg suggesting a different pathogenicity of the two species. New genotypes of Mah were identified in these birds that is important for epidemiological studies and for understanding the zoonotic role of this pathogen, as the subsp. hominissuis represents an increasing public health concern. The study provides some evidence of correlation between individual Maa genotypes and virulence which will have to be confirmed by broader studies.</p>
The impact of within-host coinfection interactions on between-host parasite transmission dynamics varies with spatial scale
<p>Within-host interactions among coinfecting parasites can have major consequences for individual infection risk and disease severity. However, the impact of these within-host interactions on between-host parasite transmission, and the spatial scales over which they occur, remain unknown. We developed and applied a novel spatially explicit analysis to parasite infection data from a wild wood mouse (<em>Apodemus sylvaticus</em>) population. We previously demonstrated a strong within-host negative interaction between two wood mouse gastrointestinal parasites, the nematode <em>Heligmosomoides polygyrus,</em> and the coccidian <em>Eimeria hungaryensis</em>, using drug-treatment experiments. Here, we show this negative within-host interaction can significantly alter the between-host transmission dynamics of <em>E. hungaryensis</em>, but only within spatially-restricted neighbourhoods around each host. However, for the closely related species <em>E. apionodes</em>, which experiments show does not interact strongly with <em>H. polygyrus</em>, we did not find any effect on transmission over any spatial scale. Our results demonstrate that the effects of within-host coinfection interactions can ripple out beyond each host to alter the transmission dynamics of the parasites, but only over local scales that likely reflect the spatial dimension of transmission. Hence there may be knock-on consequences of drug treatments impacting the transmission of non-target parasites, altering infection risks even for non-treated individuals in the wider neighbourhood.</p>
Fig. 1 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions
Fig. 1. FIV infection is common in lions of Kruger National Park. Within the sample population, 72.8% (142/195) of lions were infected with FIV. Prevalence of FIV infection was similar between males and females (75.6% versus 70.2%; n = 74 and 121, respectively), but increased with host age (a). For ease of visualization, age has been broken up by life stage into cubs (0–2yrs), subadults (2.1–4yrs), young adults (4.1–6yrs), prime adults (6.1–8yrs), and seniors (>8yrs) based on previous age classifications (Schaller, 1976). Regional prevalence of FIV was highest in the central region and lowest in the north (b). The map to the right shows locations where lion prides were sampled.
Fig. 4 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions
Fig. 4. FIV has strong direct and indirect effects on overall health. The final path model (a) shows only statistically significant relationships between manifest variables (rectangles) and latent variables (circles) for FIV infection, immune response (IMM), coinfections with hemoparasites (Hemoparasites), co-infections with gastrointestinal parasites (Helminths), and morbidity (Morbidity). Note that the parameter βx,z between each variable of interest represents the path coefficient obtained from least squares regression examining the relationship between one latent variable and the next (for example, FIV to IMM). Blue arrows represent positive relationships, whereas red arrows denote negative relationships. Final sample size was 106 lions.
Fig. 3 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions
Fig. 3. FIV significantly increases the prevalence of select gastrointestinal and hemoparasitic coinfections, as well as overall parasite richness for both groups. Graph (a) shows the prevalence of coinfecting parasites isolated in lions from this study. Sample size for the parasite groups included is as follows: n = 114 for gastrointestinal parasites; n = 190 for hemoparasites; and n = 195 for viral parasites. Coinfections are broken down by FIV status (positive versus negative). The two additional graphs illustrate the relationship between FIV status and gastrointestinal parasite richness (b) and hemoparasite richness (c).
Fig. 2 in Equal contributions of feline immunodeficiency virus and coinfections to morbidity in African lions
Fig. 2. FIV has broad effects on lion health and is associated with progressive immune impairment. Box (2a) above provides a complete list of the health metrics measured for the purposes of this study. Arrows to the right of each variable summarize the directionality of statistically significant changes with FIV infection. Descriptive statistics and reference values can be found in Table 2. Complete model output can be found in supplementary tables S1–S4. For ease of visualization, each parameter has been broken into categories of clinical relevance. To the right, age-related changes in lymphocyte profiles are shown for total lymphocyte counts in FIV-positive versus FIV-negative lions (b); as well as specific lymphocyte subsets in FIV-positive lions (c). Due to small sample size for lymphocyte subsets, subadults, and cubs have been included together under the 'juvenile' category.
