Root-Knot and Root-Lesion Nematode Suppression by Cover Crops, Poultry Litter, and Poultry Litter Compost.

Experiments using soil-incorporated cover crops and amendments of poultry litter (PL) and PL compost to suppress root-knot (RKN) and root-lesion nematodes were conducted in response to increasing nematode populations in Maryland's potato production areas. Identical experiments were established in microplots infested with Meloidogyne incognita or Pratylenchus penetrans. Treatments consisted of 12 3-year rotational sequences comprising potato (year 1) and cucumber (year 2) followed by a moderately RKN-resistant or susceptible soybean cultivar, castor bean, grain sorghum, or sorghum sudangrass; PL or PL compost were amended to some of the RKN-susceptible soybean and sorghum sudangrass plots. In the third year of the rotation, potato followed by soybean was planted in all 12 treatments. The RKN-resistant soybean, castor bean, sorghum sudangrass, and fallow or tillage decreased the populations of M. incognita compared with microplots where RKN-susceptible soybean had been grown. However, RKN populations quickly recovered. Root-lesion nematode was reduced in the spring of 2001 following application of high rates of PL and PL compost in 2000. In the fall of 2001, sorghum sudangrass alone or in combination with PL or PL compost, grain sorghum, or fallow or tillage reduced root-lesion nematodes compared with either soybean cultivar. No treatment affected root-lesion nematode the following year. The use of cover crops and PL compost is an effective method to reduce nematode populations only if successively incorporated into rotational cropping sequences.

CCR5 and CXCR4 expression on memory and naive T cells in HIV-1 infection and response to highly active antiretroviral therapy.

OBJECTIVE: To measure CCR5 and CXCR4 chemokine receptor expression on CD4 and CD8 T cells in HIV-1 infection and to relate levels to the distribution of CD45RO memory and CD45RA-naive subsets, measures of disease activity, and response to highly active antiretroviral therapy (HAART). DESIGN: Fourteen untreated HIV-1-infected patients, 18 patients at 3-to 4-weeks after beginning HAART, and 35 uninfected control subjects were studied. METHODS: Four-color cytofluorometry with appropriate conjugated monoclonal antibodies (mAbs) was performed to define CD45RA and CD45RO subsets of CD4 and CD8 T cells and measure their expression of CCR5, CXCR4, and CD38. RESULTS: HIV-1-infected patients had higher CCR5 levels and lower CXCR4 levels on CD4 and CD8 T cells and their CD45RO/CD45RA subsets than control subjects did. However, CCR5 elevation was statistically significant only for CD4 T cells and their subsets, and CXCR4 depression was significant for CD8 T cells and their subsets (and for CD4:CD45RO cells). The elevation of CCR5 and depression of CXCR4 were not due to shifts in CD45RO/CD45RA subset proportions but to upregulation or downregulation within the subsets. CCR5 elevation on CD4 T cells was significantly restored toward normal by HAART, but the CXCR4 depression was not. CCR5 expression but not CXCR4 expression correlated with other measures of immunodeficiency (CD4 T-cell levels), active infection (viral load), and cellular activation (CD38). CONCLUSIONS: CCR5 elevation is a concomitant of immune activation and viral replication that occurs in HIV-1 infection, but the relation of CXCR4 depression to severity of infection, disease progression, and response to therapy remains undefined.

Declining CD4+ T-lymphocyte counts are associated with increased risk of enteric parasitosis and chronic diarrhea: results of a 3-year longitudinal study.

From January 1991 through September 1994, we observed people who were infected with HIV to assess the impact of enteric parasite-associated diarrhea. Respondents answered comprehensive questionnaires covering clinical and epidemiologic information and provided stool specimens monthly, which were examined unstained as well as stained with trichrome, chromotrope 2R, and with Kinyoun carbol-fuchsin, and with indirect immunofluorescence for Cryptosporidium. In all, 602 participants, who were interviewed, provided stool specimens at 3254 monthly visits. Parasites were associated with 50 of 354 (14.1%) acute diarrheal episodes (lasting < or = 28 days) and with 97 of 279 (34.8%) chronic episodes (lasting > 28 days). A parasite was associated with 31 of 222 (14.0%) episodes that occurred when CD4+ counts were > or = 200 cells/microl and with 150 of 566 (26.5%) episodes that occurred when CD4+ counts were < 200 cells/microl. The most commonly identified parasite was C. parvum, which was associated with 18 of 354 (5.1%) acute episodes and 36 (12.9%) of the 279 chronic episodes of diarrhea. In this patient population, enteric protozoan parasites were commonly associated with illness, particularly as immunosuppression worsened, and were more likely to be associated with chronic rather than acute diarrhea.