Multispecies coinfections and presence of antibiotics shape resistance and fitness costs in a pathogenic bacterium
<p>Increasing antimicrobial resistance (AMR) poses a challenge for treatment of bacterial diseases. In real life, bacterial infections are typically <span>embedded within complex multispecies communities and influenced by the environment, which can shape </span>costs and benefits of AMR. However, knowledge of such interactions and their implications for AMR <em>in vivo</em> is limited. <span>To address this knowledge gap, we investigated fitness-related traits of a pathogenic bacterium (</span><em>Flavobacterium</em> <em>columnare</em><span>)</span> <span>in its fish host, capturing the effects of bacterial antibiotic resistance, multispecies coinfections</span> <span>(metazoan fluke </span><span><em>Diplostomum</em> <em>pseudospathaceum</em></span><span>), and antibiotic exposure. </span>We quantified real-time replication and virulence of sensitive and resistant bacteria and demonstrate that both bacteria can benefit from coinfection in terms of persistence and replication, depending on the coinfecting partner and antibiotic presence. We also show that antibiotics can benefit resistant bacteria by increasing bacterial replication under coinfection with flukes. These results emphasize the importance of diverse, inter-kingdom coinfection interactions and antibiotic exposure in shaping costs and benefits of AMR, supporting their role as significant contributors to the spread and long-term persistence of resistance.</p>
Data for: Age structure eliminates the impact of coinfection on epidemic dynamics in a freshwater zooplankton system
<p>Parasites often coinfect host populations, and, by interacting within hosts, might change the trajectory of multi-parasite epidemics. However, host-parasite interactions often change with host age, raising the possibility that within-host interactions between parasites might also change, influencing the spread of disease. We measured how heterospecific parasites interacted within zooplankton hosts and how host age changed these interactions. We then parameterized an epidemiological model to explore how age-effects altered the impact of coinfection on epidemic dynamics. In our model, we found that in populations where epidemiologically relevant parameters did not change with age, the presence of a second parasite altered epidemic dynamics. In contrast, when parameters varied with host age (based on our empirical measures), there was no longer a difference in epidemic dynamics between singly and coinfected populations, indicating that variable age structure within a population eliminates the impact of coinfection on epidemic dynamics. Moreover, infection prevalence of both parasites was lower in populations where epidemiologically relevant parameters changed with age. Given that host-population age structure changes over time and space, these results indicate that age-effects are important for understanding epidemiological processes in coinfected systems and that studies focused on a single age group could yield inaccurate insights.</p>
Multispecies coinfections and presence of antibiotics shape resistance and fitness costs in a pathogenic bacterium
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Data from: Is the local environment more important than within-host interactions in determining coinfection?
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Young male blackcaps with blood parasite coinfections cope with oxidative stress favouring anthocyanin-rich food during migratory fattening
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Data for: Age structure eliminates the impact of coinfection on epidemic dynamics in a freshwater zooplankton system
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Heterogeneous mosquito exposure increases Plasmodium vivax and Plasmodium falciparum coinfections: a modelling study
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Order of arrival and nutrient supply alter outcomes of coinfection with two fungal pathogens
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The impact of within-host coinfection interactions on between-host parasite transmission dynamics varies with spatial scale
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Data from: Diversity and composition of viral communities: coinfection of barley and cereal yellow dwarf viruses in California grasslands 2000 - 2005
Most species host multiple pathogens, yet field studies rarely examine the processes determining pathogen diversity within a single host or the effects of coinfection on pathogen dynamics in natural systems. Coinfection can affect pathogen transmission and virulence. In turn, coinfection can be regulated within hosts by interactions such as cross-protective immunity or at broader spatial scales via vector distributions. Using a general model, we demonstrate that coinfection by a group of vectored pathogens is highest with abundant generalist vectors and weak cross-protection and coinfection- induced mortality. Using these predictions, we investigate the distribution of five coexisting aphid-vectored, viral pathogens (barley and cereal yellow dwarf luteoviruses and poleroviruses) in a native perennial grass (Elymus glaucus) in both space (700 km) and time (4 years). Observed coinfection rates were much higher than expected at random, suggesting that within-host processes exerted weak effects on within-host pathogen diversity. Covariance among viruses in space and time was highest for viral species sharing a vector. Temporal correlation arose from the synchronous invasion of two viruses transmitted by a shared aphid species. On the basis of our modeling and empirical results, we expect that factors external to individual hosts may affect the coinfection dynamics in other communities hosting vectored pathogens.
Data from: Quantitative PCR as a marker for preemptive therapy and its role in therapeutic control in Trypanosoma cruzi/HIV coinfection
<p><strong>Background: </strong><em>Trypanosoma cruzi</em> and HIV coinfection can evolve with depression of cellular immunity and increased parasitemia. We applied quantitative PCR (qPCR) as a marker for preemptive antiparasitic treatment to avoid fatal Chagas disease reactivation and analyzed the outcome of treated cases.</p> <p><strong>Methodology:</strong> This mixed cross-sectional and longitudinal study included 171 Chagas disease patients, 60 coinfected with HIV. Of these 60 patients, ten showed Chagas disease reactivation, confirmed by parasites identified in the blood, cerebrospinal fluid, or tissues, 12 exhibited high parasitemia but no reactivation, and 38 had low parasitemia and no reactivation.</p> <p><strong>Results</strong>: We showed, for the first time, the success of the timely introduction of benznidazole in the non-reactivated group with high levels of parasitemia detected by qPCR and the absence of parasites in reactivated cases with at least 58 days of benznidazole. HIV+ and HIV+ without reactivation had a 4.0 – 5.1 higher chance of having parasitemia than HIV seronegative cases. A positive correlation was found between parasite and viral loads. Remarkably, treated <em>T. cruzi/</em>HIV-coinfected patients had 77.3% conversion from positive to negative parasitemia compared to 19.1% of untreated patients. Additionally, untreated patients showed ~13.6 times higher odds of having positive parasitemia in the follow-up period compared with treated patients. Treated and untreated patients showed no differences regarding the evolution of Chagas disease. The main factors associated with all-cause mortality were higher parasitemia, lower CD4 counts/µL, higher viral load, and absence of antiretroviral therapy.</p> <p><strong>Conclusion</strong>: We recommend qPCR prospective monitoring of <em>T. cruzi</em> parasitemia in HIV+ patients and point out the value of pre-emptive therapy for patients with temporary high parasitemia. In parallel, an early antiretroviral therapy introduction is advisable, aiming at viral load control, immune response restoration, and major survival. We also suggest an earlier antiparasitic treatment for all coinfected patients, followed by effectiveness analysis alongside antiretroviral therapy.</p>
Data from: Diversity and composition of viral communities: coinfection of barley and cereal yellow dwarf viruses in California grasslands
Most species host multiple pathogens, yet field studies rarely examine the processes determining pathogen diversity within a single host or the effects of coinfection on pathogen dynamics in natural systems. Coinfection can affect pathogen transmission and virulence. In turn, coinfection can be regulated within hosts by interactions such as cross-protective immunity or at broader spatial scales via vector distributions. Using a general model, we demonstrate that coinfection by a group of vectored pathogens is highest with abundant generalist vectors and weak cross-protection and coinfection- induced mortality. Using these predictions, we investigate the distribution of five coexisting aphid-vectored, viral pathogens (barley and cereal yellow dwarf luteoviruses and poleroviruses) in a native perennial grass (Elymus glaucus) in both space (700 km) and time (4 years). Observed coinfection rates were much higher than expected at random, suggesting that within-host processes exerted weak effects on within-host pathogen diversity. Covariance among viruses in space and time was highest for viral species sharing a vector. Temporal correlation arose from the synchronous invasion of two viruses transmitted by a shared aphid species. On the basis of our modeling and empirical results, we expect that factors external to individual hosts may affect the coinfection dynamics in other communities hosting vectored pathogens.
Data from: Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns
<p>By altering the abundance, diversity, and distribution of species — and their pathogens — globalization may inadvertently select for more virulent pathogens. In Brazil's Atlantic Forest, a hotspot of amphibian biodiversity, the global trade has facilitated the co-occurrence of previously isolated enzootic and panzootic lineages of the pathogenic amphibian-chytrid (<em>Batrachochytrium dendrobatidis</em>, 'Bd') and generated new virulent recombinant genotypes ('hybrid'). Epidemiological data indicate that amphibian declines are most severe in hybrid zones, suggesting that coinfections are causing more severe infections or selecting for higher virulence. We investigated how coinfections involving these genotypes shaped virulence and transmission. Overall, coinfection favored the more virulent and competitively superior panzootic genotype, despite dampening its transmission potential and overall virulence. However, for the least virulent and least competitive genotype, coinfection increased both overall virulence and transmission. Thus, by integrating experimental and epidemiological data, our results provide a mechanistic insight into how globalization can select for, and propel, the emergence of introduced hypervirulent lineages, such as the globally distributed panzootic lineage of Bd.</p>
Nitazoxanide Plus Ribavirin and Peginterferon for Therapy of Treatment Naive HCV Genotype 1 and HIV Coinfected Subjects
ClinicalTrials.gov study NCT00991289. IPD Sharing: Not stated. Countries: 2. Publications: 2.
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